Tryptic Soy Agar + LT + Cephase – ICR [Pack of 120]

Description

Ten settle plates each with a diameter of 90 mm are triple-bagged in transparent, hydrogen peroxide impermeable sleeves. The product is gamma-irradiated in the final packaging at a dose of 9-20 kGy. The sleeves consist of polypropylene with a barrier of PE-EVOH-PE.
The formulation of the basic medium (Soybean-Casein Digest Agar) is prepared according to the recommendations of the current European, Japanese and United States Pharmacopoeia (EP, 2.6.12.; JP, 4.05 and USP, 61) and supplemented with neutralizers.
Further plate designs are available with the identical media formulation:
• TSA Contact + LT + Cephase – ICR+ (article number 146539): 55 mm lockable contact plates, triple-bagged, gamma-irradiated; intended for microbial monitoring of dry, sanitized surfaces and personnel in Clean Rooms and Isolators. The plate design allows aerobic, microaerophilic and anaerobic incubation.
• TSA + LT + Cephase – ICR+ (article number 146700, only available upon request): 90 mm lockable settle plates; triple-bagged; gamma-irradiated; intended for microbial monitoring of air (passive and active) and fingerprints of personnel in Clean Rooms and Isolators. The plate design allows aerobic, microaerophilic and anaerobic incubation.

Mode of Action
Tryptic Soy Agar (TSA, Soybean Casein Digest Agar) is a complex medium for cultivation and isolation of a wide range of bacteria, yeasts and molds. The medium is supplemented with pyruvate to provide an efficient neutralization of hydrogen peroxide for use in Isolators. Internal studies confirmed the neutralization efficiency of the neutralizers lecithin and polysorbate (Tween®) 80 for disinfectants containing the following active agents:
• Alcohol (70 % ethanol or isopropyl alcohol)
• Aldehydes
• Chlorine (e.g. sodium hypochlorite)
• Dichloroisocyanurate
• Glucoprotamine
• Hydrogen Peroxide
• Peracetic acid

• Phenolic compounds
• Low concentrated quaternary ammonium compounds

The neutralizing efficiency towards residues of disinfectants in use should be validated at the application
site. For neutralization of high concentrated quaternary ammonium compounds and/or polyhexamethylene
biguanides the use of Neutralizer A Contact Plates is recommended (article number 146697).

The combination of a specific broad spectrum cephalosporinase and penicillinase provides inactivation of β-lactam antibiotics such as penicillins and cephalosporins, including cephalosporins of the 3rd and 4th generation, as well as carbapenems. Since the given activities are defined for cephalosporin C and penicillin G, enzyme activity concerning other antibiotics is not specified. Specification should be determined experimentally using a defined amount of the concerning antibiotic.
The table below shows the inhibition zone of S. aureus against different ß-lactam antibiotics using antibiotic discs in an agar diffusion test.

The appearance of the medium is clear and yellowish. The pH value is in the range of 7.1-7.5. The medium can be adjusted and/or supplemented according to the performance criteria required.

Application and Interpretation
The plates are introduced into Clean Rooms grade A or B by removing one bag in each material lock. For use in Isolators the inner bag has a hole in the sealing to hang up the bag during decontamination. Do not leave plates which are unprotected (unwrapped) in an Isolator during decontamination.
Each plate is provided with a label including a data matrix code for paperless plate identification. The code consists of a two-dimensional 20-digit serial number, which harbors the following information:
Digits 1-3: here code 714 (corresponds to article 146076); digits 4-9: lot number; digits 10-14: batch specific individual number; digits 15-20: expiry date (YY/MM/DD).

Please check each agar plate before using it on sterility and pay attention to aseptic handling to avoid false positive results. The plates may be used for passive or active air monitoring as described in USP chapter <1116> or ISO 14698. For active air sampling please follow the guidance of the air sampler.

Typically, 1000 liter of air are sampled for quantification of CFU. The exposure time of opened settle plates should be validated with respect to the environmental conditions of the sampling area such as flow rates, temperatures and relative humidity to preclude desiccation.

Afterwards the plates are closed and transferred to an incubator. To protect the plates from secondary contamination during transport and incubation outside of the Clean Room zone, sterile transport bags (article number 146509) may be used.

Several recommendations are given by different guidelines for incubation: according to USP <1116> the plates used for environmental monitoring should be incubated between 20 and 35 °C for not less than 72 hours.

According to the FDA Aseptic Guide the plates for determination of the total aerobic bacterial count should be incubated at 30 to 35 °C for 48 to 72 hours, while the plates for determination of the total yeast and mold count should be incubated at 20 to 25 °C for 5 to 7 days.

Individual incubation conditions can be chosen and should be validated at the application side. For anaerobic incubation we recommend to use the lockable version (146700) in „VENT“ position, which facilitates the gas exchange within the plate. Finally, the number of CFU per plate is examined. Grown colonies are recommended to be identified.

Storage and Shelf Life

The product can be used for sampling until the expiry date if stored upright, protected from light and properly sealed at +15 °C to +25 °C. Condensation can be prevented by avoiding quick temperature shifts and mechanical stress. The testing procedures as described on the CoA can be started up to the expiry date printed on the label.

Disposal

Please mind the respective regulations for the disposal of used culture medium (e.g. autoclave for 20 min at 121 °C, disinfect, incinerate etc.).