Kang Xin, Wang Feng, Xie Zhihong, Li Huande
The Clinical Pharmacy and Pharmacology Institute, Second Xiangya Hospital, Central South University, Changsha 410011, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Mar 1;877(7):645-8. doi: 10.1016/j.jchromb.2009.01.001. Epub 2009 Jan 9.
A high performance liquid chromatography (HPLC) method was developed for the simultaneous determination of rosiglitazone and gemfibrozil in human plasma using alpha-asarone as an internal standard (IS). Plasma samples were pretreated by protein precipitation. The analytes were separated on a Macherey-Nagel Nucleodur C(18) (250 mm x 4.6 mm, 5 microm) column using acetonitrile and 30 mmol/l ammonium acetate solution (including 0.1% methanoic acid) as mobile phase which was delivered at 1.2 ml/min. A gradient elution program was adopted to adjust proportion of solvent in mobile phase. A time program was used to regulate conditions of fluorescence detection. The method was validated over the concentration range of 5.0-751.3 ng/ml for rosiglitazone and 0.5-75.4 microg/ml for gemfibrozil with acceptable accuracy, precision and extraction recoveries. This method is suitable for routine therapeutic drug monitoring and pharmacokinetic interaction study of the two drugs.
建立了一种以α-细辛醚为内标,同时测定人血浆中罗格列酮和吉非贝齐的高效液相色谱法。血浆样品采用蛋白沉淀法进行预处理。分析物在Macherey-Nagel Nucleodur C(18)(250 mm×4.6 mm,5 µm)柱上分离,以乙腈和30 mmol/L醋酸铵溶液(含0.1%甲酸)为流动相,流速为1.2 ml/min。采用梯度洗脱程序调节流动相中溶剂的比例。使用时间程序调节荧光检测条件。该方法在罗格列酮浓度范围为5.0 - 751.3 ng/ml和吉非贝齐浓度范围为0.5 - 75.4 μg/ml内进行了验证,具有可接受的准确度、精密度和提取回收率。该方法适用于这两种药物的常规治疗药物监测和药代动力学相互作用研究。