Fibers with polypyrrole and polythiophene phases for isolation and determination of adrenolytic drugs from human plasma by SPME-HPLC

被引:39
作者
Olszowy, Pawel [1 ]
Szultka, Malgorzata [1 ]
Ligor, Tomasz [1 ]
Nowaczyk, Jacek [2 ]
Buszewski, Boguslaw [1 ]
机构
[1] Nicholas Copernicus Univ, Dept Environm Chem & Bioanalyt, Fac Chem, Torun, Poland
[2] Nicholas Copernicus Univ, Dept Phys Chem & Physicochem Polymers, Fac Chem, Torun, Poland
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2010年 / 878卷 / 24期
关键词
Solid-phase microextraction; Electropolymerization; Adrenolytic drugs; Liquid chromatography; PERFORMANCE LIQUID-CHROMATOGRAPHY; SAMPLE PREPARATION; MICROEXTRACTION; EXTRACTION; MS;
D O I
10.1016/j.jchromb.2010.06.033
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, polypyrrole (PPy) and polythiophene (PTh) SPME coatings and their ability to extract selected adrenolytic drugs with different physico-chemical properties from standard solutions and human plasma samples were evaluated. In measurements metoprolol, oxprenolol, mexiletine, propranolol, and propaphenon were investigated. The main parameters such as extraction time, desorption conditions and pH influence were examined. Inter-day precisions were in range 0.1-2.0%, 1.1-2.9%, 1.3-2.6%, 0.1-2.6% and 0.3-2.1% for metoprolol, oxprenolol, mexiletine, propranolol and propaphenon, respectively. Accuracies were less than 15%, which was evaluated by analyzing preparation samples of five replicates. The method was successfully applied to human plasma samples spiked with selected adrenolytic drugs. The method was linear in the concentration range from 1 to 10 mu g/ml for all of studied adrenolytic drugs using human plasma samples. The PTh-SPME coating displayed higher extraction efficiency towards the target analytes in comparison to PPy-SPME. The reproducibility of the extraction using polypyrrole and polythiophene fibers was confirmed by variation coefficients lower than 8% and 3%, respectively. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:2226 / 2234
页数:9
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