The Ayurvedic Pharmacopoeia of India: Part - Ii (Formulations) Volume - I First Edition Monographs Ebook V.1.0
The Ayurvedic Pharmacopoeia of India: Part - Ii (Formulations) Volume - I First Edition Monographs Ebook V.1.0
The Ayurvedic Pharmacopoeia of India: Part - Ii (Formulations) Volume - I First Edition Monographs Ebook V.1.0
OF INDIA
PART - II (FORMULATIONS)
VOLUME - I
First Edition
MONOGRAPHS
e-BOOK V.1.0
GOVERNMENT OF INDIA
MINISTRY OF HEALTH AND FAMILY WELFARE
DEPARTMENT OF AYURVEDA, YOGA & NATUROPATHY, UNANI, SIDDHA AND HOMOEOPATHY,
NEW DELHI
2008
AVALEHA
AVALEHA
General Description:
Avaleha or Lehya is a semi-solid preparation of drugs, prepared with addition of jaggery, sugar or sugar-candy and boiled with
prescribed juices or decoction.
Jaggery, sugar or sugar-candy is dissolved in the liquid and strained to remove the foreign particles. This solution is boiled over a
moderate fire. When pressed between two fingers if P¡ka
becomes thready ( Tantuvat
), or when it sinks in water without getting easily dissolved,
it should be removed from the fire. Fine powders of drugs are then added in small quantities and stirred continuously to form a homogenous
mixture. Ghee or oil, if mentioned, is added while the preparation is still hot and mixed well. Honey, if mentioned is added when the preparation
becomes cool and mixed well.
The Lehya should neither be hard nor a thick fluid. When pulp of the drugs is added and ghee or oil is present in the preparation, this can
be rolled between the fingers. When metals are mentioned, the Bhasmas of the metals are used. In case of drugs like Bhall¡taka, purification
process is to be followed.
The Lehya should be kept in glass or porcelain jars. It can also be kept in a metal container which does not react with it. Normally,
Lehyas should be used within one year.
1. Astangavaleha
1. AâÙË×GËVALEHA
AFI, Part-II, 3:1
Definition:
AâÙË×GËVALEHA is a semisolid preparation made with the ingredients in the Formulation composition given below.
Formulation Composition:
1. Ka¶phala Myrica esculenta Buch-Ham. Ex. D.Don. (API-Vol:3/92) (St.Bk) 1 part
2. PuÀkaram£la (PuÀkara) Inula racemosa Hook.f (API-Vol:4/102) (Rt.) 1 part
3. ᤴg¢ (Karka¶a¿¤´g¢) Pistacia chinensis Burgo (API-Vol:1/66) (Gl.) 1 part
4. Yam¡n¢ (Yav¡n¢) Trachyspermum ammi (Linn.) Sprague ex Turril. (API-Vol:1/129) (Fr.) 1 part
5. K¡rav¢ (K¤À¸aj¢raka) Carum carvi Linn (API-Vol:1/73) (Fr.) 1 part
6. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 1 part
7. Marica Piper nigrum Linn. (API-Vol:3/115) (Fr.) 1 part
8. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 1 part
9. Madhu Honey 12 parts
10. Ërdraka (Svarasa) Zingiber officinale Rosc (API-Vol:2/12) (Rz.) Fresh Juice of Rz. Q.S.
for Bh¡van¡
Method of preparation:
Wash, dry and powder the ingredients 1 to 8 separately and pass through sieve number 85.
Wash and peelËrdraka, grind it, squeeze the juice and filter it through a muslin cloth to collect svarasa.
Mix the powdered ingredients 1 to 8 thoroughly, levigate with Ërdraka svarasa and later dry the mixture.
Add honey and stir thoroughly to form an Avaleha.
Pack it in tightly closed containers to protect from light and moisture.
Description:
A blackish brown coloured semisolid sticky paste, odour pleasant, and taste bitter, astringent and spicy.
Identification:
Microscopy:
Take about 5 g, wash thoroughly with water. Pour out the water without loss of material; repeat the process, each time rejecting the supernatant
and keeping the sediment. Take a few mg of the sediment, stain with iodine solution and mount in 50 per cent glycerin; clarify a few mg with
chloral hydrate wash in water and mount in 50 percent glycerin. Observe the following characters in different mounts.
Various types of stone cells solitary or in a group of 12 to 15, with narrow and broad lumen some filled with prismatic crystals of calcium
oxalate, pitted fibre sclereids, pitted parenchyma, oil cells, group of parenchymatous cells with prismatic crystals of calcium oxalate, fragments
of fibres ( Ka¶phala ); several collapsed epidermal cells, tissue fragments with yellowish brown contents, and large tannin-filled sacs associated
with vascular bundles ( Karka¶a¿¤´g¢
); elongated or spindle shaped stone cells with broad lumen isolated or in groups of 2 to 8 ( Pippal¢
);
fragments of hypodermis in surface view, stone cells varying in sizes, shapes and thickness, mostly present in groups, interspersed among
parenchyma cells (Marica); groups of parenchymatous cells, densely packed with starch grains, isolated starch grains, simple, oval to rod
shaped, measuring 15 to 70 µ in length, hilum eccentric, lamellae distinct, yellow coloured oleo resin cells, non-lignified septate fibres, some of
them bearing marks of adjacent cells pressing against them, 30 to 50 µ broad, ( áu¸¶h¢
); striated epidermal debris, fragments of vittae in surface
view showing honey comb like epithelial layers, groups of mesocarpic stone cell layer with polygonal cells not much longer than broad;
transversely much elongated thin walled parenchymatous cell layer, with cells interlocked in a regular V joint with neighbouring cell ( K¤À¸aj
¢raka); prismatic crystals of calcium oxalate, measuring 70 to 100 µ in dia and septate fibres (PuÀkara); papillose epidermal cells in surface view
with puckered radially striated cuticle, epidermal cells with broken trichome bases, unicellular, small club shaped simple trichomes (Yav¡n¢).
Thin layer chromatography:
Extract 5 g of Avaleha in 75 ml n-hexane under reflux on a water-bath for 30 min. Filter and concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate (9 : 1) as
mobile phase. After development, allow the plate to dry in air and examine under ultraviolet light (254 nm). It shows major spots at R f 0.14,
0.22, 0.26, 0.34.
Physico-chemical parameters:
Loss on drying: Not more than 32.0 per cent, Appendix 2.2.10.
Total ash: Not more than 2.70 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 0.50 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 51.0 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 47.0 per cent, Appendix 2.2.8.
pH (1% aqueous solution): 6.3 to 6.6, Appendix 3.3.
Other requirements:
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed amber coloured containers, protected from light and moisture.
Therapeutic uses: V¡takaphajvara (Fever due to V¡ta doÀa and Kapha doÀa), K¡sa (Cough), áv¡sa (Dyspnoea), Aruc¢ (Tastelessness),
Chardi (Emesis)
Dose: 3 to 5 g daily in divided doses.
Anupāna: Water.
2. Bhallataka modaka
2. BHALLËTAKËDI MODAKA
AFI, Part-I, 3:21
Definition:
BHALLËTAKËDI MODAKA is a solid preparation made in the form of lumps, with the ingredients given in the Formulation composition.
Formulation composition:
1. Bhall¡taka (áuddha) Semecarpus anacardium Linn (API-Vol:2/19) (Fr.) 1 part
2. Tila Sesamum indicum linn (API-Vol:4/128) (Sd.) 1 part
3. Pathy¡ (Har¢tak¢) Terminalia chebula Retz. (API-Vol:1/47) (P.) 1 part
4. Gu·a Jaggery 6 parts
Method of preparation:
Description:
Black coloured roughly spherical lumps, firm, but crushing under pressure, with the characteristic odour of Bhall¡taka and bitter, astringent
taste.
Identification:
Microscopy:
Weigh 5 g of the sample, and mix with 50 ml of water in a beaker with gentle warming, till the sample gets completely dispersed in water.
Centrifuge the mixture and decant supernatant. Wash the sediment with distilled water and centrifuge again. Decant the supernatant. Collect the
sediment. Mount a few mg in 50 per cent glycerine and observe the following characters.
Pathy¡); fragments
Fragments of crisscross fibres, epidermal tissue of cells with slightly beaded walls, and occasionally divided by a thin septa (
of epidermis in surface view with elongated cells having lignified walls and mesocarp tissue showing oil cavities, (Bhall¡taka); cells of
endosperm filled with oil globules and aluerone grains, occasionally sectional view of epidermal debris, with palisade like cells (Tila).
a) Extract 10 g of crushed Modaka with 75 ml of methanol under reflux for 30 min. Filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate : formic acid :
methanol (3 : 3 : 0.8 : 0.2 ) as mobile phase. After development, allow the plate to dry in air and spray with anisaldehyde-sulphuric acid reagent
followed by heating at 1100 for about 10 min. It shows major spots at Rf 0.12 (blue), 0.32 (blue), 0.34 (light brown, gallic acid), 0.45 (blue), 0.52
(light brown), 0.67 (violet), 0.82 (violet) and 0.90 (violet) under visible light.
b) Extract 10 g of crushed Modaka with 75 ml of n-hexane on a water-bath for 30 min. Filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate (7 : 3) as mobile phase.
After development, allow the plate to dry in air and spray with anisaldehyde-sulphuric acid reagent followed by heating 1100 for about 10 min.
It shows major spots at Rf 0.47 (purple), 0.69 (dark blue) and 0.7 (purple) under visible light.
Physico-chemical parameters:
Total Ash: Not more than 2.5 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than, 0.25 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 65.0 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 75.0 per cent, Appendix 2.2.8.
Reducing sugars: 23 to 24 per cent, Appendix 5.1.3.1.
Non reducing sugars: 56 to 58 per cent, Appendix 5.1.3.3.
pH (5% aqueous solution): 4 to 4.5, Appendix 3.3.
Total tannins: Not less than 5 per cent, Appendix 5.1.2.
Assay:
The formulation contains not less than 5 per cent gallic acid when assayed by the following method.
Estimation of gallic acid: Dissolve 10 mg of gallic acid in 100 ml of methanol in a volumetric flask. From this stock solution, prepare standard
solutions of 15 to 75 µµg / ml by transferring aliquots (1.5 to 7.5 ml) of stock solution to 10 ml volumetric flasks and adjusting the volume to 10
ml with methanol.
Apply 10 µµl of each standard solution corresponding to 150 ng to 750 ng of gallic acid on a TLC plate. Develop the plate to a distance of 8 cm
using toluene : ethyl acetate : formic acid : methanol (3 : 3 : 0.8 : 0.2 ) as mobile phase. After development, dry the plate and scan in TLC
scanner at wavelength of 280 nm. Note the area under the curve for peak corresponding to gallic acid and prepare the calibration curve by
plotting peak area vs amount of gallic acid.
Hydrolyze accurately weighed about 5 g of crushed Modaka by refluxing with 50 ml of 2N hydrochloric acid on a water-bath. Filter, add equal
amount of water, transfer to a separating funnel and extract with diethyl ether (20 ml x 4). Collect the diethyl ether layer and dry. Dissolve the
residue in 25 ml of methanol. Apply 10 µµl on a TLC plate and develop, dry and scan the plate as described in the preceding paragraph for
calibration curve of gallic acid. Note area under the curve for a peak corresponding to gallic acid. Calculate the amount of gallic acid in the test
solution from the calibration curve of gallic acid.
Other requirements:
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Pitt¡r¿a (Anorectal growth due to Pitta DoÀa)
Dose: 2 to 5 g daily in divided doses.
BILVËDI LEHA is a semisolid preparation made with the ingredients in the Formulation composition given below.
Formulation Composition:
1. Bilva - m£la Aegle marmelos Corr. (API-Vol:3/29) (Rt.) 1536 g
2. Water for decoction 12.28 l
reduced to 3.072 l
3. J¢r¸a Gu·a (Pur¡¸a Gu·a) Old jaggery 768 g
4. Ghana (Must¡) Cyperus rotundus Linn. (API-Vol:3/129) (Rt. Tr.) 12 g
5. Dh¡nya (Dh¡nyaka) Coriandrum sativum Linn (API-Vol:1/30) (Fr.) 12 g
6. J¢raka (áveta j¢raka) Cuminum cyminum Linn (API-Vol:1/106) (Fr.) 12 g
7. T¤¶¢ (S£kÀmail¡) Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) (Sd.) 12 g
8. Tvak Cinnamomum zeylanicum Blume (API-Vol:1/113) (St. Bk.) 12 g
9. Ke¿ara (N¡gak®¿ara) Mesua ferrea Linn (API-Vol:2/118) (Stmn.) 12 g
10. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 12 g
11. Marica Piper nigrum Linn. (API-Vol:3/115) (Fr.) 12 g
12. Pippal¢ Piper longum Linn. (API-Vol:4/91) (Fr.) 12 g
Method of Preparation:
Take raw material of pharmacopoeial quality.
Wash, dry, powder ingredient number 1 ( Kv¡tha Dravya) of the formulation composition and pass through sieve number 44 to obtain coarse
powder.
Clean, dry, powder the ingredients number 4 to 12 ( PrakÀepa Dravya) of the formulation composition and pass through sieve number 85 to
obtain fine powder.
Add specified amounts of water to the Kv¡tha Dravya, heat, reduce to one fourth and filter through muslin cloth.
Add jaggery to the Kv¡tha, boil to dissolve and filter through muslin cloth.
Reduce the Kv¡tha to thicker consistency by gentle boiling and stirring continuously during the process.
Continue heating till the preparation attains the consistency of leha confirmed by the formation of a soft ball that doesn't disperse in water.
Remove from heat source and allow to cool to room temperature.
Add fine powders of PrakÀepa Dravya , mix thoroughly to prepare a homogeneous mass.
Pack it in tight closed containers to protect from light and moisture.
Description:
Dark brown semisolid paste with a spicy pleasant odour and sweet, astringent taste.
Identification:
Microscopy:
Take about 5 g of Avaleha and wash twice or thrice with about 20 ml of water, each time rejecting the supernatant; take a few mg of the
sedimented material, stain with iodine solution and mount in 50 per cent glycerin; clarify a few mg with chloral hydrate and mount in 50 per
cent glycerin. Observe the following characters in different mounts.
Multicellular, multiseriate trichomes, fragments of vittae in surface view showing epithelial tissue elongated along the long axis of the vittae, and
mesocarpic stone cell layer with cells much longer than broad ( áveta J¢raka); groups of slightly wavy parenchymatous cells, each cell contains 1
to 3 rosette crystal of calcium oxalate, groups of bulbous perisperm cells packed with starch grains which also shows in the middle tiny prismatic
crystal of calcium oxalate, epidermal and hypodermal cells crossing each other at right angle ( S£kÀmail¡); fragments of fibres with very narrow
lumen, not over 600 μ long and not over 45 μ broad, parenchyma cells containing minute acicular crystals of calcium oxalate, stone cells of
varying shapes and sizes with thickened walls on three sides, oil cells ( Tvak ); crushed pieces of anther lobes containing pollen grains, pollen
grains tricolporate, measuring 25 to 55 μ in dia, unicellular and multicellular uniseriate trichomes several showing a funneling tip or branching,
groups of endothecial cells of anther lobe ( N¡gak®sara
); group of parenchymatous cells, densely packed with starch grains, isolated starch
grains, simple, oval to rod shaped, measuring 15 to 70 μ in length, hilum eccentric, lamellae distinct, yellow coloured oleo resin cells, non-
lignified, septate fibres some of them bearing marks of adjacent cells pressing against them, 30 to 50 μ broad, (áu¸¶h¢
); tissue debris consisting
of packed regular rows of fibre-sclereids of fairly uniform size, and narrow scalariformed vessel showing laterally placed simple perforation
( Must¡
); lignified cells, isolated or in small groups measuring 130 to 190 µ in dia with broad lumen, in groups of 2 to 8 (Pippal¢
); fragments of
hypodermis in surface view with stone cells varying in sizes, shapes and thickness, present in groups, interspersed among parenchymatous cells
(Marica); group of sclerenchymatous cells, crisscrossing each other, epidermal tissue with fairly large cells showing stomata and octahedrons of
calcium oxalate crystals, large, pentagonal, sclerenchymatous cell layer (Dh¡ny¡).
Extract 5 g of Avaleha with 75 ml of n-hexane under reflux on a water-bath for 30 min. Filter and concentrate to 10 ml and carry out the thin
layer chromatography. Apply 10 µl of the extract on TLC plate. Develop the plate to a distance of 8 cm using toluene : ethyl acetate (8 : 2) as
mobile phase. After development, allow the plate to dry in air and examine under ultraviolet light (366 nm). It shows major spots at R f 0.23, 0.30
(both blue), 0.53 (fluorescent blue) 0.65 and 0.73 (both blue).
Physico-chemical parameters:
Loss on drying: Not more than 20.0 per cent, Appendix 2.2.10.
Total ash: Not more than 2.30 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 0.22 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 6.8 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 66.0 per cent, Appendix 2.2.8.
pH (1% aqueous solution): 5.8 to 6.7, Appendix 3.3.
Other requirements:
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Aruc¢ (Aversion to food), Agnim¡ndya (Digestive impairment), Praseka (Excessive salivation), Chardi (Emesis)
Dose: 6 g to be licked up 2 to 3 times in small quantities each time.
4. Citraka haritaki
4. CITRAKA HARÌTAKÌ
AFI, Part-I, 3:10AFI, Part-I, 3:10
Definition:
CITRAKA HARÌTAKÌ is a semisolid preparation made with the ingredients in the Formulation composition given below:
Formulation Composition:
1. Citraka - Kv¡tha Plumbago zeylanica Linn. (API-Vol:1/29) (Rt. ) 4.800 l
2. Ëmalak¢ - Kv¡tha Emblica officinalis Gaertn. (API-Vol:1/4) (P. ) 4.800 l
3. Gu·£c¢ - Kv¡tha Tinospora cordifolia (Willd.) Miers. (API-Vol:1/41) (St.) 4.800 l
4. Da¿am£la - Kv¡tha 4.800 l
a. Bilva Aegle marmelos Corr (API-Vol:4/10) (Rt./St. Bk.)
b. Agnimantha Premna mucronata (Official substitute) (API-Vol:3/3) (Rt./St. Bk.)
c. áyon¡ka Oroxylum indicum Vent. (API-Vol:3/209) (Rt./St. Bk.)
d. K¡¿mar¢ (Gambh¡r¢) Gmelina arborea Linn (API-Vol:4/31) (Rt./St. Bk.)
e. P¡¶al¡ Stereospermum suaveolens (L.F) DC (API-Vol:4/87) (Rt./St. Bk.)
f. á¡lapar¸¢ Desmodium gangeticum DC. (API-Vol:3/178) (Pl.)
g. P¤¿nipar¸¢ Uraria picta Desv. (API-Vol:4/99) (Pl.)
h. ávadaÆÀ¶r¡ (GokÀura) Tribulus terrestris Linn (API-Vol:1/38) (Pl.)
i. B¤hat¢ Solanum indicum Linn (API-Vol:2/27) (Pl.)
j. K¡¸¶ak¡r¢ Solanum surattense Burm.f. (API-Vol:1/59) (Pl.)
5. Pathy¡ (Har¢tak¢) c£r¸a Terminalia chebula Retz. (API-Vol:1/47) (P.) 3.07 kg
6. Gu·a Jaggery 4.80 kg
7. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) Rz. 96 g
8. Marica Piper nigrum Linn. (API-Vol:3/115) Fr. 96 g
9. Pippal¢ Piper longum Linn (API-Vol:4/91) Fr. 96 g
10. Tvak Cinnamomum zeylanicum Blume (API-Vol:1/113) St. Bk. 96 g
11. El¡ (S£kÀmail¡) Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) Sd. 96 g
12. Patra (Tejapatra) Cinnamomum tamala (Buch-Ham)Nees & Eberm. (API-Vol:1/115) Lf. 96 g
13. KÀ¡ra (Yava) Hordeum vulgare Linn (API-Vol:5/146) Water soluble Ash of Pl. 24 g
14. Madhu Honey 384 g
Note: Stem bark of the ingredient number 4 [(a) to (e)] has been used.
Method of Preparation:
Wash, dry and powder the ingredients numbered 1 to 4 ( Kv¡tha Dravya) of the Formulation composition separately and pass through sieve no.
44 to obtain a coarse powder.
Dry and powder the ingredient number 5 separately and ingredients number 7 to 13 ( PrakÀepa Dravyas) of the Formulation composition to a fine
powder and pass through sieve no. 85.
Add required amount of water to the Kv¡tha Dravya, heat, reduce to one fourth and filter through muslin cloth.
Mix all theKv¡thas together. Add Jaggery, boil to dissolve and filter through a muslin cloth.
Reduce the Kv¡tha to a thicker consistency by gentle boiling; add cūrņa of Pathy¡ and stir thoroughly during the process.
Add the powdered PrakÀepa Dravya no. 7 to 13 while hot at 50 , mix thoroughly to prepare a homogeneous mass.
0
Blackish brown, semisolid paste with spicy, pleasant odour and bitter-astringent taste.
Identification:
Microscopy:
·
Take about 5 g of the sample, wash thoroughly and repeatedly in warm water to remove Gu a and Madhu, each time rejecting the supernatant,
and saving the residue without loss. Take the sediment in distilled water, mix thoroughly, allow to settle, and throw off supernatant. Take a few
mg of the sediment, stain with iodine solution, mount in glycerin (50 per cent); take a few mg of sediment, clear in chloral hydrate, wash, and
mount in glycerine (50 per cent). Observe the following characters in different mounts.
Large parenchyma cells containing elliptical, elongated starch grains, up to 50 μ in length, with hilum at one end; broad, short vessel debris,
áu¸¶h¢
resin cells, fragments of non-lignified septate fibres that show dentation on one wall ( ); fragments from hypodermis with groups of stone
cells interspersed among parenchyma tissue from hypodermis, dark coloured groups of very thick walled polygonal stone cells from testa
(Marica); long uniseriate multicellular fragile trichomes, spindle shaped, large lumened sclerenchyma cells, isolated or in small groups (Pippal
¢); perisperm cells with bulbous projections, packed with minute starch grains aggregates, carrying tiny prisms or clusters of calcium oxalate;
large, elongated cells of aril tissue
(S£kÀmail¡); fragments of fibres with narrow lumen not over 600 μ long or over 45 μ midwidth, stone cells lignified on three sides only,
parenchyma cells containing minute acicular crystals of calcium oxalate (Tvak); pieces of leaf epidermis with thick cuticle and sunken stomata,
showing stomata and a few unicellular or bicellular short stout trichomes (Tejapatra); crisscross layers of fibres, polygonal cells of epidermis
showing slight beading and transverse septa, large stone cells with pits (Har¢tak¢).
Extract 5 g of Avaleha with 75 ml (25 ml x 3) of n-hexane under reflux on a water-bath for 30 min. Reflux hexane-extracted marc with 75 ml of
chloroform (25 ml x 3), filter and concentrate the combined chloroform extract to 10 ml and carry out the thin layer chromatography. Apply 10
µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate : formic acid (9.8 : 0.2 : 0.04) as mobile
phase. After development, allow the plate to dry in air and examine under ultraviolet light (366 nm). It shows major spots at Rf 0.36, 0.46 (both
blue) and 0.27 (yellow). Spray the plate with anisaldehyde sulphuric acid reagent and heat it at 1100 for about 10 min. It shows major spots at R f
0.12, 0.18 (both green), 0.36 (blue) and 0.40 (greenish blue) under visible light.
Physico-chemical parameters:
Loss on drying: Not more than 36.0 per cent Appendix 2.2.10.
Total ash: Not more than 4.7 per cent Appendix 2.2.3.
Acid-insoluble ash: Not more than 1.0 per cent Appendix 2.2.4.
Alcoholic-soluble extractive: Not less than 21.0 per cent Appendix 2.2.7.
Water-soluble extractive: Not less than 67.0 per cent Appendix 2.2.8.
pH (1% aqueous solution) : 6.4 to 6.6 Appendix 3.3.
Other requirements:
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Gulma (Abdominal lump), Ud¡varta (Upward movement of gases), P¢nasa (Chronic Rhinitis/Sinusitis), K¡sa (Cough),
áv¡sa (Dyspnoea), Ar¿a (Piles), Agnim¡ndya (Loss of appetite), KÀaya (Pthisis), K¤mi (Helminthiasis / Worm infestation)
Dose: 6 to 12 g daily in divided dose.
Method of preparation:
Description:
Semisolid, chocolate brown colored sticky paste, taste sweet with non-specific pleasant odour.
Identification:
Microscopy:
Extract 5 g of Cyavanaprāśa successively with 75 ml each of n-hexane, chloroform and methanol under reflux on a water-bath for 30 min drying
the marc after each extraction. Filter each extract and discard the chloroform extract. Concentrate the other two extracts to 10 ml and carry out
thin layer chromatography. Apply 10 µl each of hexane and methanol extracts separately on two TLC plates and develop the plates to a distance
of 8 cm using toluene : ethyl acetate (8.5 : 1.5) as mobile phase for hexane extract and ethyl acetate : methanol : water (15 : 1 : 1) for methanol
extract. After development, allow the plates to dry in air and examine under ultraviolet light (254 nm). The hexane extract shows major spots at
Rf 0.10, 0.16, 0.23 and 0.30; and methanol extract shows major spots at Rf 0.10, 0.47 and 0.81.
Physico-chemical parameters:
Other requirements:
Therapeutic uses: K¡sa (Cough), áv¡sa (Dyspnoea), KÀata kÀ¢¸a (Debility due to chest injury), Svarabheda (Hoarseness of voice), KÀaya
(Pthisis), H¤droga (Heart disease), Agnim¡ndya (Loss of appetite), Uroroga (Disease of thorax), V¡tarakta (Gout), Pip¡s¡ (Thirst), M
£traroga (Urinary diseases), áukra DoÀa (Abnormalities in semen), Jar¡ (Senility/progeriasis). Used as a Ras¡yana (Rejuvenating agents),
Medhya (Brain tonic/ Nootropic), Sm¤tiprada (Memory provider)
Dose: 25 g daily in divided doses .
Anupana: Water, Milk.
6. Kalyanavaleha
6. KALYËÛËVALEHA
AFI, Part-II, 3:4
Definition:
KALYËÛËVALEHA is a semisolid preparation made with the ingredients of the Formulation composition given below.
Formulation composition:
1. Haridr¡ Curcuma longa Linn. (API-Vol:1/45) (Rz.)1 part
2. Vac¡ Acorus calamus Linn (API-Vol:2/168) (Rz.)1 part
3. Ku˦ha Saussurea lappa CB. Clarke (API-Vol:1/76) (Rt.)1 part
4. Pippal¢ Piper Longum Linn (API-Vol:4/91) (Fr.)1 part
5. Vi¿vabheÀaja (áu¸¶h¢) Zingiber officinale Roxb. (API-Vol:1/103) (Rz.)1 part
6. Aj¡j¢ (áveta J¢raka) Cuminum cyminum Linn (API-Vol:1/106) (Fr.)1 part
7. Ajamod¡ Apium leptophyllum (Pers.) F.V.M.ex Benth (API-Vol:1/2) (Fr.)1 part
8. YaÀ¶imadhuka (YaÀ¶¢) Glycyrrhiza glabra Linn (API-Vol:1/127) (Rt. )
1 part
9. Saindhava Lava¸a Rock salt 1 part
10. Sarpi (Gogh¤ta) Clarified butter from cow's milk Q.S. 6 parts
Method of preparation:
Semisolid paste, yellowish-brown in color with pungent odour, astringent and salty taste.
Identification:
Microscopy:
Take about 5 g of Avaleha, wash thoroughly with n-hexane; repeat twice; take the sediment and wash with hot water to remove salt. Clarify a
few mg with chloral hydrate and mount in 50 per cent glycerine; boil a few mg in 2 per cent potassium hydroxide solution , wash, and mount in
glycerine; mount a few mg in iodine solution; observe the following characters in different mounts.
Groups of yellow coloured, suberized, angular parenchymatous cells, patches of pitted parenchyma with beaded cell walls, pits simple, patches
of thick walled, angular cells filled with very small simple and compound, starch grains, multicellular, multiseriate trichomes, fragments of vittae
(áveta J¢raka); patches of thick walled angular or slightly wavy parenchyma, pitted parenchyma, parenchymatous cells with reticulate
thickenings, oil cells, unicellular, simple and glandular trichomes and fragments of vittae showing large polygonal epitheial cells (Ajamod¡);
groups of parenchymatous cells, densely packed with starch grains, isolated starch grains, simple, oval to rod shaped, measuring 15 to 70 μ in
length, hilum eccentric, lamellae distinct; yellow coloured oleo resin cells, non-lignified, septate fibres some of them bearing marks of adjacent
(áu¸¶h¢); groups of large perisperm cells packed with minute starch grains, elongated stone cells
cells pressing against them, 30 to 50 μ broad,
measuring 130 to 190 µ in dia with broad lumen isolated or in groups (Pippal¢); groups of polygonal and elongated parenchymatous cells,
orange or brownish resin cells, branched tracheids, inulin crystals (Ku˦ha) groups of large parenchymatous tissues with cells filled with
spheroidal starch grains which are mostly single, rarely in 2 or 3 groups, 2 to 10 µ in dia, interrupted by aerenchymatous space, oil cells with
suberized walls (Vac¡); crystal fibres and pitted vessels showing honeycomb structure (YaÀ¶imadhu); cells with yellow pigment turning red in
sulphuric acid 50 per cent, and cells with large starch grains, partially gelatinised (Haridr¡).
Chemical tests:
a) Treat the Avaleha with concentrated sulphuric acid; orange red colour develops indicating the presence of curcuminoids (Haridr¡).
b) Treat the Avaleha with 10% solution of sodium hydroxide or potassium hydroxide; red to violet colour develops indicating the presence of
curcuminoids (Haridr¡)
Physico-chemical parameters:
Loss on drying: Not more than 5.5 per cent, Appendix 2.2.10.
Total ash: Not more than 12.0 per cent, Appendix 2.2.3.
Acid- insoluble ash: Not more than 2.0 per cent, Appendix 2.2.4.
Alcohol- soluble extractive: Not less than 46.0 per cent, Appendix 2.2.7.
Water- soluble extractive: Not less than 11.0 per cent, Appendix 2.2.8.
pH (1% aqueous solution): 5.1 and 5.3, Appendix 3.3.
Starch: Not less than 42.0 per cent, Appendix 2.2.14.
Other requirements:
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Svarabheda (Hoarseness of voice), M£kat¡ (Aphasia)
Dose: 12 g daily in divided doses.
Anupāna: Water.
7. Kushmanda Rasayana
7. KÍâMËÛÚAKA RASËYANA (Synonym: KuÀm¡¸·a Kha¸·a)
AFI, Part-I, 3:7
Definition:
KÍâMËÛÚAKA RASËYANA is a semisolid avaleha preparation made with the ingredients in the Formulation composition given below
Formulation composition:
1. K£Àm¡¸·a Benincasa hispida (Thunb)Cogn. (API-Vol:4/55) (Fresh Fr.) 4.8kg
2. Gh¤ta Clarified butter from cow's milk 768g
3. Kha¸·a Sugar candy 4.8kg
4. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 96g
5. ᤴgavera (áu¸¶h¢) Zingiber officinale Roxb. (API-Vol:1/103) (Rz. ) 96g
6. J¢raka (áveta J¢raka) Cuminum cyminum Linn (API-Vol:1/106) (Fr.) 96g
7. Tvak Cinnamomum zeylanicum Blume (API-Vol:1/113) (St.Bk. ) 24g
8. El¡ (S£kÀmail¡) Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) (Sd. ) 24g
9. Patra (Tejapatra) Cinnamomum tamala (Buch-Ham) Nees & Eberm. (API-Vol:1/115) (Lf. ) 24g
10. Marica Piper nigrum Linn. (API-Vol:3/115) (Fr.) 24g
11. Dh¡nya (Dh¡nyaka) Coriandrum sativum Linn (API-Vol:1/30) (Fr.) 24g
12. KÀaudra (Madhu ) Honey 384g
13. Jala Water Q.S.
Method of preparation:
Take all ingredients of pharmacopoeial quality.
Wash, dry, powder the ingredients number 4 to 11 ( PrakÀepa) separately and pass through sieve number 85.
Take fresh mature fruit of K£Àm¡¸·a, remove skin and seeds and cut in to small pieces of 2.5 to 5 cm. Add double the quantity of water. Heat
till
K£Àm¡¸·a pieces become soft to make PiÀ¶i maintaining temperature between 90 to 100 . Strain the liquid through muslin cloth.
0 0
Keep the strained liquid separately and crush the boiled pieces of K£Àm¡¸·a in an end runner mill to make a fine paste, fry in Gh¤ta with
constant stirring maintaining temperature between 800 to 900 till the mixture turns brown. Take due care to avoid over roasting or under roasting
ofPi˦i
Add sugar to the strained liquid and heat to make "two-thread sugar syrup".
Add the fried paste of K£Àm¡¸·a to the syrup, heat with constant stirring maintaining temperature between 900to 1000 and observe the mixture
for formation of soft bolus, which does not disperse in water. Stop heating and allow to cool to 500.
Add fine powders of ingredients ( PrakÀepa) numbered 4 to 11. Mix thoroughly to prepare a homogeneous blend, allow to cool it to room
temperature and add Madhu .
Pack it in tightly closed containers to protect from light and moisture.
Description:
Semi solid, malleable, sticky preparation, dark brown in color with spicy odour and pungent, sweet taste.
Identification:
Microscopy:
Weigh about 5 g of the sample, stir with 50 ml of a defatting solvent in a beaker. Pour off the solvent without loss of material and repeat the
process till free fromGh¤ta . Wash the sediment in warm water similarly, pour out water. Wash the sediment with distilled water and centrifuge
at medium speed. Decant the supernatant. Take a few mg of the sediment, warm in chloral hydrate and mount in glycerine (50 per cent). Mount
a few mg in iodine solution. Observe the following characters in different mounts.
áu¸¶h¢); multicellular,
Sac-shaped starch grains with eccentric hilum, non-lignified xylem fibres and xylem vessels with reticulate thickenings (
multiseriate trichomes and sclereid layer from mesocarp (J¢raka); U-shaped stone cells with thickenings on three sides (Tvak); bulbous
perisperm cells containing starch grains and small prisms of calcium oxalate within (El¡); fragments of multicellular uniseriate, short, stout
trichomes and leaf epidermal fragments with sunken paracytic stomata (Tejapatra); highly thickened stone cells with narrow lumen from testa
and groups of stone cells interspersed among parenchyma tissue from hypodermis (Marica); groups of fusiform fibres of sclerenchyma
crisscrossing with each other (Dh¡nyaka).
Extract 5 g of sample with 75 ml of ethyl acetate under reflux on a water-bath for 30 min. Filter, concentrate the filtrate to 10 ml and carry out
the thin layer chromatography. Apply 10 µl of the extract on two separate TLC plates and develop the plates to a distance of 8 cm using
toluene : ethyl acetate (7 : 3) as mobile phase. After development, allow the plates to dry in air and examine one plate under ultraviolet light at
254 nm. It shows major spots at Rf 0.11, 0.24 (piperine), 0.42 and 0.47, when observed at 366 nm it shows major spots at Rf 0.10 (blue), 0.20
(green), 0.24 (blue, piperine), 0.33 (green), 0.37 (blue), 0.48 (blue) and 0.59 (blue). Derivatize the plate with modified Dragendorff's reagent and
observe under visible light. It shows orange-coloured spots at R f 0.24 (piperine), 0.27 and 0.83. Spray the second plate with anisaldehyde-
sulphuric acid reagent followed by heating at 1100 for about 10 min and examine under visible and ultraviolet light. Under visible light, it shows
major spots at Rf 0.24 (green, piperine), 0.37 (violet), 0.47 (violet), 0.51 (violet) and 0.59 (violet). Under ultraviolet light (366 nm), it shows
major spots at Rf 0.24, (fluorescent yellow, piperine), 0.26 (red), 0.36 (red), 0.46 (pink), 0.60 (red) and 0.70 (red).
Physico-chemical parameters:
Total Ash: Not more than 1.0 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 0.2 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 45 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 75 per cent, Appendix 2.2.8
Reducing sugars: 67 to 70 per cent, Appendix 5.1.3.1.
Non-reducing sugars: 5.6 to 5.8 per cent, Appendix 5.1.3.3.
pH (5% aqueous solution): 4.0 to 4.5, Appendix 3.3.
Assay:
The formulation contains not less than 0.008 per cent of piperine when assayed by the following method.
Estimation of piperine: Dissolve 5 mg of piperine in methanol and make up the volume to 100 ml in a volumetric flask. Pipette out aliquots of
0.8 to 4.8 ml into 10 ml volumetric flasks and adjust the volume in each flask with methanol to prepare standard solutions of 4 to 24 µg / ml.
Apply 10 µµl of each standard solution on TLC plate. Develop the plate to a distance of 10 cm using dichloromethane : ethyl acetate (7.5 : 1) as
mobile phase. After development, dry the plate in air and scan in the TLC scanner at a wavelength of 337 nm. Note the area under the curve for a
peak corresponding to piperine and prepare the calibration curve by plotting peak area vs concentration of piperine.
Extract, accurately weighed, about 5 g of K£Àm¡¸·aka Ras¡yana in 25 ml portions of ethyl acetate (4 to 5 times), until it tests negative to
modified Dragendorff's reagent. Filter, concentrate the combined extract and adjust the volume to 25 ml in a volumetric flask. Apply 10 µµl of
the test solution on TLC plate. Develop, dry and scan the plate as described in the preceding paragraph for calibration curve of piperine. Record
area under the curve for a peak corresponding to piperine. Calculate the amount of piperine in the test solution from the calibration curve of
piperine.
Other requirements:
Therapeutic uses: K¡sa (Cough), áv¡sa (Dyspnoea), UrakÀata (Chest wound), KÀaya (Pthisis), Pur¡¸ajvara (Chronic fever), Raktapitta
(Bleeding disorders), Chardi (Emesis), T¤À¸¡(Thirst), Jvara (Fever), áukra KÀaya (Deficiency of semen), Daurbalya (Weakness), K¡r¿ya
(Emaciation), Svarabheda (Hoarseness of voice), Vaivar¸ya (Discoloration)
Dose: 20 g daily in divided doses.
Description:
Dark brown coloured, semi solid, malleable, sticky preparation with a pungent, slightly sweet and sour taste.
Identification:
Microscopy:
Take about 5 g of sample, wash in two or three increments of hot water and centrifuge. Decant the supernatant and mount a small portion of the
sediment in 50 per cent glycerine; observe the following characters. Prisms and raphides of calcium oxalate, cells filled with pinkish pigment ( M
¤dv¢k¡); simple starch grains with concentric hilum and polygonal perisperm cells filled with starch grains (Pippal¢).
Thin layer chromatography:
Extract 20 g of the Avaleha with a combination of 50 ml of a mixture of diethyl ether : chloroform (2 : 1) and 5 ml methanol. Filter, concentrate
to 10 ml and carry out the thin layer chromatography. Apply 10 µl of the extracts on TLC plate and develop the plate to a distance of 8 cm using
toluene : ethyl acetate : formic acid (4 : 2.5 : 0.7 ) as mobile phase. Allow the plate to dry in air and examine under ultraviolet light (254 nm).
The plate shows major spots at Rf 0.41, 0.58, 0.64 (piperine), 0.74. Under ultraviolet light (366 nm) the plate shows major spots at Rf 0.45
(blue), 0.55 (brown), 0.64 (Blue, piperine), 0.84 (red), 0.88 (red) and 0.93 (blue). Spray the plate with anisaldehyde-sulphuric acid reagent
followed by heating at 1100 for about 10 min. It shows major spots at R f 0.40 (brown), 0.52 (purple), 0.58 (yellow), 0.64 (blue, piperine), 0.68
(purple) and 0.75 (violet) under visible light.
Physico-chemical parameters:
Total Ash: Not more than 1.0 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 0.2 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 30.0 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 90.0 per cent, Appendix 2.2.8.
Total tannins: 0.4 to 0.56 per cent, Appendix 5.1.2.
Total phenolics: 0.7 to 0.8 per cent, Appendix 5.1.1.
Total sugar: 70 to 73 per cent, Appendix 5.1.3.2.
Reducing sugars: 50 to 51 per cent, Appendix 5.1.3.1.
Non-reducing sugars: 20 to 23 per cent, Appendix 5.1.3.3.
pH (5% aqueous solution): 4.0 to 4.3, Appendix 3.3.
Assay:
The formulation contains not less than 2.0 per cent gallic acid when assayed by the following method.
Estimation of gallic acid: Dissolve 10 mg of gallic acid in 100 ml of methanol in a volumetric flask. From this stock solution, prepare standard
solutions of 15 to 75 µµg / ml by transferring aliquots (1.5 to 7.5 ml) of stock solution to 10 ml volumetric flasks and adjusting the volume to 10
ml with methanol.
Apply 10 µµl each of standard solution corresponding to 150 ng to 750 ng of gallic acid on a TLC plate and develop the plate to a distance of 8
cm using toluene : ethyl acetate : formic acid : methanol (3 : 3 : 0.8 : 0.2 ) as mobile phase. After development, dry the plate and scan in TLC
scanner at a wavelength of 337 nm. Note the area under the curve for a peak corresponding to gallic acid and prepare the calibration curve by
plotting peak area vs amount of gallic acid.
Hydrolyze accurately weighed about 5 g avaleha by refluxing with 50 ml of 2N hydrochloric acid on a water-bath. Filter, add equal amount of
water, transfer to a separating funnel and extract with diethyl ether (20 ml x 4). Collect the diethyl ether layer and dry. Dissolve the residue in
methanol and make up the volume to 25 ml in a volumetric flask.
Apply 10 µµl on TLC plate and develop, dry and scan the plate as described in the preceding paragraph for calibration curve of gallic acid. Note
area under the curve for a peak corresponding to gallic acid in each track of test solution. Calculate the amount of gallic acid in the test solution
from the calibration curve of gallic acid.
Other requirements:
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: K¡sa (Cough)
Dose: 25 g daily in divided doses.
Method of preparation:
Crush the fresh Ëmalak¢, strain through a muslin cloth to obtain juice.
Take fresh áat¡var¢ roots and wash. Remove the outer layer (epiblema) and express the juice with the help of juicer. Add sugar ( Sit¡) to the
mixture of above juices, heat till syrup forms. Add áodhita P£ga phala powder with continuous stirring till it becomes a thick paste. Remove the
utensil from the fire and stir continuously while adding PrakÀepa Dravya. Allow to cool down into granules. Spread the granules in a stainless
steel tray and allow to dry.
Pack the granules in tightly closed containers to protect from light and moisture.
Description:
Light brown granules with pleasant odour and spicy, sweet, acrid and astringent taste.
Identification:
Extract 5 g of P£ga Kha¸·a successively with 75 ml each of n-hexane and chloroform under reflux on a water-bath for 30 min; drying the marc
between two extractions. Filter, concentrate each extract to 10 ml and carry out the thin layer chromatography. Apply 10 µl of each extract
separately on two TLC plates and develop the plates to a distance of 8 cm using hexane : ethyl acetate (9 : 1) as mobile phase for hexane
extract and toluene : ethyl acetate : formic acid (5 : 5 : 1) for chloroform extract. After development, allow the plates to dry in air and examine
under ultraviolet light. The hexane extract shows major spots at Rf 0.20, 0.29, 0.48 and 0.61 under ultraviolet light (254 nm). The chloroform
extract shows major spots at Rf 0.28, 0.33, 0.56 and 0.62 under ultraviolet light (254 nm) and at 366 nm it shows major spots at R f 0.27, 0.42
(both blue), 0.49, 0.52 (both red) and 0.73 (green).
Physico-chemical parameters:
Loss on drying: Not more than 5 per cent, Appendix 2.2.10.
Total ash: Not more than 2.40 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 1.00 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 17.0 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 69.0 per cent, Appendix 2.2.8.
pH (1% aqueous solution): 5.0 to 5.5, Appendix 3.3.
Other requirements:
Therapeutic uses:
Chardi (Emesis), á£la (Pain / colic), Amlapitta (Hyperacidity), M£rcch¡(Syncope), Vandhy¡roga (Infertility), Pradara (Excessive vaginal
discharge), P¡¸·u (Anaemia), Rakt¡r¿a (Bleeding piles), GarbhadoÀa (Foetal anomaly), Jar¡ (Senility), áukra KÀaya (Oligospermia),
Agnim¡ndya (Loss of appetite), T¤¶ (Thirst), Daurbalya (Weakness), Aj¢r¸a (Dyspepsia), Vi¶sanga (Constipation), M£trasa´ga (Obstruction
in urinary tract), YakÀm¡ (Tuberculosis), Balya (Improves strength / immunity), Var¸ya (Improve complexion), D¤À¶i (Improves vision.)
Dose: 12 g daily in divided doses.
Description:
Semi solid, malleable, dark brown, sticky preparation with spicy odour and pungent, sweet taste
Identification:
Microscopy:
Weigh about 5 g of the sample, stir with 50 ml of a defatting solvent in a beaker. Pour out the solvent without loss of material and repeat the
process till removal of theGh¤ta.Wash the sediment in warm water similarly, and pour out the water. Wash the sediment with distilled water and
centrifuge at medium speed. Decant the supernatant. Take a few mg of the sediment, warm in chloral hydrate and mount in glycerine (50 per
cent). Mount a few mg in iodine solution. Observe the following characters in different mounts.
Sac-shaped starch grains with eccentric hilum, non-lignified xylem fibres and xylem vessels with reticulate thickenings (áu¸¶h¢); multicellular,
multiseriate trichomes and sclereid layer from mesocarp (J¢raka); U-shaped stone cells with thickening on three sides (Tvak); bulbous perisperm
cells containing starch grains and small prisms of calcium oxalate within (El¡); fragments of multicellular uniseriate short stout trichomes and
leaf epidermal fragments with sunken paracytic stomata (Tejapatra); highly thickened stone cells with narrow lumen from testa, and groups of
stone cells interspersed among parenchyma tissue from hypodermis (Marica); groups of fusiform fibres of sclerenchyma crisscrossing with each
other (Dh¡nyaka).
Physico-chemical parameters:
Total Ash: Not more than 0.1 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 0.05 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 25 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 50 per cent, Appendix 2.2.8.
Starch content: Not less than 3 per cent, Appendix 2.2.14.
Total sugars: 80 to 90 per cent, Appendix 5.1.3.2.
Reducing sugars: 62 to 65 per cent, Appendix 5.1.3.1.
Non-reducing sugars: 18 to 20 per cent, Appendix 5.1.3.3.
pH (10% aqueous solution): 4.0 to 4.3, Appendix 3.3.
Assay:
The formulation contains not less than 0.003 per cent of piperine, when assayed by the following method.
Estimation of piperine: Dissolve 5 mg of piperine in methanol and make up the volume to 100 ml in a volumetric flask. From this stock solution,
pipette out aliquots of 0.8 to 4.8 ml into 10 ml volumetric flask and make up the volume with methanol to prepare standard solutions of 4 to 24
µg / ml. Apply 10 µµl of each standard solution (corresponding to 40 to 240 ng of piperine) on TLC plate. Develop the plate to a distance of 8
cm using dichloromethane : ethyl acetate (7.5 : 1). After development, dry the plate and scan in a TLC scanner at a wavelength of 337 nm.
Record the area under the curve for a peak corresponding to piperine and prepare the calibration curve by plotting peak area vs amount of
piperine.
Extract accurately weighed about 5 g S£ra¸¡valeha in ethyl acetate (25 ml x 5). Filter the extracts, pool, concentrate and adjust the volume to 25
ml in a volumetric flask. Apply 10 mml of test solution on TLC plate and develop, dry and scan the plate as described in the proceeding
paragraph for calibration curve of piperine. Calculate the amount of piperine in the test solution from the calibration curve of piperine.
Other requirements:
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Mand¡gni (Dyspepsia), M£·hav¡ta (Obstructed movement of V¡ta doÀa), Ar¿a (Piles etc.)
Dose: 20 g daily in divided doses.
Description:
Dark brown coloured, semi solid, malleable, sticky preparation with odour of ghee; taste bitter and pungent.
Identification:
Microscopy:
Take about 5 g of sample dissolve in sufficient quantity of n-hexane for removal of ghee. Repeat the procedure with two further increments of
solvent pouring out solvent each time, wash the sediment with warm water, followed by cold water repeatedly till a clear sediment is obtained.
Take a few mg of the sediment, mount in 50 per cent glycerine and observe the following characters. Simple starch grains with concentric hilum,
abundant polygonal perisperm cells packed with starch grains ( Pippal¢); multicellular, uniseriate, warty covering trichomes, sessile glandular
trichomes with quadricellular head, fragments of lower epidermis showing the presence of diacytic stomata, cigar-shaped crystoliths (V¡s¡).
Extract 5 g of Avaleha with 100 ml of methanol under reflux on a water-bath for 30 min. Filter, concentrate to 25 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using ethyl acetate : methanol : ammonia
(8 : 2 : 0.2) as mobile phase. After development, allow the plate to dry in air and examine under ultraviolet light. It shows major spots at R f 0.34
(vasicine), 0.74, 0.96 (piperine) under ultraviolet light (254 nm) and at Rf 0.77 (fluorescent blue), 0.89 (blue), 0.96 (fluorescent blue - piperine)
under ultraviolet light (366 nm). Derivatise the plate with modified Dragendorff's reagent and observe under visible light. It shows two orange
coloured spots at Rf 0.34 and 0.96.
Physico-chemical parameters:
Loss on drying: Not more than 12.16 per cent, Appendix 2.2.10.
Total Ash: Not more than 2.5 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 0.15 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 20 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 60 per cent, Appendix 2.2.8.
Total sugar: 83 to 88 per cent, Appendix 5.1.3.2.
Reducing sugars: 44 to 45 per cent, Appendix 5.1.3.1.
Non-reducing sugars: 38 to 43 per cent, Appendix 5.1.3.3.
pH (10% aqueous solution): 4.35 to 4.9, Appendix 3.3.
Assay:
The formulation contains not less than 0.2 per cent of vasicine and not less than 0.2 per cent of piperine when assayed by the following methods.
Estimation of vasicine: Dissolve 2 mg of vasicine in 25 ml of methanol in a volumetric flask. From this stock solution pipette out aliquots of 2 to
6 ml and make up the volume to 5 ml in volumetric flasks with methanol. Apply 10 mml of each standard solution (corresponding to 320 to 960
ng of vasicine) on TLC plate. Develop the plate to a distance of 8 cm using ethyl acetate : methanol : ammonia (8 : 2 : 0.2) as mobile phase.
After development, dry the plate and scan in TLC scanner at a wavelength of 298 nm. Note the peak area under the curve for a peak
corresponding to vasicine and prepare the calibration curve by plotting peak area vs amount of vasicine.
Extract accurately weighed about 5 g of V¡s¡valeha in methanol (25 ml x 5). Filter the extract, pool, concentrate and adjust the volume to 25 ml.
Apply 10 mml of test solution on TLC plate and develop, dry and scan the plate as described in the preceeding paragraph for calibration curve of
vasicine. Calculate the amount of vasicine in the test solution from the calibration curve of vasicine.
Estimation of piperine: Dissolve 5 mg of piperine in 100 ml of methanol. From this stock solution, pipette out 0.8 to 4.8 ml aliquots into 10 ml
volumetric flasks and make up the volume with methanol to prepare standard solutions of 4 to 24 µg / ml. Apply 10 mml of each standard
solution (corresponding to 40 to 240 ng) on TLC plate and develop the plate to a distance of 8 cm using dichloromethane : ethyl acetate (7.5 : 1)
as mobile phase. After development, dry the plate and scan in TLC scanner at a wavelength of 337 nm. Note the peak area under the curve for a
peak corresponding to piperine and prepare the calibration curve by plotting peak area vs amount of piperine.
Extract accurately weighed about 5 g of V¡s¡valeha with ethyl acetate (25 ml x 5). Filter the extract, pool, concentrate and adjust the volume to
25 ml in a volumetric flask. Apply 10 mml of test solution on TLC plate and develop, dry and scan the plate as described in the preceding
paragraph for calibration curve of piperine. Calculate the amount of piperine in the test solution from the calibration curve of piperine.
Other requirements:
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: K¡sa (Cough), áv¡sa (Dyspnoea), Jvara (Fever), Raktapitta (Bleeding disorders), R¡jayakÀm¡ (Tuberculosis), P¡r¿va¿
£la (Intercostal neuralgia and pleurodynia), H¤t¿£la (Angina pectoris)
Dose: 12 g daily in divided doses.
Description:
A blackish brown, semisolid sticky paste with bitter and astringent taste and spicy pleasant odour.
Identification:
Microscopy:
·
Take about 5 g of the Avaleha and wash it with warm water till gu a and honey are removed. Collect the sediment. Clarify a small amount of
residue with chloral hydrate solution, wash in cold water, and mount in glycerin. Take a few mg, add iodine solution water, and mount in
glycerin. Observe following character in different mounts.
Fragments of hypodermis in surface view, stone cells varying in sizes, shapes and thickness, mostly present in groups interspersed among
parenchyma ( Marica); fragments of fibres with very narrow lumen, not over 600 μ long and not over 45 μ broad; parenchyma cells containing
minute acicular crystal of calcium oxalate, stone cells varying shape and size, smaller ones somewhat rectangular; oil cells present (Tvak);
groups of slightly wavy parenchymatous cells, each cell containing 1 to 3 rosette crystals of calcium oxalate, groups of perisperm cells bulbous
in shape packed with starch grains which also shows in middle tiny prismatic crystals of calcium oxalate; epidermal and hypodermal cells
S£kÀmail¡
crossing each other at right angle ( ); groups of parenchymatous cells, densely packed with starch grains, isolated starch grains, simple,
oval to rod shaped upto 75 μ in length, hilum eccentric, lamellae distinct; yellow coloured oleo resin cells, non-lignified, septate fibres some of
them bearing marks of adjacent cells pressing against them ( áu¸¶h¢); stone cells with broad lumen in groups of 2 to 8 (Pippal¢ ); crushed pieces
of anther lobes containing pollen grains, each tricolporate measuring upto 55 μ in dia., groups of epidermal cells of anther lobe (N¡gake¿ara);
groups of angular epidermal parenchytamous cells with sunken stomata, oil cells and oil globules seen, unicellular and bicellular trichomes
( Tejapatra).
Thin layer chromatography:
Extract 5 g of sample with n-hexane (25 ml x 3) under reflux on a water bath for 30 min, filter, concentrate to 10 ml and carry out thin layer
chromatography. Apply 10 µl of the extract on TLC plate. Develop the plate to a distance of 8 cm using tolune : ethyl acetate (8 : 2) as mobile
phase. After development, allow the plate to dry in air and examine under ultra violet light (366 nm). It shows major spots at R f 0.28 (blue), 0.43
and 0.58 (faint blue). Spray the plate with anisaldehyde- sulphuric acid reagent followed by heating at 1100 about for 10 min. It shows major
spots at Rf 0.21 (green), 0.43 (blue) and 0.58 (brown) under visible light.
Physico-chemical parameters:
Loss on drying: Not more than 23.0 per cent, Appendix 2.2.10.
Total ash: Not more than 4.0 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 0.15 per cent, Appendix 2.2.4.
Sulphated Ash: Not more than 0.41 per cent, Appendix 2.2.6.
Alcohol-soluble extractive: Not less than 20.0 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 68.7 per cent, Appendix 2.2.8.
pH of 1% aqueous solution : 5.5 and 5.6, Appendix 3.3.
Other requirements:
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses:K¡sa (cough), Prati¿y¡ya (Coryza), áv¡sa (Asthma), SvarakÀaya (aphasia), P¢nasa (Chronic rhinitis / Sinusitis) and
R¡jayakÀm¡ (Tuberculosis.)
Dose: 5 to 15 g
Anupāna: Water, Milk.
CHURNA
CÍRÛA
General Descripition:
In cases where Pārada and Gandhaka are mentioned, prepare Kajjalī and add other drugs, one by one, according to the formula.
´
In general the aromatic drugs like Hi gu [Asafoetida] etc. should be fried before they are converted to fine powders.
Specific care should be taken in case of Salts and Sugars. Formulations with hygroscopic components should not usually be prepared
during rainy seasons. If so, specific precautions should be taken during storage.
C£r¸as should be stored in air tight containers. Polyethylene and foil packing also provides damp proof protection.
Special precaution for storage should be taken in cases of formulations with salts, sugars and KÀāras.
13. Amalakyadi churna
13. ËMALAKYËDI CÍRÛA
AFI, Part-I, 7:3
Definition:
ËMALAKYËDI CÍRÛA is a powder preparation made with the ingredients in the Formulation composition given below.
Formulation composition:
1. Ëmala (Ëmalak¢) Phyllanthus emblica (Emblica officinalis) (API-Vol:1/111) (P.) 1 Part
2. Citraka Plumbago zeylanica Linn (API-Vol:1/29) (Rt.) 1 Part
3. Pathy¡ (Har¢tak¢) Terminalia chebula Retz. (API-Vol:1/47) (P.) 1 Part
4. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 1 Part
5. Saindhava lava¸a Rock salt 1 Part
Method of preparation:
Description:
Brown-coloured, smooth powder with pleasant odour and salty, spicy taste. The powder completely pass on through sieve number 44 and not
less than 50 per cent pass on through sieve number 85.
Identification:
Microscopy:
Take about 2 g of C£r¸a , and wash it thoroughly with water to remove salt, pour out the water without loss of material and mount in glycerine;
warm a few mg with chloral hydrate, wash and mount in glycerine; treat a few mg with iodine in potassium iodide solution and mount in
glycerine. Observe the following characters in the different mounts.
Thin walled epidermis with paracytic stomata, brachysclereids with pitted wide lumen, silica crystals in epidermal cells (Ëmalak¢); cork cells in
surface view, uniseriate and multiseriate ray parenchyma cells, bifurcated short fibres and pitted vessels ( Citraka); Prismatic and druses of
calcium oxalate crystals, groups of sclereids, criss-cross layers of fibres, thin walled fibres and broad lumen with pegged tip ( Har¢tak¢);
perisperm cells packed with starch grains and minute crystals of calcium oxalate, uniseriate multicellular trichomes (Pippal¢).
Extract 4 g of C£r¸a in alcohol (25 ml x 3) under reflux on a water-bath for 30 min, filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate (5 : 2) as
mobile phase. After development, allow the plate to dry in air and examine under ultraviolet light (254 nm). It shows major spots at R f. 0.43
(light green), 0.50 (green) and 0.85 (pale green).
Physico-chemical parameters:
0
Loss on drying at 105 : Not more than 10 per cent, Appendix 2.2.10.
Total ash: Not more than 27 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 0.6 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 25 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 46 per cent, Appendix 2.2.8.
pH (10% aqueous solution): 3 to 4, Appendix 3.3.
Assay:
Sodium: Not less than 6 per cent w/w, Appendix 5.2.9.
Other requirements:
Microbial limits: Appendix 2.4.
Aflatoxin: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic Uses: Aruc¢ (Anorexia), Agnim¡ndya (Dyspepsia), Jvara (Fever), Aj¢r¸a (Indigestion)
Dose: 5 to 10 g daily in divided doses.
Anupāna: Water.
14. Avipathikara churna
14. AVIPATTIKARA CÍRÛA
AFI, Part- I, 7:2
Definition:
AVIPATTIKARA CÍRÛA is a powder preparation made with the ingredients in the Formulation composition given below.
Formulation composition:
1. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 1 Part
2. Marica Piper nigrum Linn. (API-Vol:3/115) (Fr.) 1 Part
3. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 1 Part
4. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) (P.) 1 Part
5. Bibh¢taka Terminalia belerica Roxb. (API-Vol:1/26) (P.) 1 Part
6. Ëmalak¢ Emblica officinalis Gaertn. (Phyllanthus emblica) (API-Vol:1/4) (P.) 1 Part
7. Must¡ Cyperus rotundus Linn. (API-Vol:3/129) (Rz.) 1 Part
8. Vi·a (Vi·a Lava¸a) _ 1 Part
9. Vi·a´ga Embelia ribes Burm.f. (API-Vol:1/123) (Fr.) 1 Part
10. El¡ (S£kÀmail¡) Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) (Sd.) 1 Part
11. Patra (Tejapatra) Cinnamomum tamala (Buch-Ham)Nees & Eberm. (API-Vol:1/115) (Lf.) 1 Part
12. Lava´ga Syzygium aromaticum (Linn.) Merr M.Perry. (API-Vol:1/80) (Fl.Bd.) 11Parts
13. Triv¤t Operculina turpethum (Linn.) Silva Manso. (API-Vol:3/213) (Rt.) 44 Parts
14. áarkar¡ Cane sugar 66 Parts
Method of preparation:
Take all ingredients of pharmacopoeial quality.
Clean, dry and powder the ingredients numbered 1 to 7 and 9 to 13 individually in a pulverizer and pass through sieve number 85. Prepare fine
· ¸
powder of Vi a lava a and áarkar¡ separately and pass through sieve number 85. Weigh separately each powdered ingredient, mix together in
specified ratio and pass through sieve number 44 to obtain a homogeneous blend. Pack it in tightly closed containers to protect from light and
moisture.
Description:
Light brown, fine powder, odour characteristic of clove, with a sweet, spicy and pungent taste. The powder completely pass on through sieve
number 44 and not less than 50 per cent pass on through sieve number 85.
Identification:
Extract 4 g of sample in alcohol (25 ml x 3) under reflux on a water-bath for 30 min, filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate (5 : 2) as
mobile phase. After development allow the plate to dry in air and examine under ultraviolet (366 nm). It shows major spots at R f 0.11, 0.23, 0.35
(all blue) and 0.72 (fluorescent blue). Spray the plate with vanillin-sulphuric acid reagent followed by heating at 1100 for about 10 min and
observe under visible light. The plate shows major spots at Rf 0.49, 0.54, (both violet), 0.65 and 0.73 (both pale violet).
Physico-chemical parameters:
0
Loss on drying at 105 : Not more than 7 per cent, Appendix 2.2.10.
Total ash: Not more than 6 per cent, Appendix 2.2.3.
Acid- insoluble ash: Not more than 0.5 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 20 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 53 per cent, Appendix 2.2.8.
pH (10%) aqueous solution: 4 to 6, Appendix 3.3.
Total sugars: Not less than 39 per cent, Appendix 5.1.3.2.
Reducing sugars: Not less than 4 per cent, Appendix 5.1.3.1.
Other requirements:
Microbial load: Appendix 2.4.
Aflatoxin: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Agnim¡ndya (Digestive impairment), Malabandha (Constipation), Amlapitta (Hyperacidity), Ar¿a (Piles), M£trabandha
(Retention of urine), Prameha (Metabolic disorder)
Dose: 10 g daily in divided doses.
Description:
¢
Pale brown powder, odour characteristic of Pippal and taste slightly pungent followed by a tingling sensation. The powder completely passes
on through sieve number 44 and not less than 50 per cent pass on through sieve number 85.
Identification:
Microscopy:
Take a few mg of C£r¸a and warm with chloral hydrate, wash and mount in glycerine; wash a few mg of C£r¸a in water and mount in
glycerine; treat a few mg of C£r¸a with iodine solution and mount in glycerine; observe the following characters in the different mounts.
Parenchyma cells with reddish brown contents, starch grains simple, circular to oval upto 30 µ, narrow vessels with lateral simple perforation,
walls reticulate, pitted and spiral vessels, regularly arranged sclereids from scale leaf (Must¡); multicellular uniseriate trichomes, perisperm
cells packed with starch grains and minute crystals of calcium oxalate, spindle shaped, elongated stone cells with wide lumen (Pippal¢); starch
grains, simple and compound with 2 to 4 components, upto 65µ in size, parenchyma cells with starch grains and cork cells in surface view
( AtiviÀ¡); collapsed thin walled epidermal cells, tissue fragments with yellowish brown contents and large tannin containing sacs associated
with vascular bundles ( Karka¶a¿¤´g¢).
Thin Layer Chromatography:
Extract 4 g of C£r¸a in alcohol (25 ml x 3) under reflux on a water-bath for 30 min filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8cm using toluene : ethyl acetate (5 : 1.5) as
mobile phase. After development allow the plate to dry in air and examine under ultraviolet light (254 nm). It shows major spots at R f 0.31, 0.37,
0.45, 0.60 (all green), 0.74 (light green) and 0.91 (blue). Under ultraviolet light (366 nm), it shows major spot at Rf 0.65 (fluorescent blue). Spray
the plate with vanillin-sulphuric acid reagent followed by heating at 1100 for about 10 min and observe under visible light. The plate shows
major spots at Rf 0.36, 0.50 (both grey), 0.61 (blue), 0.68 (grey) and 0.81 (pink).
Physico-chemical parameters:
0
Loss on drying at 105 : Not more than 9 per cent, Appendix 2.2.10.
Total ash: Not more than 7 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 2.5 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 14 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 16 per cent, Appendix 2.2.8.
pH (10% aqueous solution): 5 to 5.3, Appendix 3.3.
Other requirements:
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: At¢s¡ra (Diarrhoea), Chardi (Vomiting), K¡sa (Cough), áv¡sa (Dyspnoea), Jvara (Fever), B¡la áoÀa (Emaciation in
children)
Dose: 0.5 to 1 g daily in divided dose.
Anupāna: Honey.
16. Eladi churna
16. ELËDI CÍRÛA
AFI, Part-I, 7:5
Definition:
ELËDI CÍRÛA is a powder preparation made with the ingredients in the Formulation composition given below.
Formulation composition:
1. El¡ (S£kÀmail¡) Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) (Sd.) 1 Part
2. Lava´ga Syzygium aromaticum (Linn.) Merr M.Perry. (API-Vol:1/80) (Fl.Bd.) 1 Part
3. Gajake¿ara (N¡gake¿ara) Mesua ferrea Linn (API-Vol:2/118) (Stmn.) 1 Part
4. Kolamajj¡ (Kola) Zyzyphus jujuba Lam. (API-Vol:3/94) (Rp.Fr.Pp.) 1 Part
5. L¡ja (á¡li) Oryza sativa Linn (API-Vol:2/145) (Sd.) 1 Part
6. Priya´gu Callicarpa macrophylla Vahl (API-Vol:2/143) (InFl. ) 1 Part
7. Ghana (Must¡) Cyperus rotundus Linn. (API-Vol:3/129) (Rt.Tr) 1 Part
8. Candana (áveta Candana) Santalum album Linn. (API-Vol:3/207) (Ht.Wd.) 1 Part
9. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 1 Part
Method of preparation:
Description:
Brown-coloured, smooth powder with characteristic odour of El¡
, and a spicy, pungent taste. The powder completely pass on through sieve
number 44 and not less than 50 per cent pass on through sieve number 85.
Identification:
Microscopy:
Take a few mg of C£r¸a and warm with chloral hydrate, wash and mount in glycerine; wash a few mg in water and mount in glycerine; treat a
few mg with iodine solution and mount in glycerine; observe the following characters in the different mounts.
Perisperm cells with bulbous projections, packed with starch grains and also carrying minute calcium oxalate crystals, fragments of aril tissue
with elongated cells and orange coloured sclerenchymatous cells ( El¡); pollen grains tetrahedral, spherical, biconvex, measuring 15 to 20 μ in
dia, spindle shaped fibres, parenchyma with oil cells and anther wall with cluster crystals of calcium oxalate (Lava´ga); numerous golden
yellow pollen grains upto 50 μ in dia and fragments of anther wall (N¡gake¿ara); circular to oval thin walled, reddish brown cells of mesocarp,
polygonal epicarp cells in surface view (kola); endosperm cells packed with minute starch grains in clusters (á¡li); fragments of stellate hairs,
elliptical, oval and circular pollen grains with clear exine, yellowish in colour, upto 30 μ in dia, spiral vessels (Priya´gu); circular to oval starch
grains measuring upto 30 μ in dia, narrow vessel with scalariform thickness, oblique pore, regular arrangement of parallel short fibres from
scale leaf ( Must¡
); abundant fragments of thick walled fibres isolated or associated with pitted vessel with tail ( áveta Candana
); oval to
elongated stone cells, measuring upto 300 μ in length, perisperm cells packed with starch grains and minute calcium oxalate crystals,
multicellular uniseriate trichome ( Pippal¢).
Thin Layer Chromatography:
Extract 4 g of sample in alcohol (25 ml x 3) under reflux on a water-bath for 30 min, filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate, develop the plate to a distance of 8 cm using toluene : ethyl acetate (5 : 1.5) as mobile
phase. After development allow the plate to dry in air and examine under ultraviolet light (254 nm). It shows major spots at R f 0.54, 0.71 (both
blue) and 0.92 (fluorescent blue). Spray the plate with vanillin-sulphuric acid reagent followed by heating at 1100 for about 10 min and observe
under visible light. The plate shows major spots at Rf 0.56 (grey), 0.71 (orange), 0.92 (grey).
Physico-chemical parameters:
0
Loss on drying at 105 : Not more than 10 per cent, Appendix 2.2.10.
Total ash: Not more than 7 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 2 per cent, Appendix 2.2.4.
Water-soluble extractive: Not less than 18 per cent, Appendix 2.2.8.
Alcohol-soluble extractive: Not less than 10 per cent, Appendix 2.2.7.
pH (10% aqueous solution): 5 to 7, Appendix 3.3.
Other requirements:
Microbial limit: Appendix 2.4.
Aflatoxin: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Formulation composition:
1. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 1 part
2. Marica Piper nigrum Linn. (API-Vol:3/115) (Fr.) 1 part
3. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 1 part
4. Ajamod¡ Apium leptophyllum (Pers.) F.V.M.ex Benth (API-Vol:1/2) (Fr.) 1 part
5. Saindhava Lava¸a Rock salt 1 part
6. áveta J¢raka Cuminum cyminum Linn (API-Vol:1/106) (Fr.) 1 part
7. K¤À¸a J¢raka Carum carvi Linn (API-Vol:1/73) (Fr.) 1 part
8. Hi´gu - ¿uddha Ferula foetida Regel. (API-Vol:1/49) (Exd.) 1 part
Method of preparation:
Light brown; free flowing powder with a spicy and astringent taste, odour aromatic and pleasant. The powder completely pass on through sieve
number 44 and not less than 50 per cent pass on through sieve number 85.
Identification:
Microscopy:
Take about 5g of C£r¸a and wash thoroughly with distilled water to get rid of salt; allow the material to settle, and reject the supernatant without
loss of material; take a few mg and stain with iodine solution and mount in 50 per cent glycerine to examine the starch grains. Clarify a few mg
with chloral hydrate and mount in 50 per cent glycerine; boil a few mg with 2 per cent potassium hydroxide, wash with water and mount in
glycerine. Observe the following character in different mounts.
Pippal¢); fragments of inner epidermis of pericarp in
Stone cells measuring 130 to 190 µ in dia with broad lumen, isolated in groups of 2 to 8 (
surface view, with groups of stone cells varying in sizes, shapes and thickness, interspersed among parenchymatous hypodermis (Marica);
groups of parenchymatous cells, densely packed with starch grains, isolated starch grains, simple, oval to rod shaped, measuring 15 to 70 μ in
length, hilum eccentric, lamellae distinct; yellow coloured oleo resin cells, non-lignified, sepatate fibres some of them bearing marks of adjacent
cells pressing against them, 30 to 50 μ broad, (áu¸¶h¢); striated epidermal debris, transversely much elongated, thin walled parenchymatous cells
in a regular V joint with neighbouring cell, stone cells from mesocarpic stone cell layer, not much longer than broad, epithelial cells of vittae
arranged like honey comb ( K¤À¸a J¢raka); multicellular large trichomes, stone cells of mesocarpic stone cell layer much longer than broad
(áveta J¢raka); epicarp tissue with radially striated or puckered papillose outgrowth, along with anomocytic stomata (Ajamod¡).
Physico-chemical parameters:
Loss on drying: Not more than 13.5 per cent, Appendix 2.2.10.
Total ash: Not more than 23.0 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 4.5 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 14.0 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 34.0 per cent, Appendix 2.2.8.
pH (1% aqueous solution): 6.4 to 6.6, Appendix 3.3.
Other requirements:
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Agnim¡ndya (Digestive impairment), á£la (Pain / colic), Gulma (Abdominal lump), V¡ta Roga (Diseases due to V¡ta
doÀa)
Dose: 3 to 6 g daily in divided doses.
Anupāna: Gh¤ta.
18. Navayasa churna
18. NAVËYASA CÍRÛA
AFI, Part-I, 7:17
Definition:
NAVËYASA CÍRÛA is a powder preparation made with the ingredients in the formulation composition given below.
Formulation composition:
1. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 1 part
2. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 1 part
3. Marica Piper nigrum Linn. (API-Vol:3/115) (Fr) 1 part
4. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) (P.) 1 part
5. Bibh¢taka Terminalia belerica Roxb. (API-Vol:1/26) (P.) 1 part
6. Ëmalak¢ Emblica officinalis Gaertn. (Phyllanthus emblica) (API-Vol:1/4) (P.) 1 part
7. Must¡ Cyperus rotundus Linn. (API-Vol:3/129) (Rt.Tr.) 1 part
8. Vi·a´ga Embelia ribes Burm.f. (API-Vol:1/123) (Fr.) 1 part
9. Citraka Plumbago zeylanica Linn (API-Vol:1/29) (Rt. ) 1 part
10. Ayoraja (Lauha) - bhasma (30 Pu¶i) - 9 parts
Method of preparation:
Reddish-brown powder with pungent odour and spicy, pungent taste. All pass through sieve number 44 and not less than 50 per cent pass
through sieve number 85.
Identification:
Microscopy:
Take about 5 gC£r¸a in a small beaker, add water, stir thoroughly and pass through 150 sieve to remove the Bhasma; repeat once more. Take a
few mg of the washed C£r¸a and warm with chloral hydrate, wash and mount in glycerine; wash a few mg in water and mount in glycerine;
treat a few mg with iodine solution and mount in glycerine. Observe the following characters in different mounts.
Large starch grains, oval shape upto 50 µ in size; spiral vessels and septate non lignified fibres ( áu¸¶h¢); stone cells of various shapes
interspersed with parenchyma cells from hypodermis ( Marica); groups of isolated and spindle shaped stone cells, uniseriate multicellular
trichomes (Pippal¢); groups of elongated sclereids with pits and broad lumen, crisscross fibre tissue, thin walled fibres with broad lumen and
pegged tips (Har¢tak¢); unicellular trichomes with sharp tips and bulbous base, epidermal fragment with cicatrices (Bibh¢taka); thin walled
epidermis with paracytic stomata and silica crystals, brachysclereids with pitted wide lumen, large, irregular thick walled parenchyma with
prominent corner thickening ( Ëmalak¢); scalariform vessels, starch grains upto 30 µ and regularly arranged, parallel sclereids from scale leaf
(Must¡); prismatic crystals of calcium oxalate, spiral vessels and stone cells in different shapes and sizes with prominent pits from testa and
elongated sclereids with broad lumen and pitted walls (Vi·a´ga) ; cork cells in surface view and ray parenchyma cells with pits and thin walled
fibres with pointed tips (Citraka).
Extract 4 g of c£r¸a
in alcohol (25 ml x 3) under reflux on a water-bath for 30 min, filter, concentrate to 10 ml and carry out the thin layer
chromatography Apply 10 µl of the extrct on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate (5 : 1.5) as
mobile phase. After development allow the plate to dry in air and examine under ultraviolet light (254 nm). It shows major spots at R f 0.26, 0.31,
0.43 (all blue) and 0.91 (fluorescent blue).
Physico-chemical Parameters:
0
Loss on drying at 105 : Not more than 6 per cent, Appendix 2.2.10.
Total ash: Not more than 56 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 14 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 11 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 12 per cent, Appendix 2.2.8.
pH (10% aqueous solution): 3 to 4, Appendix 3.3.
Assay:
Iron: Not less than 33 per cent, Appendix 5.2.5.
Other requirements:
Microbial limit: Appendix 2.4.
Aflatoxin: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: P¡¸·u (Anaemia), K¡mal¡ (Jaundice), Prameha (Metabolic disorder), Pi·ak¡ (Carbuncle), H¤droga (Heart disease),
KuÀ¶ha (Diseases of Skin), Ar¿a (Piles)
Dose: 2 g daily in divided doses.
Roast coarsely powdered Saindhava lava¸a (number 15) in a stainless steel pan at a low temperature till it becomes free from moisture. Prepare
fine powder and pass through sieve number 85. Clean, dry and powder the other ingredients 1 to 21 (except number 15) individually in a
pulverizer and sift through sieve number 85 mesh separately. Weigh separately each ingredient, mix together in specified ratio and pass through
sieve number 44 to obtain a homogeneous blend. Pack it in tightly closed containers to protect from light and moisture.
Description:
Yellowish brown, smooth powder, taste bitter, salty and odour pungent. The powder completely pass on through sieve number 44 and not less
than 50 per cent pass on through sieve number 85.
Identification:
Physico-chemical parameters:
0
Loss on drying at 105 : Not more than 8 per cent, Appendix 2.2.10.
Total ash: Not more than 12 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 10 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 18 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 23 per cent, Appendix 2.2.8.
pH (10% aqueous solution): 4 to 5, Appendix 3.3.
Assay:
Sodium: Not less than 0.6 per cent w/w, Appendix 5.2.9.
Other requirements
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Udara (Diseases of abdomen), Ëmav¡ta (Rheumatism), V¡tarakta (Gout), KuÀ¶ha (Diseases of Skin)
Dose: 5 g daily in divided dose.
Description:
Pale brown, smooth powder, odour pungent and taste slightly pungent with tingling sensation. The powder completely pass on through sieve
number 44 and not less than 50 per cent pass on through sieve number 85.
Identification:
Microscopy:
Take about 2 g of the C£r¸aand wash it thoroughly with water to remove the salt without loss of C£r¸a ; using the washed C£r¸a make the
following preparations: warm a few mg in chloral hydrate, wash to remove chloral hydrate and mount in glycerine; mount a few mg in
glycerine; treat a few mg with solution of iodine solution and mount in glycerine: take a few mg in a watch glass add iodine water, and drain
excess of iodine by filter paper; add a drop of sulphuric acid (2 parts in 1 part water), mount in glycerine to locate cellulosic fibres. Observe the
following characters in the different mounts:
Fragments of septate non-lignified fibres, broad spiral and reticulate vessels and oval shaped starch grains upto 50 µ in size ( áu¸¶h¢
); groups of
elongated thick walled sclereids with pits and broad lumen, crisscross thin walled fibres with broad lumen and pegged tips, polygonal epidermal
cells with slight beading and dividing septum ( Har¢tak¢); uniseriate, multicellular trichomes, perisperm cells packed with starch grains and
minute crystals of calcium oxalate, isolated, elongated stone cells with broad lumen (Pippal¢); Prismatic crystals of calcium oxalate and rosette
crystals of calcium oxalate, vessels with regular bordered pits appearing like honey comb, stone cells and thick walled cellulosic fibres with
broken ends and very narrow lumen ( Triv¤t).
Thin Layer Chromatography:
Extract 4 g of sample in alcohol (25 ml x 3) under reflux on a water-bath for 30 min filter concentrate to 10 ml and carry out the Thin Layer
Chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate (5 : 2) as
mobile phase. After development of the plate, allow it to dry in air and examine under ultraviolet light (254 nm). It shows major spots at R f 0.46
and 0.63 (both green). Under ultraviolet light (366 nm), it shows a major spot at Rf 0.77 (fluorescent blue). Spray the plate with vanillin-
sulphuric acid reagent followed by heating at 1100 for about 10 min and observe under ultraviolet light. The plate shows a major spot at R f 0.77
(pink).
Physico-chemical parameters:
Loss on drying at 105 :
0
Not more than 10 per cent, Appendix 2.2.10.
Total ash: Not more than 22 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 3 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 20 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 35 per cent, Appendix 2.2.8.
pH (10% aqueous solution): 4.5 to 4.7, Appendix 3.3.
Assay:
Sodium: Not less than 4 per cent w/w, Appendix 5.2.9.
Other requirements:
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Ëdhm¡na (Flatulance with gurgling sound), á£la (Pain / colic), Ëmav¡ta (Rheumatism), Ar¿a (Piles), Udara Roga
(Diseases of abdomen), Vibandha (Constipation)
Dose: 3 to 5 g daily in divided dose.
Description:
Reddish brown-coloured fine powder with a pungent odour and a bitter, sweet taste. The powder completely pass on through sieve number 44
and not less than 50 per cent pass on through sieve number 85.
Identification
Thin Layer Chromatography:
Extract 4 g of C£r¸a in alcohol (25 ml x 3) under reflux on a water-bath for 30 min filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate (5 : 2) as
mobile phase. After development, allow the plate, to dry in air and examine under ultraviolet light (366 nm). It shows major spots at R f 0.18
(blue), 0.73 (fluorescent blue). Spray the plate with vanillin-sulphuric acid reagent followed by heating at 1100 for about 10 min and observe
under visible light. The plate shows major spots at Rf 0.13 (grey), 0.27 (purple), 0.33 (yellow), 0.53 (purple), 0.66 and 0.97 (both purple).
Physico-chemical parameters:
0
Loss on drying at 105 : Not more than 11 per cent, Appendix 2.2.10.
Total ash: Not more than 15 per cent, Appendix 2.2.3.
Acid-Insoluble ash: Not more than 4 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 12 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 13 per cent, Appendix 2.2.8.
pH (10% )aqueous solution: 5 to 6, Appendix 3.3.
Other requirements:
Description:
Creamish white fine powder with pleasant odour and a sweet, spicy and pungent taste. The powder completely pass on through sieve number 44
and not less than 50 per cent pass on through sieve number 85.
Identification:
Microscopy:
Take about 2 g of C£r¸a , wash thoroughly in water to remove sugar. Take a few mg of the washed C£r¸aand warm with chloral hydrate, wash
and mount in glycerine; wash a few mg in water and mount in glycerine; treat a few mg with iodine solution and mount in glycerine. Observe the
following characters in different mounts.
Surface view of epidermis showing sunken stomata with thick cuticle, palisade parenchymatous fragments, parenchyma cells filled with brown
colour cell content ( T¡l¢sa); beaker shaped stone cells upto 150 μ length, tissue from hypodermis with polygonal pitted stone cells with
interspersed among parenchyma cells, lumen circular (Marica); large starch grains upto 35 μ in dia, eccentric hilum, reticulate and spiral
vessels, septate fibres non lignified and broad lumen with sharp tips (áu¸¶h¢); spindle shaped stone cells with or without a broad lumen,
uniseriate multicellular trichome (Pippal¢); perisperm cells with bulbous projections, packed with minute starch grains and also carrying minute
calcium oxalate crystals, fragments of aril tissue from testa, orange coloured sclerenchymatous cells (El¡); fibres with thick walls narrow lumen
upto 720 μ length, lignified stone cells with thick inner walls, pitted parenchyma, acicular crystals of calcium oxalate (Tvak).
Extract 4 g of sample in alcohol (25 ml x 3) under reflux on a water-bath for 30 min filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate : formic acid
(5 : 2.5 : 0.5) as mobile phase. After development allow the plate to dry in air and examine under ultraviolet (254 nm). It shows a major spot at
Rf 0.59 and 0.64 (both grey).Under ultraviolet light (366 nm), it shows a major spot at R f 0.52(fluorescent blue). Spray the plate with vanillin-
sulphuric acid reagent followed by heating at 1100 for about 10 min and observe under visible light. The plate shows major spots at R f 0.45
(yellow), and 0.76 (orange).
Physico-chemical parameters:
0
Loss on drying at 105 : Not more than 4 per cent, Appendix 2.2.10.
Total ash: Not more than 11 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 9.5 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 12 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 68 per cent, Appendix 2.2.8.
pH (10% aqueous solution): 6 to 8, Appendix 3.3.
Total sugars: Not less than 56 per cent, Appendix 5.1.3.2.
Reducing sugars: Not less than 8 per cent, Appendix 5.1.3.1.
Other requirements:
Microbial limit: Appendix 2.4.
Aflatoxin: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Chardi (Vomiting), Ëdhm¡na (Flatulance with gurgling sound), K¡sa (Cough), áv¡sa (Asthma), Jvara (Fever), Aruc¢
(Anorexia), Aj¢r¸a (Indigestion), At¢s¡ra (Diarrhoea), áoÀa (Cachexia), Pl¢h¡(Splenic disease), Graha¸¢ (Malabsorption syndrome), P¡¸·u
(Anaemia)
Dose: 5 g daily in divided doses.
Description:
Microscopy:
Extract 4 g of sample in alcohol (25 ml x 3) under reflux on a water-bath for 30 min. Filter, concentrate to 10 ml and carry out the thin layer
chromatography. Apply 10 µl of the extract on TLC plate, develop the plate to a distance of 8 cm using toluene : ethyl acetate (5 : 1) as mobile
phase. After development of the plate, allow it to dry in air and examine under ultraviolet light (254 nm). It shows major spots at Rf 0.36, 0.55
(both green), 0.64 (fluorescent blue) and 0.72 (green). Under ultraviolet light (366 nm), it shows major spots at R f, 0.52 and 0.63 (both pale
blue). Spray the plate with vanillin-sulphuric acid reagent followed by heating at 1100 for about 10 min and observe under visible light. The
plate shows major spots at Rf 0.47, 0.62, 0.76 and 0.97 (all grey).
Test for Chloride: Dissolve 1 g of the C£r¸a in 10 ml of deionised water and filter. Acidify the filtrate with dilute nitric acid and add 5 per cent
w/v silver nitrate solution. A curdy white precipitate appears.
Physico-chemical parameters:
Loss on drying at 105 :
0
Not more than 10 per cent, Appendix 2.2.10.
Total ash: Not more than 15 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 1.8 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 34 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 42 per cent, Appendix 2.2.8.
Assay:
Other requirements
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses:Ëdhm¡na (Flatulance with gurgling sound), Gulma (Abdominal lump), Pari¸¡ma¿£la (Duodenal ulcer), Ëmav¡ta
(Rheumatism), H¤droga (Heart disease)
Dose: 5 g daily in divided doses
The medicated Gh¤ta will have the odour, colour and taste of the drugs used in the process. If a considerable amount of milk is
used in the preparation, the Gh¤ta will become thick and may solidify in cold seasons.
Gh¤tas are preserved in good quality of glass, steel or polythene containers. These medicated preparations retain the therapeutic
efficacy for sixteen months.
24. Brahmi ghrutha
24. BRËHMÌ GHÎTA
AFI, Part-I, 6:32
Definition:
BRËHMÌ GHÎTA ¤
is a semisolid preparation made with the ingredients in the formulation composition given below with Gh ta as the basic
ingredient.
Formulation composition:
1. Br¡hm¢ svarasa (br¡hm¢) Bacopa monnieri (Linn.) Wettst. (API-Vol:2/25) (Pl.) 1.536 l
2. Gh¤ta (Gogh¤ta) Clarified butter from cow's milk 768 g
3. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 12 g
4. Marica Piper nigrum Roxb. (API-Vol:1/103) (Fr.) 12 g
5. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 12 g
6. áy¡m¡ (Triv¤t) Operculina turpethum (Linn.) Silva Manso. (API-Vol:3/213) (Rt.) 12 g
7. Triv¤t (áveta Triv¤t) Operculina turpethum (Linn.) Silva Manso. (API-Vol:3/213) (Rt.) 12 g
8. Dant¢ Baliospermum montanum Muell Arg. (API-Vol:3/41) (Rt.) 12 g
9. áa¸khapuÀp¢ Convolvulvus pluricaulis Choisy (API-Vol:2/147) (W.P.) 12 g
10. N¤padruma (Ëragvadha) Cassia fistula Linn (API-Vol:5/8) (Fr.Pulp.) 12 g
11. Saptal¡ Euphorbia dracunculoides Lam (API-Vol:2/150) (Pl.) 12 g
12. K¤mihara (Vi·a´ga) Embelia ribes Burm.f. (API-Vol:1/123) (Fr.) 12 g
Method of preparation:
Take all ingredients of pharmacopoeial quality.
Take fresh Br¡hm¢ and wash thoroughly with water. Grind and filter with muslin cloth to obtain Br¡hm¢ svarasa.
Treat Gh¤ta to prepare M£rchita Gh¤ta (Appendix 6.2.8.2.).
Take the other ingredients (Kalka dravya) numbered 3 to 12, wash, dry, powder and pass through sieve number 85. Transfer the powdered
ingredients to the wet grinder and grind with sufficient quantity of water to prepare a homogeneous blend.
Take M£rchita Gh¤ta in a stainless steel vessel and heat it mildly.
Add increments of Kalka. Stir thoroughly while adding Br¡hm¢ Svarasa in the specified ratio.
Heat for 3 h with constant stirring maintaining the temperature between 500 and 900 during the first hour of heating. Stop heating and allow to
stand overnight. Start the heating next day and observe the boiling mixture for subsidence of froth (phena śānti) and constantly check the kalka
for formation of varti (Madhyama P¡ka LakÀa¸a ).
Expose the varti to flame and confirm the absence of crackling sound indicating absence of moisture. Stop heating when the kalka forms a varti
and the froth subsides. Filter while hot (about 800) through a muslin cloth and allow to cool.
Pack it in tightly closed glass containers to protect from light and moisture.
Description:
A low melting Gh¤ta, green in colour with soft, unctuous touch, pleasant odour and bitter taste.
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter, concentrate to 5 ml and carry out the
thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate :
hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows major spots at Rf 0.15 (both grey), 0.28, 0.40 and 0.51 (all light grey) under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.454 to1.465, Appendix 3.1.
Weight per ml at 400: 0.930g to 0.945g, Appendix 3.2.
Saponification value: 190 to 230, Appendix 3.10.
Iodine value: 30 to 40, Appendix 3.11.
Acid value: Not more than 2, Appendix 3.12
Peroxide value: Not more than 4, Appendix 3.13.
Congealing point: 210 to 170, Appendix 3.4.2.
Other requirements:
Mineral oil: Absent Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeuticuses: Apasm¡ra (Epilepsy), Unm¡da (Insanity), Vandhyatva (Infertility), KuÀ¶ha (Skin disorders), V¡ksvara Bha´ga (Inability
to speak properly), SÆrtikÀaya (Memory loss), Buddhi m¡ndya(Mental retardation)
Dose: 12 to 24 g daily in divided doses.
Formulation composition:
1. Bilva Aegle marmelos Corr (API-Vol:4/10) (Rt./St.Bk.) 307.6 g
2. áyon¡ka Oroxylum indicum Vent. (API-Vol:3/209) (Rt./St.Bk.) 307.6 g
3. Gambh¡r¢ Gmelina arborea Linn (API-Vol:4/31) (Rt./St.Bk.) 307.6 g
4. P¡¶al¡ Stereospermum suaveolens (L.F) DC (API-Vol:4/87) (Rt./St.Bk.) 307.6 g
5. Agnimantha Clerodendrum phlomidis Linn (Premna integrifolia) (API-Vol:3/3) (Rt./St.Bk.) 307.6 g
6. á¡lapar¸¢ Desmodium gangeticum DC. (API-Vol:3/178) (Pl.) 307.6 g
7. P¤¿nipar¸¢ Uraria picta Desv. (API-Vol:4/99) (Pl) 307.6 g
8. B¤hat¢ Solanum indicum Linn (API-Vol:2/27) (Pl.) 307.6 g
9. Ka¸¶ak¡r¢ Solanum surattense Burm.f. (API-Vol:1/59) (Pl.) 307.6 g
10. GokÀura Tribulus terrestris Linn (API-Vol:1/38) (Fr.) 307.6 g
11. Water for decoction Water 12.29 l
reduced to - 3.07 l
12. Gh¤ta (Gogh¤ta ) Clarified butter from cow's milk 768 g
13. PuÀkar¡hv¡ (PuÀkara) Inula racemosa Hook.f (API-Vol:4/102) (Rt.) 12 g
14. áa¶h¢ (áa¶¢) Hedychium spicatum Ham . Ex.Smith (API-Vol:1/99) (Rz.) 12 g
15. Bilva Aegle marmelos Corr. (API-Vol:3/29) (Rt./St.Bk.) 12 g
16. Suras¡ (Tulas¢) Ocimum sanctum Linn (API-Vol:4/128) (Pl.) 12 g
17. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 12 g
18. Marica Piper nigrum Linn. (API-Vol:3/115) (Fr.) 12 g
19. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 12 g
20. Hi´gu -¿uddha Ferula foetida Regel. (API-Vol:1/49) (Exd. ) 12 g
Method of preparation:
Note: Stem bark of the ingredients number 1 to 5 & 15 of the formulation composition has been used.
TreatHi´gu to prepare áodhita Hi´gu (Appendix 6.2.7.12.) and keep aside for addition during Snehap¡ka.
Take the other ingredients (Kalka Dravya) numbered 13 to 19 in the formulation composition, with the exception of Tulas¢, clean, dry, powder
and pass through sieve number 85. Grind Tulasī in a wet grinder.
Transfer all the Kalka dravyas (number 13 to 20) to the wet grinder and grind with sufficient quantity of water to prepare a homogeneous blend
(Kalka).
Take M£rchita Gh¤ta in a stainless steel vessel and heat mildly.
Add increments of Kalka. Stir thoroughly while adding Da¿am£la Kv¡tha.
Heat for 3 h with constant stirring maintaining the temperature between 50 and 900 during the first hour of heating. Stop heating and allow to
stand overnight. Start heating next day and observe the boiling mixture for subsidence of froth (phena śānti) and constantly check the kalka for
formation of varti ( Madhyama P¡ka LakÀa¸a ).
Expose the varti to flame and confirm the absence of crackling sound indicating absence of moisture. Stop heating when the kalka forms a varti
and the froth subsides. Filter while hot (about 800) through a muslin cloth and allow to cool.
Pack it in tightly closed glass containers to protect from light and moisture.
Description:
A low melting Gh¤ta, yellowish green in color with pleasant odour and bitter taste.
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter, concentrate to 5 ml and carry out the
thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene: ethyl acetate:
hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at Rf 0.11 (light grey), 0.38 (light grey), 0.50 (grey), 0.63 (grey), 0.70 (light grey), 0.78 (light
grey) and 0.90 (light grey) under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.450 to 1.453, Appendix 3.1.
Weight per ml at 400: 0.910 g to 0.940 g, Appendix 3.2.
Saponification value: 180 to 210, Appendix 3.10.
Iodine value: 120 to 150, Appendix 3.11.
Acid value: Not more than 3, Appendix 3.12.
Peroxide value: Not more than 6, Appendix 3.13.
Congealing point: 220 to 170 Appendix 3.4.2.
Other requirements:
Mineral oil Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflotoxins: Appendix 2.7.
Storage: Pack it in tightly closed containers to protect from light and moisture.
Therapeutic uses: V¡taja K¡sa (Cough due to V¡ta doÀa), Kaphaja K¡sa (Cough due to Kapha doÀa), V¡takapha Roga (Diseases due to
V¡ta Kapha doÀa), S£tik¡ roga (Puerperal disorders), Hasta P¡da d¡ha (Burning sensation in palms & soles.)
Dose: 12 g daily in divided doses.
Formulation composition:
1. Bilva Aegle marmelos Corr (API-Vol:4/10) (Rt./St.Bk.) 240 g
2. áyon¡ka Oroxylum indicum Vent. (API-Vol:3/209) (Rt./St.Bk.) 240 g
3. Gambh¡r¢ Gmelina arborea Linn (API-Vol:4/31) (Rt./St.Bk.) 240 g
4. P¡¶al¡ Stereospermum suaveolens (L.F) DC (API-Vol:4/87) (Rt./St.Bk.) 240 g
5. Agnimantha Clerodendrum phlomidis Linn (Premna integrifolia) (API-Vol:3/3) (Rt./St.Bk.) 240 g
6. á¡lapar¸¢ Desmodium gangeticum DC. (API-Vol:3/178) (Pl.) 240 g
7. P¤¿nipar¸¢ Uraria picta Desv. (API-Vol:4/99) (Pl.) 240 g
8. B¤hat¢ Solanum indicum Linn (API-Vol:2/27) (Pl.) 240 g
9. Ka¸¶ak¡r¢ Solanum surattense Burm.f. (API-Vol:1/59) (Pl.) 240 g
10. GokÀura Tribulus terrestris Linn (API-Vol:1/38) (Pl.) 240 g
11. Water for decoction Water 12.29 l
reduced to - 3.07 l
12. KÀ¢ra (Godugdha) Cow's milk 3.072 l
13. Pippal¢ Piper longum Linn (API-Vol:4/91) (Fr.) 21.33 g
14. Pippal¢ m£la Piper longum Linn (API-Vol:2/133) (Rt.) 21.33 g
15. Cavya Piper chaba Vahl. (API-Vol:2/29) (Rt.) 21.33 g
16. Citraka Plumbago zeylanica Linn (API-Vol:1/29) (Rt.) 21.33 g
17. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 21.33 g
18. KÀ¡ra (Yava) Hordeum vulgare Linn (API-Vol:2/175) (Ash of Pl.) 21.33 g
19. Sarpi (Gogh¤ta ) Clarified butter from cow's milk 768 g
Method of preparation:
Pulverize Da¿am£la ingredients 1 to 10. (Kv¡tha dravya) to coarse powder, add specified quantity of water, keep for four hours, heat and reduce
the volume to one fourth. Filter with muslin cloth to obtain Da¿am£la Kv¡tha.
Take the other ingredients (Kalka Dravya) numbered 13 to 18 of the formulation composition, powder and pass through sieve number 85.
Transfer the powdered ingredients to wet grinder and grind with sufficient quantity of water to prepare a homogeneous blend (Kalka)
Take M£rchita Gh¤ta in a stainless steel vessel and heat mildly.
Add increments of Kalka. Stir thoroughly while adding Da¿am£la kv¡tha and Godugdha.
Heat for 3 h with constant stirring maintaining the temperature between 500and 900 during the first hour of heating. Stop heating and allow to
stand overnight.
Start heating next day and observe the boiling mixture for subsidence of froth ( Phena ¿¡nti) and constantly check the kalka for formation of varti
(Madhyama p¡ka lakÀa¸a ).
Expose the varti to flame and confirm the absence of crackling sound indicating absence of moisture. Stop heating when the kalka forms a varti
and the froth subsides. Filter while hot (about 800) through a muslin cloth and allow to cool.
Pack it in tightly closed glass containers to protect from light and moisture.
Description:
A low melting Gh¤ta, yellowish green in color with pleasant odour and bitter and astringent taste.
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter and concentrate to 5 ml and carry out
the thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene: ethyl acetate:
hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at Rf 0.12 (grey), 0.19 (grey), 0.35 (grey), 0.71 (light brown), 0.8 (brown) and 0.92 (brown)
under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.448 to 1.530, Appendix 3.1.
Weight per ml at 400: 0.910 g to 0.940g, Appendix 3.2.
Saponification value: 180 to 210, Appendix 3.10.
Iodine value: 30 to 47, Appendix 3.11.
Acid value: Not more than 3, Appendix 3.12.
Peroxide value: Not more than 6, Appendix 3.13.
Congealing point: 220 to 170, Appendix 3.4.2.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Pack it in tightly closed containers to protect from light and moisture.
Therapeutic uses: Agnim¡ndya (Loss of appetite), P¡¸·u (Anaemia), K¡sa (Cough), Aj¢r¸a (Indigestion), Jvara (Fever), Pl¢haroga (Spleen
disease)
Dose: 12 g daily in divided doses.
Formulation composition:
1. Dh¡tr¢ rasa (Ëmalak¢) Phyllanthus emblica (Emblica officinalis Gaertn.) (API-Vol:1/4) P. 768 ml
2. Vid¡r¢ rasa (Vid¡r¢) Pueraria tuberosa DC (API-Vol:2/173) Rt.Tr. 768 ml
3. IkÀu rasa Saccharum officinarum Linn (API-Vol:4/33) St.(Juice) 768 ml
4. áat¡var¢ rasa (áat¡var¢) Asparagus racemosus Willd (API-Vol:4/108) Rt. 768 ml
5. K£Àm¡¸·aka ras (K£Àm¡¸·a) Benincasa hispida (Thunb)Cogn. (API-Vol:4/55) Fr.P. 768 ml
6. Sarpi (Gogh¤ta ) Clarified butter from cow's milk 768 ml
7. KÀ¢ra (Godugdha) Cow's milk 768 ml
8. M¤dv¢k¡ (Dr¡kÀ¡) Vitis vinifera Linn. (API-Vol:3/45) Dr.Fr. 24 g
9. YaÀ¶y¡hvaya (YaÀ¶¢) Glycyrrhiza glabra Linn (API-Vol:1/127) Rt. 24 g
10. Candana (áveta Candana) Santalum album Linn. (API-Vol:3/207) Ht.Wd. 24 g
11. Sit¡ Sugar candy 24 g
Method of preparation:
Description:
Medicated Gh¤ta, greenish yellow in color with pleasant odour and sweet taste.
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter, concentrate to 5 ml and carry out the
thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene: ethyl acetate:
hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at Rf 0.39 (light grey), 0.62 (light grey), 0.68 (light grey), 0.79 (light grey) and 0.88 (light grey)
under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.465 to 1.466, Appendix 3.1.
Weight per ml at 400: 0.910 g to 0.920 g, Appendix 3.2.
Saponification value: 175 to 205, Appendix 3.10.
Iodine value: 35 to 45, Appendix 3.11.
Acid value: Not more than 2, Appendix 3.12.
Peroxide value: Not more than 2, Appendix 3.13.
Congealing point: 210 to 170, Appendix 3.4.2.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Pittaja Gulma (Lump due to Pitta doÀa), Pittaja P¡¸·u (Anemia due to Pitta doÀa), Mada (Intoxication), M£rcch¡
(Syncope), Mad¡ty¡ya (Alcoholism), Unm¡da (Insanity), Raktapitta (Bleeding disorders), As¤gdara (Excessive bledding from vaginal tract),
Vandhyatva (Infertility), V¡tarakta (Gout), Pittavik¡ra (Disorders of Pitta doÀa), Asthi Sr¡va (Discharge from bone)
Dose: 12 g daily in divided doses.
Anupāna: Mixed with equal quantity of sugar and administer with warm milk and warm water.
28. Jaatyaadi ghrutha
28. JËTYËDI GHÎTA (Synonym Vra¸a áodhan¡di Gh¤ta)
AFI, Part-I, 6:11
Definition:
JËTYËDI GHÎTA is a medicated preparation made with the ingredients in the formulation composition given below with Gh¤ta as the basic
ingredient.
Formulation composition:
1. J¡t¢ patra (J¡t¢) Jasminum officinale Linn. Var. grandiflorum (API-Vol:3/71) Lf. 14.76 g
2. Nimba patra Azadirachta indica A. Juss (API-Vol:2/124) Lf. 14.76 g
3. Pa¶ola patra Trichosanthes dioica Lf. 14.76 g
4. Ka¶uk¡ Picrorrhiza kurroa Royle ex Benth. (API-Vol:2/85) Rz. 14.76 g
5. D¡rv¢ (D¡ruharidr¡) Berberis aristata DC (API-Vol:2/33) St. 14.76 g
6. Ni¿¡ (Haridr¡) Curcuma longa Linn. (API-Vol:1/45) Rz. 14.76 g
7. S¡riva (áveta S¡riv¡) Hemidesmus indicus (Linn.) R.Br. (API-Vol:1/107) Rt. 14.76 g
8. MaµjiÀ¶h¡ Rubia cordifolia Linn. (API-Vol:3/112) Rt. 14.76 g
9. Abhaya (U¿¢ra ) Vetiveria zizaniodes (Linn.) Nash. (API-Vol:3/219) Rt. 14.76 g
10. Siktha (Madh£cchiÀ¶a ) Bee's wax 14.76 g
11. Tuttha Copper sulphate 14.76 g
12. Madhuka (YaÀ¶¢) Glycyrrhiza glabra Linn (API-Vol:1/127) Rt. 14.76 g
13. Nakt¡hv¡ (Karaµja) Pongamia pinnata (Linn.) Merr. (API-Vol:1/63) Sd. 14.76 g
14. Sarpi (Gogh¤ta ) Clarified butter from cow's milk 768 g
15. Water Water 3.07 l
Method of preparation:
Pack it in tightly closed glass containers to protect from light and moisture.
Description:
A low melting Gh¤ta, yellowish green in color, unctuous to touch with pleasant odour.
Identification:
Physico-chemical parameters:
0
Refractive index at 40 : 1.452 to 1.464, Appendix 3.1.
Weight per ml at 400: 0.910g to 0.935g, Appendix 3.2.
Saponification value: 190 to 210, Appendix 3.10.
Iodine value: 35 to 45, Appendix 3.11.
Acid value: Not more than 3, Appendix 3.12.
Peroxide value: Not more than 5, Appendix 3.13.
Congealing point: 210 to 170, Appendix 3.4.2.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: For local application in Marm¡¿rita vra¸a (Ulcers in vital points), Kled¢ Vra¸a (Oozing / weeping ulcer), Gambh¢ra
Vra¸a (Deep-rooted ulcers), Saruja Vra¸a (Painful ulcers), Raktaja Vra¸a (Bleeding ulcers), DuÀ¶a vra¸a (Non-healing ulcers)
Dose: For application on various types of wounds and ulcers.
29. Kalyaanaka ghrutha
29. KALYËÛAKA GHÎTA
AFI, Part-I, 6:7
Definition:
KALYËÛAKA GHÎTA is a medicated preparation made with the ingredients in the formulation composition given below with Gh¤ta as the
basic ingredient.
Formulation composition:
1. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) P. 12 g
2. Bibh¢taka Terminalia belerica Roxb. (API-Vol:1/26) P. 12 g
3. Ëmalak¢ Phyllanthus emblica (Emblica officinalis Gaertn.) (API-Vol:1/4) P. 12 g
4. Vi¿¡l¡ (Rakta Indrav¡ru¸¢) Citrullus colocynthis Schrad. (Official Substitute) (API-Vol:3/65) Fr. 12 g
5. Bhadrail¡ (Sth£lail¡) Amomum subulatum Roxb (API-Vol:2/158) Sd. 12 g
6. Devad¡ru Cedrus deodara (Roxb.) Loud (API-Vol:4/23) Ht.Wd 12 g
7. Elav¡luka Prunus avium Linn.f. (API-Vol:5/31) St.Bk 12 g
8. áveta S¡riv¡ Hemidesmus indicus (Linn.) R.Br. (API-Vol:1/107) Rt. 12 g
9. K¤À¸a S¡riv¡ Cryptolepis buchanani Roem & Schult (API-Vol:4/47) Rt. 12 g
10. Haridr¡ Curcuma longa Linn. (API-Vol:1/45) Rz. 12 g
11. D¡ruharidr¡ Berberis aristata DC (API-Vol:2/33) St. 12 g
12. á¡lapar¸¢ Desmodium gangeticum DC. (API-Vol:3/178) Rt. 12 g
13. P¤¿nipar¸¢ Uraria picta Desv. (API-Vol:4/99) Rt. 12 g
14. Phalin¢ (Priya´gu) Callicarpa macrophylla Vahl (API-Vol:2/143) Infl. 12 g
15. Nata (Tagara) Valeriana wallichii (API-Vol:1/109) Rt 12 g
16. B¤hat¢ Solanum indicum Linn (API-Vol:2/27) Pl. 12 g
17. Ku˦ha Saussurea lappa CB. Clarke (API-Vol:1/76) Rt 12 g
18. MaµjiÀ¶h¡ Rubia cordifolia Linn. (API-Vol:3/112) St 12 g
19. N¡gakesara Mesua ferrea Linn (API-Vol:2/118) Stmn. 12 g
20. D¡·ima - Phala tvak Punica granatum Linn (API-Vol:4/16) P. 12 g
21. Vella (Vi·a´ga) Embelia ribes Burm.f. (API-Vol:1/123) Fr. 12 g
22. T¡l¢sapatra (T¡l¢sa) Abies webbiana Lindl (API-Vol:4/126) Lf. 12 g
23. El¡ (S£kÀmail¡) Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) Sd. 12 g
24. M¡lat¢ mukula (J¡t¢) Jasminum officinale Linn. Var. grandiflorum (API-Vol:3/71) Fl. 12 g
25. Utpala Nymphaea stellata Willd. (API-Vol:3/221) Fl. 12 g
26. Dant¢ Baliospermum montanum Muell Arg. (API-Vol:3/41) Rt 12 g
27. Padmaka Prunus cerasoides D.Don. (API-Vol:3/145) Ht. Wd 12 g
28. Hima (Rakta Candana) Pterocarpus santalinus Linn. (API-Vol:3/155) Ht. Wd 12 g
29. Sarpi (Gogh¤ta ) Clarified butter from cow's milk 768 g
Method of preparation:
Description:
A low melting Gh¤ta, yellowish green in color with pleasant odour and bitter taste.
Identification:
Physico-chemical parameters:
0
Refractive index at 40 : 1.450 to 1.461, Appendix 3.1.
Weight per ml at 400: 0.920g to 0.940g, Appendix 3.2.
Saponification value: 180 to 210, Appendix 3.10.
Iodine value: 33 to 45, Appendix 3.11.
Acid value: Not more than 4.5, Appendix 3.12.
Peroxide value: Not more than 6, Appendix 3.13.
Congealing point: 220 to 170, Appendix 3.4.2.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Absent, Appendix 2.4.
Aflatoxins: Absent, Appendix 2.7.
Storage: Pack it in tightly closed containers to protect from light and moisture.
Therapeutic uses: K¡sa (Cough), P¡¸·u (Anaemia), Apasm¡ra (Epilepsy), Bh£tonm¡da (Exogenous psychosis), B¡lagraha (Specific
disorders of children), ViÀavik¡ra (Disorders due to poison), Gara ViÀa (Slow/accumulated poison), Vandhyatva (Infertility), Yoni Roga
(Diseases of the female genital tract), Ka¸·£ (Itching), áopha (Oedema), Meda (Adipose tissue), Moha (Delusion), Jvara (Fever), Sm¤ti
Daurbalya (Weak memory) and Daurbalya.
Dose: 12 g daily in divided doses.
Formulation composition:
1. Gomaya svarasa Water extract of fresh cow dung 3.07 l
2. KÀ¢ra (Godugdha) Cow's milk 3.07 l
3. Dadhi (Godadhi) Curd from cow's milk 3.07 kg
4. M£tra (Gom£tra) Urine of cow 3.07 l
5. Havi (Gogh¤ta) Clarified butter from cow's milk 768 g
Method of preparation:
Description:
A low melting Gh¤ta, light yellow in color with phenolic odour.
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter, concentrate to 5 ml and carry out the
thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene: ethyl acetate:
hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at Rf 0.15 (light grey), 0.22 (brownish grey), 0.30 (light grey), 0.50 (light grey), 0.63 (brownish
grey), 0.70 (grey) and 0.82 (brownish grey) under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.450 to 1.455, Appendix 3.1.
Weight per ml at 400: 0.915 g to 0.950 g, Appendix 3.2.
Saponification value: 200 to 225, Appendix 3.10.
Iodine value: 35 to 45, Appendix 3.11.
Acid value: Not more than 3, Appendix 3.12.
Peroxide value: Not more than 2, Appendix 3.13.
Congealing point: 210 to 170, Appendix 3.4.2.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Apasm¡ra (Epilepsy), Jvara (Fever), Unm¡da (Insanity), K¡mal¡ (Jaundice)
Dose: 12 g daily in divided dose.
Formulation composition:
1. Nimba Azadirachta indica A.Juss (API-Vol:5/119) St.Bk. 480 g
2. Pa¶ola Trichosanthes dioica Lf. 480 g
3. Vy¡ghr¢ (Ka¸¶ak¡r¢) Solanum surattense Burm.f. (API-Vol:1/59) Pl. 480 g
4. Gu·£c¢ Tinospora cordifolia (Willd.) Miers. (API-Vol:1/41) St. 480 g
5. V¡saka (V¡s¡) Adhatoda vasica Medic (API-Vol:4/138) Rt. 480 g
6. Water for decoction Water 12.29 l
reduced to 3.07 l
7. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) P. 128 g
8. Bibh¢taka Terminalia bellerica Roxb. (API-Vol:1/26) P. 128 g
9. Ëmalak¢ Phyllanthus emblica (Emblica officinalis Gaertn.) (API-Vol:1/4) P. 128 g
10. Gh¤ta (Gogh¤ta) Clarified butter from cow's milk 768 g
Method of preparation:
Description:
A low melting Gh¤ta, greenish yellow color with pleasant odour and bitter taste.
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter concentrate to 5 ml and carry out the
thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene: ethyl acetate:
hexane (6: 3: 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at Rf 0.13 (light grey), 0.20 (light grey), 0.28 (light grey), 0.37 (light grey), 0.57 (light grey) and
0.89 (brown) under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.450 to 1.452, Appendix 3.1.
Weight per ml at 400: 0.910 g to 0.930 g, Appendix 3.2.
Saponification value: 180 to 210, Appendix 3.10.
Iodine value: 30 to 40, Appendix 3.11.
Acid value: Not more than 3, Appendix 3.12.
Peroxide value: Not more than 3, Appendix 3.13.
Congealing point: 210 to 170 Appendix 3.4.2.
Other requirements:
Therapeutic uses: DuÀ¶a vra¸a (Non-healing ulcers), KuÀ¶ha (Leprosy/skin diseases), V¡tavy¡dhi (Disorders due to vitiated V¡ta doÀa),
Pittavy¡dhi (Diseases due to vitiated Pitta doÀa), Kaphavik¡ra (Disorders due to vitiated Kapha doÀa), K¤mi (Worm infestation), Ar¿a (Piles
and), K¡sa (Cough)
Dose: 12 g daily in divided doses.
Anupāna: Warm milk, Warm water.
32. Phala ghrutha
32. PHALA GHÎTA
AFI, Part-I, 6:30
Definition:
PHALA GHÎTA is a medicated preparation made with the ingredients in the formulation composition given below with Gh¤ta as the basic
ingredient.
Formulation composition:
1. MaµjiÀ¶h¡ Rubia cordifolia Linn. (API-Vol:3/112) Rt. 12 g
2. Ku˦ha Saussurea lappa CB. Clarke (API-Vol:1/76) Rt. 12 g
3. Tagara Valeriana wallichii (API-Vol:1/109) Rt. 12 g
4. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) P. 12 g
5. Bibh¢taka Terminalia bellerica Roxb. (API-Vol:1/26) P. 12 g
6. Ëmalak¢ Phyllanthus emblica (Emblica officinalis Gaertn.) (API-Vol:1/4) P. 12 g
7. áarkar¡ Sugar 12 g
8. Vac¡ Acorus calamus Linn (API-Vol:2/168) Rz. 12 g
9. Haridr¡ Curcuma longa Linn. (API-Vol:1/45) Rz. 12 g
10. D¡ruharidr¡ Berberis aristata DC (API-Vol:2/33) St. 12 g
11. Madhuka (YaÀ¶¢) Glycyrrhiza glabra Linn (API-Vol:1/127) Rt. 12 g
12. Med¡ Asparagus racemosus (Official substitute) Rt.Tr. 12 g
13. D¢pyaka (Yav¡ni) Trachyspermum ammi (Linn.) Sprague ex Turril. (API-Vol:1/129) Fr. 12 g
14. Ka¶urohi¸¢ (Ka¶uk¡) Picrorhiza kurroa Royle ex Benth. (API-Vol:2/85) Rz./ Rt.12 g
15. Payasy¡ (K¿ira Vid¡r¢) Ipomoea digitata Linn. (API-Vol:5/88) Rt.Tr. 12 g
16. Hi´gu Ferula foetida Regel. (API-Vol:1/49) Exd. 12 g
17. K¡kol¢ Lilium polyphyllum D.Don.
[Withania somnifera (Official substitute)] (API-Vol:3/79) Rt. 12 g
18. V¡jigandh¡ (A¿vagandh¡) Withania somnifera Dunal (API-Vol:1/15) Rt. 12 g
19. áat¡var¢ Asparagus racemosus Willd (API-Vol:4/108) Rt.Tr. 12 g
20. Gh¤ta (Gogh¤ta) Clarified butter from cow milk 768 g
21. KÀ¢ra (Godugdha) Cow's milk 3.072 l
Method of preparation:
After complete cooling add powdered sugar, stir vigorously for dissolution.
Pack it in tightly closed glass containers to protect from light and moisture.
Description:
A low melting Gh¤ta, greenish yellow in color with pleasant odour and astringent taste.
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter, concentrate to 5 ml and carry out the
thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate :
hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at R f 0.094 (light grey), 0.19 (light grey), 0.25 (light grey), 0.28 (light grey), 0.53 (light grey),
0.80 (light grey) and 0.97 (brownish grey) under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.440 to 1.450, Appendix 3.1.
Weight per ml at 400: 0.910g to 0.940g, Appendix 3.2
Saponification value: 185 to 210, Appendix 3.10.
Iodine value: 35 to 42, Appendix 3.11.
Acid value: Not more than 3, Appendix 3.12.
Peroxide value: Not more than 4, Appendix 3.13.
Congealing point: 220 to 170 Appendix 3.4.2.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: áukra Vik¡ra (Disorders of the áukra dh¡thu), Yoni Vik¡ra (Disorders of female genital tract), Vandhyatva (Infertility),
Garbhi¸¢roga (Diseases during pregnancy), K¡r¿ya (Emaciation), Uttara Vasti (Vaginal Douche)
Dose: 12 g daily in divided doses.
Formulation composition:
1. Aj¡kÀ¢ra Goat's milk 3.07 l
2. Abhay¡ (Har¢tak¢) Terminalia chebula Retz. (API-Vol:1/47) P. 24 g
3. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) Rz. 24 g
4. Marica Piper nigrum Linn. (API-Vol:3/115) Fr. 24 g
5. Pippal¢ Piper Longum Linn (API-Vol:4/91) Fr. 24 g
6. P¡¶h¡ Cissampelos pareira Linn (API-Vol:1/92) Rt. 24 g
7. Ugr¡ (Vac¡) Acorus calamus Linn (API-Vol:2/168) Rz. 24 g
8. áigru Moringa oleifera Lam (API-Vol:4/110) Rt.Bk. 24 g
9. Saindhava lava¸a Rock Salt 24 g
10. Water Water 3.07 l
11. Sarpi (Gogh¤ta) Clarified butter from cow's milk 768 g
Method of preparation:
Description:
A low melting Gh¤ta, greenish yellow in color with pleasant odour and bitter taste.
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 40 0 for 3 h. Cool, separate the alcohol layer, filter, concentrate to 5 ml and carry out the
thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate :
hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows eight spots at R f 0.09 (light grey), 0.29 (light grey), 0.42 (grey), 0.52 (brown), 0.55 (light grey), 0.59
(light grey), 0.66 (grey) and 0.69 (light grey) under visible light.
Physico-chemical parameters:
Refractive index at 400: 1.450 to 1.453, Appendix 3.1.
Weight per ml at 400: 0.910g to 0.940g, Appendix 3.2.
Saponification value: 180 to 210, Appendix 3.10.
Iodine value: 40 to 53, Appendix 3.11.
Acid value: Not more than 3.5, Appendix 3.12.
Peroxide value: Not more than 5, Appendix 3.13.
Congealing point: 210 to 170 Appendix 3.4.2.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Improves V¡k (Speech), Medh¡ (Intelligence), Sm¤ti (Memory), J¡¶har¡gni (Appetite)
Dose: 12 g daily in divided dose.
Formulation composition:
1. Trika¸¶aka (GokÀura) Tribulus terrestris Linn (API-Vol:1/40) Fr. 768 g
2. Water for decoction Water 12.29 l
reduced to 3.07 l
3. El¡ (S£kÀmail¡) Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) Sd. 9.14 g
4. Girijatu (áil¡jatu) Exd. From rock crevices 9.14 g
5. áil¡bheda (PaÀ¡¸abheda) Bergenia ciliata (Haw) Sternb. (API-Vol:1/90) Rz. 9.14 g
6. YaÀ¶¢ Glycyrrhiza glabra Linn (API-Vol:1/127) Rt. 9.14 g
7. Var¢ (áat¡var¢) Asparagus racemosus Willd (API-Vol:4/108) Rt. 9.14 g
8. Darbha Imperata cylindrica (Linn) Beauv. (API-Vol:5/21) Rt. 9.14 g
9. Dr¡kÀ¡ Vitis vinifera Linn. (API-Vol:3/45) Dr. Fr. 9.14 g
10. Ambu (Hr¢v®ra) Coleus vettiveroides Rt. 9.14 g
11. áau¸·¢ (Pippal¢) Piper Longum Linn (API-Vol:4/91) Fr. 9.14 g
12. Vasuka Calotropis procera (Ait.) R.Br. (Official substitute) (API-Vol:1/8) Pl. 9.14 g
13. Va¿ira (Cavya) Piper chabaVahl. (API-Vol:2/29) Rt. 9.14 g
14. K¡¿a Saccharaum spontaneum Linn. (API-Vol:3/88) Rt. 9.14 g
15. IkÀu M£la Saccharum officinale Linn (API-Vol:4/33) Rt. 9.14 g
16. Matsy¡kÀik¡ (Matsy¡kÀ¢) Alternanthera sessilis (Lilnn.) R.Br (API-Vol:2/104) Pl. 9.14 g
17. Dugdha (Godugdha ) Cow's milk 768 g
18. Gh¤ta (Gogh¤ta) Calrified butter from cow's milk 768 g
Method of preparation:
Description: A low melting Gh¤ta, greenish in color with pleasant odour and bitter taste.
Identification:
Thin layer chromatography:
Extract 2 g ofTrika¸¶aka Gh¤ta with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter, concentrate to 5 ml and carry
out the thin layer chromatography. Apply 10 µl of the extract on TLC plate. Develop the plate to a distance of 8 cm using toluene : ethyl acetate
: hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at Rf 0.33 (brown), 0.62 (yellow), 0.68 (grey), 0.80 and 0.90 (light brown) under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.451 to 1.452, Appendix 3.1.
Weight per ml at 400: 0.910g to 0.930g, Appendix 3.2.
Saponification value: 200 to 225, Appendix 3.10.
Iodine value: 35 to 45, Appendix 3.11.
Acid value: Not more than 4, Appendix 3.12.
Peroxide value: Not more than 5, Appendix 3.13.
Congealing point: 220 to 180 Appendix 3.4.2.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: M£trak¤cchra (Dysuria), Prameha (Metabolic disorder), A¿mar¢ (Urinary calculus), M£tra áarkar¡ (Gravel in urine), M
£tradoÀa (Urinary disorders), M£tr¡d¡ha (Burning micturition)
Dose: 12 g daily in divided doses.
Formulation composition:
1. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) P. 12 g
2. Bibh¢taka Terminalia bellerica Roxb. (API-Vol:1/26) P. 12 g
3. Ëmalak¢ Phyllanthus emblica (Emblica officinalis Gaertn.) (API-Vol:1/4) P. 12 g
5. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) Rz. 12 g
6. Marica Piper nigrum Linn. (API-Vol:3/115) Fr. 12 g
7. Pippal¢ Piper Longum Linn (API-Vol:4/91) Fr. 12 g
8. Dr¡kÀ¡ Vitis vinifera Linn. (API-Vol:3/45) Dr.Fr. 12 g
9. Madhuka (YaÀ¶¢) Glycyrrhiza glabra Linn (API-Vol:1/127) Rt. 12 g
10. Ka¶urohi¸¢ (Ka¶uk¡) Picrorhiza kurroa Royle ex Benth. (API-Vol:2/85) Rz./Rt 12 g
11. Prapau¸·ar¢ka Nelumbo nucifera Gaertn (API-Vol:2/69) Fl. 12 g
12. S£kÀmail¡ Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) Sd. 12 g
13. Vi·a´ga Embelia ribes Burm.f. (API-Vol:1/123) Fr. 12 g
14. N¡gak®¿ara Mesua ferrea Linn (API-Vol:2/118) Stmn. 12 g
15. N¢l°tpala (Utpala) Nymphaea stellata Willd. (API-Vol:3/221) Fl. 12 g
16. áveta S¡riv¡ Hemidesmus indicus (Linn.) R.Br. (API-Vol:1/107) Rt. 12 g
17. K¤Àna S¡riv¡ Cryptolepis buchanani Roem & Schult (API-Vol:4/47) Rt. 12 g
18. Candana (áveta Candana) Santalum album Linn. (API-Vol:3/207) Ht.Wd 12 g
19. Haridr¡ Curcuma longa Linn. (API-Vol:1/45) Rz. 12 g
20. D¡ruharidr¡ Berberis aristata DC (API-Vol:2/33) St. 12 g
21. Gh¤ta (Gogh¤ta) Clarified butter from cow's milk 768 g
22. Payasa (Godugdha) Cow's milk 768 g
23. *Triphal¡ rasa kvatha Kv¡tha of Emblica officinalis, Terminalia chebula, Terminalia bellirica 2.3 l
* Equal parts of Har¢tak¢, Ëmalak¢ and Bibh¢taka.
Method of preparation:
Take all ingredients of pharmacopoeial quality.
Wash and dry all the herbal raw materials thoroughly.
Take the other ingredients numbered 1 to 19 in the formulation composition ( Kalka dravya), powder and pass through sieve number 85. Transfer
the powdered ingredients to wet grinder and grind with sufficient quantity of water to prepare a homogeneous blend (Kalka)
Take M£rchita Gh¤ta in a stainless steel vessel and heat it mildly. Add increments of Kalka. Stir thoroughly while adding Triphal¡ kvatha and
Godugdha in the specified ratio.
Heat for 3 h with constant stirring maintaining the temperature between 500 and 900 during the first hour of heating. Stop heating and allow to
stand overnight.
Start heating next day and observe the boiling mixture for subsidence of froth ( Phena ¿¡nti) and constantly check the Kalka for formation of
varti (Madhyama p¡ka lakÀa¸a).
Expose the varti to flame and confirm the absence of crackling sound indicating absence of moisture. Stop heating when the Kalka forms into a
varti and the froth subsides. Filter while hot (about 800) through a muslin cloth and allow to cool.
Pack it in tightly closed glass containers to protect from light and moisture.
Description:
A low melting Gh¤ta, green in colour, unctuous to touch with pleasant odour and bitter taste.
Identification:
Physico-chemical parameters:
0
Refractive index at 40 : 1.452 to 1.455, Appendix 3.1.
Weight per ml at 400: 0.910g to 0.935g, Appendix 3.2.
Saponification value: 200 to 225, Appendix 3.10.
Iodine value: 35 to 45, Appendix 3.11.
Acid value: Not more than 3, Appendix 3.12.
Peroxide value: Not more than 5, Appendix 3.13.
Congealing point: 210 to 170 Appendix 3.4.2
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Arbuda (Tumours), K¡mal¡ (Jaundice), Timira (Cataract), Visarpa (Erysipelas), Pradara (Excessive vaginal discharge),
Netraruj¡(Pain in eyes), Netrasr¡va (Lacrimation), K¡sa (Cough), Ka¸·£ (Itching), Rakta DoÀa (Disorders of Blood), ávayathu (Oedema),
Kh¡litya (Alopecia), Ke¿a Patana (Falling of hair), ViÀama Jvara (Intermittent fever), Arma (Pterygium), áukla Netra Roga (Eye disorders
related to sclera), Vartma Roga (Disorders of eyelids)
Dose: 12 g daily in divided doses. It can also be used in different Netra Kriyā kalpas.
Guggulu is an exudate (Niry¡sa) obtained from the plant Commiphora mukul. Preparations having the exudates as main effective
ingredient are known as Guggulu. There are five different varieties of Guggulu described in the Ayurvedic texts. However two of the varieties,
namely, MahiÀ¡kÀa and Kanaka Guggulu are usually preferred for medicinal preparations. MahiÀ¡kÀa Guggulu is dark greenish brown and
Kanaka Guggulu is yellowish brown in color.
Before using, Guggulu is cleaned in the following manner:
1.Sand, stone, plant debris, glass etc. are first removed.
2.It is then broken into small pieces.
3.It is thereafter bundled in a piece of cloth and boiled in Dol¡ Yantra containing
any one of the following fluids.
a. Gom£tra,
b. Triphal¡ kaÀ¡ya.,
c. Nirgu¸·¢ patra Svarasa with Haridr¡ C£r¸a,
d. V¡s¡patra KaÀ¡ya,
e. V¡s¡patra Svarasa and
f. Dugdha.
The boiling of Guggulu in Dol¡ Yantra is carried on until all the Guggulu passes into the fluid through the cloth. By pressing with
fingers, much of the fluid that can pass through is taken out. The residue in the bundle is discarded. The fluid is filtered and again boiled till it
forms a mass. This mass is dried and then pounded with a pestle in a stone mortar, adding ghee in small quantities till it becomes waxy.
Guggulucleaned as above, is soft, waxy and brown in color. Characteristics of preparations of Guggulu vary depending on the other
ingredients added to the preparations.
Guggulu is kept in glass or porcelain jars free from moisture and stored in a cool place. The potency is maintained for two years when
prepared with ingredients of plant origin and indefinitely when prepared with metals and minerals.
36. Kaishore guggulu
36. KAIáORA GUGGULU (Va¶¢)
AFI, Part-I, 5:2
Definition:
KAIáORA GUGGULU is a Va¶¢ preparation made with the ingredients in the formulation composition given below with Guggulu as the
basic ingredient.
Formulation composition:
1. Guggulu - ¿uddha Commiphora wightii (Arn.) Bhand. (API-Vol:1/43) Exd.768 g
2. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) P. 256 g
3. Bibh¢taka Terminalia bellerica Roxb. (API-Vol:1/26) P. 256 g
4. Ëmalak¢ Phyllanthus emblica (Emblica officinalis Gaertn.) (API-Vol:1/4) P. 256 g
5. Chinnaruh¡ (Gu·£c¢) Tinospora cordifolia (Willd.) Miers. (API-Vol:1/41) St. 1.54 kg
6. Water for decoction Water 12.29 1
reduced to 6.14 1
7. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) P. 8 g
8. Bibh¢taka Terminalia bellerica Roxb. (API-Vol:1/26) P. 8 g
9. Ëmalak¢ Phyllanthus emblica (Emblica officinalis Gaertn.) (API-Vol:1/4) P. 8 g
10. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) Rz. 24 g
11. Marica Piper nigrum Linn. (API-Vol:3/115) Fr. 24 g
12. Pippal¢ Piper longum Linn (API-Vol:4/91) Fr. 24 g
13. K¤miripu (Vi·a´ga) Embelia ribes Burm.f. (API-Vol:1/123) Fr. 24 g
14. Triv¤t Operculina turpethum (Linn.) Silva Manso. (API-Vol:3/213) Rt. 12 g
15. Dant¢ Baliospermum montanum Muell Arg. (API-Vol:3/41) Rt. 12 g
16. Am¤t¡ (Gu·£c¢) Tinospora cordifolia (Willd.) Miers. (API-Vol:1/41) St. 48 g
17. Gh¤ta (Gogh¤ta) Calrified butter from cow's milk 384 g
Method of preparation:
Pack it in tightly closed glass containers to protect from light and moisture.
Description:
Spherical pills, dark brown in color with pleasant odour, taste astringent and sweetish.
Identification:
Microscopy:
Take about 5 g of the sample, powder it and add n-hexane (20 ml), stir for 10 min thoroughly over a water-bath; pour out hexane. Repeat the
process thrice adding fresh quantities of hexane; discard hexane. Wash the sediment in hot water thoroughly. Take a few mg of the washed
material, stain with iodine solution and mount in 50 per cent glycerine. Clarify a few mg with chloral hydrate and mount in 50 per cent
glycerine. Observe the following characters in different mounts.
Groups of parenchymatous epidermal cells having beaded walls, several showing a thin cross wall, crisscross layer of sclerenchymatous fibres
(Har¢tak¢); short, unicellular, thick walled trichomes with sharp tips and bulbous bases and fragments of polyhedral epidermis showing
cicatrices (Bibh¢taka); thin walled cells of epidermal tissue with paracytic stomata and containing silica crystals, brachysclereids with pitted
wide lumen, parenchymatous tissue with large irregular thick walled cells showing corner thickenings (Ëmalak¢); groups of parenchymatous
cells, densely packed with starch grains, isolated starch grains, simple, oval to rod shaped, measuring 15 to 70 μ in length, hilum eccentric,
lamellae distinct, yellow coloured oleo-resin cells, non-lignified, septate fibres some of them bearing marks of adjacent cells pressing against
them, 30 to 50 μ broad ( Su¸¶h¢); fragments of inner epidermis in surface view with group of stone cells, interspersed amidst parenchyma
( Marica
); spindle shaped or elongated stone cells showing narrow boundary and broad lumen isolated or in groups of 2 to 8 ( Pippal¢ ); groups of
polygonal, non lignified, thick walled brown coloured cells of testa in surface view, palisade like thick walled cells of testa in transverse view
measuring 55 to 80 µ in length and 15 to 30 µ in width, thick walled polygonal cells filled with yellowish brown content of mesocarp cells
almost square in shape, measuring 25 to 45 µ in dia ( Vi·a´ga); cortical parenchymatous cells containing rosette crystals of calcium oxalate,
broken, thick rod-like cellulosic fibres, fragments of typically honeycomb like pitted vessels, resin canals lined with epithelium (Triv¤t); cork
cells in surface and transverse view several with tannin or red colouring matter (Dant¢); parenchymatous cells filled with starch grains, starch
grains abundant, single and compound, ovoid, elliptical, hilum, mostly irregular in shape, measuring 5 to 10 µ in dia, fragments of bordered
pitted vessels ( Gu·£c¢).
Thin layer chromatography:
Extract 5 g of powdered vatis (vatti powder) in 75 ml of n- hexane under reflux on a water-bath for 30 min. Filter and concentrate the extract to
10 ml and carry out the thin layer chrmotography. Apply 10 µl of n-hexane extract on TLC plate and develop the plate to a distance of 8 cm
using n-hexane : ethyl acetate (8.5 : 1.5) as mobile phase. After development, allow the plate to dry in air and examine under ultraviolet light
(366 nm). It shows major spots at Rf 0.10, 0.17 (both blue), 0.25 (fluorescent blue) and 0.46 (blue).
Physico-chemical parameters:
Loss on drying: Not more than 13.0 per cent Appendix 2.2.10.
Total ash: Not more than 9.0 per cent Appendix 2.2.3.
Acid-insoluble ash: Not more than 2.0 per cent Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 40.0 per cent Appendix 2.2.7.
Water-soluble extractive: Not less than 34.0 per cent Appendix 2.2.8.
pH (1% aqueous solution): 4.0 to 4.5 Appendix3.3.
Other requirements:
Therapeutic uses: Mand¡gni (Dyspepsia), Vibandha (Constipation), V¡ta¿o¸ita (Gout), Pramehapi·aka (Diabetic carbuncle), Vra¸a
(Ulcer), K¡sa (Cough), KuÀ¶ha (Diseases of Skin), Gulma (Abdominal lump), ávayathu (Oedema), P¡¸·u (Anaemia), Meha (Excessive flow
of urine),
Jar¡d°Àa (Geriatric disorder)
Dose: 3 g daily in divided doses.
Spherical, soft, blackish brown coloured pills with pleasant odour and sweet taste.
Identification:
Microscopy:
Take about five pills, crush, wash with water, clear in chloral hydrate, wash in water and mount in glycerin (80 per cent) and observe the
following characters:
Group of isodiameric or slightly elongated stone cells with moderately thickened walls, interspersed with thin walled polygonal parenchyma
Marica); groups of elongated, spindle shaped, wide lumened lignified stone cells (Pippal¢); groups of stone cells, oval shape, striated walls
cells (
with minute central lumen (D¡·ima).
Extract 5 g of the powdered pills with 70 ml of ethanol in soxhlet apparatus on a water-bath for 6 h, filter and carry out thin layer
chromatography. Apply 7.5 µl of the extract on TLC plate. Develop the plate to a distance of 8 cm using ethyl acetate : n-hexane : formic acid
(4 : 6 : 0.1) as mobile phase. After development, allow the plate to dry in air and examine under ultraviolet light (254 nm). It shows major spots
at Rf 0.14, 0.20 and 0.34 (fluorescent green). Spray the plate with anisaldehyde- sulphuric acid reagent and heat at 1100 for about 10 min. The
plate shows major spots at Rf 0.80 (blue), 0.65 (light violet), 0.52 (violet) and 0.11 (green) under visible light.
Physico-chemical parameters:
Loss on drying at 110 :
0
Not more than 10 per cent, Appendix 2.2.10.
Total ash: Not more than 6 per cent, Appendix 2.2.3.
Acid-insoluble ash: Not more than 1 per cent, Appendix 2.2.4.
Alcohol-soluble extractive: Not less than 9 per cent, Appendix 2.2.7.
Water-soluble extractive: Not less than 46 per cent, Appendix 2.2.8.
Assay:
Not less than 2.83 per cent of piperine when assayed by the following method.
Estimation of Piperine: Dissolve 2.5 mg of piperine in a mixture of methanol : chloroform (1 : 1) and make up the volume to 25 ml in a
volumetric flask. Apply 2, 5, 8, 11, 14, 17 µl of solution on TLC plate and develop the plate a distance of to 8 cm using acetone : n-hexane (3 :
7) as mobile phase. After development, dry the plate in a current of hot air and scan in the TLC scanner at a wavelength of 338 nm. Note the
peak area and prepare the calibration curve by plotting peak area vs concentration of piperine.
Extract accurately weighed about 6 g powder of vatis in 100 ml of alcohol in a Soxhlet apparatus for 6 h. Filter the extract while hot and dry
completely and weigh. Take 25 mg of extract in a volumetric flask and dissolve in a mixture of methanol : chloroform (1 : 1) and make up the
volume to 25 ml. Apply 3 µl of the test solutions on TLC plate. Develop, dry and scan the plate as described in the proceeding paragraph for
calibration curve of piperine. Record area under the curve for a peak corresponding to piperine in the test solution. Calculate the amount of
piperine in the test solution from the calibration curve of piperine.
Other requirements:
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Description:
Fine powder, passing through sieve number 100; hygroscopic, odour faint and taste saline; freely soluble in water.
Identification:
An aqueous solution yields the reactions characteristic of sodium and potassium, Appendix 5.2.12.
Physico-chemical parameters:
0
Loss on drying at 110 : Not more than 4 per cent, Appendix 2.2.10.
Acid-insoluable ash : Not more than 1 per cent, Appendix 2.2.4.
pH (10%aqeous solution) : 10 to 11, Appendix 3.3.
Assay:
Sodium : Not less than 4 per cent, Appendix 5.2.9.
Potassium : Not less than 29 per cent, Appendix 5.2.9.
Iron : Not less than 1.2 per cent, Appendix 5.2.5.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Gulma (Abdominal lump), Udara á£la (Pain in the abdomen), Graha¸¢ (Malabsorption syndrome), ViÀ£cik¡ (Gastro-
enteritis with piercing pain), Alasaka (Intestinal atony), Aj¢r¸a (Dyspepsia), Aruc¢ (Tastelessness), Ën¡ha (Distention of abdomen due to
obstruction to passage of urine and stool), Ar¿a (Piles), áarkar¡(Gravel in urine), A¿mar¢ (Urinary calculus), K¤mi (Helminthiasis),
Antarvidradhi (Hernia), áv¡sa (Asthma)
Dose: 125 to 500 mg daily in divided dose.
Anupāna: Water.
39. Arka lavana
39. ARKA LAVAÛA
AFI, Part-I, 10:1
Definition:
ARKA LAVAÛA is a preparation made with the ingredients in the formulation composition given below.
Formulation composition:
1. Arka patra (Arka) Calotropis procera (Ait.) R.Br. (API-Vol:1/10) Lf. 1 part
2. Lava¸a (Saindhava Lava¸a) Rock Salt 1 part
Method of Preparation:
Description:
A fine powder, passing through sieve number 100; grey in colour, odourless, taste salty.
Identification:
An aqueous solution yields reactions characteristic of sodium, potassium, calcium, chloride and sulphate, Appendix 5.2.12.
Physico-chemical parameters:
0
Loss on drying at 110 : Not more than 1 per cent, Appendix 2.2.10.
Acid- insoluble ash: Not more than 3 per cent, Appendix 2.2.4.
pH (10% aqueous solution): 9 to 10, Appendix 3.3.
Assay:
Sodium: Not less than 31 per cent, Appendix 5.2.9.
Potassium: Not less than 0.3 per cent, Appendix 5.2.9.
Iron: Not less than 0.11 per cent, Appendix 5.2.5.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Gulma (Abdominal lump), Udara Roga (Diseases of abdomen), Pl¢hodara (Splenomegaly), Yak¤todara (Enlargement of
Liver)
Dose: 1g daily in divided doses.
Description:
Fine powder, passing through sieve number 100; hygroscopic, odour less, taste salty.
Identification:
i) An aqueous solution yields the reactions characteristic of sodium, potassium, carbonate, sulphate, chloride and bicarbonate, Appendix 5.2.12.
ii) A solution in dilute hydrochloric acid gives reactions characteristic of calcium, and magnesium, Appendix 5.2.12.
Physico-chemical parameters:
0
Loss on drying at 110 : Not more than 6 per cent, Appendix 2.2.10.
Acid- insoluble ash: Not more than 1 per cent, Appendix 2.2.4.
pH (10% aqueous solution): 10 to 11, Appendix 3.3.
Assay:
Sodium: Not less than 14 per cent, Appendix 5.2.9.
Potassium: Not less than 2 per cent, Appendix 5.2.9.
Iron: Not less than 1.6 per cent, Appendix 5.2.5.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Vibandha (Constipation), Ëdhm¡na (Flatulence), Gulma (Abdominal lump), Ud¡varta (Upward movement of gases),
Ar¿a (Piles), P¡¸·u (Anaemia), Udara Roga (Diseases of abdomen), K¤mi (Helminthiasis), Mutr¡gh¡ta (Urinary obstruction), A¿mar¢
(Urinary calculus), áopha (Oedema), H¤droga (Heart disease), Graha¸¢ (Malabsorption syndrome), Meha (Excessive flow of urine), Pl
¢haruj¡(Pain due to splenic disease), Ën¡ha (Distention of abdomen), áv¡sa (Asthma), K¡sa (Cough), Agnim¡ndya (Digestive impairment)
Dose: 1 g daily in divided doses.
Anupāna: Gh¤ta.
41. Moolaka kshaara
41. MÍLAKA KâËRA
AFI, Part-I, 10:10
Definition:
MÍLAKA KâËRA is a powder preparation made with the ingredients in the formulation composition given below.
Formulation composition:
1. M£laka bhasma (M£laka) Raphanus sativus Linn (API-Vol:2/109) Pl. 1 part
2. Water Water 6 parts
Method of preparation:
Description: Fine powder, passing through sieve number 100; hygroscopic, odourless, taste salty; freely soluble in water.
Identification:
An aqueous solution yields the reactions characteristic of sodium and potassium, Appendix 5.2.12.
Physico-chemical parameters:
0
Loss on drying at 110 : Not more than 1 per cent, Appendix 2.2.10.
Acid- insoluble ash: Not more than 1 per cent, Appendix 2.2.4.
pH (10% aqueous solution): 10 to 11, Appendix 3.3.
Assay:
Sodium: Not less than 4 per cent, Appendix 5.2.9.
Potassium: Not less than 28 per cent, Appendix 5.2.9.
Iron: Not less than 2.2 per cent, Appendix 5.2.5.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: M£trak¤cchra (Dysuria), A¿mar¢ (Urinary calculus), Gulma (Abdominal lump), V¡tavik¡ra (Disorders due to Vata doÀa)
Dose: 1g daily in divided doses.
Anupāna: Water.
42. Palasha kshaara
42. PALËáA KâËRA
AFI, Part-I, 10:9
Definition:
PALËáA KâËRA is a white alkaline preparation made with the ingredients in the formulation composition given below.
Formulation composition:
1. Pal¡¿a bhasma (pal¡¿a) Butea monosperma (Lam ) Kuntze (API-Vol:4/78) Pl. 1 part
2. Jala Water 6 parts
Method of preparation:
Description:
Fine powder, passing through sieve number 100; hygroscopic, odourless, taste saline; freely soluble in water.
Identification:
An aqueous solution yields the reactions characteristic of sodium and potassium, Appendix 5.2.12.
Physico-chemical parameters:
0
Loss on drying at 110 : Not more than 6 per cent, Appendix 2.2.10.
Acid- insoluble ash: Not more than 1 per cent, Appendix 2.2.4.
pH (10% aqueous Solution): 10 to 12, Appendix 3.3.
Assay:
Sodium: Not less than 0.8 per cent, Appendix 5.2.9.
Potassium: Not less than 35 per cent, Appendix 5.2.9.
Iron: Not less than 1.2 per cent, Appendix 5.2.5.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Agnim¡ndya (Digestive impairment), Gulma (Abdominal lump), Pl¢hayak¤tv¤ddhi (Spleno-hepatomegaly), M£trak¤cchra
(Dysuria), A¿mar¢ (Urinary calculus), áarkar¡ (Gravel in urine), Graha¸¢ (Malabsorption syndrome), Ën¡ha (Distention of abdomen due to
obstruction to passage of urine and stool), ViÀ£cik¡ (Gastro-enteritis with piercing pain)
Description:
Greyish white, fine powder, passing through sieve number 100; hygroscopic, odourless, taste saline; freely soluble in water.
Identification:
An aqueous solution yields the reactions characteristic of sodium and potassium, Appendix 5.2.12.
Physico-chemical parameters:
Loss on drying at 1100: Not more than 4 per cent, Appendix 2.2.10.
Acid-insoluble ash: Not more than 1 per cent, Appendix 2.2.4.
pH (10% aqueous solution): 9 to 10, Appendix 3.3.
Assay:
Sodium: Not less than 17 per cent, Appendix 5.2.9.
Potassium: Not less than 16 per cent, Appendix 5.2.9.
Iron: Not less than 1.5 per cent, Appendix 5.2.5.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Ëdhm¡na (Flatulance), Ën¡ha (Distention of abdomen due to obstruction to passage of urine and stool), á£la (Pain /
colic), Udara (Diseases of abdomen), Gulma (Abdominal lump), Pl¢h¡maya (Splenic disease), M£trak¤cchra (Dysuria)
Dose: ½ to 1 g daily in divided dose.
Formulation composition:
1. Bal¡ Sida cordifolia Linn. (Rt.) 256 g
2. Gu·£c¢ Tinospora cordifolia (Willd.) Miers. (API-Vol:1/41) (St.) 256 g
3. Surap¡dapa (Devad¡ru) Cedrus deodara ( Roxb.) Loud (API-Vol:4/23) (Ht.Wd.) 256 g
4. Water for decoction Water 12.29 l
reduced to 3.072 l
5. Ja¶¡ (Ja¶am¡Æs¢) Nardostachys jatamansi DC (API-Vol:1/51) (Rt./Rz.) 16 g
6. Ëmaya (KuÀ¶ha) Saussurea lappa CB. Clarke (API-Vol:1/76) (Rt.) 16 g
7. Candana (Raktacandana) Pterocarpus santalinus Linn. (API-Vol:3/155) (Ht.Wd.) 16 g
8. KunduruÀka (Kunduru) Boswellia serrata Roxb (API-Vol:4/50) (Exd.) 16 g
9. Nata (Tagara) Valeriana wallichii (API-Vol:1/109) (Rt./Rz.) 16 g
10. A¿vagandh¡ Withania somnifera Dunal (API-Vol:1/15) (Rt.) 16 g
11. Sarala Pinus roxburghii Sargent. (API-Vol:3/189) (Ht.Wd.) 16 g
12. R¡sn¡ Pluchea lanceolata Oliver & Hiem.
[Alpinia galanga (Official Substitute)] (API-Vol:3/162) (Rz.) 16 g
13. Taila (Tila) Sesamum indicum linn (API-Vol:4/128) (Oil.) 768 g
Method of preparation:
Filter while hot (about 800) through a muslin cloth and allow to cool.
Pack it in tightly closed containers to protect from light and moisture.
Description: A medicated oil, dark reddish brown in color with pleasant odour.
Identification:
Physico-chemical parameters:
0
Refractive index at 40 : 1.455 to 1.460, Appendix 3.1.
Weight per ml at 400: 0.915 g to 0.930 g, Appendix 3.2.
Saponification value: 180 to 195, Appendix 3.10.
Iodine value: 80 to 100, Appendix 3.11.
Acid value: Not more than 5, Appendix 3.12.
Peroxide value: Not more than 5, Appendix 3.13
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: In conditions of V¡tarakta (Gout), Raktagata V¡ta (Hypertension), áopha (Oedema), Skandhagata V¡ta (Frozen
shoulder)
Dose: External application for Abhya´ga.
45. Dhanvantari taila
45. DHËNVANTARA TAILA (Synonym Bal¡ Taila)
AFI, Part-I, 8:22
Definition:
DHËNVANTARA TAILA is a liquid preparation made with the ingredients in the formulation composition given below with Tila Taila as
the basic ingredient.
Formulation composition:
1. Bal¡ m£la (Bal¡) Sida cordifolia Linn. (Rt.) 4.608 kg
2. Water for decoction Water 36.864 l
reduced to 4.608 l
3. PayaÅ (Godugdha ) Cow's milk 4.608 l
4. Yava Hordeum vulgare Linn (API-Vol:2/175) (Sd.) 59.07 g
5. Kola Zyzyphus jujuba Lam. (API-Vol:3/94) (Fr.) 59.07 g
6. Kulattha Vigna unquiculata (Linn.) Walp. (Dolichos biflorus) (API-Vol:1/75) (Sd.) 59.07 g
7. Bilva Aegle marmelos Corr (API-Vol:4/10) (Rt./St.Bk.) 59.07 g
8. áyon¡ka Oroxylum indicum Vent. (API-Vol:3/209) (Rt./St.Bk.) 59.07 g
9. Gambh¡r¢ Gmelina arborea Linn (API-Vol:4/31) (Rt./St.Bk.) 59.07 g
10. P¡¶al¡ Stereospermum suaveolens (L.F) DC (API-Vol:4/87) (Rt./St.Bk.) 59.07 g
11. Ga¸ik¡rik¡ (Laghu Agnimantha) Clerodendrum phlomidis Linn (API-Vol:3/3) (Rt./St.Bk.) 59.07 g
12. á¡lapar¸¢ Desmodum gangeticum DC. (API-Vol:3/178) (Rt./St.Bk.) 59.07 g
13. P¤¿nipar¸¢ Uraria picta Desv. (API-Vol:4/99) (Rt./St.Bk.) 59.07 g
14. B¤hat¢ Solanum indicum Linn (API-Vol:2/27) (Rt./St.Bk.) 59.07 g
15. Ka¸¶ak¡r¢ Solanum surattense Burm.f. (API-Vol:1/59) (Rt./St.Bk.) 59.07 g
16. GokÀura Tribulus terrestis Linn (API-Vol:1/40) (Rt./St.Bk.) 59.07 g
17. Water for decoction Water 6.144 l
reduced to 768 ml
18. Taila (Tila) Sesamum indicum linn (API-Vol:4/128) (Oil. ) 768 ml
19. Med¡ Polygonatum cirrhifolium Royle.
[Asparagus racemosus (Official substitute)] (Rt.Tr ) 6g
20. Mah¡med¡ [Asparagus racemosus (Official substitute) ] (Rt.Tr.) 6g
21. D¡ru (Devad¡ru) Cedrus deodara ( Roxb.) Loud (API-Vol:4/23) (Ht.Wd.) 6g
22. MaµjiÀ¶h¡ Rubia cordifolia Linn. (API-Vol:3/112) (Rt.) 6g
23. K¡kol¢ Lilium polyphyllum D.Don.
Withania somnifera (Official substitute) (API-Vol:3/79) (Sub.Rt.) 6g
24. KÀ¢rak¡kol¢ Fritillaria royelei Hook
Withania somnifera (Official substitute) (API-Vol:5/86) (Sub.Rt.) 6g
25. Candana (Raktacandana) Pterocarpus santalinus Linn. (API-Vol:3/155) (Ht.Wd.) 6g
26. á¡riv¡ (áveta S¡riv¡) Hemidesmus indicus (Linn.) R.Br. (API-Vol:1/107) (Rt.) 6g
27. Ku˦ha Saussurea lappa CB. Clarke (API-Vol:1/76) (Rt.) 6g
28. Tagara Valeriana wallichii (API-Vol:1/109) (Rt./Rz.) 6g
29. J¢vaka Malaxis acuminata D.Don
Pueraria tuberose (Official substitute) (API-Vol:5/52) (Rt.Tr.) 6g
30. ÎÀabhaka Pueraria tuberose (Official substitute) 6g
31. Saindhava lava¸a Rock Salt 6g
32. K¡l¡nus¡r¢ (Tagara) Valeriana wallichii (API-Vol:1/109) (Rt./Rz.) 6g
33. áaileya Parmelia perlata ( Huds.) Ach. (API-Vol:3/172) (Pl.) 6g
34. Vac¡ Acorus calamus Linn (API-Vol:2/168) (Rz.) 6g
35. Agaru Aquilaria agallocha Roxb. (API-Vol:4/4) (Ht.Wd.) 6g
36. Punarnav¡ (Rakta Punarnav¡) Boerhaavia diffusa Linn. (API-Vol:3/157) (Rt.) 6g
37. A¿vagandh¡ Withania somnifera Dunal (API-Vol:1/15) (Rt.) 6g
38. Var¢ (áat¡var¢) Asparagus racemosus Willd (API-Vol:4/108) (Rt.Tr.) 6g
39. KÀ¢ra¿ukla (KÀ¢ravid¡r¢) Ipomoea digitata Linn. (API-Vol:5/88) (Rt.Tr.) 6g
40. YaÀ¶¢ Glycyrrhiza glabra Linn (API-Vol:1/127) (Rt.) 6g
41. Har¢tak¢ Terminalia chebula Retz. (API-Vol:1/47) (P.) 6g
42. Bibh¢taka Terminalia bellerica Roxb. (API-Vol:1/26) (P.) 6g
43. Ëmalak¢ Emblica officinalis Gaertn. (Phyllanthus emblica) (API-Vol:1/4) (P.) 6g
44. áat¡hv¡ Anethum sowa Roxb.ex Flem . (API-Vol:2/153) (Fr.) 6g
45. S£rpapar¸i (M¡Àapar¸¢) Teramnus labialis Spreng. (API-Vol:3/118) (Pl.) 6g
46. El¡ (S£kÀmail¡) Elettaria cardamomum (Linn.) R.Br. (API-Vol:1/101) (Sd.) 6g
47. Tvak Cinnamomum zeylanicum Blume (API-Vol:1/113) (St.Bk.) 6g
48. Patra (Tejapatra) Cinnamomum tamala (Buch-Ham)Nees & Eberm. (API-Vol:1/115) (Lf.) 6g
Method of preparation:
Start heating next day, stir and constantly check the Kalka by rolling between the fingers. Stop heating when the Kalka breaks down into pieces
on attempting to form a varti (Khara p¡ka lakÀa¸a ), and at the appearance of froth over the oil. Expose the varti to flame and confirm the absence
of crackling sound indicating absence of moisture.
Filter while hot (about 800) through a muslin cloth and allow to cool.
Pack it in tightly closed containers to protect from light and moisture.
Description:
Identification:
Physico-chemical parameters:
0
Refractive index at 40 : 1.465 to 1.465, Appendix 3.1.
Weight per ml at 400: 0.930 g to 0.940 g, Appendix 3.2.
Saponification value: 180 to 195, Appendix 3.10.
Iodine value: 100 to 120, Appendix 3.11.
Acid value: Not more than 4, Appendix 3.12.
Peroxide value: Not more than 5, Appendix 3.13.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: V¡ta Roga (Diseases due to V¡ta doÀa), PakÀavadha (Hemiplegia), Sarv¡´ga V¡ta (Quadriplegia), Dh¡tu KÀaya (Tissue
wasting), S£tik¡ Roga (Puerperal diseases), B¡la Roga (Diseases of children), External application for Abhya´ga
Dose: Internally 6 to 12 ml daily in divided doses; as well as external application Q.S.
46. Gandharvahastaadi taila
46. GANDHARVAHASTA TAILA
AFI, Part-I, 8:12
Definition:
GANDHARVAHASTA TAILA is a liquid preparation made with the ingredients in the formulation composition described below with Tila
Taila as the basic ingredient.
Formulation composition:
1. Gandharvahasta M£la (Era¸·a) Ricinus communis Linn (API-Vol:1/34) (Rt.) 4.800 kg
2. Yava Hordeum vulgare Linn (API-Vol:2/175) (Sd.) 3.072 kg
3. N¡gara (áu¸¶h¢) Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 96 g
4. Water for decoction Water 24.58 l
reduced to 6.14 l
5. KÀ¢ra (Godugdha) Cow's milk 1.54 l
6. Era¸·a taila Ricinus communis Linn (API-Vol:1/34) (Oil.) 768 g
7. Gandharvahasta m£la (Era¸·a) Ricinus communis Linn (API-Vol:1/34) (Rt.) 192 g
8. áu¸¶h¢ Zingiber officinale Roxb. (API-Vol:1/103) (Rz.) 48 g
Method of preparation:
Description:
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer and filter. Concentrate to 5 ml and carry
out the thin layer chromatography. Apply 10 µl of the extract on TLC plate. Develop the plate to a distance of 8 cm using toluene : ethyl acetate
: hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at Rf 0.45 (light grey), 0.52 (grey), 0.75 (dark brown) and 0.81 (dark brown) under visible light.
Physico-chemical parameters:
Refractive index at 400: 1.451 to 1.460, Appendix 3.1.
Weight per ml at 400: 0.975 g to 0.985 g, Appendix 3.2.
Saponification value: 180 to 200, Appendix 3.10.
Iodine value: 75 to 100, Appendix 3.11.
Acid value: Not more than 4, Appendix 3.12.
Peroxide value: Not more than 2, Appendix 3.13.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses:Vidradh¢ (Abscess), Pl¢h¡(Enlargement of spleen), Gulma (Abdominal lump), Ud¡varta (Upward movement of gases),
áopha (Oedema), Udara (Diseases of abdomen), Mah¡v¡ta Roga (Major neurological disorders)
Dose: 6 to12 ml daily in divided doses
Formulation composition:
1. Ko¶¶am (KuÀ¶ha) Saussurea lappa CB. Clarke (API-Vol:1/76) (Rt.) 21.0 g
2. Cukku (áu¸¶h¢) Zingiber officinale Roxb. (API-Vol:1/103) (Rz ) 21.0 g
3. Vayambu (Vac¡) Acorus calamus Linn (API-Vol:2/168) (Rz.) 21.0 g
4. áigru Moringa oleifera Lam (API-Vol:4/114) (St.Bk ) 21.0 g
5. La¿una Allium sativum Linn. (API-Vol:3/108) (Bl.) 21.0 g
6. K¡rto¶¶i (Himsr¡) Capparis spinosa Linn. (API-Vol:5/41) (Rt.) 21.0 g
7. Devadruma-(Devad¡ru) Cedrus deodara (Roxb.) Loud (API-Vol:4/23) (Ht.Wd.) 21.0 g
8. Siddh¡rtha (SarÀapa) Brassica campestris Linn. (API-Vol:3/193) (Sd.) 21.0 g
9. Suvah¡ (R¡sn¡) Pluchea lanceolata Oliver & Hiem.
Alpinia galanga (Official substitute) (API-Vol:3/162) (Rz.) 21.0 g
10. Tilaja (Tila) Sesamum indicum linn (API-Vol:4/128) (Oil.) 768 g
11. Dadhi (Godadhi ) Curd from cow's milk 768 g
12. Ciµc¡ rasa (Ciµc¡) Tamarindus indica Linn (API-Vol:4/14) (Lf.) 3.072 g
Method of preparation:
Take all ingredients of pharmacopoeial quality.
Wash and dry all the herbal raw materials except ingredient 12 thoroughly.
Treat Tila Taila to prepare M£rchita Taila (Appendix 6.2.8.3).
svarasa through muslin cloth.
Collect fresh leaves of ingredient number 12, wash thoroughly, grind and express
Take the other ingredients (Kalka dravyas) with the exception of La¿una and SarÀapa, dry, powder and pass through sieve number 85. Grind
La¿una and SarÀapa separately, add the powdered ingredients and grind with sufficient quantity of water to prepare a homogeneous blend.
(Kalka)
Take M£rchita Taila in a stainless steel vessel and heat it mildly.
Add increments of Kalka. Stir thoroughly while adding the Svarasa and Godadhi.
Heat for 3 h with constant stirring maintaining the temperature between 50 and 900 during the first hour of heating. Stop heating and allow to
stand overnight.
Start heating next day, stir and constantly check the Kalka by rolling between the fingers. Stop heating when the Kalka breaks down into pieces
on attempting to form a varti ( khara p¡ka lakÀa¸a ), and at the appearance of froth over oil. Expose the varti to flame and confirm the absence of
crackling sound indicating absence of moisture.
Filter while hot (about 800) through a muslin cloth and allow to cool.
Pack it in tightly closed containers to protect from light and moisture.
Description:
Identification:
Physico-chemical parameters:
0
Refractive index at 40 : 1.461 to 1.463, Appendix 3.1.
Weight per ml at 400: 0.920 to 0.940 g, Appendix 3.2.
Saponification value: 150 to 175, Appendix 3.10.
Iodine value: 75 to 100, Appendix 3.11.
Acid value: Not more than 8, Appendix 3.12.
Peroxide value: Not more than 4, Appendix 3.13.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Ëmav¡ta (Rheumatism), V¡ta Roga (Diseases due to V¡ta doÀa), A´gastambha (Stiffness of body), External application
for Abhya´ga
48. Ksheerabala taila
48. KâÌRABALË TAILA
AFI, Part-I, 8:11
Definition:
KâÌRABALË TAILA is a liquid preparation made with the ingredients in the Formulation composition given below with Tila Taila as the
basic ingredient.
Formulation composition:
1. Bal¡ kaÀ¡ya Sida cordifolia Linn. (Rt.) 16 Parts
2. Bal¡ kalka Sida cordifolia Linn (Rt.) 1 Part
3. Taila (Tila) Sesamum indicum linn (API-Vol:4/128) (Oil.) 4 Parts
4. KÀ¢ra (Godugdha) Cow's milk 4 Parts
5. Jala Water 16 Parts
Method of preparation:
stand overnight.
Start heating next day, stir and constantly check the Kalka by rolling between the fingers. Stop heating when the Kalka breaks down into pieces
on attempting to form a varti (khara p¡ka lakÀa¸a ), and at the appearance of froth over the oil. Expose the varti to flame and confirm the absence
of crackling sound indicating absence of moisture. Filter while hot (about 800) through a muslin cloth and allow to cool.
Pack it in tightly closed containers to protect from light and moisture.
Description:
Identification:
Extract 2 g of the sample with 20 ml of alcohol at about 400 for 3 h. Cool, separate the alcohol layer, filter, concentrate to 5 ml and carry out the
thin layer chromatography. Apply 10 µl of the extract on TLC plate and develop the plate to a distance of 8 cm using toluene : ethyl acetate :
hexane (6 : 3 : 1) as mobile phase. After development, allow the plate to dry in air and spray with ethanol-sulphuric acid reagent followed by
heating at 1100 for about 10 min. It shows spots at Rf 0.42 (brown), 0.57 (brown), 0.70 (grey) and 0.80 (light grey) under visible light.
Physico-chemical parameters:
0
Refractive index at 40 : 1.451 to 1.460, Appendix 3.1.
Weight per ml at 400: 0.930 g to 0.945 g, Appendix 3.2.
Saponification value: 185 to 200, Appendix 3.10.
Iodine value: 75 to 100, Appendix 3.11.
Acid value: Not more than 6.5, Appendix 3.12.
Peroxide value: Not more than 2, Appendix 3.13.
Other requirements:
Mineral oil: Absent, Appendix 3.15.
Microbial Limits: Appendix 2.4.
Aflatoxins: Appendix 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: V¡tarakta (Gout), V¡ta Roga (Diseases due to V¡ta doÀa), áukra DoÀa (Vitiation of ¿ukra dh¡tu), RajodoÀa (Menstrual
disorder), K¡r¿ya (Emaciation), Svarabheda (Hoarseness of voice),
External application for Abhya´ga, Nasya (Nasal drops), P¡na (Oral use), Bastiprayoga (Enema)
Dose: 6 to 12 ml daily in divided doses.
Formulation composition:
1. Saindhava lava¸a Rock salt 28 g
2. Arka Calotropis procera (Ait.) R.Br. (API-Vol:1/8) (Rr.) 28 g
3. Marica Piper nigrum Linn. (API-Vol:3/115) (Ft.) 28 g
4. Jvalan¡khya (Citraka) Plumbago zeylanica Linn (API-Vol:1/29) (Rt.) 28 g
5. M¡rkava (Bh¤´gar¡ja) Eclipta alba Hassk (API-Vol:2/21) (Pl.) 28 g
6. Haridr¡ Curcuma longa Linn. (API-Vol:1/45) (Rz.) 28 g
7. D¡ruharidr¡ Berberis aristata DC (API-Vol:2/33) (St.) 28 g
8. Taila (Tila) Sesamum indicum linn (API-Vol:4/128) (Oil.) 768 g
9. Jala Water 3.072 l
Method of preparation:
Description:
Identification:
Extract 25 ml of the formulation in a separatory funnel with methanol (20 ml x 3 ). Pool the methanolic extracts, concentrate and make up the
volume to 20 ml and carry out the Thin Layer Chromatography. Apply 20 µl on TLC plate. Develop the plate to a distance of 8 cm using toluene
: ethyl acetate (7 : 3) as mobile phase. After development allow the plate to dry in air and examine under ultraviolet light (254 nm). It shows
major spots at Rf 0.29, 0.35, 0.50, 0.60, 0.75, 0.82 and 0.90. Under ultraviolet light (366 nm), the plate shows fluorescent spots at Rf 0.10 (light
blue), 0.13 (light blue), 0.30 (light green), 0.35 (yellow), 0.53 (blue), 0.68 (light blue), 0.75 (light green), 0.86 (blue). Spray the plate with
anisaldehyde-sulphuric acid reagent followed by heating at 1100 for about 10 min. It shows major spots at Rf 0.15 (light violet), 0.35 (brown),
0.50 (light violet), 0.60 (light violet), 0.70 (light blue violet), 0.80 (red), 0.87 (light brown) and 0.97 (light violet) under visible light.
Physico-chemical parameters:
Refractive index at 250: 1.473 to 1.478, Appendix 3.1.
Weight per ml at 250: 0.950 to 0.951 g, Appendix 3.2.
Saponification value: 185 to 200, Appendix. 3.10.
Iodine value: 100 to 115, Appendix 3.11.
Acid value: Not more than 5.0, Appendix 3.12.
Peroxide value: Not more than 6, Appendix 3.13.
Other requirements:
Mineral oil Absent, Appendix 3.15.
Microbial limits: Appendix 2.4.
Aflatoxins: Appendix. 2.7.
Storage: Store in a cool place in tightly closed containers, protected from light and moisture.
Therapeutic uses: Kaphav¡taja N¡·¢ Vra¸a (Sinus due to Kapha DoÀa and V¡ta DoÀa)
Dose: As prescribed by the physician for Abhya´ga (External use).
LEPA
LEPA
Lepas are semi-solid preparations intended for external application to the skin or certain mucous membranes for emollient, protective,
therapeutic or prophylactic purposes where a degree of occlusion is desired. They usually consist of solutions or dispersions of one or more
medicaments in suitable bases.
The base should not produce irritation or sensitization of the skin, nor should it retard wound healing; it should be smooth, inert,
odourless, physically and chemically stable and compatible with the skin and with incorporated medicaments.
The proportions of the base ingredients should be such that the ointment is not too soft or too hard for convenient use. The consistency
should be such that the ointment spreads and softens when stress is applied.
50. Daarvi malahar
50. DËRVÌ MALAHARA (GEL)
Based on Caraka Cikitsa 25/93
Definition:
DËRVÌ MALAHARA is a semisolid preparation made with the ingredients given in the Formulation composition.
Formulation Composition:
1. Ras¡µjana Berberis aristata DC /B. asiatica/B. lycium (API-Vol:2/33) Root extract 2 g
2. Spha¶ik¡ Alum or Potable Alums 1g
3. Tragacanth 2g
4. Xanthan gum FF 1g
5. Propylene glycol 4 ml
6. Methyl paraben 0.17 g
7. Propyl paraben 0.03 g
8. Disodium edentate 0.01 g
9. Peppermint oil 0.05 ml
10. Jala Water 100ml
Method of Preparation:
Description:
Identification:
Test for Berberine: Dissolve about 2 g of D¡rv¢ Malahara in 20 ml of water and filter. Take about 2 ml of the filtrate and add 1 ml of
concentrated nitric acid. A dark red colour is formed.
Test forSpha¶ik¡ : Dip a spatula in the water solution of D¡rv¢ Malahara. Take it out and let it dry. Hold spatula in a nonluminous flame; a
violet colour is imparted to the flame.
Physico-chemical parameters:
pH (5% aqueous solution) : 3.7 to 4.2 Appendix 3.3.
Assay:
Sample contains not less than 0.08 per cent of berberine when assayed by the following method.
Estimation of Berberine: Dissolve about 25 mg of accurately weighed Berberine hydrochloride in water and makeup the volume to 25 ml in a
volumetric flask. Transfer 1, 2,3,4,5 and 6 ml of this stock solution separately to six 25 ml- volumetric flasks and makeup the volume in each to
25 ml.
Apply in triplicate 1 µl of each dilution on a TLC plate. Develop the plate to a distance of 8 cm using n-propanol : formic acid : water (8.1: 0.1:
1.8) as mobile phase. After development, dry the plate in air and scan at 343 nm in a TLC scanner. Note the area under the curve for peak
corresponding to berberine and prepare the calibration curve by plotting peak area vs amount of berberine hydrochloride.
Dissolve accurately weighed about 1 g of D¡rv¢ Malahara in 5 ml of distilled water and make up the volume to 25 ml in a volumetric flask with
distilled water. Filter the solution and discard the first 5 ml of the solution. Collect the next 5 ml of solution and use for analysis. Apply 1 µl of
solution in triplicate on a TLC plate and develop, dry and scan the plate as described in preceding paragraph for calibration curve of berberine.
Calculate the amount of berberine in the test solution from the calibration curve of berberine hydrochloride and determine the concentration of
berberine in the D¡rv¢ Malahara.
Other requirements:
Microbial limits: Appendix. 2.4.
Aflatoxins: Appendix. 2.7.
Dose: 2g twice a day to be applied with applicator in vagina.
Storage: At room temperature.
Therapeutic uses: áveta Pradara (Leucorrhoea), Yonika¸·£ (Itching), Yoni ¿otha(Vaginitis and other wounds and ulcers)
Precaution: Discontinue if there is any irritation or discomfort.