Issue 14, 2024

A screening method for the quantitative determination of selective androgen receptor modulators (SARMs) in capsules by high resolution 19F- and 1H-NMR spectroscopy

Abstract

A new method for rapid determination of the content of selective androgenic receptor modulators (SARMs) andarine, cardarine, ligandrol, ostarine and S-23 in capsules by 1H- and 19F-high resolution nuclear magnetic resonance spectroscopy was described and validated. Specificity, linearity, accuracy, precision, detection and quantification limits were considered as validation parameters. Full 1H-, 13C- and 19F-NMR structural assignment of the SARMs is provided as a tool for self-standing identification without a reference standard. Amounts of 7–15 mg of SARMs/capsule were detected in different products with an intermediate precision of 0.8–1.7% in 4 to 20 minutes of analysis time. The validation results and rapidity of analysis confirm the applicability of the method for large-scale screening. The statistical analysis of the results from 19F- and 1H-quantitative NMR showed that both approaches were equally effective, thus expanding the potential use of the methodology to non-fluorinated SARMs. At present, no SARM has been approved for human consumption; however, SARMs are actually used by bodybuilders and recreational athletes, who purchase them even though the risk–benefit ratio of these molecules has not been definitively established.

Graphical abstract: A screening method for the quantitative determination of selective androgen receptor modulators (SARMs) in capsules by high resolution 19F- and 1H-NMR spectroscopy

Supplementary files

Article information

Article type
Paper
Submitted
31 Jan 2024
Accepted
07 Mar 2024
First published
22 Mar 2024

Anal. Methods, 2024,16, 2135-2146

A screening method for the quantitative determination of selective androgen receptor modulators (SARMs) in capsules by high resolution 19F- and 1H-NMR spectroscopy

A. Maccelli, A. Borioni, F. Aureli, M. C. Gaudiano, L. Manna and M. Raimondo, Anal. Methods, 2024, 16, 2135 DOI: 10.1039/D4AY00188E

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