2018
DOI: 10.1016/j.tiv.2018.03.016
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Role of the equine CYP3A94, CYP3A95 and CYP3A97 in ketamine metabolism in presence of medetomidine, diazepam and methadone studied by enantioselective capillary electrophoresis

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Cited by 7 publications
(10 citation statements)
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“…No reaction was observed in the presence of canine or human liver microsomes as well as purified uridine‐5'‐diphospho‐glucuronosyl‐transferase. A chiral CE method was used for the investigation of the kinetics of the in vitro demethylation of ketamine to norketaime by the equine cytochrome P450 (CYP) isoenzymes CYP3A94, CYP3A95, and CYP3A97 as well as equine liver microsomes [142]. The effect of the benzodiazepine diazepam, the α 2 ‐receptor agonist medetomidine, and the opiate methadone on the ketamine metabolism was also studied.…”
Section: Ce In Stereoisomer Analysis Of Pharmaceuticalsmentioning
confidence: 99%
“…No reaction was observed in the presence of canine or human liver microsomes as well as purified uridine‐5'‐diphospho‐glucuronosyl‐transferase. A chiral CE method was used for the investigation of the kinetics of the in vitro demethylation of ketamine to norketaime by the equine cytochrome P450 (CYP) isoenzymes CYP3A94, CYP3A95, and CYP3A97 as well as equine liver microsomes [142]. The effect of the benzodiazepine diazepam, the α 2 ‐receptor agonist medetomidine, and the opiate methadone on the ketamine metabolism was also studied.…”
Section: Ce In Stereoisomer Analysis Of Pharmaceuticalsmentioning
confidence: 99%
“…Drug metabolism studies in presence of fungi were undertaken with albendazole [66], risperidone [67], propranolol [68], midodrine [69], zopiclone [70], hydroxyzine [71], and oxcarbazepine [72]. The fate of ketamine [46,60,76,79–81,83,84] and tetrabenazine [82] were also studied in presence of inhibitors or drugs that are typically coadministrated in clinical practice.…”
Section: Applicationsmentioning
confidence: 99%
“…The use of a recombinant single CYP enzyme instead of organ microsomes provides information about the possible involvement of a specific enzyme in a metabolic step together with its stereospecificity when an appropriate chiral assay is used. Using chiral CE, this was successfully shown for CYP enzymes involved in the metabolism of fluoxetine [74], verapamil [75], ketamine [76][77][78][79][80][81]83], and norketamine [78,81]. Liver microsomes were incubated with ketamine [46,47,60,73,78,80,83,84], norketamine [47,78], tetrabenazine [82], and fenbendazole [62].…”
Section: Assessment Of Drug Metabolism and Inhibition In Vitromentioning
confidence: 99%
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“…Therefore, the development of an efficient and reliable method for the analysis of the drugs in different samples like pharmaceutical preparations, clinical or criminal examinations and biological fluids is crucial for the analysts. 6 Up to now, diverse approaches such as capillary electrophoresis, 7,8 gas chromatography (GC), 9,10 and high performance liquid chromatography [11][12][13][14][15] have been developed for the determination of these types of drugs. Among these methods, chromatographic techniques are preferred due to the possibility of simultaneous determination of several anti-seizures in different samples.…”
Section: Introductionmentioning
confidence: 99%