Search Results - "Yoda, Noriaki"
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Prediction of drug intestinal absorption in human using the Ussing chamber system: A comparison of intestinal tissues from animals and humans
Published in European journal of pharmaceutical sciences (01-01-2017)“…An adequate evaluation system for drug intestinal absorption is essential in the pharmaceutical industry. Previously, we established a novel prediction system…”
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Changes of drug pharmacokinetics mediated by downregulation of kidney organic cation transporters Mate1 and Oct2 in a rat model of hyperuricemia
Published in PloS one (05-04-2019)“…The effects of hyperuricemia on the expression of kidney drug transporters and on the pharmacokinetics of several substrate drugs were examined. We first…”
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Constitutive androstane receptor transcriptionally activates human CYP1A1 and CYP1A2 genes through a common regulatory element in the 5′-flanking region
Published in Biochemical pharmacology (15-01-2010)“…Phenobarbital has long been known to increase cellular levels of CYP1A1 and CYP1A2 possibly through a pathway(s) independent of aryl hydrocarbon receptor. We…”
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Delamanid Does Not Inhibit or Induce Cytochrome P450 Enzymes in Vitro
Published in Biological & pharmaceutical bulletin (01-11-2014)“…Delamanid is a new drug for the treatment of multidrug-resistant tuberculosis. Individuals who are co-infected with human immunodeficiency virus and…”
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5
Metabolic Mechanism of Delamanid, a New Anti-Tuberculosis Drug, in Human Plasma
Published in Drug metabolism and disposition (01-08-2015)“…The metabolism of delamanid (OPC-67683, Deltyba), a novel treatment of multidrug-resistant tuberculosis, was investigated in vitro using plasma and purified…”
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Inhibitory Potential of Twenty Five Anti-tuberculosis Drugs on CYP Activities in Human Liver Microsomes
Published in Biological & pharmaceutical bulletin (01-09-2015)“…The direct inhibitory potential of twenty five anti-tuberculosis drugs on eight CYP-specific reactions in human liver microsomes was investigated to predict in…”
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Comparison of p450 enzymes between cynomolgus monkeys and humans: p450 identities, protein contents, kinetic parameters, and potential for inhibitory profiles
Published in Current drug metabolism (01-02-2013)“…Cynomolgus monkeys are used to predict human pharmacokinetic and/or toxic profiles in the drug developmental stage. Cynomolgus P450s exhibit a high degree of…”
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8
Delamanid Does Not Inhibit or Induce Cytochrome P450 Enzymes in Vitro
Published in Biological and Pharmaceutical Bulletin (01-11-2014)“…Delamanid is a new drug for the treatment of multidrug-resistant tuberculosis. Individuals who are co-infected with human immunodeficiency virus and…”
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9
Evaluation of intestinal metabolism and absorption using the Ussing chamber system equipped with intestinal tissue from rats and dogs
Published in European journal of pharmaceutics and biopharmaceutics (01-01-2018)“…[Display omitted] The purpose of this study was to evaluate the intestinal metabolism and absorption in a mini-Ussing chamber equipped with animal intestinal…”
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Absorption, distribution and excretion of the anti‐tuberculosis drug delamanid in rats: Extensive tissue distribution suggests potential therapeutic value for extrapulmonary tuberculosis
Published in Biopharmaceutics & drug disposition (01-05-2017)“…Delamanid (OPC‐67683, Deltyba™, nitro‐dihydro‐imidazooxazoles derivative) is approved for the treatment of adult pulmonary multidrug‐resistant tuberculosis…”
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11
Characterization of intestinal and hepatic P450 enzymes in cynomolgus monkeys with typical substrates and inhibitors for human P450 enzymes
Published in Xenobiotica (01-08-2012)“…Cynomolgus monkeys are widely used to predict human pharmacokinetic and/or toxic profiles in the drug developmental stage. Characterization of cynomolgus…”
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