Microbial Air Samplers for Meaningful Cleanroom Environmental Monitoring

T. Eaton
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Abstract

Airborne microbiological concentrations within pharmaceutical cleanrooms are determined by sampling and to maximise the detection of any airborne microbes, it is essential that the sampling is undertaken in locations where there is greatest contamination risk using air samplers that have a verified and appropriate performance. Sampler performance can be assessed by review of both the physical and biological collection efficiencies that are determined by testing. The physical collection efficiency is the ability to collect particles of various sizes and the biological collection efficiency assesses the collection of viable microbes that includes the losses caused by the physical collection efficiency and the detrimental effect that the sampling has on the viability of the captured microbes. Due to the limitations of the established biological collection efficiency test method, this efficiency is only determined for microbes of sub-micron size which are not representative of the larger microbe-carrying particles typically present with cleanrooms. Samplers with a low physical collection efficiency for sub-micron particles are likely to have a poor performance when this test method is utilised and in an attempt to remove this bias from the testing the ‘biological efficiency’, is often reported. This is a measure of the likelihood that any captured microbes would survive, but is often mistaken for the biological collection efficiency and samplers may be utilised in the false belief that they have an appropriate performance. This article provides information regarding air sampler performance testing and reviews the test results reported by the same independent specialist testing company, therefore negating issues resulting from different testing methods, for three different air samplers. The results that are used to determine the ‘biological efficiency’ are examined to provide information relating to the biological collection efficiency of each sampler and to also provide additional information relating to the physical collection efficiency. Improvements to enhance the air sampler testing procedures, to enable a better direct comparison of the performance of different samplers, are suggested.
微生物空气采样器用于有意义的洁净室环境监测
制药洁净室内的空气微生物浓度是通过采样来确定的,为了最大限度地检测任何空气微生物,必须在污染风险最大的地方进行采样,使用具有验证和适当性能的空气采样器。采样器的性能可以通过审查由测试确定的物理和生物收集效率来评估。物理收集效率是收集各种大小颗粒的能力,生物收集效率评估活菌的收集,包括物理收集效率造成的损失和采样对捕获微生物活力的有害影响。由于已建立的生物收集效率测试方法的局限性,该效率仅针对亚微米大小的微生物确定,而这些微生物不能代表洁净室中通常存在的较大的携带微生物的颗粒。当使用这种测试方法时,对亚微米颗粒的物理收集效率较低的采样器可能具有较差的性能,并且在试图从测试中消除这种“生物效率”的偏差时,经常报道。这是衡量任何捕获的微生物存活的可能性,但经常被误认为是生物收集效率,采样器可能被错误地认为它们具有适当的性能。本文提供了有关空气采样器性能测试的信息,并审查了同一家独立专家测试公司报告的测试结果,因此否定了三种不同空气采样器不同测试方法导致的问题。检查用于确定“生物效率”的结果,以提供与每个采样器的生物收集效率有关的信息,并提供与物理收集效率有关的额外信息。建议改进空气采样器的测试程序,以便更好地直接比较不同采样器的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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