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首页> 外文期刊>Journal of liquid chromatography and related technologies >Application of an expanded model procedure for transfer of TLC screening methods for substandard and fake drugs designed for use in developing countries to quantitative HPTLC-densitometry methods
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Application of an expanded model procedure for transfer of TLC screening methods for substandard and fake drugs designed for use in developing countries to quantitative HPTLC-densitometry methods

机译:将扩展的模型程序应用于为发展中国家设计的次标准和假药的TLC筛选方法转移到定量HPTLC密度测定法中

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摘要

Transfer of four rapid thin-layer chromatography (TLC) screening methods used to detect substandard and fake pharmaceutical products to quantitative high-performance TLC (HPTLC)-densitometry methods is demonstrated using an expanded version of a model procedure that was published earlier. These methods for mebendazole, diphenhydramine hydrochloride, amodiaquine, and artesunate are contained in a Compendium of methods by Kenyon and Layloff and/or Minilab method manuals from Global Pharma Health Fund E.V. for use in countries with limited resources. A new HPTLC-densitometry method was also developed for amitriptyline hydrochloride, for which there was no Compendium or Minilab method that could be transferred. These quantitative methods use Merck HPTLC silica gel 60 F 254 glass plates, automated standard and sample solution application, and automated densitometry for detection, identification, and quantification. Standard and sample solution preparation and application procedures for obtaining calibration curves and bracketed samples are described. Additions to the previous model procedure include peak identity and purity checks by spectral comparison. HPTLC gives better efficiency, selectivity, and resolution than TLC, and the new methods overcome the deficiencies in technology related to manual application and visual zone comparison that do not allow the Compendium and Minilab TLC procedures to support regulatory compliance actions. These new methods can be fully validated according to International Conference on Harmonization (ICH) guidelines or by interlaboratory studies if their applications require.
机译:使用先前发布的模型程序的扩展版本,证明了将用于检测不合格药品和假药的四种快速薄层色谱(TLC)筛选方法转移到定量高性能TLC(HPTLC)密度测定法中。这些用于苯达唑,盐酸苯海拉明,阿莫地喹和青蒿琥酯的方法包含在Kenyon和Layloff的方法纲要和/或Global Pharma Health Fund E.V.的Minilab方法手册中。供资源有限的国家使用。还开发了一种新的用于盐酸阿米替林的HPTLC密度测定法,该方法没有可移植的Compendium或Minilab方法。这些定量方法使用默克HPTLC硅胶60 F 254玻璃板,自动标准液和样品溶液的应用以及自动光密度法进行检测,鉴定和定量。描述了用于获得校准曲线和带括号的样品的标准溶液和样品溶液的制备以及应用程序。对先前模型程序的补充包括通过光谱比较进行峰鉴定和纯度检查。 HPTLC提供了比TLC更好的效率,选择性和分离度,新方法克服了与手动应用和可视区域比较相关的技术缺陷,这些缺陷使Compendium和Minilab TLC程序无法支持法规遵从行为。这些新方法可以根据国际协调会议(ICH)指南或通过实验室间研究(如果需要应用)进行充分验证。

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