Department of Chemistry, University of Mazandaran, Babolsar 47416-95447, Iran.
J Pharm Biomed Anal. 2012 Mar 5;61:44-9. doi: 10.1016/j.jpba.2011.11.019. Epub 2011 Nov 25.
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.
一种简单、廉价且高效的样品制备技术,三相中空纤维液相微萃取(HF-LPME),随后进行高效液相色谱-紫外检测(HPLC-UV),用于分析人血浆中的华法林。华法林从 pH=2.3 的 11.0ml 水溶液(供体相)中被萃取到固定在多孔中空纤维壁孔中的 1-辛醇中,然后用 pH=11.0 的接受相(位于中空纤维的内腔中)萃取到接受相。萃取后,接受相直接注入 HPLC 系统进行定量分析。考察并优化了影响 HF-LPME 的不同因素,包括有机萃取溶剂的性质、供体相和接受相的 pH、搅拌速度、萃取时间以及向样品溶液(供体相)中加盐。在优化条件下(1-辛醇为有机溶剂,pH(供体)=2.3,pH(接受)=11.0,搅拌速度为 1000rpm,萃取时间为 30min,不添加盐),检测限(LOD)为 5ngml(-1),富集因子为 225。校准曲线在 15-550ngml(-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%。该方法成功应用于治疗该药的患者血浆样品中华法林的分析,并观察到出色的样品净化效果。