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Drug testing and analysis2020; 13(2); 299-317; doi: 10.1002/dta.2918

Detection and identification of ACP-105 and its metabolites in equine urine using LC/MS/MS after oral administration.

Abstract: ACP-105 is a novel nonsteroidal selective androgen receptor modulator (SARM) with a tissue-specific agonist effect and does not have side effects associated with the use of common androgens. This research reports a comprehensive study for the detection of ACP-105 and its metabolites in racehorses after oral administration (in vivo) and postulating its structures using mass spectrometric techniques. To obtain the metabolic profile of ACP-105, a selective and reliable LC-MS/MS method was developed. The chemical structures of the metabolites were determined based on their fragmentation pattern, accurate mass, and retention time. Under the current experimental condition, a total of 19 metabolites were detected in ACP-105 drug administered equine urine samples. The study results suggest the following: (1) ACP-105 is prone to oxidation, which gives corresponding monohydroxylated, dihydroxylated, and trihydroxylated metabolites; (2) along with oxidation, there is a possibility of elimination of water molecule (dehydration) from the third position of the tropine moiety, resulting in the dehydrated analogs of corresponding monohydroxylated, dihydroxylated, and trihydroxylated metabolites; (3) from the study on the metabolites using LC-MS/MS, it is clear that the fragmentation pattern is identical and a great number of fragment ions are common in all the metabolites and the parent drug. (4) The ACP-105 and its metabolites were detected for up to 72 h; thus, the result is a valuable tool for evaluating its use and/or misuse in sport.
Publication Date: 2020-09-06 PubMed ID: 32852865DOI: 10.1002/dta.2918Google Scholar: Lookup
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  • Journal Article

Summary

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The research article is about a study on the detection and identification of ACP-105 and its metabolites in racehorse urine samples. The study used liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) method to detect and establish the metabolic profile of ACP-105 and its possible impacts in sports.

Development of the LC-MS/MS Method

  • The researchers developed a reliable and selective LC-MS/MS method to obtain the metabolic profile of ACP-105, a novel nonsteroidal selective androgen receptor modulator (SARM).
  • They used this method to evaluate the fragmentation patterns, accurate mass, and retention time to determine the chemical structures of the metabolites found in the equine urine samples after the administration of ACP-105.

Findings

  • Under the experimental conditions of this study, a total of 19 metabolites were detected in the urine samples of horses after they were administered ACP-105.
  • One finding suggests that ACP-105 is prone to oxidation, resulting in various monohydroxylated, dihydroxylated, and trihydroxylated metabolites.
  • Along with oxidation, the researchers found that there is a possibility of dehydration from the third position of the tropine moiety. As a result, dehydrated analogs of the corresponding monohydroxylated, dihydroxylated, and trihydroxylated metabolites were produced.

Implications

  • One significant observation from the metabolite study via LC-MS/MS is that the fragmentation pattern is identical in all metabolites and the parent drug, with a great number of fragment ions shared between them.
  • Moreover, the detection of ACP-105 and its metabolites was possible for up to 72 hours after administration. This finding suggests that this method could be a valuable tool for evaluating potential use or misuse of ACP-105 in sports, especially since these substances have tissue-specific agonistic effects and do not trigger side-effects associated with common androgens.

Cite This Article

APA
Subhahar MB, Karakka Kal AK, Philip M, K Karatt T, N I, Vazhat RA, M P MA. (2020). Detection and identification of ACP-105 and its metabolites in equine urine using LC/MS/MS after oral administration. Drug Test Anal, 13(2), 299-317. https://doi.org/10.1002/dta.2918

Publication

ISSN: 1942-7611
NlmUniqueID: 101483449
Country: England
Language: English
Volume: 13
Issue: 2
Pages: 299-317

Researcher Affiliations

Subhahar, Michael Benedict
  • Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.
Karakka Kal, Abdul Khader
  • Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.
Philip, Moses
  • Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.
K Karatt, Tajudheen
  • Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.
N, Ibrahimwaseem
  • Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.
Vazhat, Ramees Abdulla
  • Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.
M P, Muhammed Ajeebsanu
  • Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

MeSH Terms

  • Administration, Oral
  • Androgens / administration & dosage
  • Androgens / metabolism
  • Androgens / urine
  • Animals
  • Azabicyclo Compounds / administration & dosage
  • Azabicyclo Compounds / metabolism
  • Azabicyclo Compounds / urine
  • Chromatography, Liquid / methods
  • Doping in Sports
  • Female
  • Horses / urine
  • Male
  • Substance Abuse Detection / methods
  • Tandem Mass Spectrometry / methods

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Citations

This article has been cited 2 times.
  1. Broberg MN, Knych H, Bondesson U, Pettersson C, Stanley S, Thevis M, Hedeland M. Investigation of Equine In Vivo and In Vitro Derived Metabolites of the Selective Androgen Receptor Modulator (SARM) ACP-105 for Improved Doping Control. Metabolites 2021 Feb 1;11(2).
    doi: 10.3390/metabo11020085pubmed: 33535528google scholar: lookup
  2. Fijałkowska O, Jurowski K. Toxicity of ACP-105: a substance used as doping in sports: application of in silico methods for prediction of selected toxicological endpoints. Arch Toxicol 2025 Apr;99(4):1485-1503.
    doi: 10.1007/s00204-025-03962-zpubmed: 40064700google scholar: lookup