Literature DB >> 25065924

Rapid quantitative chiral amphetamines liquid chromatography-tandem mass spectrometry: method in plasma and oral fluid with a cost-effective chiral derivatizing reagent.

Matthew N Newmeyer1, Marta Concheiro2, Marilyn A Huestis3.   

Abstract

Methamphetamine is a widely abused psychostimulant containing a chiral center. Consumption of over-the-counter and prescription medications may yield positive amphetamines results, but chiral separation of l- and d-methamphetamine and its metabolite amphetamine can help determine whether the source was licit or illicit. We present the first LC-MS/MS method with precolumn derivatization for methamphetamine and amphetamine chiral resolution in plasma and oral fluid collected with the Oral-Eze(®) and Quantisal™ devices. To 0.5mL plasma, 0.75mL Oral-Eze, or 1mL Quantisal specimen racemic d11-methamphetamine and amphetamine internal standards were added, followed by protein precipitation. Samples were centrifuged and supernatants loaded onto pre-conditioned Phenomenex(®) Strata™-XC Polymeric Strong Cation solid phase extraction columns. After washing, analytes were eluted with 5% ammonium hydroxide in methanol. The eluate was evaporated to dryness and reconstituted in water. Derivatization was performed with 1-fluoro-2,4-dinitrophenyl-5-l-alanineamide (Marfey's reagent) and heating at 45°C for 1h. Derivatized enantiomer separations were performed under isocratic conditions (methanol:water, 60:40) with a Phenomenex(®) Kinetex(®) 2.6μm C18 column. Analytes were identified and quantified by two MRM transitions and their ratio on a 3200 QTrap (AB Sciex) mass spectrometer in ESI negative mode. In all three matrices, the method was linear for all enantiomers from 1 to 500μg/L, with imprecision and accuracy of ≤11.3% and 85.3-108%, respectively. Extraction efficiencies ranged from 67.4 to 117% and matrix effects from -17.0 to 468%, with variation always ≤19.1%. Authentic plasma and OF specimens were collected from an IRB-approved study that included controlled Vicks(®) VapoInhaler™ administration. The present method is sensitive, selective, economic and rapid (separations accomplished in <10min), and improves methamphetamine result interpretation. Published by Elsevier B.V.

Entities:  

Keywords:  Amphetamines; Chiral analysis; Marfey's reagent; Oral fluid; Plasma

Mesh:

Substances:

Year:  2014        PMID: 25065924      PMCID: PMC4150735          DOI: 10.1016/j.chroma.2014.06.096

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  21 in total

Review 1.  Illegal or legitimate use? Precursor compounds to amphetamine and methamphetamine.

Authors:  F Musshoff
Journal:  Drug Metab Rev       Date:  2000-02       Impact factor: 4.518

2.  Enantioselective trace analysis of amphetamine in human plasma by gas chromatography/negative ion chemical ionization mass spectrometry.

Authors:  Hans-Jörg Leis; Gerald N Rechberger; Günter Fauler; Werner Windischhofer
Journal:  Rapid Commun Mass Spectrom       Date:  2003       Impact factor: 2.419

3.  Drug testing in blood: validated negative-ion chemical ionization gas chromatographic-mass spectrometric assay for determination of amphetamine and methamphetamine enantiomers and its application to toxicology cases.

Authors:  Frank T Peters; Thomas Kraemer; Hans H Maurer
Journal:  Clin Chem       Date:  2002-09       Impact factor: 8.327

4.  Multiclass analysis of illicit drugs in plasma and oral fluids by LC-MS/MS.

Authors:  M Sergi; E Bafile; D Compagnone; R Curini; G D'Ascenzo; F S Romolo
Journal:  Anal Bioanal Chem       Date:  2008-11-04       Impact factor: 4.142

5.  High-performance liquid chromatographic-mass spectrometric determination of methamphetamine and amphetamine enantiomers, desmethylselegiline and selegiline, in hair samples of long-term methamphetamine abusers or selegiline users.

Authors:  Kenichi Nishida; Shinzi Itoh; Naohide Inoue; Keiko Kudo; Noriaki Ikeda
Journal:  J Anal Toxicol       Date:  2006-05       Impact factor: 3.367

6.  Development and validation of LC-HRMS and GC-NICI-MS methods for stereoselective determination of MDMA and its phase I and II metabolites in human urine.

Authors:  Andrea E Schwaninger; Markus R Meyer; Marilyn A Huestis; Hans H Maurer
Journal:  J Mass Spectrom       Date:  2011-07       Impact factor: 1.982

7.  Stereoselectivity in the human metabolism of methamphetamine.

Authors:  Linghui Li; Tom Everhart; Peyton Jacob Iii; Reese Jones; John Mendelson
Journal:  Br J Clin Pharmacol       Date:  2010-02       Impact factor: 4.335

8.  Simultaneous enantiomeric determination of MDMA and its phase I and phase II metabolites in urine by liquid chromatography-tandem mass spectrometry with chiral derivatization.

Authors:  Keiko Nakanishi; Munehiro Katagi; Kei Zaitsu; Noriaki Shima; Hiroe Kamata; Akihiro Miki; Hajime Kato; Ken-Ichi Harada; Hitoshi Tsuchihashi; Koichi Suzuki
Journal:  Anal Bioanal Chem       Date:  2012-09-26       Impact factor: 4.142

9.  Negative-ion chemical ionization gas chromatography-mass spectrometry assay for enantioselective measurement of amphetamines in oral fluid: application to a controlled study with MDMA and driving under the influence cases.

Authors:  Frank T Peters; Nele Samyn; Thomas Kraemer; Wim J Riedel; Hans H Maurer
Journal:  Clin Chem       Date:  2007-03-01       Impact factor: 8.327

10.  Concentrations and ratios of amphetamine, methamphetamine, MDA, MDMA, and MDEA enantiomers determined in plasma samples from clinical toxicology and driving under the influence of drugs cases by GC-NICI-MS.

Authors:  F T Peters; N Samyn; M Wahl; T Kraemer; G De Boeck; H H Maurer
Journal:  J Anal Toxicol       Date:  2003 Nov-Dec       Impact factor: 3.367

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  3 in total

1.  Oral fluid with three modes of collection and plasma methamphetamine and amphetamine enantiomer concentrations after controlled intranasal l-methamphetamine administration.

Authors:  Matthew N Newmeyer; Marta Concheiro; Jose Luiz da Costa; Ronald Flegel; David A Gorelick; Marilyn A Huestis
Journal:  Drug Test Anal       Date:  2015-03-18       Impact factor: 3.345

2.  A High-Resolution Magic Angle Spinning NMR Study of the Enantiodiscrimination of 3,4-Methylenedioxymethamphetamine (MDMA) by an Immobilized Polysaccharide-Based Chiral Phase.

Authors:  Juliana C Barreiro; Márcio W Paixão; Tiago C Lourenço; Quezia B Cass; Tiago Venâncio
Journal:  PLoS One       Date:  2016-09-26       Impact factor: 3.240

Review 3.  Chiral Drug Analysis in Forensic Chemistry: An Overview.

Authors:  Cláudia Ribeiro; Cristiana Santos; Valter Gonçalves; Ana Ramos; Carlos Afonso; Maria Elizabeth Tiritan
Journal:  Molecules       Date:  2018-01-28       Impact factor: 4.411

  3 in total

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