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引用本文:康美娟,李辉,赵霞.中国药包材微生物检查方法及标准的合理性探讨[J].中国现代应用药学,2023,40(10):1435-1440.
KANG Meijuan,LI Hui,ZHAO Xia.Discussion on the Rationality of Methods and Standards of Microbiological Examination for Pharmaceutical Packaging Materials in China[J].Chin J Mod Appl Pharm(中国现代应用药学),2023,40(10):1435-1440.
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中国药包材微生物检查方法及标准的合理性探讨
康美娟1, 李辉2,3, 赵霞4
1.西安石油大学, 西安 710065;2.陕西科技大学, 西安 710021;3.陕西盛德泰林生物安全技术检测有限公司, 西安 710065;4.中国食品药品检定研究院, 北京 100050
摘要:
《国家药包材标准》2015年版收载了130个药包材标准,在保障药包材及药品质量安全方面发挥了重要作用。然而,随着中国药典2020年版的修订和对药包材微生物限度检查认识的不断提高,当前药包材标准中的5类29种微生物和无菌检查方法及限度标准的合理性存在一定问题。本文从药包材微生物标准的项目设置、检查方法等方面分析存在的问题,提出优化项目等7个方面的修订建议,探讨建立基于风险的药包材微生物检查方法及标准的可行性,以期为中国药包材微生物检查方法及标准体系的完善提供参考。
关键词:  药包材  药包材标准  中国药典  微生物限度  无菌  接收质量限
DOI:10.13748/j.cnki.issn1007-7693.20221986
分类号:R953
基金项目:陕西省重点研发计划项目(2019SF-062);国家药典委员会药品标准提高项目(2018-15)
Discussion on the Rationality of Methods and Standards of Microbiological Examination for Pharmaceutical Packaging Materials in China
KANG Meijuan1, LI Hui2,3, ZHAO Xia4
1.Xi'an Shiyou University, Xi'an 710065, China;2.Shaanxi University of Science and Technology, Xi'an 710021, China;3.Shaanxi Shengde Tailin Biological Safety Technical Testing Co., Ltd., Xi'an 710065, China;4.National Institutes for Food and Drug Control, Beijing 100050, China
Abstract:
The National Standards for Pharmaceutical Packaging Materials 2015 edition contained 130 standards for pharmaceutical packaging materials, which played an important role in ensuring the quality and safety of pharmaceutical packaging materials and drugs. However, with the revision of the Chinese Pharmacopoeia 2020 edition and the continuous improvement of the understanding of the microbial limit testing of pharmaceutical packaging materials, there are certain rationality problems in the 29 microbiological examination methods in 5 categories pharmaceutical packaging material standards. This paper analyzes the existing problems from the aspects of project setting and methods of microbial standards for pharmaceutical packaging materials, puts forward 7 suggestions such as optimizing projects, and discusses the feasibility of establishing risk-based microbial inspection methods and standards for pharmaceutical packaging materials. In order to provide a reference for the improvement of the microbiological inspection methods and standard system of pharmaceutical packaging materials in China.
Key words:  pharmaceutical packaging materials  standards for pharmaceutical packaging materials  Chinese Pharmacopoeia  microbial limit  sterility  acceptance quality limit
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