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首页> 外文期刊>Analytica chimica acta >Electromembrane extraction of polar basic drugs from plasma with pure bis(2-ethylhexyl) phosphite as supported liquid membrane
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Electromembrane extraction of polar basic drugs from plasma with pure bis(2-ethylhexyl) phosphite as supported liquid membrane

机译:以纯亚磷酸双(2-乙基己基)酯为载体的液膜从血浆中电萃取极性碱性药物

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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.
机译:使用纯的亚磷酸双(2-乙基己基)酯(DEHPi)作为支撑液膜(SLM),首次研究了从人血浆中极性碱性药物的电膜萃取(EME)。选择极性碱性药物间氨基,苯甲idine,索他洛尔,苯丙醇胺,麻黄碱和甲氧苄啶作为模型分析物,并从300 mL人体血浆中提取,通过10 mL DEHPi作为SLM,并从100 mL 10 mM甲酸中提取。受体溶液。 SLM上的萃取电位为100 V,萃取进行20分钟。在EME之后,通过高效液相色谱-紫外检测(HPLC-UV)分析受体溶液。与文献中报道的有关极性碱性药物的其他SLM相比,DEHPi的SLM在与血浆接触时高度稳定,并且穿过SLM的系统电流很容易保持在50 mA以下。因此,样品和受体溶液中的电解保持在可接受的水平,没有有害的后果。对于极性模型分析物,其log P范围从-0.40到1.32,从人血浆中的回收率在25-91%范围内。强大的氢键和偶极相互作用可能是导致模型分析物有效转移到SLM中的原因,这是有关在SLM中不使用任何离子载体的高极性分析物有效EME的首次报道。 (C)2016 Elsevier B.V.保留所有权利。

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