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Transport Charcoal Medium
Intended Use
For transportation of clinical specimens.
Composition**
| Ingredients | g / L |
|---|---|
| Sodium thioglycollate | 0.900 |
| Sodium β-glycerophosphate | 10.000 |
| Charcoal | 10.000 |
| Calcium chloride anhydrous | 0.100 |
| Methylene blue | 0.002 |
| Agar | 3.000 |
Final pH (at 25°C): 7.4±0.2
**Formula adjusted, standardized to suit performance parameters
Directions
Suspend 24.0 grams in 1000 ml purified/distilled water. Heat to boiling to dissolve the medium completely. Dispense in screw capped tubes with constant stirring to maintain charcoal particles in suspension. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Shake gently to distribute charcoal particles evenly, just before the medium gels. Cool the tubed medium in an upright position.
Principle And Interpretation
Muffett, Young and Stuart (1) described a medium and method for transporting gonococcal specimens from the site of collection to the laboratory. Stuart, Toshach and Potsula (2) elaborated upon the rationale of their transport method and presented the formulation in which they observed that coliform organisms were occasionally encountered in gonococcal specimens and that they were able to propagate in the transport medium and overgrow the gonococci.
Transport Medium with Charcoal is a modified medium based on the transport medium originally developed by Moffett et al (1) and Stuart et al (2) and is formulated for the transportation of clinical specimens containing moulds, yeasts and bacteria especially gonococci. Transport media is generally formulated to provide enrichment to maintain viability of the organisms. Transport Charcoal Medium is devoid of inorganic phosphate buffer but contains glycerophosphate and methylene blue in addition to thioglycollate. Small amount of agar together with sodium thioglycollate creates a reduced atmosphere in the medium. Charcoal neutralizes the toxic metabolic products. Like the Amies Transport Medium (3), this medium is also semisolid and reductive thereby inhibiting the contaminants and avoiding the toxic oxidative effects. As compared to the fresh specimen or direct inoculation, transport medium will not show optimal growth. The specimen will be undoubtedly preserved during transportation and also the viability of the organisms will be maintained but it will diminish over time. Some growth of contaminants also may occur during longer period of transport. After transportation, the specimen should be inoculated in proper medium as soon as possible.
Type of specimen
Clinical samples : pathological samples.
Specimen Collection and Handling
For clinical samples follow appropriate techniques for handling specimens as per established guidelines (4,5). After use, contaminated materials must be sterilized by autoclaving before discarding.
Warning and Precautions
In Vitro diagnostic Use only. For professional use only. Read the label before opening the container. Wear protective gloves/protective clothing/eye protection/face protection. Follow good microbiological lab practices while handling specimens and culture. Standard precautions as per established guidelines should be followed while handling clinical specimens. Safety guidelines may be referred in individual safety data sheets
Limitations
- The specimen will be preserved and the viability of the organisms will be also maintained during transport, but over the time it will diminish.
- Therefore direct inoculation of the specimen is advised.
- Some growth of accompanying contaminants may also occur during longer period of transit.
- The specimen should be inoculated into a proper medium as soon as possible.
Performance and Evaluation
Performance of the medium is expected when used as per the direction on the label within the expiry period when stored at recommended temperature.
Quality Control
Appearance: Grey to black homogeneous free flowing powder
Gelling: Semisolid, comparable with 0.3% Agar gel.
Colour and Clarity of prepared medium: Black coloured opaque gel forms in tubes as butts
Reaction: Reaction of 2.4% w/v aqueous solution at 25°C. pH : 7.4±0.2
pH: 7.20-7.60
Cultural Response: Cultural characteristics observed after an incubation at 25-30°C for 5 days upon subculturing on Tryptone Soya Agar (M290).
| Organism | Inoculum (CFU) | Growth on Tryptone Soya Agar (M290) |
|---|---|---|
| Klebsiella pneumoniae ATCC 13883 (00097*) | 50-100 | luxuriant |
| Pseudomonas aeruginosa ATCC 27853 (00025*) | 50-100 | luxuriant |
| Salmonella Typhi ATCC 6539 | 50-100 | luxuriant |
| Shigella flexneri ATCC 12022 (00126*) | 50-100 | luxuriant |
| Staphylococcus aureus subsp. aureus ATCC 25923 (00034*) | 50-100 | luxuriant |
| Vibrio cholerae ATCC 15748 | 50-100 | luxuriant |
| Neisseria gonorrhoea ATCC 43069 | 50-100 | good |
| Neisseria meningitidis ATCC 13090 | 50-100 | good |
Key : (*) Corresponding WDCM numbers.
Storage and Shelf Life
Store between 10-30°C in a tightly closed container and the prepared medium at 5-25°C. Use before expiry date on the label. On opening, product should be properly stored dry, after tightly capping the bottle in order to prevent lump formation due to the hygroscopic nature of the product. Improper storage of the product may lead to lump formation. Store in dry ventilated area protected from extremes of temperature and sources of ignition. Seal the container tightly after use. Product performance is best if used within stated expiry period.
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 (4,5).
Reference
- Moffett M., Young J. and Stuart R. D., 1948, Brit. Med. J., 2:241.
- Stuart R. D., Toshach S. R. and Patsula T. M., 1954, Can. J. Public Health, 45:73.
- Amies C. S., 1967, Can. J. Public Health, 58:296.
- Isenberg, H.D. Clinical Microbiology Procedures Handbook 2nd Edition.
- 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.
| Product Name | Transport Charcoal Medium |
|---|---|
| SKU | M315 |
| Product Type | Regular |
| Physical Form | Powder |
| Origin | Chemically defined |
| Packaging type | HDPE |
| References | 1. Tinsdale G. F. W., 1947, J. Pathol. Bacteriol., 59:461. 2.Billings E., 1956, An investigation of Tinsdale Tellurite Medium: its usefulness and mechanisms of halo-formation, M.S.thesis, University of Michigan, Ann Arbor, Mich. 3.Moore M. S. and Parsons E. I., 1958, J. Infect. Dis., 102:88. 4.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. I, Williams and Wilkins, Baltimore. 5.Murray P. R., Baron E. J., Jorgensen J. H., Pfaller M. A., Yolken R. H., (Eds.), 8th Ed., 2003, Manual of ClinicalMicrobiology, ASM, Washington, D.C 6.Isenberg, (Eds.), 1992, Clinical Microbiology Procedures Handbook, Vol. 1, American Society for Microbiology, Washington, D.C. |
| Customized Product Available | No |








