在线水质生物负载分析仪的微生物验证替代方案。

Olivia L Venhuizen, Cynthia E Martindale, Feng Jin Liew, James Cannon, Arundhati Samanta, Mike J Scaramozzino
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引用次数: 0

摘要

背景:梅特勒-托利多 7000RMS 分析仪是一种生物荧光颗粒计数器 (BFPC),用于实时监测纯净水 (PW) 的生物负载结果:目标:使用 13 种微生物和低强度荧光聚苯乙烯珠对分析仪进行验证:方法:在验证过程中,将符合纯净水 (PW) 质量标准的实验室水系统连接到 7000RMS 上,使用注射泵将不同浓度的微生物和荧光聚苯乙烯珠引入分析仪。通过传统的膜过滤 (MF) 方法收集和检测样品,并将菌落形成单位 (CFU) 平板计数结果与 7000RMS 分析仪的自动荧光单元 (AFU) 进行比较。验证研究的设计遵循了《美国药典》(USP)第(1)章、《欧洲药典》(EP)第 5.1.6 (2)章、《PDA 技术报告 33》(3)中的指导。概念和策略改编自 EP 第 2.6.12 章《非无菌产品的微生物检查》:微生物计数测试》,EP 10.2 (4),《欧洲药典》第 2.6.1 章《无菌》,EP 10.2 (5),《美国药典》第 2.6.12 章《非无菌产品的微生物检查:微生物计数测试》:微生物计数测试 (6)、USP 无菌测试 (7)、日本药典 (JP) 一般信息 G8 章水:结果和结论:结果和结论:7000RMS 符合准确度、特异性、精密度、检测限 (LOD)、定量限 (LOQ)、线性度和量程等所有预定的验证验收标准。此外,7000RMS 还根据 USP 证明了与 MF 方法的性能等同性,但缺乏与 CFU.Highlights 的相关性:该验证方法突出显示了 7000RMS 与传统的药典 MF 检测方法相比,具有卓越的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Alternative Microbiological Validation for an Online Water Bioburden Analyzer.

Background: The Mettler-Toledo 7000RMS analyzer is a bio-fluorescent particle counter (BFPC) used to monitor real-time bioburden results from purified water (PW).

Objective: Validation of the analyzer using 13 microorganisms and a low-intensity, fluorescent, polystyrene bead.

Methods: During the execution of the validation, a laboratory water system that met PW quality standards was connected to the 7000RMS, and a syringe pump was used to introduce various concentrations of microorganisms and fluorescent polystyrene beads to the analyzer. Samples were collected and tested via the traditional membrane filtration (MF) method and the colony-forming unit (CFU) plate count results were compared to the auto-fluorescent unit (AFU) of the 7000RMS analyzer. The validation study was designed to follow the guidance in United States Pharmacopeia (USP) Chapter <1223>, European Pharmacopeia (EP) Chapter 5.1.6, and parenteral drug association (PDA) Technical Report 33. Concepts and strategies were adapted from EP Chapter 2.6.12 Microbiological Examination of Non-Sterile Products: Microbial Enumeration Tests, EP Chapter 10.2, EP Chapter 2.6.1 Sterility, USP Chapter <61> Microbiological Examination of Non-Sterile Products: Microbial Enumeration Tests, USP Chapter <71> Sterility Tests, and Japanese Pharmacopoeia (JP) General Information Chapter G8 Water: Quality Control of Water for Pharmaceutical Use.

Results: All pre-determined validation acceptance criteria for accuracy, specificity, precision, LOD, LOQ, linearity, and range were met.

Conclusions: The 7000RMS demonstrated performance equivalence to the MF method per USP <1223> but characteristically lacked correlation to the CFU.

Highlights: This validation approach highlights the superior capabilities of the 7000RMS when compared against the traditional compendial MF testing method for PW.

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