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Analytical Method Development and Validation for the Quantification of Acetone and Isopropyl Alcohol in the Tartaric Acid Base Pellets of Dipyridamole Modified Release Capsules by Using Headspace Gas Chromatographic Technique

机译:顶空气相色谱技术定量分析双嘧达莫修饰释放胶囊酒石酸碱微丸中丙酮和异丙醇的分析方法

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摘要

A simple, sensitive, accurate, robust headspace gas chromatographic method was developed for the quantitative determination of acetone and isopropyl alcohol in tartaric acid-based pellets of dipyridamole modified release capsules. The residual solvents acetone and isopropyl alcohol were used in the manufacturing process of the tartaric acid-based pellets of dipyridamole modified release capsules by considering the solubility of the dipyridamole and excipients in the different manufacturing stages. The method was developed and optimized by using fused silica DB-624 (30 m × 0.32 mm × 1.8 µm) column with the flame ionization detector. The method validation was carried out with regard to the guidelines for validation of analytical procedures Q2 demanded by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). All the validation characteristics were meeting the acceptance criteria. Hence, the developed and validated method can be applied for the intended routine analysis.
机译:建立了一种简单,灵敏,准确,可靠的顶空气相色谱法,用于定量测定双嘧达莫缓释胶囊的酒石酸基药丸中的丙酮和异丙醇。考虑到双嘧达莫和赋形剂在不同制造阶段的溶解度,将残留的溶剂丙酮和异丙醇用于双嘧达莫修饰释放胶囊的酒石酸基小丸的生产过程中。该方法是通过使用带有火焰电离检测器的熔融石英DB-624(30μm××0.32μmm××1.8μm)色谱柱开发和优化的。方法验证是根据国际人用药品技术要求协调委员会(ICH)要求的分析程序验证指南Q2进行的。所有验证特征均符合验收标准。因此,可以将开发和验证的方法应用于预期的常规分析。

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