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Sample preparation with fiber‐in‐tube solid‐phase microextraction for capillary electrophoretic separation of tricyclic antidepressant drugs in human urine
Author(s) -
Jinno Kiyokatsu,
Kawazoe Maki,
Saito Yoshihiro,
Takeichi Tsutomu,
Hayashida Makiko
Publication year - 2001
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/1522-2683(200109)22:17<3785::aid-elps3785>3.0.co;2-u
Subject(s) - chromatography , solid phase microextraction , extraction (chemistry) , chemistry , nortriptyline , capillary electrophoresis , sample preparation , gas chromatography , fiber , solid phase extraction , capillary action , materials science , mass spectrometry , gas chromatography–mass spectrometry , amitriptyline , medicine , organic chemistry , composite material , anesthesia
Solid‐phase microextraction (SPME) is a solvent‐free sample preparation technique using a thin coating attached to the surface of a fused silica‐fiber as the extraction medium, which has been successfully applied to the analysis of a wide variety of compounds by coupling to gas chromatography (GC). In recent years, in‐tube SPME using GC capillary column as the extraction medium has also been developed and coupled with liquid chromatography (LC) for the preconcentration of nonvolatile compounds. In this study, an on‐line interface between the fiber‐in‐tube SPME and capillary electrophoresis (CE) has been developed, and the preconcentration and separation of four tricyclic antidepressant (TCA) drugs, amitriptyline, imipramine, nortriptyline, and desipramine, were performed with the hyphenated system. Under the optimized condition, a better extraction performance than conventional in‐tube SPME was obtained, even the length of the extraction medium was much shorter. The results clearly indicated that the fiber was working effectively as an extraction medium. For the separation of these four TCAs, capillary electrophoretic separation with β‐cyclodextrin as the buffer additive has been employed and the application of the developed system to the analysis of complex sample mixtures in a biological matrix is also demonstrated.