In vitro immunosuppressive activity of tacrolimus dihydrodiol precursors obtained by chemical oxidation and identification of a new metabolite of SDZ-RAD by electrospray and electrospray-linked scan mass spectrometry

J Mass Spectrom. 2001 Aug;36(8):889-901. doi: 10.1002/jms.190.

Abstract

Different tacrolimus epoxides and dihydrodiol epoxides arising from the chemical oxidation of the parent drug are described. Open-chain tautomeric forms involving the lactone function were identified for the tacrolimus epoxides. Moreover, the identification by electrospray and electrospray linked scan mass spectrometry of an SDZ-RAD C16-C27 O-demethyl 17, 18-19, 20-21, 22 tris-epoxide new metabolite isolated from pig liver microsomes is reported. The in vitro immunosuppressive activity, using mixed lymphocyte reactions of the two macrolide reported oxidation compounds are discussed.

MeSH terms

  • Animals
  • Biotransformation
  • Cells, Cultured
  • Chromatography, High Pressure Liquid / methods
  • Everolimus
  • Humans
  • Immunosuppressive Agents / pharmacokinetics
  • Immunosuppressive Agents / pharmacology
  • Lactones / chemistry
  • Lymphocyte Culture Test, Mixed
  • Lymphocytes / drug effects
  • Lymphocytes / immunology*
  • Microsomes, Liver / metabolism*
  • Models, Molecular
  • Molecular Conformation
  • NADP / metabolism
  • Oxidation-Reduction
  • Sirolimus / analogs & derivatives*
  • Sirolimus / chemistry
  • Sirolimus / pharmacokinetics*
  • Sirolimus / pharmacology*
  • Spectrometry, Mass, Electrospray Ionization / methods
  • Stereoisomerism
  • Swine
  • Tacrolimus / chemistry
  • Tacrolimus / pharmacokinetics*
  • Tacrolimus / pharmacology*

Substances

  • Immunosuppressive Agents
  • Lactones
  • NADP
  • Everolimus
  • Sirolimus
  • Tacrolimus