Development of a microfluidic-chip system for liquid-phase microextraction based on two immiscible organic solvents for the extraction and preconcentration of some hormonal drugs

被引:28
作者
Asl, Yousef Abdossalami [1 ]
Yamini, Yadollah [1 ]
Seidi, Shahram [2 ]
机构
[1] Tarbiat Modares Univ, Dept Chem, POB 14115-175, Tehran, Iran
[2] KN Toosi Univ Technol, Dept Analyt Chem, Fac Chem, Tehran, Iran
关键词
Microfluidic chip; Two immiscible organic solvents; Levonorgestrel; Dydrogesterone; Medroxyprogesterone; HOLLOW-FIBER MICROEXTRACTION; OPTICAL EMISSION-SPECTROMETRY; ELECTROMEMBRANE EXTRACTION; WATER SAMPLES; MEMBRANE; CHROMATOGRAPHY; SOLIDIFICATION; ALUMINUM; URINE;
D O I
10.1016/j.talanta.2016.07.063
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the present study, for the first time, an on-chip liquid phase microextraction (LPME) coupled with high performance liquid chromatography was introduced for the analysis of levonorgestrel (Levo), dydrogesterone (Dydo) and medroxyprogesterone (Medo) as the model analytes in biological samples. The chip-based LPME set-up was composed of two polymethyl methacrylate (PMMA) plates with micro fabricated channels and a microporous membrane sandwiched between them to separate the sample solution and acceptor phase. These channels were used as a flow path for the sample solution and a thin compartment for the acceptor phase, respectively. In this system, two immiscible organic solvents were used as supported liquid membrane (SLM) and acceptor phase, respectively. During extraction, the model analytes in the sample solution were transported through the SLM (n-dodecane) into the acceptor organic solvent (methanol). The new set-up provided effective and reproducible extractions using low volumes of the sample solution. The effective parameters on the extraction efficiency of the model analytes were optimized using one variable at a time method. Under the optimized conditions, the new set-up provided good linearity in the range of 5.0-500 mu g L-1 for the model analytes with the coefficients of determination (r(2)) higher than 0.9909. The relative standard deviations (RSDs%) and limits of detection (LODs) values were less than 6.5% (n=5) and 5.0 mu g L-1, respectively. The preconcentration factors (PFs) were obtained using 1.0 mL of the sample solution and 20.0 mu L of the acceptor solution higher than 19.9-fold. Finally, the proposed method was successfully applied for the extraction and determination of the model analytes in urine samples. (C) 2016 Elsevier B.V. All rights reserved.
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页码:592 / 599
页数:8
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