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在停滞条件下通过电场在支撑液膜上进行逐滴微萃取。

Drop-to-drop microextraction across a supported liquid membrane by an electrical field under stagnant conditions.

作者信息

Petersen Nickolaj Jacob, Jensen Henrik, Hansen Steen Honoré, Rasmussen Knut Einar, Pedersen-Bjergaard Stig

机构信息

Department of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, University of Copenhagen, DK-2100 Copenhagen, Denmark.

出版信息

J Chromatogr A. 2009 Feb 27;1216(9):1496-502. doi: 10.1016/j.chroma.2008.12.079. Epub 2008 Dec 30.

Abstract

Electromembrane extraction (EME) of basic drugs from 10 microL sample volumes was performed through an organic solvent (2-nitrophenyl octyl ether) immobilized as a supported liquid membrane (SLM) in the pores of a flat polypropylene membrane (25 microm thickness), and into 10 microL 10 mM HCl as the acceptor solution. The driving force for the extractions was 3-20 V d.c. potential sustained over the SLM. The influence of the membrane thickness, extraction time, and voltage was investigated, and a theory for the extraction kinetics is proposed. Pethidine, nortriptyline, methadone, haloperidol, and loperamide were extracted from pure water samples with recoveries ranging between 33% and 47% after only 5 min of operation under totally stagnant conditions. The extraction system was compatible with human urine and plasma samples and provided very efficient sample pretreatment, as acidic, neutral, and polar substances with no distribution into the organic SLM were not extracted across the membrane. Evaluation was performed for human urine, providing linearity in the range 1-20 microg/mL, and repeatability (RSD) in average within 12%.

摘要

从10微升样品体积中对碱性药物进行电膜萃取(EME),是通过固定在25微米厚的扁平聚丙烯膜孔中的有机溶剂(2-硝基苯基辛基醚)作为支撑液膜(SLM),并进入10微升10 mM盐酸作为接受液来实现的。萃取的驱动力是施加在支撑液膜上的3 - 20 V直流电势。研究了膜厚度、萃取时间和电压的影响,并提出了萃取动力学理论。在完全静止的条件下仅操作5分钟后,从纯水样品中萃取了哌替啶、去甲替林、美沙酮、氟哌啶醇和洛哌丁胺,回收率在33%至47%之间。该萃取系统与人尿和血浆样品兼容,并提供了非常有效的样品预处理,因为未分配到有机支撑液膜中的酸性、中性和极性物质不会穿过膜被萃取。对人尿进行了评估,线性范围为1 - 20微克/毫升,平均重复性(相对标准偏差)在12%以内。

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