Formula
Sodium Thioglycollate, 1.0 g
Sodium Phosphate, dibasic, 1.15 g
Sodium Chloride, 3.0
g
Potassium Chloride, 0.2
g
Potassium Phosphate, monobasic, 0.2 g
Magnesium Sulfate, heptahydrate, 0.1 g
L-Cysteine, 1.0
g
Resazurin, 1.0
mg
Gelrite, 4.0
g
Distilled Water, 1000.0
ml
Final pH 7.3 +/- 0.2 at 25 degrees C.
Final
volume 6.0 ml +/- 0.6.
Precautions
For IN VITRO DIAGNOSTIC USE only. Approved biohazard precautions and aseptic
techniques should be observed when using this product. This product is for use only by properly
trained and qualified personnel.
Sterilize all biohazard waste prior to disposal.
Storage and Shelf Life
Storage: Upon receipt store at room temp, in original
packaging until use. Avoid overheating
or freezing. Do not use medium if there
are signs of deterioration (discoloration or evaporation), oxygen exposure or
contamination.
The
expiration date applies to the product in its original packaging and stored as
directed. Do not use product past the
expiration date shown on the container.
Shelf Life: 6 months from
date of manufacture.
Procedure
Specimen Collection:
Specimens for anaerobic culture should be protected from air (oxygen)
during collection, transport and processing of specimens. Consult appropriate references for detailed instructions
concerning collection and transport of anaerobes.
Methods for Use: Anaerobic Transport Medium Surgery Packs are suitable for use as a transport and holding medium
for clinical specimens collected as tissue samples or fluid specimens aspirated
into syringes. With any clinical
specimen, Anaerobic Transport Medium Surgery Packs should be inoculated by aseptic technique immediately at
or after collection. For tissue samples,
open tube by screw cap and place tissue on the surface of the semisolid medium,
inserting the tissue into the agar column is not necessary. Immediately close tube. Contact with air of tube contents should be
minimized. For syringe specimens, the
rubber septum in the cap should be disinfected and the fluid specimen directly
injected into the tube at a slow rate.
Once inoculated, keep at room temperature and deliver to the laboratory
for processing as soon as possible.
Swabs are not recommended for use as anaerobic specimen collection
devices, however this medium can accommodate swabs, if necessary. Detailed instructions for processing
anaerobic cultures can be found in the appropriate references.
Sterile Pack (AS-914):
The contents and outer surface of the tube are sterile. The envelope is peeled apart, an individual,
wearing sterile gloves removes the tube, which then can be taken into the
surgical area.
Materials Required But Not Provided
Standard
microbiological supplies and equipment such as loops, paper points,
disinfectant, syringes with needles, sterile forceps, saline blanks, slides,
staining supplies, microscope, incinerator/autoclave, incubators, anaerobic
chamber, other culture media and serological and biochemical reagents.
Limitations
Anaerobic Transport Medium Surgery Packs are designed as a holding medium to
maintain viability of microorganisms contained within a specimen during transport. This medium will not provide complete
information for identification of bacterial isolates. Additional test procedures and media are
required for complete identification.
Specimens should be transported and processed in the laboratory in a timely
manner, since delay may result in overgrowth by one organism present in a
specimen from polymicrobic infections.
Consult reference materials for additional information.
Quality Control
If used properly this medium should maintain the
viability of microorganisms present within a clinical specimen until
transported and processed within the laboratory.
The following organisms are routinely used for
quality assurance testing at Anaerobe Systems.
For determining the holding capacity of Anaerobic Transport Medium Surgery Packs for each isolate listed
below, an ATCC strain, from 24-hour growth, is inoculated into the media
aerobically and held overnight. In an
anaerobic environment, each organism is streaked, onto Anaerobic Brucella Blood
Agar, to obtain isolated colonies.
Plates are incubated for 35 –37oC for 48 hours and growth is
observed.
|
Organism Tested
|
ATCC #
|
Results
|
Time (Hours)
|
|
Bacteroides fragilis
|
25285
|
Growth
|
24 h
|
|
Porphyromonas levii
|
29147
|
Growth
|
24 – 48 h
|
|
Bacteroides vulgatus
|
8482
|
Growth
|
24 h
|
|
Fusobacterium nucleatum
|
25586
|
Growth
|
24 h
|
|
Fusobacterium necrophorum
|
25286
|
Growth
|
24 h
|
|
Clostridium perfringens
|
13124
|
Growth
|
24 h
|
|
Clostridium novyi
|
7659
|
Growth
|
24 – 48 h
|
|
Peptostreptococcus anaerobius
|
27337
|
Growth
|
24 h
|
|
|
|
** For AS-914 the following organisms are used:
|
|
Propionibacterium acnes
|
6919
|
Growth
|
24 – 48 h
|
|
Staphylococcus aureus
|
25923
|
Growth
|
24 h
|
User
Quality Control: The final determination to the extent and quantity of user
laboratory quality control must be determined by the end user.
If
sterility testing is to be performed on this product the appropriate percentage
of the original shipment amount should be incubated anaerobically and
aerobically for 48 – 96 hours.
If
the holding capacity of this medium is to be tested for performance, it is
recommended that the following ATCC organisms be evaluated for growth.
|
Organism
|
Growth in
|
|
|
Hours
|
|
B. fragilis
|
24 hrs
|
|
P. levii
|
48 hrs
|
|
C. perfringens
|
24 hrs
|
|
F. necrophorum
|
24 hrs
|
|
S. aureus
|
24 hrs
|
Physical appearance:
Anaerobic Transport Medium Surgery Packs should appear as a
clear translucent semi solid media.
References
1. Dowell, V. R., Jr. and T. M. Hawkins. 1974. Laboratory Methods in Anaerobic Bacteriology. CDC Laboratory Manual. USDHEW C.D.C. Atlanta, GA 30333.
2.
Dowell, V. R., Jr. and G. L. Lombard. 1977. Presumptive Identification of Anaerobic Non-spore forming Gram-negative
Bacilli. USDHEW, CDC. Atlanta, GA 30333.
3.
Dowell, V. R., Jr., G. L. Lombard, F. S. Thompson and A. Y. Armfield. 1977. Media for the Isolation, Characterization
and Identification of Obligately Anaerobic Bacteria. USDHEW, CDC, Atlanta, GA 30333.
4.
Engelkirk, P. G., Duben-Engelkirk, J. and Dowell, V. R. 1992. Principles and Practices of Clinical
Anaerobic Bacteriology. Star
Publishing Co., Belmont, CA 94002.
5.
Holdeman, L. V., F. P. Cato and W. E. C. Moore. 1977. Anaerobe Laboratory Manual. Virginia Polytechnic Institute and State University. Blacksburg, VA 24061
6. Jousimeis-Somer, H. R., Summanen, P., Citron, D. M., Baron, E. J.,
Wexler, H. M. and S. M. Finegold. 2002. Wadsworth – KYL
Anaerobic Bacteriology Manual. Star
Publishing Co., Belmont, CA 94002.
7.
QA for commercially prepared microbiological culture media – Second
Edition; 1996 Approved Standard. NCCLS
document M22-A2. NCCLS, 940 West Valley Road, Suite
1400,
Wayne, PA 19087-1898.