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Screening and Quantitative Determination of Twelve Acidic and Neutral Pharmaceuticals in Whole Blood by Liquid-Liquid Extraction and Liquid Chromatography-Tandem Mass Spectrometry
Author(s) -
Kirsten Wiese Simonsen,
Anni Steentoft,
Margaret Buck,
Lars Hestbjerg Hansen,
Kristían Línnet
Publication year - 2010
Publication title -
journal of analytical toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.161
H-Index - 76
eISSN - 1945-2403
pISSN - 0146-4760
DOI - 10.1093/jat/34.7.367
Subject(s) - chromatography , chemistry , chlorzoxazone , mass spectrometry , detection limit , extraction (chemistry) , high performance liquid chromatography , liquid chromatography–mass spectrometry , piroxicam , meprobamate , medicine , biochemistry , alternative medicine , cytochrome p450 , metabolism , pathology , cyp2e1 , anesthesia
We describe a multi-method for simultaneous identification and quantification of 12 acidic and neutral compounds in whole blood. The method involves a simple liquid-liquid extraction, and the identification and quantification are performed using liquid chromatography-tandem mass spectrometry. The method was fully validated for salicylic acid, paracetamol, phenobarbital, carisoprodol, meprobamate, topiramate, etodolac, chlorzoxazone, furosemide, ibuprofen, warfarin, and salicylamide. The method also tentatively includes thiopental, theophylline, piroxicam, naproxen, diclophenac, and modafinil, but these drugs were not included in the full validation program and are not described in detail here. Limit of quantitation was 1 mg/kg for the compounds with coefficients of variation of < 20%, except for furosemide, which had a coefficient of variation of 32% at limit of quantitation. The measuring interval was wide for most components. Extraction efficiencies were high, reflecting the high-yield capacity of the method.

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