A simple procedure for the quantitative determination in hair samples of 13 common drugs of abuse or metabolites (morphine, 6-acetylmorphine, codeine, amphetamine, methamphetamine, 3,4- methylenedioxy-amphetamine, 3,4-methylenedioxymethamphetamine, 3,4- methylenedioxyethylamphetamine, benzoylecgonine, cocaine, buprenorphine, methadone and 9- tetrahydrocannabinol) has been developed and fully validated. The analytes were extracted from the matrix by a simple overnight incubation with methanol at 55°C. An aliquot of the extract was directly injected into an ultra-high performance liquid chromatography system equipped with Waters Acquity UHPLC BEH C18 column (100 mm × 2.1 mm, 1.7 μm). The mobile phase eluted with a linear gradient (water/formic acid 5mM : acetonitrile; v:v) from 98:2 to 0:100 in 4.5 min, followed by isocratic elution at 100% B for 1.0 min. The flow rate was 0.6 mL/min and the total run time was 8.0 min including re-equilibration at the initial conditions. The compounds were revealed by a triple quadrupole mass spectrometer operating in the selected reaction monitoring mode. The absence of matrix interferents, together with excellent repeatability of both retention times and relative abundances of diagnostic transitions, allowed the correct identification of all analytes tested. The method proved linear in the interval from the limit of quantification to 5.0 ng/mg (1.0 ng/mg for 9-tetrahydrocannabinol) with correlation coefficient values ranging from 0.9970 to 0.9997. Quantitation limits were below the cut-off values recommended by the Society of Hair Testing and ranged from 0.02 to 0.08 ng/mg. Application of the present UHPLC-MS/MS procedure and instrumentation to hair analysis allows high sample-throughput, together with excellent sensitivity and selectivity, in workplace drug-screening controls and forensic investigations. These qualities, combined with minimal sample workup, make the cost of this screening affordable for most private and public administrations.

Simultaneous determination in hair of multiclass drugs of abuse (including THC) by ultrahigh performance liquid chromatography - tandem mass spectrometry

GERACE, ENRICO;A. Salomone;VINCENTI, Marco
2012-01-01

Abstract

A simple procedure for the quantitative determination in hair samples of 13 common drugs of abuse or metabolites (morphine, 6-acetylmorphine, codeine, amphetamine, methamphetamine, 3,4- methylenedioxy-amphetamine, 3,4-methylenedioxymethamphetamine, 3,4- methylenedioxyethylamphetamine, benzoylecgonine, cocaine, buprenorphine, methadone and 9- tetrahydrocannabinol) has been developed and fully validated. The analytes were extracted from the matrix by a simple overnight incubation with methanol at 55°C. An aliquot of the extract was directly injected into an ultra-high performance liquid chromatography system equipped with Waters Acquity UHPLC BEH C18 column (100 mm × 2.1 mm, 1.7 μm). The mobile phase eluted with a linear gradient (water/formic acid 5mM : acetonitrile; v:v) from 98:2 to 0:100 in 4.5 min, followed by isocratic elution at 100% B for 1.0 min. The flow rate was 0.6 mL/min and the total run time was 8.0 min including re-equilibration at the initial conditions. The compounds were revealed by a triple quadrupole mass spectrometer operating in the selected reaction monitoring mode. The absence of matrix interferents, together with excellent repeatability of both retention times and relative abundances of diagnostic transitions, allowed the correct identification of all analytes tested. The method proved linear in the interval from the limit of quantification to 5.0 ng/mg (1.0 ng/mg for 9-tetrahydrocannabinol) with correlation coefficient values ranging from 0.9970 to 0.9997. Quantitation limits were below the cut-off values recommended by the Society of Hair Testing and ranged from 0.02 to 0.08 ng/mg. Application of the present UHPLC-MS/MS procedure and instrumentation to hair analysis allows high sample-throughput, together with excellent sensitivity and selectivity, in workplace drug-screening controls and forensic investigations. These qualities, combined with minimal sample workup, make the cost of this screening affordable for most private and public administrations.
2012
899
154
159
http://www.sciencedirect.com/science/article/pii/S1570023212002723
Hair; Ultra-high performance liquid chromatography; Multidrugs; Validation
D. Di Corcia; F. D’Urso; E. Gerace; A. Salomone; M. Vincenti
File in questo prodotto:
File Dimensione Formato  
Di Corcia_JCB_2012_postprint.pdf

Open Access dal 07/05/2014

Tipo di file: POSTPRINT (VERSIONE FINALE DELL’AUTORE)
Dimensione 825.68 kB
Formato Adobe PDF
825.68 kB Adobe PDF Visualizza/Apri
DiCorcia_2012_JCB_multianalyte hair UHPLC.pdf

Accesso riservato

Tipo di file: PDF EDITORIALE
Dimensione 563.33 kB
Formato Adobe PDF
563.33 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/104960
Citazioni
  • ???jsp.display-item.citation.pmc??? 13
  • Scopus 59
  • ???jsp.display-item.citation.isi??? 58
social impact