Keywords: سینتیک متابولیت; pharmacokinetic/pharmacodynamic models; pharmacokinetics/pharmacodynamics; pharmacokinetics; metabolism; metabolite kinetics; clinical pharmacokinetics; population pharmacokinetics;
مقالات ISI سینتیک متابولیت (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: سینتیک متابولیت; HPLC; mathematical model; metabolite kinetics; pharmacokinetics; prodrugs; A; pre-exponential factor; ÎEa; standard error of the activation energy; Ea; activation energy; k; reaction rate constant; k1; rate constant for the reaction TREO â S,S-EBDM;
Keywords: سینتیک متابولیت; valproic acid; carnitine; renal clearance; β-oxidation; pharmacokinetics; metabolism; metabolite kinetics; renal excretion; drug interaction; glucuronide;
Keywords: سینتیک متابولیت; bioanalysis; disposition; elimination; HPLC; metabolite kinetics; pharmacokinetics; prodrugs; AUC0ââ; area under the plasma drug concentration-time profile from zero to infinity; Cltot; total clearance; Cmax; maximal concentration of a drug in plasm
Keywords: سینتیک متابولیت; Toremifene; Tamoxifen; Metabolite kinetics; Bioactivation; CYP2D6; CYP3A4; CYP2C9; Pharmacogenomics; PolymorphismsTOR, toremifene; TAM, tamoxifen; SERM, selective estrogen receptor modulator; SSRI, selective serotonin reuptake inhibitor; 4OH, 4-hydroxy; N
Keywords: سینتیک متابولیت; Pharmacokinetics; Absorption; Distribution; Clearance; Metabolite kinetics; Pharmacodynamics
Intravenous Administration of Stable-Labeled N-Acetylcysteine Demonstrates an Indirect Mechanism for Boosting Glutathione and Improving Redox Status
Keywords: سینتیک متابولیت; N-acetylcysteine (NAC); glutathione (GSH); redox ratio; stable-label; prodrugs; metabolism; metabolite kinetics; preclinical pharmacokinetics; pharmacodynamics;
Activation of Prodrug Treosulfan at pH 7.4 and 37°C Accompanied by Hydrolysis of Its Active Epoxides: Kinetic Studies with Clinical Relevance
Keywords: سینتیک متابولیت; HPLC; mathematical model; metabolite kinetics; pharmacokinetics; prodrugs; refractive index;
CYP-dependent Metabolism of Antitumor Pyrazolo[3,4-d]pyrimidine Derivatives Is Characterized by an Oxidative Dechlorination Reaction
Keywords: سینتیک متابولیت; anticancer agents; cytochrome P450; CYP3A4; liver microsomes; metabolite kinetics; metabolite identification
Simultaneous measurement of heroin and its metabolites in brain extracellular fluid by microdialysis and ultra performance liquid chromatography tandem mass spectrometry
Keywords: سینتیک متابولیت; Heroin; Metabolite kinetics; Microdialysis; Opiates; Pharmacokinetics; Retrodialysis
Effects of Normothermic Hepatic Ischemia-Reperfusion Injury on the In Vivo, Isolated Perfused Liver, and Microsomal Disposition of Chlorzoxazone, a Cytochrome P450 2E1 Probe, in Rats
Keywords: سینتیک متابولیت; hepatic ischemia-reperfusion injury; pharmacokinetics; isolated perfused rat liver; hepatobiliary disposition; microsomes; cytochrome P450 2E1; cytochrome P450 reductase; chlorzoxazone; hepatic metabolism; metabolite kinetics;
Population pharmacokinetic analysis of ropivacaine and its metabolite 2â²,6â²-pipecoloxylidide from pooled data in neonates, infants, and children
Keywords: سینتیک متابولیت; local anaesthetics; ropivacaine; metabolite kinetics; paediatric anaesthesia; population pharmacokinetics; regional anaesthetic techniques;
Physiologically based mechanistic modelling to predict complex drug–drug interactions involving simultaneous competitive and time-dependent enzyme inhibition by parent compound and its metabolite in both liver and gut—The effect of diltiazem on the time-c
Keywords: سینتیک متابولیت; Multiple drug–drug interactions; Metabolite kinetics; Mechanism-based inhibition; Simulation; Diltiazem
Oral Sulfasalazine as a Clinical BCRP Probe Substrate: Pharmacokinetic Effects of Genetic Variation (C421A) and Pantoprazole Coadministration
Keywords: سینتیک متابولیت; ABC transporters; clinical pharmacokinetics; drug interactions; metabolite kinetics; pharmacogenetics;
Species Differences in Inhibition Potential of Nonsteroidal Anti-Inflammatory Drugs Against Estradiol 3β-Glucuronidation Between Rats, Dogs, and Humans
Keywords: سینتیک متابولیت; inhibition; glucuronosyltransferases (UGT); metabolite kinetics; microsomes; drug interactions;