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Optimizing the extraction, separation and quantification of tricyclic antidepressant drugs in human plasma with CE-ESI-TOF-MS using cationic-coated capillaries
Uppsala University, Sweden.
Uppsala universitet. (INTERACT)ORCID-id: 0000-0003-1819-1709
Uppsala University, Sweden.
Uppsala University, Sweden.
2011 (engelsk)Inngår i: Electrophoresis, ISSN 0173-0835, E-ISSN 1522-2683, Vol. 32, nr 6-7, s. 647-658Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

In this study, the extraction and CE-ESI-TOF-MS analysis of tricyclic antidepressant (TCA) drugs imipramine, desipramine, clomipramine and norclomipramine in human plasma has been optimized. The CE capillaries were modified with omega-iodo-alkyl ammonium salt (M7C4I coating) to reduce analyte adsorption to the silica wall. The use of a strong cation exchange (SCX) solid-phase extraction (SPE) column specifically designed for the extraction of basic drug species from biofluids gave very clean extracts with high and reproducible recoveries. The extraction recoveries were ranging between 87 and 91% with % RSD values of 0.5-1.7% (n = 3). The obtained strong cation exchange-SPE extracts of the TCA in human plasma only contained the analytes of interest. The optimized CE separation conditions were obtained by adding ACN and acetic acid to the sample while using an aqueous BGE. The CE-ESI-TOF-MS analysis was performed within 6 min for all TCA analytes under the optimized condition with peak efficiencies up to 1.4 x 10(5) plates/m and an average % RSD of the migration times of the analytes of 0.3% (n = 5). The presented method can readily be used for the extraction and quantification of basic drug species in human biological fluids and in pharmaceutical formulations.

sted, utgiver, år, opplag, sider
Wiley-Blackwell, 2011. Vol. 32, nr 6-7, s. 647-658
Emneord [en]
CE, Human plasma, Mass spectrometry, Quantification, Tricyclic anti-depressant drugs
HSV kategori
Identifikatorer
URN: urn:nbn:se:kau:diva-46874DOI: 10.1002/elps.201000566ISI: 000288602000001PubMedID: 21341290OAI: oai:DiVA.org:kau-46874DiVA, id: diva2:1037513
Tilgjengelig fra: 2016-10-16 Laget: 2016-10-16 Sist oppdatert: 2019-06-17bibliografisk kontrollert

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