Review and comparison of acceptance criteria for Senna and its preparations according to BP (2015 and 2020) and USP-NF (39-34 and 43-38)

Q4 Pharmacology, Toxicology and Pharmaceutics Infarma Pharmaceutical Sciences Pub Date : 2021-12-27 DOI:10.34172/ps.2021.80
L. Khodaie, Saurabh Bhatia, A. Al-Harrasi
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Abstract

Background: Quality and quantity assurance of herbs are global concerns. This study aimed to classify and compare the monographs and test procedures of Senna parts and preparations according to two editions of BP and USP-NF. The monographs and specifications were compared to suggest an applicable approach to extract relevant data. Methods: BP 2015 and 2020, USP-NF 39-34 and 43-38, as well as scientific databases were used for literature review. Results: the results of this study were classified in 3 tables; table 1 classified specifications of herbal monographs in pharmacopeias. Table 2 classified various identification tests, measurement methods, and standard phytochemicals for quantitative assays. Table 3 outlined and categorized related physicochemical and contamination tests for quality assurance according to two editions of BP and USP-NF. In both editions of USP-NF, only sennosides powder and tablets were required to be analyzed for heavy metals. Hence, microbial contamination tests were merely included for leaves and pods of Senna. In both editions of BP, assessment of microbial contamination was merely included in the monograph of dry extract of Senna, not for the rest of monographs. Comparing two editions of BP indicated that in BP 2020, LC and HPTLC methods were added to assure the quality of pods and leaflets of Senna species. Conclusion: preparation of tabular data will assist analysts to extract desired information and guidelines to prepare licensed herbal products. This approach could be applicable to select relevant tests according to the facilities and equipment of laboratories.
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根据BP(2015和2020)和USP-NF(39-34和43-38)审查和比较塞纳及其制剂的验收标准
背景:草药的质量和数量保证是全球关注的问题。本研究旨在根据BP和USP-NF两个版本对塞纳部位和制剂的专著和试验方法进行分类和比较。比较了专著和规范,提出了一种适用的方法来提取相关数据。方法:采用BP 2015、2020、USP-NF 39-34、43-38以及科学数据库进行文献综述。结果:本研究结果分为3个表;表1药典中草药专著分类规范。表2分类了用于定量分析的各种鉴定试验、测量方法和标准植物化学物质。表3根据两个版本的BP和USP-NF概述并分类了质量保证的相关理化和污染测试。在两个版本的USP-NF中,仅要求对sen皂苷粉末和片剂进行重金属分析。因此,微生物污染检测仅包括番泻叶和豆荚。在两个版本的BP中,微生物污染的评估仅包括在番泻叶干提取物的专论中,而不是在其他专论中。比较两个版本的BP表明,在BP 2020中增加了LC和HPTLC方法,以保证番泻豆荚和小叶的质量。结论:表格数据的准备将有助于分析人员提取所需的信息和指南,以制备许可的草药产品。该方法可适用于根据实验室的设施和设备选择相关试验。
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来源期刊
CiteScore
0.10
自引率
0.00%
发文量
17
审稿时长
10 weeks
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