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基于超分子溶剂的苯二氮䓬类药物中空纤维液相微萃取

Supramolecular solvent-based hollow fiber liquid phase microextraction of benzodiazepines.

作者信息

Rezaei Fatemeh, Yamini Yadollah, Moradi Morteza, Daraei Bahram

机构信息

Department of Chemistry, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Iran.

出版信息

Anal Chim Acta. 2013 Dec 4;804:135-42. doi: 10.1016/j.aca.2013.10.026. Epub 2013 Oct 19.

Abstract

A new, efficient, and environmental friendly hollow fiber liquid phase microextraction (HF-LPME) method based on supramolecular solvents was developed for extraction of five benzodiazepine drugs. The supramolecular solvent was produced from coacervation of decanoic acid aqueous vesicles in the presence of tetrabutylammonium (Bu4N(+)). In this work, benzodiazepines were extracted from aqueous samples into a supramolecular solvent impregnated in the wall pores and also filled inside the porous polypropylene hollow fiber membrane. The driving forces for the extraction were hydrophobic, hydrogen bonding, and π-cation interactions between the analytes and the vesicular aggregates. High-performance liquid chromatography with photodiode array detection (HPLC-DAD) was applied for separation and determination of the drugs. Several parameters affecting the extraction efficiency including pH, hollow fiber length, ionic strength, stirring rate, and extraction time were investigated and optimized. Under the optimal conditions, the preconcentration factors were obtained in the range of 112-198. Linearity of the method was determined to be in the range of 1.0-200.0 μg L(-1) for diazepam and 2.0-200.0 μg L(-1) for other analytes with coefficient of determination (R(2)) ranging from 0.9954 to 0.9993. The limits of detection for the target benzodiazepines were in the range of 0.5-0.7 μg L(-1). The method was successfully applied for extraction and determination of the drugs in water, fruit juice, plasma and urine samples and relative recoveries of the compounds studied were in the range of 90.0-98.8%.

摘要

基于超分子溶剂开发了一种新型、高效且环境友好的中空纤维液相微萃取(HF-LPME)方法,用于萃取5种苯二氮䓬类药物。超分子溶剂由癸酸水囊泡在四丁基铵(Bu4N(+))存在下凝聚而成。在本研究中,苯二氮䓬类药物从水样中萃取到浸渍在壁孔中且填充在多孔聚丙烯中空纤维膜内部的超分子溶剂中。萃取的驱动力是分析物与囊泡聚集体之间的疏水、氢键和π-阳离子相互作用。采用配有光电二极管阵列检测的高效液相色谱(HPLC-DAD)对药物进行分离和测定。研究并优化了影响萃取效率的几个参数,包括pH值、中空纤维长度、离子强度、搅拌速率和萃取时间。在最佳条件下,预富集因子在112 - 198范围内。该方法的线性范围为:地西泮1.0 - 200.0 μg L(-1),其他分析物2.0 - 200.0 μg L(-1),测定系数(R(2))范围为0.9954至0.9993。目标苯二氮䓬类药物的检测限在0.5 - 0.7 μg L(-1)范围内。该方法成功应用于水、果汁、血浆和尿液样品中药物的萃取和测定,所研究化合物的相对回收率在90.0 - 98.8%范围内。

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