Determination of methadone and EDDP in oral fluid using the dried saliva spots sampling approach and gas chromatography-tandem mass spectrometry

被引:0
作者
Andreia Ribeiro
Margarida Prata
Cristiana Vaz
Tiago Rosado
José Restolho
Mário Barroso
André R. T. S. Araújo
Eugenia Gallardo
机构
[1] Faculdade de Ciências da Saúde da Universidade da Beira Interior (CICS-UBI),Centro de Investigação em Ciências da Saúde
[2] Instituto Politécnico da Guarda (IPG),Escola Superior de Saúde
[3] Universidade da Beira Interior,Laboratório de Fármaco
[4] Nal von Minden,Toxicologia
[5] GmbH,UBIMedical
[6] Instituto de Medicina Legal e Ciências Forenses - Delegação do Sul,Serviço de Química e Toxicologia Forenses
[7] Unidade de Investigação para o Desenvolvimento do Interior do IPG (UDI/IPG),LAQV, Requimte, Departamento de Ciências Químicas, Laboratório de Química Aplicada, Faculdade de Farmácia
[8] Universidade do Porto,undefined
来源
Analytical and Bioanalytical Chemistry | 2019年 / 411卷
关键词
Methadone; EDDP; Oral fluid; Dried saliva spots; GC-MS/MS;
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学科分类号
摘要
The present work describes the development and validation of a novel approach to determine methadone (MTD) and its main metabolite (EDDP) in oral fluid samples, using the dried saliva spots (DSS) sampling approach and gas chromatography-tandem mass spectrometry (GC-MS/MS). Oral fluid samples (50 μL) were applied into Whatman™ 903 protein saver filter paper cards and were allowed to dry overnight. The extraction was carried out by immersion of the spot in 1 mL of isopropyl alcohol with agitation for 1 min. Afterwards, the extract was centrifuged for 15 min at 3500 rpm and the supernatant evaporated to dryness and reconstituted with 50 μL of methanol. The procedure was considered linear in the range of 10 to 250 ng/mL for both compounds, with determination coefficients greater than 0.99. Intra- and inter-day precision and accuracy revealed coefficients of variation (CVs) lower than 15% at the studied concentrations, with mean relative errors within ± 15% of the nominal concentrations. Recoveries ranged from 45 to 74%. The limits of detection and quantification were 5 and 10 ng/mL respectively for both analytes. All studied parameters complied with the defined criteria and the method enabled the successful determination of MTD and EDDP in oral fluid samples from patients undergoing opiate substitution/maintenance therapy.
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页码:2177 / 2187
页数:10
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