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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >HPTLC methods to assay active ingredients in pharmaceutical formulations: A review of the method development and validation steps
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HPTLC methods to assay active ingredients in pharmaceutical formulations: A review of the method development and validation steps

机译:用于测定药物制剂中活性成分的HPTLC方法:方法开发和验证步骤的回顾

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摘要

High-performance thin-layer chromatography (HPTLC) is still increasingly finding its way in pharmaceutical analysis in some parts of the world. With the advancements in the stationary phases and the introduction of densitometers as detection equipment, the technique achieves for given applications a precision and trueness comparable to high-performance liquid chromatography (HPLC). In this review, the literature is surveyed for developed and validated HPTLC methods to assay active ingredients in pharmaceutical formulations published in the period 2005-2011. Procedures and approaches for method development, validation and quantitative assays are compared with the standard ways of conducting them. Applications of HPTLC in some other areas are also briefly highlighted.
机译:高性能薄层色谱(HPTLC)在世界某些地区仍在越来越多地用于药物分析中。随着固定相的发展以及作为检测设备的光密度计的引入,该技术在给定的应用中实现了与高效液相色谱(HPLC)相当的精度和真实性。在本综述中,对2005-2011年间发表的已开发和验证的HPTLC方法进行了调查,以分析药物制剂中的活性成分。将方法开发,验证和定量分析的程序和方法与执行它们的标准方法进行比较。还简要介绍了HPTLC在其他一些领域的应用。

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