Enantiomeric resolution of three profen drugs using direct thin-layer chromatographic method

IF 1.1 4区 化学 Q4 CHEMISTRY, ANALYTICAL
Bhaskar Vallamkonda, PhanikumarReddy Satti, Dipak Kumar Das, Gaurav Sharma, Suman Yadav, Vinod Kumar Vashistha
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引用次数: 0

Abstract

This study presents the enantiomeric resolution of three profen drugs, viz., flurbiprofen (FLB), fenoprofen, and zaltoprofen by employing sitafloxacin (SIT) as a chiral selector within a direct thin-layer chromatography (TLC) method. Chromatographic resolution of three drugs was carried out using a mobile phase consisting of acetonitrile‒methanol‒trimethylamine (6:3:1, V/V, pH 8.5), with a stationary phase maintained at pH 5. Analytical validation of the FLB enantiomeric resolution exhibited consistent recovery rates, with coefficient of variation (%CV) values consistently below 2%. Furthermore, the method demonstrated sensitivity, with low limits of detection and quantification values of 0.058 and 0.172 µg per spot, respectively, for FLB enantiomers, indicating reliable detection at low concentrations. The analytical data validate the effectiveness and reliability of the developed TLC method for the enantiomeric resolution of profen drugs, offering significant implications for pharmaceutical research and development.

Abstract Image

用直接薄层色谱法解析三种泼尼松药物的对映体
本研究采用直接薄层色谱(TLC)方法,以西他沙星(SIT)作为手性选择剂,对氟匹洛芬(FLB)、非诺洛芬和扎洛芬这三种泼尼松类药物的对映体进行了解析。采用乙腈-甲醇-三甲胺(6:3:1, V/V, pH 8.5)组成的流动相,固定相的 pH 值保持在 5,对三种药物进行了色谱解析。FLB 对映体解析的分析验证结果表明回收率稳定,变异系数 (%CV) 值始终低于 2%。此外,该方法灵敏度高,FLB 对映体的检出限和定量限分别为 0.058 微克/点和 0.172 微克/点,表明在低浓度下也能进行可靠的检测。这些分析数据验证了所开发的 TLC 方法在解析呋喃苯类药物对映体方面的有效性和可靠性,对药物研究和开发具有重要意义。
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来源期刊
CiteScore
2.20
自引率
18.80%
发文量
66
审稿时长
>12 weeks
期刊介绍: JPC - Journal of Planar Chromatography - Modern TLC is an international journal devoted exclusively to the publication of research papers on analytical and preparative planar chromatography. The journal covers all fields of planar chromatography, on all kinds of stationary phase (paper, layer, gel) and with various modes of migration of the mobile phase (capillary action or forced flow).
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