Li Min, Fan Liu-Yin, Zhang Wei, Sun Ji, Cao Cheng-Xi
Laboratory of Analytical Biochemistry and Bioseparation, School of Life Science and Biotechnology, Shanghai Jiao Tong University, 800 Dongchuan Road, Minhang, 200240 Shanghai, PR China.
J Pharm Biomed Anal. 2007 Jan 4;43(1):387-92. doi: 10.1016/j.jpba.2006.07.003. Epub 2006 Aug 9.
A capillary zone electrophoresis (CZE) method was developed for the quantitative analysis of lovastatin (Lvt) in capsule of monascus-Chinese medicine. Lvt in the capsule was separated using an electrolyte system consisting of 16% ethanol (v/v) in 60 mM Gly-sodium hydroxide buffer, pH 10.5, 16 kV applied voltage, 238 nm detection wavelength with a capillary of 51 cm x 75 microm i.d (43 cm to detector). Under the optimized conditions, the linear response of Lvt concentration ranges from 4.0 to 240 microg/mL with high correlation coefficient (r=0.9998, n=9), the limits of detection (LOD) and quantification (LOQ) for Lvt are 0.73 and 2.42 microg/mL, the precision values (expressed as R.S.D.) of intra-day and inter-day are 1.40-2.12% and 1.47-3.88%, respectively. The recoveries of the analyte at three concentration levels are 90.28-100.71%. The developed method can be well used for the quantification of Lvt in the drug in commercial formulations.
建立了一种毛细管区带电泳(CZE)法,用于定量分析中药红曲胶囊中的洛伐他汀(Lvt)。胶囊中的Lvt采用由60 mM甘氨酸 - 氢氧化钠缓冲液(pH 10.5)中含16%乙醇(v/v)组成的电解质体系进行分离,施加电压16 kV,检测波长238 nm,使用内径75 μm、总长51 cm(至检测器长度为43 cm)的毛细管。在优化条件下,Lvt浓度的线性响应范围为4.0至240 μg/mL,相关系数高(r = 0.9998,n = 9),Lvt的检测限(LOD)和定量限(LOQ)分别为0.73和2.42 μg/mL,日内和日间精密度值(以相对标准偏差R.S.D.表示)分别为1.40 - 2.12%和1.47 - 3.88%。在三个浓度水平下分析物的回收率为90.28 - 100.71%。所建立的方法可很好地用于商业制剂中该药物中Lvt的定量分析。