Background: Volumetric Absorptive Microsampling (VAMS) is emerging as a valuable technique in the collection of dried biological specimens, offering a potential alternative to traditional sampling methods. The objective of this study was to assess the suitability of 30 μL VAMS for the measurement of endogenous steroid hormones. Methods: A novel LC-MS/MS method was developed for the quantification of 18 analytes in VAMS samples, including main endogenous free steroids and phase II metabolites of androgens. The method underwent validation in accordance with ISO/IEC 17025:2017 and World Anti-Doping Agency (WADA) requirements. Subsequently, it was applied to authentic VAMS samples obtained from 20 healthy volunteers to assess the stability of target analytes under varying storage conditions. Results: The validation protocol assessed method's selectivity, matrix effect, extraction recovery, quantitative performance, carry-over and robustness. The analysis of authentic samples demonstrated the satisfactory stability of monitored steroids in VAMS stored at room temperature, 4 °C, -20 °C and -80 °C for up to 100 days and subjected to up to 3 freezing-thawing cycles. Conclusions: The validated LC-MS/MS method demonstrated its suitability for the measurement of steroids in dried blood VAMS. The observed stability of steroidal compounds suggests promising prospects for future applications of VAMS, both in anti-doping contexts and clinical research.

LC-MS/MS measurement of endogenous steroid hormones and phase II metabolites in blood volumetric absorptive microsampling (VAMS) for doping control purposes

Ponzetto, Federico
First
;
Parasiliti-Caprino, Mirko;Leoni, Laura;Marinelli, Lorenzo;Nonnato, Antonello;Ghigo, Ezio;Mengozzi, Giulio;Settanni, Fabio
Last
2024-01-01

Abstract

Background: Volumetric Absorptive Microsampling (VAMS) is emerging as a valuable technique in the collection of dried biological specimens, offering a potential alternative to traditional sampling methods. The objective of this study was to assess the suitability of 30 μL VAMS for the measurement of endogenous steroid hormones. Methods: A novel LC-MS/MS method was developed for the quantification of 18 analytes in VAMS samples, including main endogenous free steroids and phase II metabolites of androgens. The method underwent validation in accordance with ISO/IEC 17025:2017 and World Anti-Doping Agency (WADA) requirements. Subsequently, it was applied to authentic VAMS samples obtained from 20 healthy volunteers to assess the stability of target analytes under varying storage conditions. Results: The validation protocol assessed method's selectivity, matrix effect, extraction recovery, quantitative performance, carry-over and robustness. The analysis of authentic samples demonstrated the satisfactory stability of monitored steroids in VAMS stored at room temperature, 4 °C, -20 °C and -80 °C for up to 100 days and subjected to up to 3 freezing-thawing cycles. Conclusions: The validated LC-MS/MS method demonstrated its suitability for the measurement of steroids in dried blood VAMS. The observed stability of steroidal compounds suggests promising prospects for future applications of VAMS, both in anti-doping contexts and clinical research.
2024
Inglese
Esperti anonimi
557
117890
117900
11
https://www.sciencedirect.com/science/article/pii/S0009898124001311?via=ihub
Androgens; Biomarker; Doping; LC-MS/MS; Steroids; VAMS; Whole blood
SVIZZERA
   Use of volumetric absorptive microsampling (VAMS) for the quantification of novel blood markers of EAAS doping
   Non presente
   WADA WORLD ANTI-DOPING AGENCY
   --

   IMPLEMENTATION OF A BLOOD STEROIDAL MODULE IN THE FRAMEWORK OF THE ATHLETE BIOLOGICAL PASSPORT
   Non presente
   Partnership for Clean Competition
   non presente
1 – prodotto con file in versione Open Access (allegherò il file al passo 6 - Carica)
262
10
Ponzetto, Federico; Parasiliti-Caprino, Mirko; Leoni, Laura; Marinelli, Lorenzo; Nonnato, Antonello; Nicoli, Raul; Kuuranne, Tiia; Ghigo, Ezio; Mengoz...espandi
info:eu-repo/semantics/article
open
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1967390
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