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发展中国家即时药物质量保证:小规模随机阿莫西林样本的液相色谱和红外光谱定量比较。

Toward Point-of-Care Drug Quality Assurance in Developing Countries: Comparison of Liquid Chromatography and Infrared Spectroscopy Quantitation of a Small-Scale Random Sample of Amoxicillin.

机构信息

Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario, Canada.

Faculty of Law, University of Ottawa, Ottawa, Ontario, Canada.

出版信息

Am J Trop Med Hyg. 2018 Aug;99(2):477-481. doi: 10.4269/ajtmh.17-0779. Epub 2018 Jun 7.

DOI:10.4269/ajtmh.17-0779
PMID:29893196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6090331/
Abstract

Substandard antibiotics are thought to be a major threat to public health in developing countries and a cause of antimicrobial resistance. However, assessing quality outside of a laboratory setting, using simple equipment, is challenging. The aim of this study was to validate the use of a portable Fourier transform infrared (FT-IR) spectrometer for the identification of substandard antibiotics. Results are presented for amoxicillin packages from Haiti, Ghana, Sierra Leone, Democratic Republic of Congo, India, Papua New Guinea, and Ethiopia collected over the course of 6 months in 2017, including two field trips with the FT-IR to Ghana and Sierra Leone. Canadian samples were used as a control. Regarding drug quality, of 290 individual capsules of amoxicillin analyzed, 13 were found to be substandard with total active pharmaceutical ingredients (API) lying outside the acceptable range of 90-110%. Of these 13, four were below 80% API. The FT-IR reliably identified these outliers and was found to yield results in good agreement with the established pharmacopeia liquid chromatography protocol. We conclude that the portable FT-IR may be suitable to intercept substandard antibiotics in developing countries where more sophisticated techniques are not readily available.

摘要

劣质抗生素被认为是发展中国家公共卫生的主要威胁,也是导致抗微生物药物耐药性的一个原因。然而,在实验室环境之外,使用简单的设备来评估质量是具有挑战性的。本研究的目的是验证使用便携式傅里叶变换红外(FT-IR)光谱仪来识别劣质抗生素的可行性。本研究结果展示了 2017 年 6 个月期间在海地、加纳、塞拉利昂、刚果民主共和国、印度、巴布亚新几内亚和埃塞俄比亚收集的阿莫西林药品,包括两次使用 FT-IR 对加纳和塞拉利昂的实地考察。加拿大的样本被用作对照。在药物质量方面,分析了 290 个单独的阿莫西林胶囊,发现其中 13 个不符合标准,总活性药物成分(API)超出了 90-110%的可接受范围。其中 4 个的 API 低于 80%。FT-IR 能够可靠地识别这些异常值,并且与已建立的药典液相色谱法协议得出的结果非常吻合。我们得出结论,在那些更复杂的技术不易获得的发展中国家,便携式 FT-IR 可能适合拦截劣质抗生素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/f438259e901a/tpmd170779f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/4d9e4e5d87ff/tpmd170779f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/07cfe7f2fde4/tpmd170779f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/17821fe089c8/tpmd170779f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/f438259e901a/tpmd170779f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/4d9e4e5d87ff/tpmd170779f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/07cfe7f2fde4/tpmd170779f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/17821fe089c8/tpmd170779f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6737/6090331/f438259e901a/tpmd170779f4.jpg

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