Direct coupling in-tube solid-phase microextraction with mass spectrometry using polymer coated open-tubular column for rapid analysis of antiepileptic drugs in biofluids

被引:10
|
作者
Hu, Wei [1 ,2 ]
Zhou, Wei [1 ,4 ]
Wang, Chenlu [1 ]
Liu, Zichun [1 ]
Chen, Zilin [1 ,2 ,3 ]
机构
[1] Wuhan Univ, Zhongnan Hosp, Sch Pharmaceut Sci, Dept Orthoped Trauma & Microsurg, Wuhan 430072, Peoples R China
[2] Hubei Prov Engn & Technol Res Ctr Fluorinated Phar, Minist Educ, Key Lab Combinatorial Biosynth & Drug Discovery, Wuhan 430071, Peoples R China
[3] Wuhan Univ, Sch Pharmaceut Sci, Wuhan 430071, Peoples R China
[4] Univ Waterloo, Dept Chem, Waterloo, ON N2L 3G1, Canada
基金
中国国家自然科学基金;
关键词
In tube solid-phase microextraction; Mass spectrometry; Direct coupling; Open tubular column; Antiepileptic drugs; IONIZATION;
D O I
10.1016/j.aca.2022.340775
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Development of high-throughput and rapid screening analytical method is in high demand for anti-doping and clinical point-of-care (POC) analysis. Solid-phase microextraction and mass spectrometry direct coupling (SPME-MS) has been proved as a rapid and effective way for target analysis in complex sample matrixes. An online direct coupling of in-tube SPME (IT-SPME) with MS using polymer coated open-tubular column has been developed in this work. A sharp stainless -steel needle was attached at the end of the SPME column, which enables the direct ionization of the analytes after elution from the IT-SPME column. Itaconic acid-benzene co-polymer was in-situ grown on the inner surface of the fused silica capillary and used as extraction phase. This column has low backpressure and provides both hydrophobic and weak cationic exchange interaction with the target analytes due to the chemical properties. The developed online IT-SPME-MS method showed good extraction performance towards various target analytes and good reusability at least for 60 times. As a proof-of-concept application, the above method was applied for the analysis of antiepileptic drugs (AEDs) in both plasma and urine samples with linear range (1 ng/mL-200 ng/mL), good linearity (R2 >= 0.99), and good reproducibility (intra-day RSDs less than 4.36%, inter-day RSDs less than 6.55%). The method exhibited high enrichment factors be-tween 187 and 204 for the two AEDs and high sensitivity for the analysis of human plasma samples and urine samples.
引用
收藏
页数:6
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