1. Academic Validation
  2. Comprehensive metabolic study of IOX4 in equine urine and plasma using liquid chromatography/electrospray ionization Q Exactive high-resolution mass spectrometer for the purpose of doping control

Comprehensive metabolic study of IOX4 in equine urine and plasma using liquid chromatography/electrospray ionization Q Exactive high-resolution mass spectrometer for the purpose of doping control

  • Drug Test Anal. 2022 Feb;14(2):233-251. doi: 10.1002/dta.3172.
Hideaki Ishii 1 2 Mariko Shibuya 1 Yat-Ming So 3 Jenny K Y Wong 3 Emmie N M Ho 3 Kanichi Kusano 4 Yu Sone 4 Takahiro Kamiya 5 Ai Wakuno 5 Hideki Ito 5 Kenji Miyata 6 Masayuki Yamada 1 Gary Ngai-Wa Leung 1
Affiliations

Affiliations

  • 1 Drug Analysis Department, Laboratory of Racing Chemistry, Utsunomiya, Tochigi, Japan.
  • 2 Department of Pharmaceutical Sciences, Tohoku University Hospital, Sendai, Miyagi, Japan.
  • 3 Racing Laboratory, The Hong Kong Jockey Club, Sha Tin Racecourse, Sha Tin, N.T., Hong Kong.
  • 4 Veterinarian Section, Equine Department, JRA, Minato, Tokyo, Japan.
  • 5 Equine Veterinary Clinic, Horse Racing School, Japan Racing Association, Shiroi, Chiba, Japan.
  • 6 JRA Equestrian Park Utsunomiya Office, Utsunomiya, Tochigi, Japan.
Abstract

IOX4 is a hypoxia-inducible factor prolyl hydroxylase (HIF-PHD) inhibitor, which was developed for the treatment of anemia by exerting hematopoietic effects. The administration of HIF-PHD inhibitors such as IOX4 to horses is strictly prohibited by the International Federation of Horseracing Authorities and the Fédération Équestre Internationale. To the best of our knowledge, this is the first comprehensive metabolic study of IOX4 in horse plasma and urine after a nasoesophageal administration of IOX4 (500 mg/day, 3 days). A total of four metabolites (three mono-hydroxylated IOX4 and one IOX4 glucuronide) were detected from the in vitro study using homogenized horse liver. As for the in vivo study, post-administration plasma and urine samples were comprehensively analyzed with liquid chromatography/electrospray ionization high-resolution mass spectrometry to identify potential metabolites and determine their corresponding detection times. A total of 10 metabolites (including IOX4 glucuronide, IOX4 glucoside, O-desbutyl IOX4, O-desbutyl IOX4 glucuronide, four mono-hydroxylated IOX4, N-oxidized IOX4, and N-oxidized IOX4 glucoside) were found in urine and three metabolites (glucuronide, glucoside, and O-desbutyl) in plasma. Thus, the respective quantification methods for the detection of free and conjugated IOX4 metabolites in urine and plasma with a biphase enzymatic hydrolysis were developed and applied to post-administration samples for the establishment of elimination profiles of IOX4. The detection times of total IOX4 in urine and plasma could be successfully prolonged to at least 312 h.

Keywords

IOX4; LC/ESI-HRMS; doping control; equine; metabolic study.

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