Li Zhiling, Chen Fan, Wang Xuedong, Wang Chengjun
College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, China.
Biomed Chromatogr. 2013 Feb;27(2):254-8. doi: 10.1002/bmc.2784. Epub 2012 Jun 26.
An environmentally friendly ionic liquids dispersive liquid-liquid microextraction (IL-DLLME) method coupled with high-performance liquid chromatography (HPLC) for the determination of antihypertensive drugs irbesartan and valsartan in human urine samples was developed. The HPLC separations were accomplished in less than 10 min using a reversed-phase C(18) column (250 × 4.60 mm i.d., 5 µm) with a mobile phase containing 0.3 % formic acid solution and methanol (v/v, 3:7; flow rate, 1.0 mL/min). UV absorption responses at 236 nm were linear over a wide concentration range from 50 µg/mL to the detection limits of 3.3 µg/L for valsartan and 1.5 µg/L for irbesartan. The effective parameters on IL-DLLME, such as ionic liquid types and their amounts, disperser solvent types and their volume, pH of the sample and extraction time were studied and optimized. The developed IL-DLLME-HPLC was successfully applied for evaluation of the urine irbesartan and valsartan profile following oral capsules administration.
建立了一种环境友好的离子液体分散液液微萃取(IL-DLLME)与高效液相色谱(HPLC)联用的方法,用于测定人尿液样本中的抗高血压药物厄贝沙坦和缬沙坦。使用反相C(18)柱(250×4.60 mm内径,5 µm),流动相为含0.3%甲酸溶液和甲醇(v/v,3:7;流速1.0 mL/min),在不到10分钟内完成HPLC分离。在236 nm处的紫外吸收响应在50 µg/mL至缬沙坦的检测限3.3 µg/L和厄贝沙坦的检测限1.5 µg/L的宽浓度范围内呈线性。研究并优化了IL-DLLME的有效参数,如离子液体类型及其用量、分散剂溶剂类型及其体积、样品pH值和萃取时间。所建立的IL-DLLME-HPLC成功应用于口服胶囊给药后尿液中厄贝沙坦和缬沙坦谱的评估。