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凝胶挤出模块片剂制剂中残留溶剂的静态顶空气相色谱分析

Static headspace gas chromatographic analysis of the residual solvents in gel extrusion module tablet formulations.

作者信息

Li Zhong, Han Yieng-Hau, Martin Gregory P

机构信息

Merck Research Laboratories, West Point, PA 19486, USA.

出版信息

J Pharm Biomed Anal. 2002 May 15;28(3-4):673-82. doi: 10.1016/s0731-7085(01)00657-4.

Abstract

A rapid static headspace-gas chromatographic (SHS-GC) method was developed and validated for the quantitation of residual solvents in pharmaceutical gel extrusion module (GEM) tablet formulations. A static headspace sampling technique was utilized to overcome the difficulties imposed by direct injection methods. A Rtx-1701 megabore capillary column was selected to achieve optimal resolution among organic volatile chemicals used commonly in the manufacturing of GEM tablets, residual solvents in the active ingredient and excipients, and other formulation matrix artifacts. A 50-mM pH 3.0 sodium phosphate buffer was used as a sample diluent to minimize matrix effects. The instrumental parameters of the SHS-GC method were optimized for sensitivity and precision. Quantitation was performed by external standard analysis. The SHS-GC method was validated according to regulatory requirements and produced acceptable results with respect to specificity, linearity, range, detection and quantitation limits, precision, and accuracy.

摘要

建立了一种快速静态顶空气相色谱(SHS-GC)方法,并对其进行了验证,用于定量测定药物凝胶挤出模块(GEM)片剂配方中的残留溶剂。采用静态顶空进样技术克服直接进样方法带来的困难。选用Rtx-1701大口径毛细管柱,以实现GEM片剂生产中常用有机挥发性化学品、活性成分和辅料中的残留溶剂以及其他制剂基质杂质之间的最佳分离度。使用50 mM pH 3.0的磷酸钠缓冲液作为样品稀释剂,以尽量减少基质效应。对SHS-GC方法的仪器参数进行了优化,以提高灵敏度和精密度。采用外标法进行定量分析。该SHS-GC方法根据法规要求进行了验证,在特异性、线性、范围、检测限和定量限、精密度和准确度方面均产生了可接受的结果。

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