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一种用于定量测定人血浆中低浓度盐酸苯丙醇胺及其药代动力学应用的简单灵敏的高效液相色谱法。

A simple and sensitive HPLC method for quantitation of low phenoprolamine hydrochloride concentrations in human plasma and its pharmacokinetic application.

作者信息

Zhao Libo, Hu Jiong, Chang Qing, Ke Qiulin, Xu Rong, Gu Shifen, Chen Hui, Zeng Fandian

机构信息

Institute of Clinical Pharmacology, Tongji Medical College of Huazhong University of Science and Technology, Wuhan , People's Republic of China.

出版信息

Biomed Chromatogr. 2008 Mar;22(3):333-8. doi: 10.1002/bmc.937.

Abstract

Phenoprolamine hydrochloride is a novel compound that works against a variety of types of hypertension. The purpose of this study was to develop a simple and sensitive high-performance liquid chromatographic method for quantitation of low phenoprolamine hydrochloride concentrations in human plasma and to apply it to pharmacokinetic study. The procedure involved extraction of the drug and clonidine (internal standard) from the plasma using diethyl ether. Chromatographic separations were carried out on a 4.6 x 200 mm Hypersil silica column with UV detection at 230 nm. The isocratic mobile phase, 1% ammonium acetate (pH 5.4) and methanol (0.3:99.7, v/v), was run at 1 mL/min. Extraction recovery was 84% for phenoprolamine hydrochloride at a concentration level of 200 ng/mL, and 76% for clonidine at 200 ng/mL. The method was linear in the concentration range 5-4000 ng/mL with a lower limit of quantitation of 5 ng/mL for phenoprolamine hydrochloride. Inter- and intra-day coefficients of variation were less than 10%. The validated method was successfully applied to a pharmacokinetic study in human after an oral administration of the drug, and the pharmacokinetic parameters are presented.

摘要

盐酸苯丙醇胺是一种新型化合物,可用于治疗多种类型的高血压。本研究的目的是开发一种简单、灵敏的高效液相色谱法,用于定量测定人血浆中低浓度的盐酸苯丙醇胺,并将其应用于药代动力学研究。该方法包括用乙醚从血浆中提取药物和可乐定(内标)。色谱分离在4.6×200mm的Hypersil硅胶柱上进行,在230nm处进行紫外检测。等度流动相为1%醋酸铵(pH 5.4)和甲醇(0.3:99.7,v/v),流速为1mL/min。盐酸苯丙醇胺在浓度为200ng/mL时的提取回收率为84%,可乐定在200ng/mL时的提取回收率为76%。该方法在5-4000ng/mL的浓度范围内呈线性,盐酸苯丙醇胺的定量下限为5ng/mL。日内和日间变异系数均小于10%。该验证方法成功应用于人体口服该药物后的药代动力学研究,并给出了药代动力学参数。

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