Development and Validation of a Method for Quantification of 28 Psychotropic Drugs in Postmortem Blood Samples by Modified Micro-QuEChERS and LC–MS-MS

Author:

Rodrigues Taís B1,Morais Damila R2,Gianvecchio Victor A P3,Aquino Elvis M3,Cunha Ricardo L4,Huestis Marilyn A5,Costa Jose Luiz16ORCID

Affiliation:

1. Campinas Poison Control Center, University of Campinas, Campinas, São Paulo 13083-859, Brazil

2. Analytical division, Shimadzu Brazil, Barueri, São Paulo, 06460-000, Brazil

3. Forensic Toxicology Laboratory, Institute of Legal Medicine, São Paulo State Police, São Paulo, São Paulo, 05507-060, Brazil

4. Forensic Toxicology Laboratory, Institute of Analysis and Forensic Research, São Cristóvão, Sergipe, 49100-000, Brazil

5. The Lambert Center for the Study of Medicinal Cannabis and Hemp, Institute of Emerging Health Professions, Thomas Jefferson University, Philadelphia, PA, 19107, USA

6. Faculty of Pharmaceutical Sciences, University of Campinas, Campinas, São Paulo 13083-859, Brazil

Abstract

Abstract The development of new sample preparation alternatives in analytical toxicology leading to quick, effective, automated and environmentally friendly procedures is growing in importance. One of these alternatives is the QuEChERS, originally developed for the analysis of pesticide residues, producing cleaner extracts than liquid–liquid extraction, and easier separation of aqueous and organic phases. However, there are few published studies on the miniaturization of this technique for forensic toxicology, especially in postmortem analysis. We developed and validated a modified micro-QuEChERS and LC–MS-MS assay to quantify 16 antidepressants, 7 antipsychotics and 3 metabolites and semi-quantify norfluoxetine and norsertraline in postmortem blood. The calibration curve was linear from 1 to 500 ng/mL, achieved an r > 0.99, with all standards quantifying within ±15% of target except ±20% at the limit of quantification of 1 ng/mL for 26 substances. The F test was applied to evaluate if the variance between replicates remained constant for all calibrators. Six weighting factors were analyzed (1/x, 1/x2, 1/x0,5, 1/y, 1/y2 and 1/y0,5), with the weighting factor with the lowest sum of residual regression errors (1/x2) selected. No endogenous or exogenous interferences were observed. Method imprecision and bias were <19.0% and 19.7%, respectively. Advantages of this method include a low sample volume of 100 µL, simple but effective sample preparation and a rapid 8.5-min run time. The validated analytical method was successfully applied to the analysis of 100 authentic postmortem samples.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Oxford University Press (OUP)

Subject

Chemical Health and Safety,Health, Toxicology and Mutagenesis,Toxicology,Environmental Chemistry,Analytical Chemistry

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