洗手液的微生物学、科学和监管观点

IF 0.3 Q4 PHARMACOLOGY & PHARMACY
Chong Hock Sia, Ying Ting Tan, L. Chan
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引用次数: 0

摘要

摘要:洗手液是一种用于灭活手上微生物的可擦配方。随着最近的COVID-19大流行,洗手液的生产、销售和使用激增。然而,公众对洗手液的有效性和安全性并不是很了解;因此,洗手液的使用可能不能提供足够的保护,并可能造成安全威胁。在全球范围内,安全威胁的出现和不适当的制造商声明也表明,监管框架不足以确保洗手液的最佳有效性和安全标准。本文综述了抗菌药物在洗手液中作为有效成分的活性,以及评价洗手液有效性的测试方法原理。不同的抗菌素具有不同的活性,使某些抗菌素比其他抗菌素更有用。洗手液的功效也没有专门的药典测试,测试方法的选择由制造商自行决定。据报道,大量洗手液的标签不正确或有不适当的声明。实施更严格的监管框架,发展药剂师的知识和能力,提高消费者意识和揭穿常见的神话是解决所遇到的问题的一些可能的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microbiological, scientific and regulatory perspectives of hand sanitizers
Abstract: Hand sanitizers are rub-on formulations for the purpose of inactivating microorganisms on the hands. With the recent COVID-19 pandemic, a surge in the manufacturing, sale and use of hand sanitizers is observed. However, the effectiveness and safety of hand sanitizers are not well understood by the public; thus, hand sanitizer usage may not confer adequate protection and may pose safety threats. Globally, the emergence of safety threats and inappropriate manufacturer claims also suggest that regulatory frameworks are insufficient in ensuring optimal effectiveness and safety standards for hand sanitizers. This paper presents an overview of the activity of antimicrobials as active ingredients in hand sanitizers and the principles of test methods to evaluate the effectiveness of hand sanitizers. Different antimicrobials confer different activities, rendering some more useful than others. There are also no specific compendial test for efficacy of hand sanitizers and the choice of test method is left to the discretion of manufacturers. It has also been reported that a significant number of hand sanitizers were improperly labelled or had inappropriate claims. Implementing a tighter regulatory framework, developing pharmacists’ knowledge and capabilities, raising consumer awareness and debunking common myths are some possible solutions to address the problems encountered.
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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
0
期刊介绍: The scope of GaBI Journal is broad and of interest and relevance to professionals active in clinical practice, pharmaceutical science and policy. Materials published in GaBI Journal include high quality research reports, literature reviews and case studies, all of which are peer reviewed. Manuscripts on all aspects of generic and biosimilar medicines, covering areas in clinical, fundamental, technical, manufacturing, bi-processing, economic and social aspects of pharmaceuticals and therapeutics are welcome. In addition, high quality work submitted in other formats, for example, scientific and evidence-based commentaries, may also be considered. In all cases, the emphasis is on quality, originality and knowledge contribution to those involved in health care. All manuscripts submitted to GaBI Journal are subject to a rigorous peer review process. GaBI Journal plans to be indexed in PubMed within two years, and that indexing will be retrospective. GaBI Journal is published quarterly from 2012. All articles are published in English.
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