首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Three-phase hollow fiber liquid phase microextraction of warfarin from human plasma and its determination by high-performance liquid chromatography.
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Three-phase hollow fiber liquid phase microextraction of warfarin from human plasma and its determination by high-performance liquid chromatography.

机译:人血浆中华法林的三相中空纤维液相微萃取及其高效液相色谱法测定。

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摘要

A simple, inexpensive and efficient sample preparation technique, three-phase hollow fiber liquid phase microextraction (HF-LPME), followed by high-performance liquid chromatography-ultra violet detection (HPLC-UV) was used for the analysis of warfarin in human plasma. Warfarin was extracted from 11.0 ml of aqueous solution with pH=2.3 (donor phase) into 1-octanol immobilized in the wall pores of a porous hollow fiber and then extracted into the acceptor phase with pH=11.0 located in the lumen of the hollow fiber. After the extraction, the acceptor phase was directly injected into the HPLC system for quantification. Different factors affecting the HF-LPME including nature of organic extraction solvent, pH of donor and acceptor phases, stirring rate, extraction time and salt addition to the sample solution (donor phase) were investigated and optimized. Under the optimized conditions (1-octanol as organic solvent, pH(donor)=2.3, pH(acceptor)=11.0, stirring speed of 1000 rpm, extraction time of 30 min, without addition of salt), limit of detection (LOD) of 5 ng ml(-1) and enrichment factor of 225 were obtained. The calibration curve was linear within the range of 15-550 ng ml(-1) with the square of correlation coefficient of 0.9984. The values of intra-day relative standard deviation (RSD) and inter-day RSD were 4.2% and 11.1%, respectively. The method was applied successfully for the analysis of warfarin in plasma sample from a patient under treatment with this drug and excellent sample clean-up was observed.
机译:一种简单,廉价且高效的样品制备技术,使用三相中空纤维液相微萃取(HF-LPME),然后用高效液相色谱-紫外检测(HPLC-UV)进行人血浆中的华法林分析。将华法林从11.0 ml pH = 2.3的水溶液(给体相)中提取到固定在多孔中空纤维壁孔中的1-辛醇中,然后提取到位于中空纤维内腔中的pH = 11.0的受体相中。提取后,将受体相直接注入HPLC系统进行定量。研究和优化了影响HF-LPME的不同因素,包括有机萃取溶剂的性质,供体和受体相的pH值,搅拌速率,萃取时间和向样品溶液(供体相)中添加盐的影响。在优化的条件下(1-辛醇作为有机溶剂,pH(给体)= 2.3,pH(受体)= 11.0,搅拌速度为1000 rpm,提取时间为30分钟,不添加盐),检测极限(LOD)获得5 ng ml(-1)的样品,富集因子为225。校正曲线在15-550 ng ml(-1)范围内呈线性,相关系数的平方为0.9984。日内相对标准偏差(RSD)和日间RSD的值分别为4.2%和11.1%。该方法成功地用于分析用该药物治疗的患者血浆样品中的华法林,并观察到出色的样品净化效果。

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