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Identification and quantification of the antipsychotics risperidone, aripiprazole, pipamperone and their major metabolites in plasma using ultra-high performance liquid chromatography-mass spectrometry.
Wijma, Rixt A; van der Nagel, Bart C H; Dierckx, Bram; Dieleman, Gwen C; Touw, Daan J; van Gelder, Teun; Koch, Birgit C P.
Afiliação
  • Wijma RA; Department of Hospital Pharmacy, Erasmus MC, Postal Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • van der Nagel BC; Department of Hospital Pharmacy, Erasmus MC, Postal Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • Dierckx B; Department of Child and Adolescent Psychiatry, Erasmus MC, Postal box 2040, 3000 CA, Rotterdam, The Netherlands.
  • Dieleman GC; Department of Child and Adolescent Psychiatry, Erasmus MC, Postal box 2040, 3000 CA, Rotterdam, The Netherlands.
  • Touw DJ; Department of Clinical Pharmacy and Pharmacology University Medical Center Groningen, Postal Box 30.001, 9700 RB, Groningen, The Netherlands.
  • van Gelder T; Department of Hospital Pharmacy and Internal Medicine, Erasmus MC, Postal Box 2040, 3000 CA, Rotterdam, The Netherlands.
  • Koch BC; Department of Hospital Pharmacy, Erasmus MC, Postal Box 2040, 3000 CA, Rotterdam, The Netherlands.
Biomed Chromatogr ; 30(6): 794-801, 2016 Jun.
Article em En | MEDLINE | ID: mdl-26447610
ABSTRACT
The antipsychotics risperidone, aripiprazole and pipamperone are frequently prescribed for the treatment in children with autism. The aim of this study was to validate an ultra-high performance liquid chromatography-mass spectrometry method for the quantification of these antipsychotics in plasma. An ultra-high performance liquid chromatography-mass spectrometry assay was developed for the determination of the drugs and metabolites. Gradient elution was performed on a reversed-phase column with a mobile phase consisting of ammonium acetate, formic acid in methanol or in Milli-Q ultrapure water at a flow rate of 0.5 mL/min. The method was validated according to the US Food and Drug Administration guidelines. The analytes were found to be stable enough after reconstitution and injection of only 5 µL improved the accuracy and precision in combination with the internal standard. Calibration curves of all five analytes were linear. All analytes were stable for at least 72 h in the autosampler and the high quality control of 9-OH-risperidone was stable for 48 h. The method allows quantification of all analytes. The advantage of this method is the combination of a minimal injection volume, a short run-time, an easy sample preparation method and the ability to quantify all analytes in one run. Copyright © 2015 John Wiley & Sons, Ltd.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antipsicóticos / Cromatografia Líquida de Alta Pressão / Espectrometria de Massas em Tandem Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antipsicóticos / Cromatografia Líquida de Alta Pressão / Espectrometria de Massas em Tandem Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article