School of Pharmacy, College of Pharmacy, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
J Pharm Biomed Anal. 2010 Oct 10;53(2):145-50. doi: 10.1016/j.jpba.2010.02.012. Epub 2010 Feb 16.
A rapid and simple capillary zone electrophoresis (CZE) with ultraviolet detection has been developed for simultaneous determination of regular insulin and insulin aspart in bulk and commercial injection dosage forms. The simultaneous analysis of the tested drugs was performed in phosphate buffer (80 mM; pH 6.5). The separation of regular insulin and insulin aspart was achieved at 13 kV and detection at 200 nm within 7 min with RSD for the absolute migration time reproducibility of less than 3.8% (n=10). Selectivity, linearity, precision, accuracy, limits of quantification (LOQ) and limits of detection (LOD) were evaluated as the method validation. Calibration plots were linear (r>0.999) over a range of 2.0-60.0 microg/mL for regular insulin and insulin aspart. The LOD were all 1.0 microg/mL (signal-to-noise ratio=3; injection 6.89 kPa, 7s). The small amount of sample required and the expeditiousness of the procedure can be an advantageous alternative to traditional methodology for the quantification of tested drugs in individual pharmaceutical products.
建立了一种快速、简单的毛细管区带电泳(CZE)-紫外检测法,用于同时测定原料药和商业注射剂中常规胰岛素和门冬胰岛素的含量。在磷酸盐缓冲液(80 mM;pH 6.5)中对两种药物进行同时分析。在 13 kV 的分离电压和 200nm 的检测波长下,7 min 内可实现常规胰岛素和门冬胰岛素的分离,绝对迁移时间的重现性 RSD 小于 3.8%(n=10)。采用专属性、线性、精密度、准确度、定量限(LOQ)和检测限(LOD)对方法进行了验证。常规胰岛素和门冬胰岛素的校准曲线在 2.0-60.0μg/mL 范围内呈线性(r>0.999)。两种药物的检测限均为 1.0μg/mL(信噪比=3;进样压力 6.89 kPa,7s)。与传统方法相比,该方法所需样品量少,操作简便,可作为一种有利的替代方法,用于单个药物制剂中被测药物的定量分析。