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离子液体分散液液微萃取-高效液相色谱法测定人尿中的厄贝沙坦和缬沙坦

Ionic liquids dispersive liquid-liquid microextraction and high-performance liquid chromatographic determination of irbesartan and valsartan in human urine.

作者信息

Li Zhiling, Chen Fan, Wang Xuedong, Wang Chengjun

机构信息

College of Chemistry and Materials Engineering, Wenzhou University, Wenzhou, China.

出版信息

Biomed Chromatogr. 2013 Feb;27(2):254-8. doi: 10.1002/bmc.2784. Epub 2012 Jun 26.

Abstract

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.

摘要

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。

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