Supercritical fluid chromatography-mass spectrometry in routine anti-doping analyses: Estimation of retention time variability under reproducible conditions.

Details

Serval ID
serval:BIB_FA8F22D3E66E
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Supercritical fluid chromatography-mass spectrometry in routine anti-doping analyses: Estimation of retention time variability under reproducible conditions.
Journal
Journal of chromatography. A
Author(s)
Losacco G.L., Marconetto E., Nicoli R., Kuuranne T., Boccard J., Rudaz S., Veuthey J.L., Guillarme D.
ISSN
1873-3778 (Electronic)
ISSN-L
0021-9673
Publication state
Published
Issued date
12/04/2020
Peer-reviewed
Oui
Volume
1616
Pages
460780
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Abstract
The aim of this study was to estimate the retention time variability under reproducible conditions of an SFC-MS analytical method for routine anti-doping analyses. For this purpose, a set of 51 doping agents, as neat standards and spiked in diluted urine, was used to assess their retention times variability over a period of four months, as well as the column inter-batch reproducibility. Three UHPSFC stationary phases have been employed, the Acquity UPC <sup>2</sup> Torus 2-Picolylamine (2-PIC), UPC <sup>2</sup> Viridis BEH and Acquity UPLC HSS C18 SB. Four columns, per column chemistry, have been purchased to represent three different production lots, with a total of twelve columns employed in this study. The two columns from the same lot were applied to the first part of the study (repeatability), whereas the representative of three different lots were employed in the second part (robustness). In terms of organic modifier, a mixture of 98% MeOH and 2% water containing 20 mM ammonium formate was selected in order to limit the formation of methyl-silyl ethers on the surface of the silica particles, thus potentially improving the repeatability of retention times. A comparison with an UHPLC reference analytical method was made with the same set of analytes. The average relative standard deviations (RSD%), represented in split violin plots, illustrate how two of the UHPSFC columns assessed in this study were able to generate an excellent repeatability of retention times, with results that are in a similar range of those generated by UHPLC. Moreover, the Torus 2-PIC has proven to be the best of the three stationary phases, with an impressive RSD% of 0.5% in diluted urine relative to the inter-month variability. Finally, the inter-batch reproducibility assessment has highlighted a good reproducibility of the same stationary phase belonging to different production lots for all three column chemistries assessed, with the Viridis BEH silica generating an RSD% of 0.7% in diluted urine. Higher values of RSD (%) were found for Torus 2-PIC and HSS C18 SB, respectively of 1.0% and 1.6%.
Keywords
Chromatography, Supercritical Fluid, Doping in Sports/prevention & control, Humans, Mass Spectrometry, Performance-Enhancing Substances/urine, Reproducibility of Results, Silicon Dioxide/chemistry, Substance Abuse Detection/instrumentation, Substance Abuse Detection/methods, Urinalysis/instrumentation, Urinalysis/methods, Water/chemistry, Anti-doping analyses, Identification criteria, Retention time variability, Tandem mass spectrometry, Ultra-high performance supercritical fluid chromatography
Pubmed
Web of science
Create date
03/01/2020 17:06
Last modification date
28/07/2022 6:37
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