Analysis of drugs in plasma samples from schizophrenic patients by column-switching liquid chromatography-tandem mass spectrometry with organic–inorganic hybrid cyanopropyl monolithic column

•Development of the selective organic–inorganic hybrid cyanopropyl monolithic for bioanalysis.•This capillary was reused more than 100 times as sorbent for column-switching.•The high permeability of the monolithic capillary facilitated the biological sample percolation.•Column-switching LC-MS/MS sys...

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Veröffentlicht in:Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2015-07, Vol.993-994, p.26-35
Hauptverfasser: Domingues, Diego Soares, Souza, Israel Donizeti de, Queiroz, Maria Eugênia Costa
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Sprache:eng
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Zusammenfassung:•Development of the selective organic–inorganic hybrid cyanopropyl monolithic for bioanalysis.•This capillary was reused more than 100 times as sorbent for column-switching.•The high permeability of the monolithic capillary facilitated the biological sample percolation.•Column-switching LC-MS/MS system for therapeutic drug monitoring in patients with schizophrenia.•The column-switching LC-MS/MS method presented LLOQs values at sub-therapeutic levels. This study reports on the development of a rapid, selective, and sensitive column-switching liquid chromatography-tandem mass spectrometry (LC-MS/MS) method to analyze sixteen drugs (antidepressants, anticonvulsants, anxiolytics, and antipsychotics) in plasma samples from schizophrenic patients. The developed organic-inorganic hybrid monolithic column with cyanopropyl groups was used for the first dimension of the column-switching arrangement. This arrangement enabled online pre-concentration of the drugs (monolithic column) and their subsequent analytical separation on an XSelect SCH C18 column. The drugs were detected on a triple quadrupole tandem mass spectrometer (multiple reactions monitoring mode) with an electrospray ionization source in the positive ion mode. The developed method afforded adequate linearity for the sixteen target drugs; the coefficients of determination (R2) lay above 0.9932, the interassay precision had coefficients of variation lower than 6.5%, and the relative standard error values of the accuracy ranged from −14.0 to 11.8%. The lower limits of quantification in plasma samples ranged from 63 to 1250pgmL−1. The developed method successfully analyzed the target drugs in plasma samples from schizophrenic patients for therapeutic drug monitoring (TDM).
ISSN:1570-0232
1873-376X
DOI:10.1016/j.jchromb.2015.04.040