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Flutamide metabolism in four different species in vitro and identification of flutamide metabolites in human patient urine by high performance liquid chromatography/tandem mass spectrometry

Tevell, Annica (författare)
Uppsala universitet,Institutionen för läkemedelskemi,Analytisk Farmaceutisk kemi
Lennernäs, Hans (författare)
Uppsala universitet,Institutionen för farmaci
Jonsson, M. (författare)
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Norlin, Maria (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap,Farm biokemi
Lennernäs, Bo, 1963 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
Bondesson, Ulf (författare)
Uppsala universitet,Institutionen för läkemedelskemi,Analytisk Farmaceutisk Kemi
Hedeland, Mikael (författare)
visa färre...
 (creator_code:org_t)
2006-03-15
2006
Engelska.
Ingår i: Drug Metab Dispos. - : American Society for Pharmacology & Experimental Therapeutics (ASPET). - 0090-9556. ; 34:6, s. 984-92
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • A new metabolic scheme of flutamide is proposed in this article. Some patients treated with flutamide, a nonsteroidal antiandrogen, have developed severe hepatic dysfunction. Toxic metabolites have been proposed to be responsible for these negative effects. In this study, the qualitative aspects of the in vitro metabolism of flutamide in liver microsomes from human, dog, pig, and rat were evaluated. A direct comparison of the flutamide metabolism in liver and prostate microsomes from pig was made, and the in vivo metabolism of flutamide was investigated in urine from orally treated prostate cancer patients. Liquid chromatography/tandem mass spectrometry was used for analysis. The mass spectrometer was equipped with an electrospray interface and operated in the negative ion mode. In liver microsomes from pig, dog, and rat, extensive hydroxylation of flutamide occurred. One, two, or three hydroxy groups were attached, and isomeric forms were detected for both monohydroxylated and trihydroxylated drug. In pig liver microsomes, isomers of a third metabolite, hydroxylated 4-nitro-3-(trifluoromethyl)-aniline, were also found after incubation with either flutamide or 2-hydroxyflutamide. In human liver microsomes, the pharmacologically active 2-hydroxyflutamide was the only metabolite detected. Several phase I metabolites as well as four intact phase II metabolites could be recovered from the urine samples. For the first time in humans, glucuronic acid conjugates of hydroxylated 4-nitro-3-(trifluoromethyl)-aniline, and mono- and dihydroxylated flutamide were identified, together with hydroxylated 4-nitro-3-(trifluoromethyl)-aniline conjugated with sulfate. In addition, one mercapturic acid conjugate of hydroxylated flutamide, probably formed from flutamide via a reactive intermediate, was detected.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Androgen Antagonists/*metabolism/therapeutic use/urine
Animals
Antineoplastic Agents
Hormonal/*metabolism/therapeutic use/urine
Biotransformation
Chromatography
Liquid
Dogs
Flutamide/*analogs & derivatives/*metabolism/standards/therapeutic
use/urine
Glucuronidase
Humans
Male
Microsomes
Liver/metabolism
Prostate/metabolism
Prostatic Neoplasms/drug therapy/*metabolism/urine
Rats
Spectrometry
Mass
Electrospray Ionization
Swine
Androgen Antagonists/*metabolism/therapeutic use/urine

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