Electromembrane extraction of polar basic drugs from plasma with pure bis(2-ethylhexyl) phosphite as supported liquid membrane

被引:47
作者
Huang, Chuixiu [1 ]
Seip, Knut Fredrik [1 ]
Gjelstad, Astrid [1 ]
Pedersen-Bjergaard, Stig [1 ,2 ]
机构
[1] Univ Oslo, Sch Pharm, POB 1068, N-0316 Oslo, Norway
[2] Univ Copenhagen, Sch Pharmaceut Sci, Fac Hlth & Med Sci, Univ Pk 2, DK-2100 Copenhagen, Denmark
关键词
Sample preparation; Microextraction; Electromembrane extraction (EME); Polar basic drugs; Bis(2-ethylhexyl) phosphite; CONTACTLESS CONDUCTIVITY DETECTION; SCREEN-PRINTED ELECTRODE; BIOLOGICAL-FLUIDS; CAPILLARY-ELECTROPHORESIS; PHASE MICROEXTRACTION; EXHAUSTIVE EXTRACTION; SAMPLE PREPARATION; TRACE ANALYSIS; ACIDIC DRUGS; WASTE-WATER;
D O I
10.1016/j.aca.2016.06.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Electromembrane extraction (EME) of polar basic drugs from human plasma was investigated for the first time using pure bis(2-ethylhexyl) phosphite (DEHPi) as the supported liquid membrane (SLM). The polar basic drugs metaraminol, benzamidine, sotalol, phenylpropanolamine, ephedrine, and trimethoprim were selected as model analytes, and were extracted from 300 mL of human plasma, through 10 mL of DEHPi as SLM, and into 100 mL of 10 mM formic acid as acceptor solution. The extraction potential across the SLM was 100 V, and extractions were performed for 20 min. After EME, the acceptor solutions were analyzed by high-performance liquid chromatography-ultraviolet detection (HPLC-UV). In contrast to other SLMs reported for polar basic drugs in the literature, the SLM of DEHPi was highly stable in contact with plasma, and the system-current across the SLM was easily kept below 50 mA. Thus, electrolysis in the sample and acceptor solution was kept at an acceptable level with no detrimental consequences. For the polar model analytes, representing a log P range from -0.40 to 1.32, recoveries in the range 25-91% were obtained from human plasma. Strong hydrogen bonding and dipole interactions were probably responsible for efficient transfer of the model analytes into the SLM, and this is the first report on efficient EME of highly polar analytes without using any ionic carrier in the SLM. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:80 / 87
页数:8
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