Microbiological examination of non-sterile products according to the international harmonised methods/part 1: Microbial enumeration tets

被引:0
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作者
Seyfarth, Hanfried
机构
来源
PHARMAZEUTISCHE INDUSTRIE | 2006年 / 68卷 / 08期
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中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The 6(th) Supplement to the Ph.Eur. 5(th) edition contains the methods for the total viable aerobic count in pharmaceutical preparations, harmonised with the regulations in the USA and Japan. This revised text of the test includes numerous modifications compared to the previous paragraph of the Ph.Eur. 511 edition: The number of samples is clearly defined. There are new regulations concerning the amount used for the test in case of a small amount of active substance or if the preparation contains only a small amount of active substance. Prescribed as obligatory are the nutritive media: Casein soya bean digest agar for the Total Aerobic Microbial Count and Sabouraud-dextrose agar (without addition of antibiotics) for the Total Combined Yeasts/Mould Count. Control of nutrient media: The growth-promotion qualities have to be tested on each batch of ready-prepared medium and each batch of medium, prepared either from dehydrated medium or from the ingredients described. The frequency of the test of media sterility is not clearly prescribed. Regulations for incubation: Casein soya bean digest agar 3 to 5 days at 30 to 35 degrees C and Sabouraud-dextrose agar 5 to 7 days at 20 to 25 degrees C. Evaluation: The limitation of the number of colonies in case of membrane filtration is missing (up to now max. 100 CFU/filter); the count in case of plate count method is limited to < 250 bacteria, < 50 fungi resp. (previously < 300 bacteria, < 100 fungi resp.). Interpretation of results: introduction of factor 2 instead of factor 5. The recovery rate during the method validation is fixed at 50% (previously 20%).
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页码:995 / 1004
页数:10
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