Sabouraud Cycloheximide Chloramphenicol Agar: Intended Use
Sabouraud Cycloheximide Chloramphenicol Agar: Intended Use
Intended Use:
Recommended for selective isolation and cultivation of pathogenic fungi.
Composition**
Ingredients Gms / Litre
Peptone 10.000
Dextrose (Glucose) 20.000
Chloramphenicol 50mg
Cycloheximide 500mg
Agar 15.000
Final pH ( at 25°C) 6.8±0.2
**Formula adjusted, standardized to suit performance parameters
Directions
Suspend 45.54 grams in 1000 ml purified / distilled water. Heat to boiling to dissolve the medium completely. Sterilize
by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Mix well and pour into sterile Petri plates.
Caution : Cycloheximide is very toxic. Avoid skin contact or aerosol formation and inhalation.
Some pathogenic fungi may produce infective spores, which are easily dispersed in air, so examination should be carried
out in safety cabinet.
Limitations
1.Some pathogenic fungi may produce infective spores, which are easily dispersed in air, so examination should be carried
out in safety cabinet.
2.Individual organisms differ in their growth requirement and may show variable growth patterns on the medium.
Quality Control
Appearance
Cream to yellow homogeneous free flowing powder
Gelling
Firm, comparable with 1.5% Agar gel
Colour and Clarity of Prepared Medium
Light amber coloured clear to slightly opalescent gel forms in Petri plates
Reaction
Reaction of 4.5% w/v aqueous solution at 25°C. pH : 6.8±0.2
pH
6.60-7.00
Cultural Response
Cultural characteristics observed after an incubation at 25-30°C for 2-3 weeks.
Organism Inoculum Growth Recovery
(CFU)
*Aspergillus brasiliensis 50-100 none-poor
ATCC 16404 (00053*)
Candida albicans ATCC 50-100 poor-fair <=20%
10231 (00054*)
Escherichia coli ATCC >=104 inhibited 0%
25922 (00013*)
Saccharomyces cerevisiae 50-100 none-poor <=20%
ATCC 9763 (00058*)
Trichophyton 50-100 luxuriant
mentagrophytes ATCC 9533
Trichophyton rubrum ATCC 50-100 luxuriant
28191
Key : (*) - Corresponding WDCM numbers.
(#) - Formerly known as Aspergillus niger
Disposal
User must ensure safe disposal by autoclaving and/or incineration of used or unusable preparations of this product.
Follow established laboratory procedures in disposing of infectious materials and material that comes into contact
with clinical sample must be decontaminated and disposed of in accordance with current laboratory techniques ().
Reference
1. Ajello L., 1957, J. Chron. Dis., 5:545.
2. Diagnostic Procedures, 1963, 4th ed., APHA
3. Emmons C., Binford C., Uty J. and Kwon-Chung, 1970, Medical Mycology, 2nd ed., Philadelphia: Lea and Febiger.
4.. Isenberg, H.D. Clinical Microbiology Procedures Handbook. 2nd Edition
5. Jorgensen, J.H., Pfaller, M.A., Carroll, K.C., Funke, G., Landry, M.L., Richter, S.S and Warnock., D.W. (2015)
Manual of Clinical Microbiology, 11th Edition. Vol. 1.
6. MacFaddin J. F., 1985, Media For Isolation-Cultivation Identification - Maintenance of Medical Bacteria, Vol. 1, Williams
and Wilkins, Baltimore.
7. Sabouraud R., 1892, Ann. Dermatol. Syphilol., 3:1061.
CE Marking
2°C
Disclaimer :
User must ensure suitability of the product(s) in their application prior to use. Products conform solely to the information contained in
this and other related HiMedia™ publications. The information contained in this publication is based on our research and development
work and is to the best of our knowledge true and accurate. HiMedia™ Laboratories Pvt Ltd reserves the right to make changes to
specifications and information related to the products at any time. Products are not intended for human or animal or therapeutic use but
for laboratory,diagnostic, research or further manufacturing use only, unless otherwise specified. Statements contained herein should not
be considered as a warranty of any kind, expressed or implied, and no liability is accepted for infringement of any patents.
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