Optimization of carrier-mediated three-phase hollow fiber microextraction combined with HPLC-UV for determination of propylthiouracil in biological samples

被引:43
|
作者
Ebrahimzadeh, Homeira [1 ]
Asgharinezhad, Ali Akbar [1 ]
Abedi, Hamid [1 ]
Kamarei, Fahimeh [1 ]
机构
[1] Shahid Beheshti Univ, Dept Chem, Tehran, Iran
关键词
Three-phase hollow fiber microextraction; Propylthiouracil; Carrier-mediated; Biological samples; High performance liquid chromatography; LIQUID-PHASE MICROEXTRACTION; GAS-CHROMATOGRAPHY; THYREOSTAT RESIDUES; SINGLE-DROP; PRECONCENTRATION; DISPERSION; DRUGS;
D O I
10.1016/j.talanta.2011.05.015
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Carrier-mediated three-phase hollow fiber microextraction combined with high-performance liquid chromatography-ultra violet detection (HPLC-UV) was applied for the extraction and determination of propylthiouracil in biological samples. Propylthiouracil (PTU) was extracted from 7.5 mL of the basic solution (the source phase) with pH 12 into an organic phase (n-octanol containing 6% (w/v) of Aliquat 336 as the carrier) impregnated in the pores of a hollow fiber, and finally was back extracted into 24 mu L. of the acidic solution located inside the lumen of the hollow fiber (the receiving phase). The extraction was performed through the gradient of counter ion from the source to the receiving phase. The effects of different variables on the extraction efficiency were studied simultaneously using an experimental design. A half-fractional factorial design was employed for screening to determine the variables significantly affecting the extraction efficiency. Then, the factors with significant effect were optimized using a central composite design (CCD) and the response surface equations were developed. The optimal experimental conditions obtained from this statistical evaluation included: source phase, pH 12; temperature, 25 degrees C; extraction time, 40 min; counter ion concentration, 2 mol L-1 of NaClO4; organic solvent 6% of Aliquat in octanol and without salt addition in the source phase. Under the optimized conditions, the preconcentration factors were between 125 and 198 and also the limit of detections (LODs) ranged from 0.1 mu g L-1 to 0.4 mu g L-1 in different biological samples. The calibration curve was linear (r(2) = 0.998) in the concentration range of 0.5-1000 mu g L-1. Finally, the feasibility of the proposed method was successfully confirmed by extraction and determination of FTU in human plasma and urine as well as the bovine milk and meat samples in microgram per liter, and suitable results were obtained (RSDs < 6.3%). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1043 / 1049
页数:7
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