Metabolites of Doxylamine succinate in Human Urine

인체 뇨중의 숙신산 독실아민의 대사체

  • Eom, Khee-Dong (Doping Control Center, Korea Institute of Science & Technology) ;
  • Jung, Byung-Hwa (Doping Control Center, Korea Institute of Science & Technology) ;
  • Chung, Bong-Chul (Doping Control Center, Korea Institute of Science & Technology) ;
  • Slikker, William (Department of Health and Human Services, National Center for Toxicological Research) ;
  • Park, Jong-Sei (Doping Control Center, Korea Institute of Science & Technology)
  • 엄기동 (한국과학기술연구원 도핑콘트롤센터) ;
  • 정병화 (한국과학기술연구원 도핑콘트롤센터) ;
  • 정봉철 (한국과학기술연구원 도핑콘트롤센터) ;
  • ;
  • 박종세 (한국과학기술연구원 도핑콘트롤센터)
  • Published : 1992.06.29

Abstract

The metabolic profile of doxylamine, N,N-dimethyl-2-[1-phenyl-1-(2-pyridinyl)ethoxy] ethanamine, was determined in the human urine. The free fractions of extracts were obtained without hydrolysis, and the conjugated fractions of extracts were obtained with enzyme hydrolysis using ${\beta}-glucuronidase/arylsulfatase$ from Helix pomatia. The mixture of acetic anhydride/pyridine (10 : 1, v : v) was used to derivatize the urinary extracts and then analyzed by gas chromatography and mass selective detector. N-desmethyldoxylamine, doxylamine carboxylic acid, desaminohydroxydoxylamine, N, N-didesmethyldoxylamine, N-acetyl conjugates of N-desmethyl and N, N-didesmethyldoxylamine, quarternary ammonium N-glucuronide of doxylamine, N-desmethyldoxylamine N-glucuronide and unchanged doxylamine were detected in the human urine obtained after oral treatment with doxylamine succinate. $N-methyl-{\alpha}-hydroxy-2-[1-phenyl-1-(2-pyridinyl)$ ethoxy] ethanamine, which can be a key intermediate of this metabolism, was tentatively identified by the interpretation of its mass spectrum. In this study, we proposed the metabolic pathway of doxylamine in the human on the basis of our data of the identified metabolites of doxylamine.

Keywords