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手性对映体的测定依康唑和克霉唑通过胶束电动色谱法用羟丙基-β-环糊精与基于 L-赖氨酸和 L-谷氨酸的离子液体。

Enantiomeric determination of econazole and sulconazole by electrokinetic chromatography using hydroxypropyl-β-cyclodextrin combined with ionic liquids based on L-lysine and L-glutamic acid.

机构信息

Departamento de Química Analítica, Química Física e Ingeniería Química. Universidad de Alcalá. Ctra. Madrid-Barcelona Km. 33.600, 28871, Alcalá de Henares (Madrid), Spain.

Departamento de Química Analítica, Química Física e Ingeniería Química. Universidad de Alcalá. Ctra. Madrid-Barcelona Km. 33.600, 28871, Alcalá de Henares (Madrid), Spain; Instituto de Investigación Química Andrés M. del Río. Universidad de Alcalá. Ctra. Madrid-Barcelona Km. 33.600, 28871, Alcalá de Henares (Madrid), Spain.

出版信息

J Chromatogr A. 2020 Jun 21;1621:461085. doi: 10.1016/j.chroma.2020.461085. Epub 2020 Apr 19.

Abstract

Two analytical methodologies based on the combined use of hydroxypropyl-β-cyclodextrin and two different amino acid-based chiral ionic liquids (tetrabutylammonium-L-lysine or tetrabutylammonium-L-glutamic acid) in electrokinetic chromatography were developed in this work to perform the enantioselective determination of econazole and sulconazole in pharmaceutical formulations. The influence of different experimental variables such as buffer concentration, applied voltage, nature and concentration of the ionic liquid, temperature and injection time, on the enantiomeric separation was investigated. The combination of hydroxypropyl-β-cyclodextrin and tetrabutylammonium-L-lysine under the optimized conditions enabled to achieve the enantiomeric determination of both drugs with high enantiomeric resolution (3.5 for econazole and 2.4 for sulconazole). The analytical characteristics of the developed methodologies were evaluated in terms of linearity, precision, LOD, LOQ and recovery showing good performance for the determination of both drugs which were successfully quantitated in pharmaceutical formulations. This work reports the first analytical methodology enabling the enantiomeric determination of sulconazole in pharmaceutical formulations.

摘要

本工作开发了两种基于羟丙基-β-环糊精与两种不同的基于氨基酸的手性离子液体(四丁基铵-L-赖氨酸或四丁基铵-L-谷氨酸)联合使用的分析方法,用于在电泳色谱中对药物制剂中的依康唑和舒康唑进行对映选择性测定。考察了不同实验变量(缓冲液浓度、施加电压、离子液体的性质和浓度、温度和进样时间)对映体分离的影响。在优化条件下,羟丙基-β-环糊精与四丁基铵-L-赖氨酸的组合可实现两种药物的对映体测定,具有高对映体分辨率(依康唑为 3.5,舒康唑为 2.4)。所开发方法的分析特性从线性、精密度、LOD、LOQ 和回收率方面进行了评估,结果表明两种药物的测定性能良好,可成功定量药物制剂中的药物。本工作报道了首个可在药物制剂中对舒康唑进行对映体测定的分析方法。

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