Cooper J D, Muirhead D C, Taylor J E, Baker P R
Clinical Innovations Ltd., Stareton, Kenilworth, Warwickshire, UK.
J Chromatogr B Biomed Sci Appl. 1997 Nov 7;701(1):87-95. doi: 10.1016/s0378-4347(97)00339-3.
The development of the ASTED (automated sequential trace enrichment of dialysates) system to prepare plasma samples prior to high-performance liquid chromatography (HPLC) of sildenafil and its demethylated metabolite (UK-103,320) is described. Investigations to elucidate potential pitfalls of the ASTED on-line sample preparation system prior to separation of the analytes by HPLC are presented. The procedure is shown to be selective for sildenafil and UK-103,320, and linear over the range 1.00-250 ng/ml. The intra-batch imprecision (C.V.) of the method at plasma analyte concentrations of 1.00, 5.00, 50.0 and 200 ng/ml was 11.2, 3.10, 1.50, and 1.30%, respectively, and the corresponding inter-batch imprecision was estimated to be 13.5, 7.09, 3.69, and 5.43%. At these plasma analyte concentrations the overall inaccuracy (% bias) of the procedure ranged from 3.6 to 8.4%. The method showed similar assay performance for the estimation of the metabolite, UK-103,320. The application of the assay to a pharmacokinetic investigation during a clinical study is presented.
本文描述了ASTED(透析液自动连续痕量富集)系统的开发,该系统用于在对西地那非及其去甲基代谢物(UK-103,320)进行高效液相色谱(HPLC)分析之前制备血浆样本。文中还介绍了在通过HPLC分离分析物之前,对ASTED在线样品制备系统潜在缺陷的研究。结果表明,该方法对西地那非和UK-103,320具有选择性,在1.00 - 250 ng/ml范围内呈线性。该方法在血浆分析物浓度为1.00、5.00、50.0和200 ng/ml时的批内不精密度(变异系数)分别为11.2%、3.10%、1.50%和1.30%,相应的批间不精密度估计为13.5%、7.09%、3.69%和5.43%。在这些血浆分析物浓度下,该方法的总体误差(偏差百分比)范围为3.6%至8.4%。该方法在估计代谢物UK-103,320时表现出相似的分析性能。本文还介绍了该分析方法在一项临床研究中的药代动力学研究中的应用。