Search Results - "YURONG LAI"
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Organic Anion Transporter 2: An Enigmatic Human Solute Carrier
Published in Drug metabolism and disposition (01-02-2017)“…As a member of the solute carrier 22A (SLC22A) family, organic anion transporter 2 (OAT2; SLC22A7) is emerging as an important drug transporter because of its…”
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Identification of interspecies difference in hepatobiliary transporters to improve extrapolation of human biliary secretion
Published in Expert opinion on drug metabolism & toxicology (01-10-2009)“…Increasing challenges include the application of in vitro/in vivo models for prediction of safety and pharmacokinetic profiles for the compounds entering drug…”
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Clinical Probes and Endogenous Biomarkers as Substrates for Transporter Drug‐Drug Interaction Evaluation: Perspectives From the International Transporter Consortium
Published in Clinical pharmacology and therapeutics (01-11-2018)“…Drug transporters can govern the absorption, distribution, metabolism, and excretion of substrate drugs and endogenous substances. Investigations to examine…”
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Classification of Inhibitors of Hepatic Organic Anion Transporting Polypeptides (OATPs): Influence of Protein Expression on Drug–Drug Interactions
Published in Journal of medicinal chemistry (24-05-2012)“…The hepatic organic anion transporting polypeptides (OATPs) influence the pharmacokinetics of several drug classes and are involved in many clinical drug–drug…”
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Protein Abundance of Clinically Relevant Multidrug Transporters along the Entire Length of the Human Intestine
Published in Molecular pharmaceutics (06-10-2014)“…Intestinal transporters are crucial determinants in the oral absorption of many drugs. We therefore studied the mRNA expression (N = 33) and absolute protein…”
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Drug Concentration Asymmetry in Tissues and Plasma for Small Molecule-Related Therapeutic Modalities
Published in Drug metabolism and disposition (01-10-2019)“…The well accepted "free drug hypothesis" for small-molecule drugs assumes that only the free (unbound) drug concentration at the therapeutic target can elicit…”
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Editorial: Clinical trials in drug metabolism and transport: 2022
Published in Frontiers in pharmacology (13-06-2023)Get full text
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Toward a Consensus on Applying Quantitative Liquid Chromatography‐Tandem Mass Spectrometry Proteomics in Translational Pharmacology Research: A White Paper
Published in Clinical pharmacology and therapeutics (01-09-2019)“…Quantitative translation of information on drug absorption, disposition, receptor engagement, and drug–drug interactions from bench to bedside requires models…”
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Hepatic uptake of atorvastatin: influence of variability in transporter expression on uptake clearance and drug-drug interactions
Published in Drug metabolism and disposition (01-07-2014)“…Differences in the expression and function of the organic anion transporting polypeptide (OATP) transporters contribute to interindividual variability in…”
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Interindividual and Regional Variability in Drug Transporter Abundance at the Human Blood–Brain Barrier Measured by Quantitative Targeted Proteomics
Published in Clinical pharmacology and therapeutics (01-07-2019)“…For in vitro to in vivo extrapolation (IVIVE) of brain distribution of drugs that are transported at the human blood–brain barrier (BBB), it is important to…”
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Interindividual variability in the hepatic expression of the human breast cancer resistance protein (BCRP/ABCG2): effect of age, sex, and genotype
Published in Journal of pharmaceutical sciences (01-03-2013)“…Breast cancer resistance protein (BCRP), an efflux transporter expressed at the bile canalicular membrane, is responsible for the biliary clearance of many…”
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Induction of Human Intestinal and Hepatic Organic Anion Transporting Polypeptides: Where Is the Evidence for Its Relevance in Drug-Drug Interactions?
Published in Drug metabolism and disposition (01-03-2020)“…Organic anion transporting polypeptides (OATPs), expressed in human liver (OATP1B1, OATP1B3, and OATP2B1) and intestine (OATP2B1), govern the pharmacokinetics…”
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Transporter Gene Regulation in Sandwich Cultured Human Hepatocytes Through the Activation of Constitutive Androstane Receptor (CAR) or Aryl Hydrocarbon Receptor (AhR)
Published in Frontiers in pharmacology (21-01-2021)“…The induction potentials of ligand-activated nuclear receptors on metabolizing enzyme genes are routinely tested for new chemical entities. However,…”
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Mechanistic pharmacokinetic modeling for the prediction of transporter-mediated disposition in humans from sandwich culture human hepatocyte data
Published in Drug metabolism and disposition (01-05-2012)“…With efforts to reduce cytochrome P450-mediated clearance (CL) during the early stages of drug discovery, transporter-mediated CL mechanisms are becoming more…”
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Abundance of Phase 1 and 2 Drug-Metabolizing Enzymes in Alcoholic and Hepatitis C Cirrhotic Livers: A Quantitative Targeted Proteomics Study
Published in Drug metabolism and disposition (01-07-2018)“…To predict the impact of liver cirrhosis on hepatic drug clearance using physiologically based pharmacokinetic (PBPK) modeling, we compared the protein…”
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Intestinal P‐gp and Putative Hepatic OATP1B Induction: International Transporter Consortium Perspective on Drug Development Implications
Published in Clinical pharmacology and therapeutics (01-01-2021)“…There is an increasing interest in transporter induction (i.e., decreased systemic drug exposure due to increased efflux‐limited absorption or…”
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Drug-induced perturbations of the bile acid pool, cholestasis, and hepatotoxicity: mechanistic considerations beyond the direct inhibition of the bile salt export pump
Published in Drug metabolism and disposition (01-04-2014)“…The bile salt export pump (BSEP) is located on the canalicular plasma membrane of hepatocytes and plays an important role in the biliary clearance of bile…”
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Positron Emission Tomography Imaging of [11C]Rosuvastatin Hepatic Concentrations and Hepatobiliary Transport in Humans in the Absence and Presence of Cyclosporin A
Published in Clinical pharmacology and therapeutics (01-11-2019)“…Using positron emission tomography imaging, we determined the hepatic concentrations and hepatobiliary transport of [11C]rosuvastatin (RSV; i.v. injection) in…”
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