[Analysis and application thinking of standards for 500 kinds of traditional Chinese medicine formula granules on base of industrial practice].

Q3 Pharmacology, Toxicology and Pharmaceutics
Yong Liu, Jun Zhang, Xin-Hai Dong, Lin Zhou, Dong-Mei Sun, Fu-Lin Mao, Zhen-Yu Li, Lei Huang, Jin-Lai Liu
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引用次数: 0

Abstract

Following the release of the Technical Requirements on Quality Control and Standard Establishment of Traditional Chinese Medicine Formula Granules by the National Medical Products Administration in 2021, Chinese Pharmacopoeia Commission has promulgated 296 national drug standards so far, and most provinces have started the work of establishing provincial standards as supplements. The promulgation of standards fostered high-quality development of the industry. Since the implementation of national and provincial standards for more than three years, enterprises have gained deep understanding and hands-on experiences on the characteristics, technical requirements, production process, and quality control of traditional Chinese medicine(TCM) formula granules. Meanwhile, challenges have emerged restricting the high-quality development of this industry, including how to formulate quality control strategies for medicinal materials and decoction pieces, how to reduce manufacturing costs, and how to improve the pass rate and product stability under high standards. Based on the work experiences from standard management and process research, this article analyzed the distribution of sources, processing methods, dry extract rate ranges, process requirements for volatile oil-containing decoction pieces, control measures of safety indices, characteristics and trends of setting characteristic chromatograms or fingerprints, characteristics and trends of setting content ranges, and main differences between national standards and provincial standards. On the one hand, this article aims to present main characteristics for deeply understanding different indicators in standards and provide basic ideas for establishing quality and process control systems. On the other hand, from the perspective of industrial practice, suggestions are put forward on the important aspects that need to be focused on in the quality and process control of TCM formula granules.

[基于工业实践的500种中药配方颗粒标准分析及应用思考]。
自2021年国家药品监督管理局发布《中药配方颗粒剂质量控制与标准编制技术要求》以来,中国药典委员会先后颁布了296项国家药品标准,大部分省份开展了省标补充工作。标准的颁布促进了行业的高质量发展。国家和省标准实施三年多来,企业对中药配方颗粒的特点、技术要求、生产工艺、质量控制等有了深入的了解和实践经验。同时,如何制定药材和饮片的质量控制策略,如何降低生产成本,如何在高标准下提高合格率和产品稳定性,也成为制约中药饮片行业高质量发展的挑战。本文根据标准管理和工艺研究的工作经验,分析了含挥发油饮片的来源分布、炮制方法、干浸出率范围、工艺要求、安全指标的控制措施、设置特征色谱或指纹图谱的特点和趋势、设置含量范围的特点和趋势、国家标准与省标准的主要区别。一方面,本文旨在为深入理解标准中不同指标提供主要特征,为建立质量和过程控制体系提供基本思路。另一方面,从工业实践的角度,对中药配方颗粒质量和工艺控制中需要重点关注的方面提出了建议。
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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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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