Moldenhauer J E, Bass S A, Kupinski M J, Walters M L, Rubio S L
PDA J Pharm Sci Technol. 1996 Nov-Dec;50(6):391-8.
Two types of Tyvek and high density polyethylene or polypropylene packaging used for sterilization of rubber closures were evaluated for Microbial Barrier properties. The packaging evaluated was "Ready to Sterilize" (1) stoppers and a second test package (Test 2) which was designated as appropriate for a clean room, filled with washed and siliconized stoppers and then heat sealed. Each type of packaging was subjected to three different sterilization temperatures (125 degrees C, 128 degrees C and 131 degrees C) in a production sterilizer (15-18 psi). Following sterilization, a microbial barrier assessment was performed, using Bacillus subtilis niger (ATCC 9372), to determine whether the packaging could maintain a sterile barrier following sterilization. Results of the testing indicated that a microbial barrier was maintained for products in "Ready to Sterilize" packages at 125 degrees C and 128 degrees C. For products sterilized in the Test 2 container a microbial barrier could not be maintained at 128 degrees C, and no further testing was performed. Following sterilization at 131 degrees C physical defects were noted for the "Ready to Sterilize" bag and a microbial barrier could not be maintained.
对用于橡胶瓶塞灭菌的两种特卫强(Tyvek)以及高密度聚乙烯或聚丙烯包装的微生物屏障特性进行了评估。所评估的包装一种是“即待灭菌”(1)瓶塞,另一种测试包装(测试2)被指定适用于洁净室,里面装有经过清洗和硅化处理的瓶塞,然后热封。每种包装在生产灭菌器(15 - 18磅力/平方英寸)中经受三种不同的灭菌温度(125摄氏度、128摄氏度和131摄氏度)。灭菌后,使用黑曲霉(ATCC 9372)进行微生物屏障评估,以确定包装在灭菌后是否能维持无菌屏障。测试结果表明,“即待灭菌”包装中的产品在125摄氏度和128摄氏度时能维持微生物屏障。对于在测试2容器中灭菌的产品,在128摄氏度时无法维持微生物屏障,且未进行进一步测试。在131摄氏度灭菌后,“即待灭菌”袋出现物理缺陷,无法维持微生物屏障。