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Determination of methadone and EDDP in oral fluid using the dried saliva spots sampling approach and gas chromatography-tandem mass spectrometry
被引:22
|作者:
Ribeiro, Andreia
[1
]
Prata, Margarida
[1
]
Vaz, Cristiana
[2
]
Rosado, Tiago
[1
,3
]
Restolho, Jose
[1
,4
]
Barroso, Mario
[5
]
Araujo, Andre R. T. S.
[2
,6
,7
]
Gallardo, Eugenia
[1
,3
]
机构:
[1] Univ Beira Interior, Ctr Invest Ciencias Saude, Fac Ciencias Saude, Ave Infante D Henrique, P-6200506 Covilha, Portugal
[2] Inst Politecn Guarda, Escola Super Saude, Ave Rainha D Amelia S-N, P-6300749 Guarda, Portugal
[3] Univ Beira Interior, Lab Farmacotoxicol UBIMed, P-6201001 Convento De Sto, Covilha, Portugal
[4] Nal von Minden GmbH, Friedenstr 32, D-93053 Regensburg, Germany
[5] Inst Med Legal & Ciencias Forenses Delegacao Sul, Serv Quim & Toxicol Forenses, Rua Manuel Bento de Sousa 3, P-1169201 Lisbon, Portugal
[6] Unidade Invest Desenvolvimento Interior IPG UDI I, Ave Dr Francisco de Sa Carneiro 50, P-6300559 Guarda, Portugal
[7] Univ Porto, LAQV, Requimte, Dept Ciencias Quim,Lab Quim Aplicada,Fac Farm, P-4051401 Porto, Portugal
关键词:
Methadone;
EDDP;
Oral fluid;
Dried saliva spots;
GC-MS/MS;
PHASE MICROEXTRACTION;
BIOANALYTICAL METHODS;
METABOLITE EDDP;
MS/MS ANALYSIS;
ILLICIT DRUGS;
LC-MS;
BLOOD;
VALIDATION;
BUPRENORPHINE;
EXTRACTION;
D O I:
10.1007/s00216-019-01654-z
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
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 mu L) were applied into Whatman (TM) 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 1min. Afterwards, the extract was centrifuged for 15min at 3500rpm and the supernatant evaporated to dryness and reconstituted with 50 mu L 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:11
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