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Validated Enantioselective LC Method, with Precolumn Derivatization with Marfey’s Reagent, for Analysis of the Antiepileptic Drug Pregabalin in Bulk Drug Samples

机译:经验证的对映选择性LC方法,采用Marfey试剂进行柱前衍生,用于分析大批量药物样品中的抗癫痫药普瑞巴林

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摘要

An enantioselective high-performance liquid chromatographic method, with precolumn derivatization with Marfey’s chiral reagent, sodium 2,4-dinitro-5-fluorophenyl-l-alanine amide, has been developed for resolution of the enantiomers of a new antiepileptic drug, pregabalin, in the bulk drug. The diastereomers of the pregabalin enantiomers were resolved to baseline on a reversed-phase ODS column with a 60:40 (v/v) mixture of aqueous 0.2% triethylamine (pH adjusted to 3.5 with dilute orthophosphoric acid) and acetonitrile as mobile phase. Resolution between the diastereomers was not less than five. The method was extensively validated and proved to be robust. The calibration plot was indicative of an excellent linear relationship between response and concentration over the range 750 (LOQ) to 7,500 ng L?1 for the R enantiomer. The limits of detection and quantification of the R enantiomer were 250 and 750 ng L?1, respectively, for an injection volume of 10 μL. Recovery of the R enantiomer from bulk drug samples of pregabalin ranged from 97.5 to 101.76%. Solutions of pregabalin in water and in the mobile phase were found to be stable for at least 48 h. The method was found to be suitable and accurate for quantitative determination of the R enantiomer in the bulk drug. It can be also used to test the stability of samples of pregabalin.
机译:开发了一种对映选择性的高效液相色谱方法,该方法使用马菲的手性试剂2,4-二硝基-5-氟苯基-1-丙氨酸酰胺钠进行柱前衍生,用于拆分新的抗癫痫药普瑞巴林的对映体。散装毒品。普瑞巴林对映体的非对映异构体在反相ODS色谱柱上以0.2%三乙胺水溶液(用正磷酸稀溶液将pH调节至3.5)和乙腈的60:40(v / v)混合物解析为基线。非对映异构体之间的分辨率不少于五。该方法已得到广泛验证,并被证明是可靠的。校正图表明,R对映体的响应与浓度在750(LOQ)至7,500 ng L?1 范围内具有极好的线性关系。进样量为10μL时,R对映异构体的检出限和定量限分别为250和750 ng L?1 。从普瑞巴林的大宗药物样品中回收的R对映异构体的范围为97.5至101.76%。发现普瑞巴林在水中和在流动相中的溶液稳定至少48小时。发现该方法适用于定量测定散装药物中R对映异构体的方法。它也可用于测试普瑞巴林样品的稳定性。

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