The potential for complementary targeted/non-targeted screening of novel psychoactive substances in equine urine using liquid chromatography-high resolution accurate mass spectrometry

Research output: Contribution to journalJournal articleResearchpeer-review

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The potential for complementary targeted/non-targeted screening of novel psychoactive substances in equine urine using liquid chromatography-high resolution accurate mass spectrometry. / Cawley, Adam; Pasin, Daniel; Ganbat, Namuun; Ennis, Laura; Smart, Corrine; Greer, Candace; Keledjian, John; Fu, Shanlin; Chen, Alex.

In: Analytical Methods, Vol. 8, No. 8, 28.02.2016, p. 1789-1797.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Cawley, A, Pasin, D, Ganbat, N, Ennis, L, Smart, C, Greer, C, Keledjian, J, Fu, S & Chen, A 2016, 'The potential for complementary targeted/non-targeted screening of novel psychoactive substances in equine urine using liquid chromatography-high resolution accurate mass spectrometry', Analytical Methods, vol. 8, no. 8, pp. 1789-1797. https://doi.org/10.1039/c6ay00156d

APA

Cawley, A., Pasin, D., Ganbat, N., Ennis, L., Smart, C., Greer, C., Keledjian, J., Fu, S., & Chen, A. (2016). The potential for complementary targeted/non-targeted screening of novel psychoactive substances in equine urine using liquid chromatography-high resolution accurate mass spectrometry. Analytical Methods, 8(8), 1789-1797. https://doi.org/10.1039/c6ay00156d

Vancouver

Cawley A, Pasin D, Ganbat N, Ennis L, Smart C, Greer C et al. The potential for complementary targeted/non-targeted screening of novel psychoactive substances in equine urine using liquid chromatography-high resolution accurate mass spectrometry. Analytical Methods. 2016 Feb 28;8(8):1789-1797. https://doi.org/10.1039/c6ay00156d

Author

Cawley, Adam ; Pasin, Daniel ; Ganbat, Namuun ; Ennis, Laura ; Smart, Corrine ; Greer, Candace ; Keledjian, John ; Fu, Shanlin ; Chen, Alex. / The potential for complementary targeted/non-targeted screening of novel psychoactive substances in equine urine using liquid chromatography-high resolution accurate mass spectrometry. In: Analytical Methods. 2016 ; Vol. 8, No. 8. pp. 1789-1797.

Bibtex

@article{b074fa8111614e0b8a1c20cdfb3d9680,
title = "The potential for complementary targeted/non-targeted screening of novel psychoactive substances in equine urine using liquid chromatography-high resolution accurate mass spectrometry",
abstract = "The potential for liquid chromatography-high resolution accurate mass (LC-HRAM) spectrometry to identify 'unknown' compounds using non-targeted screening methods provides a potential advantage in the fight against doping in sport. This innovation comes with the requirement for assessment to support its use in the medico-legal context. A method for the LC-HRAM detection of 2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (NBOMe) compounds in equine urine was validated in order to assess the capabilities of a workflow developed for non-targeted analysis using the SIEVE{\textregistered} differential analysis software platform. Six NBOMe compounds (25B, 25C, 25D, 25E, 25H and 25I) were studied to develop and optimize the proposed non-targeted screening workflow before two additional candidates (25N and 25T2) were used as blind controls for verification. Chromatographic alignment and the integration threshold were found to be the most critical parameters for successful identification of 'unknown' responses. The proposed workflow serves as an example for anti-doping laboratories to implement fit-for-purpose non-targeted screening methods.",
author = "Adam Cawley and Daniel Pasin and Namuun Ganbat and Laura Ennis and Corrine Smart and Candace Greer and John Keledjian and Shanlin Fu and Alex Chen",
year = "2016",
month = feb,
day = "28",
doi = "10.1039/c6ay00156d",
language = "English",
volume = "8",
pages = "1789--1797",
journal = "Analytical Methods",
issn = "1759-9660",
publisher = "Royal Society of Chemistry",
number = "8",

}

RIS

TY - JOUR

T1 - The potential for complementary targeted/non-targeted screening of novel psychoactive substances in equine urine using liquid chromatography-high resolution accurate mass spectrometry

AU - Cawley, Adam

AU - Pasin, Daniel

AU - Ganbat, Namuun

AU - Ennis, Laura

AU - Smart, Corrine

AU - Greer, Candace

AU - Keledjian, John

AU - Fu, Shanlin

AU - Chen, Alex

PY - 2016/2/28

Y1 - 2016/2/28

N2 - The potential for liquid chromatography-high resolution accurate mass (LC-HRAM) spectrometry to identify 'unknown' compounds using non-targeted screening methods provides a potential advantage in the fight against doping in sport. This innovation comes with the requirement for assessment to support its use in the medico-legal context. A method for the LC-HRAM detection of 2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (NBOMe) compounds in equine urine was validated in order to assess the capabilities of a workflow developed for non-targeted analysis using the SIEVE® differential analysis software platform. Six NBOMe compounds (25B, 25C, 25D, 25E, 25H and 25I) were studied to develop and optimize the proposed non-targeted screening workflow before two additional candidates (25N and 25T2) were used as blind controls for verification. Chromatographic alignment and the integration threshold were found to be the most critical parameters for successful identification of 'unknown' responses. The proposed workflow serves as an example for anti-doping laboratories to implement fit-for-purpose non-targeted screening methods.

AB - The potential for liquid chromatography-high resolution accurate mass (LC-HRAM) spectrometry to identify 'unknown' compounds using non-targeted screening methods provides a potential advantage in the fight against doping in sport. This innovation comes with the requirement for assessment to support its use in the medico-legal context. A method for the LC-HRAM detection of 2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (NBOMe) compounds in equine urine was validated in order to assess the capabilities of a workflow developed for non-targeted analysis using the SIEVE® differential analysis software platform. Six NBOMe compounds (25B, 25C, 25D, 25E, 25H and 25I) were studied to develop and optimize the proposed non-targeted screening workflow before two additional candidates (25N and 25T2) were used as blind controls for verification. Chromatographic alignment and the integration threshold were found to be the most critical parameters for successful identification of 'unknown' responses. The proposed workflow serves as an example for anti-doping laboratories to implement fit-for-purpose non-targeted screening methods.

UR - http://www.scopus.com/inward/record.url?scp=84958948781&partnerID=8YFLogxK

U2 - 10.1039/c6ay00156d

DO - 10.1039/c6ay00156d

M3 - Journal article

AN - SCOPUS:84958948781

VL - 8

SP - 1789

EP - 1797

JO - Analytical Methods

JF - Analytical Methods

SN - 1759-9660

IS - 8

ER -

ID: 239259358