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Simultaneous determination of 75 abuse drugs including amphetamines, benzodiazepines, cocaine, opioids, piperazines, zolpidem and metabolites in human hair samples using liquid chromatography-tandem mass spectrometry.
Shin, Yongho; Kong, Tae Yeon; Cheong, Jae Cheol; Kim, Jin Young; Lee, Jae Il; Lee, Hye Suk.
Afiliación
  • Shin Y; BK21 PLUS Team for Creative Leader Program for Pharmacomics-based Future Pharmacy and Drug Metabolism and Bioanalysis Laboratory, College of Pharmacy, The Catholic University of Korea, Bucheon, Republic of Korea.
  • Kong TY; BK21 PLUS Team for Creative Leader Program for Pharmacomics-based Future Pharmacy and Drug Metabolism and Bioanalysis Laboratory, College of Pharmacy, The Catholic University of Korea, Bucheon, Republic of Korea.
  • Cheong JC; Forensic Genetics and Chemistry Division, Supreme Prosecutor's Office, Seoul, Republic of Korea.
  • Kim JY; Forensic Genetics and Chemistry Division, Supreme Prosecutor's Office, Seoul, Republic of Korea.
  • Lee JI; Forensic Genetics and Chemistry Division, Supreme Prosecutor's Office, Seoul, Republic of Korea.
  • Lee HS; BK21 PLUS Team for Creative Leader Program for Pharmacomics-based Future Pharmacy and Drug Metabolism and Bioanalysis Laboratory, College of Pharmacy, The Catholic University of Korea, Bucheon, Republic of Korea.
Biomed Chromatogr ; 33(9): e4600, 2019 Sep.
Article en En | MEDLINE | ID: mdl-31116452
A liquid chromatography-tandem mass spectrometric method for the simultaneous determination of 75 abuse drugs and metabolites, including 19 benzodiazepines, 19 amphetamines, two opiates, eight opioids, cocaine, lysergic acid diethylamide, zolpidem, three piperazines and 21 metabolites in human hair samples, was developed and validated. Ten-milligram hair samples were decontaminated, pulverized using a ball mill, extracted with 1 mL of methanol spiked with 28 deuterated internal standards in an ultrasonic bath for 60 min at 50°C, and purified with Q-sep dispersive solid-phase extraction tubes. The purified extracts were evaporated to dryness and the residue was dissolved in 0.1 mL of 10% methanol. The 75 analytes were analyzed on an Acquity HSS T3 column using gradient elution of methanol and 0.1% formic acid and quantified in multiple reaction monitoring mode with positive electrospray ionization. Calibration curves were linear (r ≥ 0.9951) from the lower limit of quantitation (2-200 pg/mg depending on the drug) to 2000 pg/mg. The coefficients of variation and accuracy for intra- and inter-assay analysis at three QC levels were 4.3-12.9% and 89.2-109.1%, respectively. The overall mean recovery ranged from 87.1 to 105.3%. This method was successfully applied to the analysis of 11 forensic hair samples obtained from drug abusers.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Drogas Ilícitas / Cromatografía Líquida de Alta Presión / Espectrometría de Masas en Tándem / Cabello Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Biomed Chromatogr Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Drogas Ilícitas / Cromatografía Líquida de Alta Presión / Espectrometría de Masas en Tándem / Cabello Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Biomed Chromatogr Año: 2019 Tipo del documento: Article