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Equine in vivo metabolite profiling of the selective androgen receptor modulator LGD-3303 for doping control

Nilsson Broberg, Malin (author)
Uppsala universitet,Analytisk farmaceutisk kemi
Knych, Heather (author)
Univ Calif Davis, Sch Vet Med, Kenneth L Maddy Equine Analyt Pharmacol Lab, Davis, CA 95616 USA.
Bondesson, Ulf (author)
Uppsala universitet,Analytisk farmaceutisk kemi
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Pettersson, Curt (author)
Uppsala universitet,Analytisk farmaceutisk kemi
Tidstedt, Borje (author)
Natl Vet Inst SVA, Dept Chem Environm & Feed Hyg, S-75189 Uppsala, Sweden.
Stanley, Scott (author)
Univ Kentucky, Gluck Equine Res Ctr, Lexington, KY 40546 USA.
Thevis, Mario (author)
German Sport Univ Cologne, Inst Biochem, Ctr Prevent Doping Res, D-50933 Cologne, Germany.
Hedeland, Mikael (author)
Uppsala universitet,Analytisk farmaceutisk kemi
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 (creator_code:org_t)
Elsevier, 2023
2023
English.
In: Journal of Pharmaceutical and Biomedical Analysis. - : Elsevier. - 0731-7085 .- 1873-264X. ; 233
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • LGD-3303 is a Selective Androgen Receptor Modulator (SARM) that is prohibited in both equine and human sports due to its anabolic properties. The aim of this study was to investigate the equine in vivo metabolite profile of LGD-3303 and identify drug metabolites that can be suitable as new and improved analytical targets for equine doping control. This was performed by an oral administration of 0.05 mg.kg(-1) LGD-3303 to horses, where blood and urine samples were collected up to 96 h after administration. The in vivo samples consisting of plasma, urine and hydrolyzed urine were analyzed utilizing ultra-high performance liquid chromatography hyphenated to a Q Exactive (TM) Orbitrap (TM) high resolution mass spectrometer with a heated electrospray ionization source. A total of eight metabolites of LGD-3303 were tentatively identified, including one carboxylated and several hydroxylated metabolites in combination with glucuronic acid conjugates. A monohydroxylated metabolite is suggested as an analytical target for doping control analysis of plasma and urine after hydrolysis with beta-glucuronidase, due to the high intensity and prolonged detection time in comparison to parent LGD-3303.

Subject headings

NATURVETENSKAP  -- Kemi -- Analytisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Analytical Chemistry (hsv//eng)

Keyword

Mass spectrometry
Selective androgen receptor modulator
LGD-3303
Doping control
Metabolites
Equine

Publication and Content Type

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