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高效液相色谱法荧光检测法测定人血浆中总游离华法林和华法林醇。

Determination of total and unbound warfarin and warfarin alcohols in human plasma by high performance liquid chromatography with fluorescence detection.

机构信息

Department of Chemistry and Industrial Chemistry, University of Pisa, Pisa, Italy.

出版信息

J Chromatogr A. 2013 Nov 1;1314:54-62. doi: 10.1016/j.chroma.2013.08.091. Epub 2013 Aug 31.

Abstract

Two analytical procedures are presented for the determination of the total content and unbound fraction of both warfarin and warfarin alcohols in human plasma. Chromatographic separation was carried out in isocratic conditions at 25°C on a C-18 reversed-phase column with a mobile phase consisting of a 70% buffer phosphate 25mM at pH=7, 25% methanol and 5% acetonitrile at a flow rate of 1.2mL/min. Fluorescence detection was performed at 390nm (excitation wavelength 310nm). Neither method showed any detectable interference or matrix effect. Inter-day recovery of the total warfarin and warfarin alcohols at a concentration level of 1000ng/mL was 89±3% and 73±3%, respectively, whereas for their unbound fraction (at a concentration level of 10ng/mL) was 66±8% and 90±7%, respectively. The intra- and inter-day precision (assessed as relative standard deviation) was <10% for both methods. The limits of detection were 0.4 and 0.2ng/mL for warfarin and warfarin alcohols, respectively. The methods were successfully applied to a pooled plasma sample obtained from 69 patients undergoing warfarin therapy.

摘要

本文介绍了两种分析方法,用于测定人血浆中华法林和华法林醇的总含量和游离分数。在 25°C 下,采用等度条件,在 C-18 反相柱上,以 70%缓冲磷酸盐 25mM(pH=7)、25%甲醇和 5%乙腈为流动相,流速为 1.2mL/min,进行色谱分离。荧光检测在 390nm(激发波长 310nm)下进行。两种方法均未显示出任何可检测的干扰或基质效应。在 1000ng/mL 浓度水平下,总华法林和华法林醇的日间回收率分别为 89±3%和 73±3%,而游离分数(在 10ng/mL 浓度水平下)的回收率分别为 66±8%和 90±7%。两种方法的日内和日间精密度(以相对标准偏差评估)均<10%。华法林和华法林醇的检测限分别为 0.4 和 0.2ng/mL。该方法成功应用于 69 名正在接受华法林治疗的患者的混合血浆样本。

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