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Fast targeted analysis of 132 acidic and neutral drugs and poisons in whole blood using LC-MS/MS.
Di Rago, Matthew; Saar, Eva; Rodda, Luke N; Turfus, Sophie; Kotsos, Alex; Gerostamoulos, Dimitri; Drummer, Olaf H.
Afiliação
  • Di Rago M; Victorian Institute of Forensic Medicine, Southbank, Victoria, Australia. Electronic address: matthew.dirago@vifm.org.
  • Saar E; Victorian Institute of Forensic Medicine, Southbank, Victoria, Australia.
  • Rodda LN; Victorian Institute of Forensic Medicine, Southbank, Victoria, Australia; Department of Forensic Medicine, Monash University, Southbank, Victoria, Australia.
  • Turfus S; Victorian Institute of Forensic Medicine, Southbank, Victoria, Australia.
  • Kotsos A; Victorian Institute of Forensic Medicine, Southbank, Victoria, Australia.
  • Gerostamoulos D; Victorian Institute of Forensic Medicine, Southbank, Victoria, Australia; Department of Forensic Medicine, Monash University, Southbank, Victoria, Australia.
  • Drummer OH; Victorian Institute of Forensic Medicine, Southbank, Victoria, Australia; Department of Forensic Medicine, Monash University, Southbank, Victoria, Australia. Electronic address: olaf.drummer@monash.edu.
Forensic Sci Int ; 243: 35-43, 2014 Oct.
Article em En | MEDLINE | ID: mdl-24794019
The aim of this study was to develop an LC-MS/MS based screening technique that covers a broad range of acidic and neutral drugs and poisons by combining a small sample volume and efficient extraction technique with simple automated data processing. After protein precipitation of 100µL of whole blood, 132 common acidic and neutral drugs and poisons including non-steroidal anti-inflammatory drugs, barbiturates, anticonvulsants, antidiabetics, muscle relaxants, diuretics and superwarfarin rodenticides (47 quantitated, 85 reported as detected) were separated using a Shimadzu Prominence HPLC system with a C18 separation column (Kinetex XB-C18, 4.6mm×150mm, 5µm), using gradient elution with a mobile phase of 25mM ammonium acetate buffer (pH 7.5)/acetonitrile. The drugs were detected using an ABSciex(®) API 2000 LC-MS/MS system (ESI+ and -, MRM mode, two transitions per analyte). The method was fully validated in accordance with international guidelines. Quantification data obtained using one-point calibration compared favorably to that using multiple calibrants. The presented LC-MS/MS assay has proven to be applicable for determination of the analytes in blood. The fast and reliable extraction method combined with automated processing gives the opportunity for high throughput and fast turnaround times for forensic and clinical toxicology.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Venenos / Espectrometria de Massas / Preparações Farmacêuticas / Cromatografia Líquida Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Forensic Sci Int Ano de publicação: 2014 Tipo de documento: Article País de publicação: Irlanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Venenos / Espectrometria de Massas / Preparações Farmacêuticas / Cromatografia Líquida Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Forensic Sci Int Ano de publicação: 2014 Tipo de documento: Article País de publicação: Irlanda