用于测定 (+/-) 西酞普兰及其 S-enantiomer 艾司西酞普兰的胶束增强荧光法和薄层色谱密度计法。

Elham A Taha, Nahla N Salama, Shudong Wang
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引用次数: 0

摘要

为测定外消旋混合物西酞普兰及其对映体 S-(+) 艾司西酞普兰,我们开发了两种灵敏且经过验证的方法。第一种方法是使用十二烷基硫酸钠作为胶束增强剂,直接测量艾司西酞普兰的本征荧光。该方法还被进一步应用于检测加标人体血浆中的艾司西酞普兰,以及常见药物和联合用药情况下的艾司西酞普兰。第二种方法是基于各种手性选择剂的 TLC 密度测定法。结果表明,最佳的 TLC 条件对鉴定和定量测定药物和药物产品中艾司西酞普兰对映体的纯度具有灵敏度和选择性。该方法可用于调查纯异构体与廉价外消旋体的掺假。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Micelle enhanced fluorimetric and thin layer chromatography densitometric methods for the determination of (+/-) citalopram and its S-enantiomer escitalopram.

Micelle enhanced fluorimetric and thin layer chromatography densitometric methods for the determination of (+/-) citalopram and its S-enantiomer escitalopram.

Micelle enhanced fluorimetric and thin layer chromatography densitometric methods for the determination of (+/-) citalopram and its S-enantiomer escitalopram.

Micelle enhanced fluorimetric and thin layer chromatography densitometric methods for the determination of (+/-) citalopram and its S-enantiomer escitalopram.

Two sensitive and validated methods were developed for determination of a racemic mixture citalopram and its enantiomer S-(+) escitalopram. The first method was based on direct measurement of the intrinsic fluorescence of escitalopram using sodium dodecyl sulfate as micelle enhancer. This was further applied to determine escitalopram in spiked human plasma, as well as in the presence of common and co-administrated drugs. The second method was TLC densitometric based on various chiral selectors was investigated. The optimum TLC conditions were found to be sensitive and selective for identification and quantitative determination of enantiomeric purity of escitalopram in drug substance and drug products. The method can be useful to investigate adulteration of pure isomer with the cheap racemic form.

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