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


Journal

Drug testing and analysis
ISSN: 1942-7611
Titre abrégé: Drug Test Anal
Pays: England
ID NLM: 101483449

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 27 01 2020
revised: 27 07 2020
accepted: 17 08 2020
pubmed: 28 8 2020
medline: 25 2 2023
entrez: 28 8 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32852865
doi: 10.1002/dta.2918
doi:

Substances chimiques

2-chloro-4-(3-hydroxy-3-methyl-8-azabicyclo(3.2.1)oct-8-yl)-3-methylbenzonitrile 0
Androgens 0
Azabicyclo Compounds 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

299-317

Informations de copyright

© 2020 John Wiley & Sons, Ltd.

Références

Mooradian AD, Morley JE, Korenman SG. Biological actions of androgens. Endocr Rev. 1987;8(1):1-28.
Mangelsdorf DJ, Thummel C, Beato M, et al. The nuclear receptor superfamily: the second decade. Cell. 1995;83(6):835-839.
Sar M, Lubahn DB, French FS, Wilson EM. Immuno-histochemical localization of the androgen receptor in rat and human tissues. Endocrinology. 1990;127(6):3180-3186.
Gao W, Bohl CE, Dalton JT. Chemistry and structural biology of androgen receptor. Chem Rev. 2005;105(9):3352-3370.
Heinlein CA, Chang C. Androgen receptor in prostate cancer. Endocr Rev. 2004;25(2):276-308.
Mohler ML, Bohl CE, Jones A, et al. Nonsteroidal selective androgen receptor modulators (SARMs): dissociating the anabolic and androgenic activities of the androgen receptor for therapeutic benefit. J Med Chem. 2009;52(12):3597-3617.
Acevedo S, Gardell L, Bradley SR, Piu F, Raber J. Selective androgens receptor modulators antagonize apolipoprotein E4-induced cognitive impairments. Lett Drug des Discovery. 2008;5(4):271-276.
Rosen J, Negro-Vilar A. Novel, non-steroidal, selective androgen receptor modulators (SARMs) with anabolic activity in bone and muscle and improved safety profile. J Musculoskelet Neuronal Interact. 2002;2:222-224.
Yarrow JF, Conover CF, McCoy SC, et al. 17-Hydroxyestra- 4, 9, 11-trien-3-one (trenbolone) exhibits tissue selective anabolic activity: effects on muscle, bone, adiposity, hemoglobin, and prostate. Am J Physiol Endocrinol Metab. 2011;300(4):E650-E660.
Haendler B, Cleve A. Recent developments in antiandrogens and selective androgen receptor modulators. Mol Cell Endocrinol. 2012;352(1-2):79-91.
Narayanan R, Mohler ML, Bohl CE, Miller DD, Dalton JT. Selective androgen receptor modulators in preclinical and clinical development. Nucl Recept Signal. 2008;6:1-26, E010.
Allan G, Lai M, Sbriscia T, et al. A selective androgen receptor modulator that reduces prostate tumor size and prevents orchidectomy-induced bone loss in rats. J Steroid Biochem Mol Biol. 2007;103(1):76-83.
Gao W, Reiser P, Coss C, et al. Selective androgen receptor modulator treatment improves muscle strength and body composition and prevents bone loss in orchidectomized rats. Endocrinology. 2005;146(11):4887-4897.
Sun C, Robl J, Wang T, et al. Discovery of potent, orally-active, and muscle-selective androgen receptor modulators based on an N-aryl-hydroxybicyclohydantoin scaffold. J Med Chem. 2006;49(26):7596-7599.
Schlienger N, Lund BW, Pawlas J, et al. Synthesis, structure-activity relationships, and characterization of novel non-steroidal and selective androgen receptor modulators. J Med Chem. 2009;52(22):7186-7191.
Grata E, Perrenoud L, Saugy M, Baume N. SARM-S4 and metabolites detection in sports drug testing: a case report. Forensic Sci Int. 2011;213(1-3):104-108.
Starcevic B, Ahrens BD, Butch AW. Detection of the selective androgen receptor modulator S-4 (andarine) in a doping control sample. Drug Test Anal. 2013;5(5):377-379.
Kintz P, Ameline A, Gheddar L, Raul J. LGD-4033, S-4 and MK-2866-testing for SARMs in hair: about 2 doping cases. Toxicologie Analy & Cliniq. 2019;31(1):56-63.
Beuck S, Schänzer W, Thevis M. Investigation of the in vitro metabolism of the emerging drug candidate S107 for doping-preventive purposes. J Mass Spectrom. 2011;46(2):112-130.
Thevis M, Geyer H, Thomas A, Schänzer W. Trafficking of drug candidates relevant for sports drug testing: detection of non-approved therapeutics categorized as anabolic and gene doping agents in products distributed via the Internet. Drug Test Anal. 2011;3(5):331-336.
Thevis M, Thomas A, Piper T, Krug O, Delahaut P, Schänzer W. Liquid chromatography-high resolution/high accuracy (tandem) mass spectrometry based identification of in vivo generated metabolites of the selective androgen receptor modulator ACP-105 for doping control purposes. Eur J Mass Spectrom. 2014;20(1):73-83.
Thevis M, Piper T, Beuck S, Geyer H, Schänzer W. Expanding sports drug testing assays: Mass spectrometric characterization of the selective androgen receptor modulator drug candidates RAD140 and ACP-105. Rapid Commun Mass Spectrom. 2013;27(11):1173-1182.
Subhahar M, Singh J, Albert PH, Kadry AM. Pharmacokinetics, metabolism and excretion of celecoxib, a selective cyclooxygenase- 2 inhibitor, in horse. J Vet Pharmacol Therap. 2019;1-7.

Auteurs

Michael Benedict Subhahar (MB)

Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

Abdul Khader Karakka Kal (AK)

Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

Moses Philip (M)

Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

Tajudheen K Karatt (T)

Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

Ibrahimwaseem N (I)

Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

Ramees Abdulla Vazhat (RA)

Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

Muhammed Ajeebsanu M P (MA)

Equine Forensic Unit, Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

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