Literature DB >> 24590313

Elucidation of in vitro phase I metabolites of droperidol using UPLC-QTOF MS.

Ling Fang1, Chao-Xian Lin, Zhi-Wei Zhu, Lin-Shu Zhao, Shu-Yao Zhang.   

Abstract

Droperidol, an antidopaminergic drug clinically used as an antiemetic and antipsychotic, has been reported to induce cardiac toxicity in patients. Due to the close relationship between drug metabolism and efficiency and toxicity, the present study aims to investigate the phase I metabolites using ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry. The NADPH-supplemented phase I incubation system was used to elucidate the in vitro phase I metabolites. Five metabolites were detected after droperidol was incubated with phase I incubation mixture, including one hydrogenated droperidol, three oxidative metabolites, and one N-dealkylated droperidol, elucidated by individual retention time and MS/MS fragmentation. Due to the existed phase II metabolic reaction, further phase II metabolism should be investigated in the future. In conclusion, the phase I metabolism of droperidol was investigated in the present study, and five new metabolites were identified. The efficiency and toxicity of these phase I metabolites should be investigated in the future.

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Year:  2014        PMID: 24590313     DOI: 10.1007/s13318-014-0185-x

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  12 in total

1.  In vitro metabolism of a novel antithrombotic compound, S002-333, and its enantiomers: quantitative cytochrome P450 phenotyping, metabolic profiling and enzyme kinetic studies.

Authors:  Amrita Saxena; Girish K Jain; Hefazat H Siddiqui; Shom S Bhunia; Anil K Saxena; Jiaur R Gayen
Journal:  Xenobiotica       Date:  2013-08-30       Impact factor: 1.908

2.  Identification of the cytochrome P450 enzymes involved in the metabolism of domperidone.

Authors:  C Simard; V Michaud; B Gibbs; R Massé; E Lessard; J Turgeon
Journal:  Xenobiotica       Date:  2004 Nov-Dec       Impact factor: 1.908

Review 3.  Droperidol analgesia for opioid-tolerant patients.

Authors:  John R Richards; Irina N Richards; Gal Ozery; Robert W Derlet
Journal:  J Emerg Med       Date:  2010-09-15       Impact factor: 1.484

4.  Assessment of the contributions of CYP3A4 and CYP3A5 in the metabolism of the antipsychotic agent haloperidol to its potentially neurotoxic pyridinium metabolite and effect of antidepressants on the bioactivation pathway.

Authors:  Amit S Kalgutkar; Timothy J Taylor; Karthik Venkatakrishnan; Emre M Isin
Journal:  Drug Metab Dispos       Date:  2003-03       Impact factor: 3.922

5.  Role of human CYP3A4 in the biotransformation of sorafenib to its major oxidized metabolites.

Authors:  Sussan Ghassabian; Tristan Rawling; Fanfan Zhou; Munikumar R Doddareddy; Bruce N Tattam; David E Hibbs; Robert J Edwards; Pei H Cui; Michael Murray
Journal:  Biochem Pharmacol       Date:  2012-04-10       Impact factor: 5.858

Review 6.  N-glucuronidation of drugs and other xenobiotics by human and animal UDP-glucuronosyltransferases.

Authors:  Sanna Kaivosaari; Moshe Finel; Mikko Koskinen
Journal:  Xenobiotica       Date:  2011-03-24       Impact factor: 1.908

Review 7.  Cardiovascular side effects of new antidepressants and antipsychotics: new drugs, old concerns?

Authors:  Pal Pacher; Valeria Kecskemeti
Journal:  Curr Pharm Des       Date:  2004       Impact factor: 3.116

8.  Studies on the metabolism of haloperidol (HP): the role of CYP3A in the production of the neurotoxic pyridinium metabolite HPP+ found in rat brain following ip administration of HP.

Authors:  K Igarashi; F Kasuya; M Fukui; E Usuki; N Castagnoli
Journal:  Life Sci       Date:  1995-11-17       Impact factor: 5.037

9.  Glucuronidation of the broad-spectrum antiviral drug arbidol by UGT isoforms.

Authors:  Jin-Hui Song; Zhong-Ze Fang; Liang-Liang Zhu; Yun-Feng Cao; Cui-Min Hu; Guang-Bo Ge; De-Wei Zhao
Journal:  J Pharm Pharmacol       Date:  2012-12-24       Impact factor: 3.765

10.  Studies on the conversion of haloperidol and its tetrahydropyridine dehydration product to potentially neurotoxic pyridinium metabolites by human liver microsomes.

Authors:  E Usuki; R Pearce; A Parkinson; N Castagnol
Journal:  Chem Res Toxicol       Date:  1996-06       Impact factor: 3.739

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