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一种用于测定药品中异维A酸及其降解产物的气相色谱法的开发。

Development of a gas chromatography method for the determination of isotretinoin and its degradation products in pharmaceuticals.

作者信息

Lima Eliana Martins, Diniz Danielle G Almeida, Antoniosi-Filho Nelson R

机构信息

Lab. Tecnologia Farmaceutica, Faculdade de Farmacia, Universidade Federal de Goias, Av. Universitaria, 74605-220 Goiania, GO, Brazil.

出版信息

J Pharm Biomed Anal. 2005 Jul 15;38(4):678-85. doi: 10.1016/j.jpba.2005.02.015.

Abstract

This paper describes the development of a gas chromatography (GC) method used for the assay of isotretinoin in its isolated form and in pharmaceutical formulations. Isotretinoin soft and hard gelatin capsules were prepared with various excipients. The performance of the proposed gas chromatography method was compared to that of traditional high performance liquid chromatography (HPLC) systems for this substance, and the GC parameters were established based on several preliminary tests, including thermal analysis of isotretinoin. Results showed that gas chromatography-flame ionization detector (GC-FID) exhibited a separation efficiency superior to that of HPLC, particularly for separating isotretinoin degradation products. This method was proven to be effectively applicable to stability evaluation assays of isotretinoin and isotretinoin based pharmaceuticals.

摘要

本文描述了一种气相色谱(GC)方法的开发,该方法用于测定异维A酸的分离形式及其药物制剂中的含量。用各种辅料制备了异维A酸软胶囊和硬胶囊。将所提出的气相色谱方法的性能与该物质的传统高效液相色谱(HPLC)系统的性能进行了比较,并基于包括异维A酸热分析在内的多项初步试验确定了GC参数。结果表明,气相色谱 - 火焰离子化检测器(GC - FID)的分离效率优于HPLC,特别是在分离异维A酸降解产物方面。该方法被证明可有效应用于异维A酸及基于异维A酸的药物的稳定性评估测定。

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