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首页> 外文期刊>PDA journal of pharmaceutical science and technology >Method for qualifying microbial removal performance of 0.1 micron rated filters. Part I: characterization of water isolates for potential use as standard challenge organisms to qualify 0.1 micron rated filters.
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Method for qualifying microbial removal performance of 0.1 micron rated filters. Part I: characterization of water isolates for potential use as standard challenge organisms to qualify 0.1 micron rated filters.

机译:鉴定0.1微米额定过滤器的微生物去除性能的方法。第一部分:水分离物的表征,这些水分离物有可能用作标准挑战生物以鉴定0.1微米级滤池。

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摘要

Although 0.1 microm rated filters intended for pharmaceutical sterilization applications have been commercially available for at least 15 years, there is no industry-wide standard for qualifying the microbial removal performance of these filters. In this article, we report on the bacterial challenge methodology used to screen four bacterial species for potential utility as a standard challenge organism to qualify 0.1 microm rated filters. These isolates were, in their natural state, demonstrated to penetrate 0.2/0.22 microm rated filters in prior studies. In the screening challenges described in this study, three out of these four candidates tested demonstrated consistent penetration of one 0.22 microm rated filter type tested (when cultured in a low nutrient medium under standard laboratory conditions). These included 6204-22 (FAME ID Acidovorax avenae citrulli), 6266-15 (FAME ID Comamonas acidovorans), and 6266-34 (FAME ID Hydrogenophaga pseudoflava). Of these, H. pseudoflava (6266-34) was chosen for additional experiments with other 0.2 microm rated filter membranes. In total, seventeen 0.2 and 0.22 microm rated filter discs, spanning five different "sterilizing grade" filter types from three different filter manufacturers were tested. H. pseudoflava penetration was observed for every filter tested. Under the same challenge conditions, H. pseudoflava was consistently retained by a 0.1 microm rated hydrophilic PVDF (polyvinylidenefluoride) filter with a specified high titer reduction claim for Acholeplasma laidlawii. In order to ensure selection of the most stable penetrative phenotype (i.e., select for nonrevertants), H. pseudoflava was subjected to three rounds of "filter cloning," and these results are described herein. The advantages of using H. pseudoflava for qualifying the microbial removal performance of 0.1 microm rated filters are also discussed.
机译:尽管用于药物灭菌的0.1微米级过滤器已经在市场上销售了至少15年,但尚无行业标准来限定这些过滤器的微生物去除性能。在本文中,我们报告了用于筛选四种细菌的细菌攻击方法,这些细菌有潜力用作标准攻击生物以鉴定0.1微米级过滤器。在以前的研究中,这些分离物以其自然状态显示可穿透0.2 / 0.22微米级别的过滤器。在这项研究中描述的筛选挑战中,测试的这四个候选对象中的三个证明了一种0.22微米额定滤器类型(在标准实验室条件下在低营养培养基中培养时)的一致渗透。这些包括6204-22(FAME ID酸果蝇),6266-15(FAME ID酸果蝇)和6266-34(FAME ID氢假单胞菌)。其中,拟假丝酵母(6266-34)被选择用于其他0.2微米额定滤膜的实验。总共测试了十七个0.2和0.22微米级的滤盘,这些滤盘跨越了来自三个不同过滤器制造商的五种不同的“灭菌等级”过滤器类型。对于每个测试的过滤器均观察到假丝酵母的渗透。在相同的挑战条件下,假丝酵母​​被0.1微米级亲水性PVDF(聚偏二氟乙烯)过滤器固定住,并具有对莱德氏无孢菌的高滴度降低要求。为了确保选择最稳定的穿透性表型(即选择非回复性表型),对假丝酵母进行了三轮“过滤器克隆”,并且在此描述了这些结果。还讨论了使用拟杆菌H鉴定0.1微米级过滤器的微生物去除性能的优势。

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