首页> 外文期刊>Journal of liquid chromatography and related technologies >DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF METFORMIN HYDROCHLORIDE AND REPAGLINIDE IN TABLET DOSAGE FORM
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DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF METFORMIN HYDROCHLORIDE AND REPAGLINIDE IN TABLET DOSAGE FORM

机译:盐酸二甲双胍同时估算盐酸二甲双胍和常产素中的rp-HPLC方法的开发与验证

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摘要

A simple, rapid, and specific reversed-phase high performance liquid chromatographic method for simultaneous estimation of Metformin hydrochloride (MET) and Repaglinide (RPG) in a tablet dosage form has been developed and validated. HPLC analysis was performed on a C_(18) column with 90:10 (v/v) acetonitrile-water as mobile phase at a flow rate of 1.0 mL min~(-1). UV detection was performed at 223 nm. Total run time was Winin; Metfonnin hydrochloride and Repaglinide were eluted with retention times of 2.72 min and 6.13 min, respectively. The method was validated for accuracy, precision, linearity, specificity, and sensitivity in accordance with ICH guidelines. Validation revealed that the method is specific, rapid, accurate, precise, reliable, and reproducible. The high recovery and low coefficients of variation confirmed the suitability of the method for simultaneous analysis of the two drugs in tablet dosage form.
机译:已经开发出并验证了一种简单,快速,特异的反相高效液相色谱法,用于同时估计盐酸二甲双胍(Met)和repaglinide(RPG)的片剂剂型,并验证。 在C_(18)柱上以90:10(v / v)乙腈 - 水作为流动率,以1.0mL min〜(-1)的流速进行HPLC分析。 UV检测在223nm处进行。 总运行时间是WININ; 盐酸梅津南甘酮和repaglinide的保留时间分别为2.72分钟和6.13分钟洗脱。 根据ICH指南,验证了该方法的准确性,精度,线性,特异性和灵敏度。 验证表明,该方法特定,快速,准确,精确,可靠,可重复。 高回收率和低的变异系数证实了该方法同时分析了两种药物剂型中的两种药物的适用性。

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