Literature DB >> 26296082

Improved sensitivity by use of gas chromatography-positive chemical ionization triple quadrupole mass spectrometry for the analysis of drug related substances.

Wim Van Gansbeke1, Michael Polet2, Fiona Hooghe1, Christophe Devos3, Peter Van Eenoo1.   

Abstract

In 2013, the World Anti-Doping Agency (WADA) drastically lowered the minimum required performance levels (MRPLs) of most doping substances, demanding a substantial increase in sensitivity of the existing methods. For a number of compounds, conventional electron impact ionization gas chromatography tandem mass spectrometry (GC-EI-MS/MS) is often no longer sufficient to reach these MRPLs and new strategies are required. In this study, the capabilities of positive ion chemical ionization (PICI) GC-MS/MS are investigated for a wide range of drug related compounds of various classes by injection of silylated reference standards. Ammonia as PICI reagent gas had superior characteristics for GC-MS/MS purposes than methane. Compared to GC-EI-MS/MS, PICI (with ammonia as reagent gas) provided more selective ion transitions and consequently, increased sensitivity by an average factor of 50. The maximum increase (by factor of 500-1000) was observed in the analysis of stimulants, namely chlorprenaline, furfenorex and phentermine. In total, improved sensitivity was obtained for 113 out of 120 compounds. A new GC-PICI-MS/MS method has been developed and evaluated for the detection of a wide variety of exogenous doping substances and the quantification of endogenous steroids in urine in compliance with the required MRPLs established by WADA in 2013. The method consists of a hydrolysis and extraction step, followed by derivatization and subsequent 1μL pulsed splitless injection on GC-PICI-MS/MS (16min run). The increased sensitivity allows the set up of a balanced screening method that meets the requirements for both quantitative and qualitative compounds: sufficient capacity and resolution in combination with high sensitivity and short analysis time. This resulted in calibration curves with a wide linear range (e.g., 48-9600ng/mL for androsterone and etiochanolone; all r(2)>0.99) without compromising the requirements for the qualitative compounds.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chemical ionization; Doping; GC–MS/MS; Sensitivity

Mesh:

Substances:

Year:  2015        PMID: 26296082     DOI: 10.1016/j.jchromb.2015.07.052

Source DB:  PubMed          Journal:  J Chromatogr B Analyt Technol Biomed Life Sci        ISSN: 1570-0232            Impact factor:   3.205


  3 in total

1.  Direct Analysis of Doping Agents in Raw Urine Using Hydrophobic Paper Spray Mass Spectrometry.

Authors:  Eduardo Luiz Rossini; Dmytro S Kulyk; Emelia Ansu-Gyeabourh; Taghi Sahraeian; Helena Redigolo Pezza; Abraham K Badu-Tawiah
Journal:  J Am Soc Mass Spectrom       Date:  2020-05-14       Impact factor: 3.109

2.  Chemical fingerprinting and quantitative monitoring of the doping drugs bambuterol and terbutaline in human urine samples using ATR-FTIR coupled with a PLSR chemometric tool.

Authors:  Faisal K Algethami; Sherif M Eid; Khadiga M Kelani; Mohamed R Elghobashy; Mohamed K Abd El-Rahman
Journal:  RSC Adv       Date:  2020-02-17       Impact factor: 3.361

Review 3.  Attenuated total reflection-Fourier transform infrared spectroscopy: a universal analytical technique with promising applications in forensic analyses.

Authors:  Khaled Alkhuder
Journal:  Int J Legal Med       Date:  2022-09-01       Impact factor: 2.791

  3 in total

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