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膜厚对在线与毛细管电泳联用的支撑液膜萃取分析复杂样品的影响。

The effect of membrane thickness on supported liquid membrane extractions in-line coupled to capillary electrophoresis for analyses of complex samples.

机构信息

Institute of Analytical Chemistry of the Czech Academy of Sciences, Veveří 97, CZ-60200 Brno, Czech Republic; Institute of Food Science and Biotechnology, Faculty of Chemistry, Brno University of Technology, Purkyňova 118, CZ-61200, Brno, Czech Republic.

Institute of Analytical Chemistry of the Czech Academy of Sciences, Veveří 97, CZ-60200 Brno, Czech Republic.

出版信息

J Chromatogr A. 2019 Jul 5;1596:226-232. doi: 10.1016/j.chroma.2019.02.067. Epub 2019 Feb 28.

DOI:10.1016/j.chroma.2019.02.067
PMID:30853166
Abstract

The effect of membrane thickness on extraction performance was systematically examined in extractions through supported liquid membranes (SLM), which were in-line coupled to capillary electrophoresis (CE). Three porous polypropylene membranes with different thickness (25, 100 and 170 μm) were used as supports for SLM extractions of model basic drugs (nortriptyline, papaverine, haloperidol and loperamide) from complex samples. The analytes were transferred through the SLMs by a pH gradient and were in-line injected, separated and quantified using a commercial CE instrument with ultraviolet (UV) detection. Transfers of the model drugs through SLM decreased with the increased membrane thickness (in the order: 25 > 100 > 170 μm) and highest transfers were achieved for the thinnest membrane. Interferences from complex sample matrices were efficiently eliminated, moreover, impregnation of the 25 μm membrane required significantly reduced volume of organic solvent. Mechanical stability of the impregnated 25 μm membrane was excellent during in-line injections, which necessitated direct contact of CE separation capillary with the SLM. Repeatability of the hyphenated SLM-CE-UV method (using the 25 μm membrane) was lower than 11% (RSD values of peak areas) and calibration curves were strictly linear in 0.5-30 μg/mL concentration range (coefficients of determination ≥ 0.997). Transfers of the basic drugs from donor solutions (standard and undiluted human urine/plasma) through the SLMs ranged from 45 to 231% and limits of detection were between 0.02 and 0.15 μg/mL.

摘要

膜厚对支撑液膜(SLM)萃取性能的影响在与毛细管电泳(CE)在线耦合的 SLM 萃取中得到了系统的考察。使用三种不同厚度(25、100 和 170 μm)的多孔聚丙烯膜作为 SLM 萃取模型碱性药物(去甲替林、罂粟碱、氟哌啶醇和洛哌丁胺)的支撑物,从复杂样品中提取。通过 pH 梯度将分析物转移通过 SLM,并使用带有紫外(UV)检测的商业 CE 仪器在线注入、分离和定量。模型药物通过 SLM 的转移随着膜厚度的增加而降低(顺序为:25>100>170 μm),最薄的膜实现了最高的转移。复杂样品基质的干扰被有效消除,此外,25 μm 膜的浸渍所需的有机溶剂体积显著减少。在在线注入过程中,浸渍的 25 μm 膜具有优异的机械稳定性,这需要 CE 分离毛细管与 SLM 直接接触。采用 25 μm 膜的 SLM-CE-UV 方法的重复性低于 11%(峰面积的 RSD 值),并且校准曲线在 0.5-30 μg/mL 浓度范围内严格线性(相关系数≥0.997)。碱性药物从供试溶液(标准和未稀释的人尿/血浆)通过 SLM 的转移率在 45%至 231%之间,检测限在 0.02 至 0.15 μg/mL 之间。

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