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用于测定舍吲哚的稳定性指示色谱法

Stability-indicating chromatographic methods for the determination of sertindole.

作者信息

El-Ragehy Nariman A, Hassan Nagiba Y, Abdelkawy Mohamed, Tantawy Mahmoud A

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr el Aini Street, 11562, Cairo, Egypt.

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr el Aini Street, 11562, Cairo, Egypt

出版信息

J Chromatogr Sci. 2014 Jul;52(6):559-65. doi: 10.1093/chromsci/bmt066. Epub 2013 Jun 2.

Abstract

In this work, two chromatographic methods have been developed and validated for the determination of sertindole (an antipsychotic agent) in the presence of its oxidative degradation product. Sertindole was subjected to stress stability studies, including acid, alkali, oxidative, photolytic and thermal degradation. The chromatographic methods included the use of thin-layer chromatography (TLC-densitometry) and high-performance liquid chromatography (HPLC). The TLC method employed aluminum TLC plates precoated with silica gel G.F254 as the stationary phase and methanol-ethyl acetate-33% ammonia (1:9:0.1, by volume) as the mobile phase, and the chromatograms were scanned at 227 nm. The developed HPLC method used a reversed-phase C18 column with isocratic elution. The mobile phase was composed of phosphate buffer pH 3.0-acetonitrile-triethylamine (45:55:0.03, by volume) and run at a flow rate of 1.0 mL/min. Quantitation was achieved with ultraviolet detection at 256 nm. The linearity ranges were found to be 2-14 µg/band and 5-200 µg/mL for TLC and HPLC, respectively. The developed methods were validated according to the International Conference on Harmonization guidelines and were applied for bulk powder and dosage forms.

摘要

在本研究中,已开发并验证了两种色谱方法,用于在存在氧化降解产物的情况下测定舍吲哚(一种抗精神病药物)。对舍吲哚进行了强制稳定性研究,包括酸、碱、氧化、光解和热降解。色谱方法包括使用薄层色谱法(薄层扫描法)和高效液相色谱法(HPLC)。薄层色谱法采用预涂硅胶G.F254的铝制薄层板作为固定相,以甲醇 - 乙酸乙酯 - 33%氨水(体积比为1:9:0.1)作为流动相,并在227 nm处扫描色谱图。所开发的高效液相色谱法使用反相C18柱进行等度洗脱。流动相由pH 3.0的磷酸盐缓冲液 - 乙腈 - 三乙胺(体积比为45:55:0.03)组成,流速为1.0 mL/min。通过在256 nm处进行紫外检测进行定量。薄层色谱法和高效液相色谱法的线性范围分别为2 - 14 μg/条带和5 - 200 μg/mL。所开发的方法根据国际协调会议指南进行了验证,并应用于原料药和剂型。

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