Search Results - "Tucker, Geoffrey T"
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Simulation and prediction of in vivo drug metabolism in human populations from in vitro data
Published in Nature reviews. Drug discovery (01-02-2007)“…The perceived failure of new drug development has been blamed on deficiencies in in vivo studies of drug efficacy and safety. Prior simulation of the potential…”
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A Re-evaluation and Validation of Ontogeny Functions for Cytochrome P450 1A2 and 3A4 Based on In Vivo Data
Published in Clinical pharmacokinetics (01-07-2014)“…Background and Objectives Current cytochrome P450 (CYP) 1A2 and 3A4 ontogeny profiles, which are derived mainly from in vitro studies and incorporated in…”
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Prediction of the clearance of eleven drugs and associated variability in neonates, infants and children
Published in Clinical pharmacokinetics (01-01-2006)“…Prediction of the exposure of neonates, infants and children to xenobiotics is likely to be more successful using physiologically based pharmacokinetic models…”
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Does age affect gastric emptying time? A model-based meta-analysis of data from premature neonates through to adults
Published in Biopharmaceutics & drug disposition (01-05-2015)“…Purpose. Gastric emptying (GE) is often reported to be slower and more irregular in premature neonates than in older children and adults. The aim of this study…”
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A Semi-Mechanistic Model to Predict the Effects of Liver Cirrhosis on Drug Clearance
Published in Clinical pharmacokinetics (01-03-2010)“…Background and Objective: Liver cirrhosis is characterized by a decrease in functional hepatocytes, lowered circulating levels of plasma proteins and…”
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In Vitro Characterization of the Human Liver Microsomal Kinetics and Reaction Phenotyping of Olanzapine Metabolism
Published in Drug metabolism and disposition (01-11-2015)“…Olanzapine (OLZ) is an atypical antipsychotic used in the treatment of schizophrenia and related psychoses. The metabolism of OLZ is complex and incompletely…”
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Assessment of algorithms for predicting drug–drug interactions via inhibition mechanisms: comparison of dynamic and static models
Published in British journal of clinical pharmacology (01-01-2011)“…WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT • The prediction of drug–drug interactions (DDIs) from in vitro data usually utilizes an average dosing interval…”
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Personalized Drug Dosage – Closing the Loop
Published in Pharmaceutical research (01-08-2017)“…A brief account is given of various approaches to the individualization of drug dosage, including the use of pharmacodynamic markers, therapeutic monitoring of…”
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Erratum to: A Re-evaluation and Validation of Ontogeny Functions for Cytochrome P450 1A2 and 3A4 Based on In Vivo Data
Published in Clinical pharmacokinetics (01-06-2015)Get full text
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Differences in Cytochrome P450-Mediated Pharmacokinetics Between Chinese and Caucasian Populations Predicted by Mechanistic Physiologically Based Pharmacokinetic Modelling
Published in Clinical pharmacokinetics (01-12-2013)“…Background International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) guidelines emphasize the…”
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Was 4β‐hydroxycholesterol ever going to be a useful marker of CYP3A4 activity?
Published in British journal of clinical pharmacology (01-07-2018)Get full text
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Letter to the editor about reporting drug concentrations and pharmacokinetics in regional anesthesia and pain medicine
Published in Regional anesthesia and pain medicine (05-02-2024)“…Whereas arterial blood drug concentrations, other than those in pulmonary vessels, will be essentially the same throughout the body, those in veins differ,…”
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When Regional Anesthesia Met Pharmacokinetics
Published in Anesthesiology (Philadelphia) (01-04-2022)“…Pharmacokinetics of Local Anaesthetic Agents. By Tucker GT, Mather LE. Br J Anaesth 1975; 47(suppl 1):213–24 Information derived from measurements of blood…”
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Implications of mechanism-based inhibition of CYP2D6 for the pharmacokinetics and toxicity of MDMA
Published in Journal of psychopharmacology (Oxford) (01-11-2006)“…The aim of this study was to model the in vivo kinetic consequences of mechanism-based inhibition (MBI) of CYP2D6 by 3,4 methylenedioxymethamphetamine (MDMA,…”
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Metformin disposition—A 40‐year‐old mystery
Published in British journal of clinical pharmacology (01-08-2020)Get full text
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Inhibition of human UDP-glucuronosyltransferase enzymes by lapatinib, pazopanib, regorafenib and sorafenib: Implications for hyperbilirubinemia
Published in Biochemical pharmacology (01-04-2017)“…[Display omitted] Kinase inhibitors (KIs) are a rapidly expanding class of drugs used primarily for the treatment of cancer. Data relating to the inhibition of…”
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Comment on: “The pharmacokinetics of metformin in patients receiving intermittent haemodialysis” by Sinnappah et al
Published in British journal of clinical pharmacology (01-08-2021)Get full text
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The British Journal of Clinical Pharmacology: The first 50 years
Published in British journal of clinical pharmacology (01-01-2024)“…The British Journal of Clinical Pharmacology celebrates its 50th anniversary of publication in 2023. Here four previous Editors‐in‐Chief and the current Editor…”
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Prediction of olanzapine exposure in individual patients using physiologically based pharmacokinetic modelling and simulation
Published in British journal of clinical pharmacology (01-03-2018)“…Aim The aim of the present study was to predict olanzapine (OLZ) exposure in individual patients using physiologically based pharmacokinetic modelling and…”
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A series acceleration algorithm for the gamma-Pareto (type I) convolution and related functions of interest for pharmacokinetics
Published in Journal of pharmacokinetics and pharmacodynamics (01-04-2022)“…The gamma-Pareto type I convolution (GPC type I) distribution, which has a power function tail, was recently shown to describe the disposition kinetics of…”
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