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Quantitation of seven sedative and analgesic drugs in whole blood from intensive care patients using liquid chromatography mass spectrometry
Natl Board Forens Med, Dept Forens Genet & Forens Toxicol, Artillerigatan 12, S-58758 Linkoping, Sweden.
Linköping University, Department of Biomedical and Clinical Sciences, Division of Clinical Chemistry and Pharmacology. Linköping University, Faculty of Medicine and Health Sciences.
Uppsala Univ, Sweden.
Uppsala Univ, Sweden.
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2021 (English)In: TOXICOLOGIE ANALYTIQUE ET CLINIQUE, ISSN 2352-0078, Vol. 33, no 4, p. 327-337Article in journal (Refereed) Published
Abstract [en]

We present the development and validation of a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for quantification of clonidine, dexmedetomidine, fentanyl, ketamine, ketobemidone, midazolam and morphine in whole blood. These are drugs predominately used in intensive care units (ICUs) but they are also encountered in forensic investigations. The analytes were recovered from 0.25 g of blood by protein precipitation with a mixture of acetonitrile and ethanol. Separation was performed on a BEH phenyl column. Mobile phases consisted of 0.05% formic acid in 10 mM ammonium formate and 0.05% formic acid in methanol, respectively, and the flow rate was 600 mu L/min. The mass spectrometer was operated in positive electrospray ionization mode with multiple reaction monitoring. Validation included selectivity, qualitative matrix effects, calibration model, limit of detection, lower limit of quantification, within- and between-day accuracy and precision, process efficiency, dilution integrity, carry over and stability. Selectivity was high and no ion suppression or enhancementwas observed in the areas were the analytes eluted. Calibration curves were linear over arange of 0.25-50 ng/g for dexmedetomidine, 0.05-50 ng/g for fentanyl and 5.0-500 ng/g formorphine and quadratic over a range of 0.5-50 ng/g for clonidine, 50-5000 ng/g for ketamine, 5.0-500 ng/g for ketobemidone and midazolam. The method showed acceptable within- and betweenday accuracies and precisions. All analytes were stable in whole blood for three weeksat 4. C. Concentrations in patient samples ranged between 42-760 ng/g for midazolam (n = 15), 0.3-1.5 ng/g for dexmedetomidine (n = 13), 0.6-6.4 ng/g for clonidine (n = 13), 8-62 ng/g for morphine (n = 16), 5-19 ng/g for ketobemidone (n = 5), 0.07-3.1 ng/g for fentanyl (n = 43), and 562000 ng/g for ketamine (n = 10). We conclude that the method was successfully validatedand applied to ante-mortem and post-mortem blood samples from critically ill adult patientsin a general ICU. (c) 2021 Societe Francaise de Toxicologie Analytique. Published by Elsevier Masson SAS. Allrights reserved.

Place, publisher, year, edition, pages
ELSEVIER MASSON SAS EDITEUR , 2021. Vol. 33, no 4, p. 327-337
Keywords [en]
Intensive care; Forensic toxicology; Analgesics; Sedatives; LC-MS/MS
National Category
Analytical Chemistry
Identifiers
URN: urn:nbn:se:liu:diva-181655DOI: 10.1016/j.toxac.2021.08.016ISI: 000721110600008OAI: oai:DiVA.org:liu-181655DiVA, id: diva2:1617535
Note

Funding Agencies|Swedish National Board of Forensic Medicine

Available from: 2021-12-07 Created: 2021-12-07 Last updated: 2021-12-07

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Ahlner, JohanKronstrand, RobertKugelberg, Fredrik
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