A validated dilute-and-shoot LC–MS-MS urine screening for the analysis of 95 illicit drugs and medicines: Insights from clinical and forensic Brazilian cases

Author:

Dos Santos Bruno Pereira12ORCID,Birk Letícia1,Schwarz Patrícia1,Sebben Viviane Cristina3,Sgaravatti Ângela Malysz14,de Gouveia Giovanna Cristiano1,Silva Petry Adriana Ubirajara56,de Menezes Francisco Paz6,Gonzaga Alexsandro Pinto6,Schlickmann Paula Flores6,Arbo Marcelo Dutra2,de Oliveira Tiago Franco1ORCID,Eller Sarah1ORCID

Affiliation:

1. Graduate Program in Health Sciences, Federal University of Health Sciences of Porto Alegre , Porto Alegre, RS 90050-170, Brazil

2. Faculty of Pharmacy, Federal University of Rio Grande do Sul , Porto Alegre, RS 90010-150, Brazil

3. Toxicological Information Center of Rio Grande do Sul , Porto Alegre, RS 90610-000, Brazil

4. General Institute of Expertise of Rio Grande do Sul , Porto Alegre, RS 90230-010, Brazil

5. Graduate Program in Pathology, Federal University of Health Sciences of Porto Alegre , Porto Alegre, RS 90050-170, Brazil

6. Division of Postmortem Inspection, Associação Hospitalar Vila Nova , Porto Alegre, RS 91750-040, Brazil

Abstract

Abstract Urine toxicological analysis is a relevant tool in both clinical and forensic scenarios, enabling the diagnosis of acute poisonings, elucidation of deaths, verification of substance use in the workplace and identification of drug-facilitated crimes. For these analyses, the dilute-and-shoot technique associated with liquid chromatography coupled with tandem mass spectrometry (LC–MS-MS) is a promising alternative since it has demonstrated satisfactory results and broad applicability. This study developed and validated a comprehensive LC–MS-MS screening method to analyze 95 illicit drugs and medicines in urine samples and application to clinical and forensic Brazilian cases. The dilute-and-shoot protocol was defined through multivariate optimization studies and was set using 100 µL of sample and 300 µL of solvent. The total chromatographic run time was 7.5 min. The method was validated following the recommendations of the ANSI/ASB Standard 036 Guideline. The lower limits of quantification varied from 20 to 100 ng/mL. Within-run and between-run precision coefficient of variations% were <20%, and bias was within ± 20%. Only 4 of the 95 analytes presented significant ionization suppression or enhancement (>25%). As proof of applicability, 839 urine samples from in vivo and postmortem cases were analyzed. In total, 90.9% of the analyzed samples were positive for at least one substance, and 78 of the 95 analytes were detected. The most prevalent substances were lidocaine (40.2%), acetaminophen (38.0%) and benzoylecgonine (31.5%). The developed method proved to be an efficient and simplified alternative for analyzing 95 therapeutic and illicit drugs in urine samples. Additionally, the results obtained from sample analysis are essential for understanding the profile of Brazilian substance use, serving as a valuable database for the promotion of health and safety public policies.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul

Publisher

Oxford University Press (OUP)

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