Shariati Shahab, Yamini Yadollah, Darabi Majid, Amini Mohsen
Department of Chemistry, Faculty of Sciences, Tarbiat Modarres University, Tehran, Iran.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Aug 15;855(2):228-35. doi: 10.1016/j.jchromb.2007.05.003. Epub 2007 May 16.
Three phase liquid phase microextraction (three phase LPME) technique coupled with HPLC-UV has been applied as a sensitive and efficient sample preparation method to determine phenylacetic acid (PAA) as a biomarker of depressive disorders and phenylpropionic acid (PPA) in biological fluids. The compounds were extracted from 3.0 ml aqueous solution with the adjustment of pH at a fixed value in the range of 2.0-3.5 (donor solution) into an organic phase (1-hexanol) layered on the surface of the donor solution and finally back-extracted into 4.0 microl of the acceptor microdrop (pH 11.1) located at the end of the microsyringe needle. After a prescribed back-extraction time, the acceptor microdrop was withdrawn into the microsyringe and then directly injected into the HPLC system. In order to achieve maximum extraction efficiency, different parameters affecting the extraction conditions were optimized. At the optimum conditions (donor solution: 2.3M Na(2)SO(4), pH 2.0-3.5; organic membrane: 95 microl of 1-hexanol; acceptor solution: 4.0 microl of 0.1M NH(3)/NH(4)(+) with pH 11.1; donor solution temperature: 45-50 degrees C; extraction time: 20 min and back-extraction time: 12 min), up to 110-fold enrichment factor was obtained. The calibration curve for these analytes was linear in the range of 1-5000 microg/l with r(2)>0.998. The intraday and interday RSD% were below 6.5% and the limits of detection (LODs) for both analytes were 0.2 microg/l (based on S/N=3). The proposed technique is a low cost, simple and sensitive method with highly clean-up effect. Finally, this technique was successfully utilized for the detection of target analytes in human urine, serum and plasma.
三相液相微萃取(三相LPME)技术结合高效液相色谱-紫外检测法已被用作一种灵敏且高效的样品前处理方法,用于测定生物体液中作为抑郁症生物标志物的苯乙酸(PAA)和苯丙酸(PPA)。将化合物从3.0 ml水溶液中提取出来,在pH值固定在2.0 - 3.5范围内(供体溶液),进入位于供体溶液表面的有机相(1-己醇),最后反萃取到位于微量注射器针头末端的4.0微升受体微滴(pH 11.1)中。在规定的反萃取时间后,将受体微滴抽回到微量注射器中,然后直接注入高效液相色谱系统。为了实现最大萃取效率,对影响萃取条件的不同参数进行了优化。在最佳条件下(供体溶液:2.3M Na₂SO₄,pH 2.0 - 3.5;有机膜:95微升1-己醇;受体溶液:4.0微升0.1M NH₃/NH₄⁺,pH 11.1;供体溶液温度:45 - 50℃;萃取时间:20分钟,反萃取时间:12分钟),获得了高达110倍的富集因子。这些分析物的校准曲线在1 - 5000微克/升范围内呈线性,r²>0.998。日内和日间相对标准偏差(RSD%)均低于6.5%,两种分析物的检测限(LOD)均为0.2微克/升(基于信噪比S/N = 3)。所提出的技术是一种低成本、简单且灵敏的方法,具有高度的净化效果。最后,该技术成功应用于人体尿液、血清和血浆中目标分析物的检测。