Drug Metabolism and Pharmacokinetics

Papers
(The median citation count of Drug Metabolism and Pharmacokinetics is 0. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-02-01 to 2025-02-01.)
ArticleCitations
Refined CYP2E1∗ Template∗∗ system to decipher the ligand-interactions160
Feature importance of machine learning prediction models shows structurally active part and important physicochemical features in drug design80
Clinical evaluation of [18F]pitavastatin for quantitative analysis of hepatobiliary transporter activity43
Protection of mice against carbon tetrachloride-induced acute liver injury by endogenous and exogenous estrogens41
Sodium citrate buffer improves pazopanib solubility and absorption in gastric acid-suppressed rat model21
CNS penetration of methotrexate and its metabolite 7-hydroxymethotrexate in mice bearing orthotopic Group 3 medulloblastoma tumors and model-based simulations for children21
Drug transporters are implicated in the diffusion of tacrolimus into the T lymphocyte in kidney and liver transplant recipients: Genetic, mRNA, protein expression, and functionality21
Development of a new assay system for bladder cancer using interactions between cytochromes P450 and serum21
Feasibility of physiologically based pharmacokinetic simulations for assessing pediatric patients after accidental drug ingestion: A case study of a 1.4-year-old girl who ingested alprazolam18
Blood concentrations of tacrolimus upon conversion from rabeprazole to vonoprazan in renal transplant recipients: Correlation with cytochrome P450 gene polymorphisms13
Adenosine deaminases acting on RNA modulate the expression of the human pregnane X receptor12
Functional characterization of human organic anion transporter 10 (OAT10/SLC22A13) as an orotate transporter12
Physiologically based pharmacokinetic model analysis of the inhibitory effect of vonoprazan on the metabolic activation of proguanil11
Dose optimization with population pharmacokinetics of ritonavir-boosted lopinavir for Thai people living with HIV with and without active tuberculosis11
A novel method for predicting the unbound valproic acid concentration11
Ataluren metabolism: Ataluren-O-1β-acyl glucuronide is a stable circulating metabolite in mouse, rat, dog and human10
Dual kinetics of OATP2B1: Inhibitory potency and pH-dependence of OATP2B1 inhibitors10
Formation of reactive metabolites of benzbromarone in humanized-liver mice10
Current progress in identifying endogenous biomarker candidates for drug transporter phenotyping and their potential application to drug development9
In vitro metabolism of the new antifungal dapaconazole using liver microsomes9
Identification and characterization of novel metabolites of F2-isoprostanes8
Potential ADME-related issues for PROTACs8
Prediction and validation of fetal exposure to dual BCRP/P-GP drug substrates using the proteomics informed efflux ratio-relative expression factor (ER-REF) approach and PBPK modeling and simulation8
Assessing victim drug-drug interaction – Reaction phenotyping of CYP and non-CYP8
Drug induced organ toxicity: Transporter roles and derisking approaches8
Prediction and validation of human hepatobiliary clearances and hepatic concentrations of transported drugs using the relative expression factor (REF) and PET imaging approaches7
Unveiling the intracellular journey: GOLGA8N-mediated subcellular trafficking of siRNA drugs and its implications on silencing efficacy7
The spectrum of hepatic clearance models, from old to new7
Modern pediatric drug development: Practical case examples and regulatory outcomes from novel applications of modelling7
Synthesis and characterization of human metabolites of the echinocandid drug rezafungin by microbial biotransformation7
The mass balance recovery, absorption, metabolism, and excretion of [14C]-orvepitant in healthy male subjects after oral dosing: radiosynthesis of [14c]-orvepitant7
Successful optimization of pharmacokinetics and pharmacodynamics of oral cyclic peptide PCSK9 inhibitors7
Preclinical evaluation of the potential for cytochrome P450 inhibition and induction by tucatinib6
UGT-mediated clearance IVIVE may be improved using relative activity factor approach6
Metabolism of DHED in vitro and in vivo to support drug optimization6
Establishment of the relay method for low-turnover compounds in hepatocyte6
Monocarboxylate transporter 10: substrate-dependent mode of transport6
The effect of traditional herbal medicine on the permeability of clarithromycin and loxoprofen in CACO-2 cell model6
A practical approach for measuring acyl glucuronide migration half life6
Development of an in vitro metabolism approach of acrylamide covalent drugs for predicting metabolism and disposition in human6
Evaluation of a cost-effective in vitro human model for predicting intrinsic hepatocyte clearance of slowly metabolized compounds5
Utilizing various plasma protein binding tools for free fraction determination of lipophilic and lipopeptide drugs5
Stereoisomer separation of drugs and biomarkers using supercritical fluid chromatography to support PK/PD studies5
Effects of genetic polymorphisms of canine CYP2D15 on in vitro hepatic metabolism and in vivo pharmacokinetics of celecoxib, and the strategy for the accurate prediction of human pharmacokinetics5
Plasma protein binding of oligonucleotides using rapid agarose gel electrophoretic mobility shift assay5
Verification of a physiologically based pharmacokinetic model of caffeine that incorporates mechanistic descriptors of absorption5
Can LS180 cells predict metabolism and drug-drug interaction potential of UGT2B17 substrates?5
Redox metabolism in intestine and liver aggravates retronecine-type pyrrolizidine alkaloids-induced liver injury5
Enriching metabolite fractions for assessment of AHR activation potential: a proof of concept study5
Dynamic free fraction: concept, methodology and impact on hepatic clearance prediction using the well-stirred model5
Relative expression versus activity factor (ref vs. raf) to estimate fractional contribution of individual UGT isoforms (FGLUC) in drug glucuronidation5
Assessment of covalent binding body burden in Hmrel human hepatocyte co-culture model for metabollically low turnover compounds5
Synthetic mRNA for ex vivo therapeutic applications4
Validation of LC-MS/MS method for the quantification of buprenorphine and its metabolites in rat’s blood, oral fluid, salivary gland and application the assay on pharmacokinetic study4
Novel food drug interaction mechanism involving acyclovir, chitosan and endogenous mucus4
Applications of model simulation in pharmacological fields and the problems of theoretical reliability4
Advancements in Microphysiological systems: Exploring organoids and organ-on-a-chip technologies in drug development -focus on pharmacokinetics related organs-4
Basic tenets for the ADME of protein therapeutics4
The characterization of the pharmacokinetic profile of anti-tumor B (ATB) in oral cancer patients4
Latest developments in nitrosamine structure-activity relationships for carcinogenicity4
Clinical studies on pharmacogenomics and DDIS involving drug transporters4
Exploration of bioactivation of a branched-chain ketoacid dehydrogenase kinase (BDK) inhibitor4
Different substrate elimination rates of model drugs pH-dependently mediated by flavin-containing monooxygenases and cytochromes P450 in human liver microsomes4
Development of template systems for ligand interactions of CYP3A5 and CYP3A7 and their distinctions from CYP3A4 template4
Effect of linker-payload design on the PK of ADCS4
Corrigendum to “Utility of Göttingen minipigs for the prediction of human pharmacokinetic profiles after intravenous drug administration” [Drug Metabol Pharmacokinet 41 (2021) 100408]4
Characterization of plasma vonoprazan and CYP3A activity using its endogenous marker and genetic variants in patients with digestive system disorders4
Understanding the role of CYP3A in the metabolism of kinase inhibitors marketed in the past decade to better manage the risk of clinical drug-drug interactions4
Jasmone, an essential oil component, is an antagonist of aryl hydrocarbon receptor in liver and intestinal cells4
Beyond non-human primates: Transgenics and PBPK models for predicting the human PK of protein therapeutics4
The refined CYP2B6-Template system for studies of its ligand metabolisms4
Story of maturation - Modelers vs models in the paediatric space4
Enzyme induction fundamentals, assays, data interpretation and in vivo translation4
Evaluation of biliary excretion process of drugs and bile acids using permeation assay by a novel in vitro hepatocyte culture system (ICHEP)3
From stratified dose adjustment to personalised dosing: Linking LCMS proteomics in tissues to more clinically practical liquid biopsy samples – Opportunities and challenges3
Mathematical modeling of affinity design goals for CIS-binding BI-specific antibody-based molecules3
In vitro and in vivo interactions between nicotine and the cannabis terpene limonene3
Pharmacokinetic interaction of caffeine and theophylline in mice3
Pharmacokinetics of ginsenosides and effect of the lactic acid bacteria on pharmacokinetics of ginsenosides in mice and human3
An approach using a gamma-distributed delay model to evaluate the anticancer effect of doxorubicin-encapsulated polymeric micelles by predictive pharmacokinetic-pharmacodynamic modeling3
An overview of CDE technical guideline for nonclinical study of ADCS: importance and strategy of studying release of payload-containing components from ADC and their further metabolism3
This is no longer just about liver: LC-MS proteomics for organ exposure brain/kidney/gut/skin/placenta3
Hepatocyte formation, reactivity, and stability differences of acyl glucuronide and acyl coenzyme a conjugates3
One size does not fit all: Preclinical tools to characterize the pharmacokinetics and biodistribution of GaINAc-siRNA3
In vitro uptake of an MC3 lipid nanoparticle formulation by mice, non-human primate, and human hepatocytes and Kupffer cells3
Human liver chimeric mouse and trasngenic animals are useful tools for quantitatively predicting clearance and drug-drug interactions in human3
Physiologically based pharmacokinetic modeling of adeno-associated viruses and the transgene product3
Understanding CYP3A4 and P-GP mediated drug-drug interactions through PBPK modeling - case example of pralsetinib3
Cannabinoid-induced drug-drug interactions with hydromorphone.3
Opportunities and challenges in drug development for retinal diseases3
Evaluation of a novel, primary human hepatocyte tri-culture model, truvivotm, for its ability to predict metabolic clearance of CYP, UGT, and AO substrates3
The practical impact of the FDA draft guidance on human mass balance studies – a year of client discussions3
Exploring the human 3D small intestinal model (epiintestinaltm) for improved prediction of oral absorption, metabolism and complex drug-drug interactions of small molecule drugs3
In vitro demonstration of antedrug mechanism of a pharmacokinetic booster to improve CYP3A4 substrates by CYP3A4-mediated metabolism inhibition2
Title page2
Strategies for enhancing oral exposure of water-insoluble compounds2
Using quantitative systems pharmacology (QSP) models to characterize the PK of novel drug modalities2
Deciphering the cell and zonal distribution of drug metabolizing enzymes and transporters in humans by single cell transcriptomics2
Prediction of human clearance using human liver microsomes and hepatocytes with 455 drugs2
Gene and oligonucleotide delivery via micro- and nanobubbles by ultrasound exposure2
Application of machine learning techniques in population pharmacokinetics/pharmacodynamics modeling2
Cytochrome P450-dependent drug oxidation activities and their expression levels in liver microsomes of chimeric TK-NOG mice with humanized livers2
Plasma protein binding in special populations: do current PBPK models correctly account for potential changes to fraction unbound?2
Comparison of clearance and metabolic pathways in suspension hepatocytes and hepatopac cultures2
What is the role of CYP1A1 in drug metabolism?2
In vivo and in vitro biotransformation of molnupiravir (MOV), An oral prodrug of the antiviral ribonucleoside analog Β-D-N4-hydroxycytidine (NHC)2
Physiologically based pharmacokinetic modeling to predict the clinical effect of azole antifungal agents as CYP3A inhibitors on azelnidipine pharmacokinetics2
Quantitative prediction of CYP3A induction-mediated drug-drug interactions in clinical practice2
DMPK perspective on quantitative model analysis for chimeric antigen receptor cell therapy: Advances and challenges2
Novel approaches and troubleshooting for developing a high-throughput oligonucleotide LC-MS method beyond the current stage2
Novel multi-tissue chips for predictive pharmacokinetic studies2
Lysosomal trapping measurement in multiple cell types using a high content imaging (HCI) system2
Imaging Mass Spectrometry (IMS) for drug discovery and development survey: Results on methods, applications and regulatory compliance2
Gene and Oligonucleotide Delivery2
Optimization of methods for reducing turnaround time and compound consumptionwith echo liquid handling and automation enabling high capacity analysis for ADME screening2
Physiologically based pharmacokinetic modeling of CYP2C8 substrate rosiglitazone and its metabolite to predict metabolic drug-drug interaction1
Species differences between rats and primates (humans and monkeys) in complex cleavage pathways of DS-8500a characterized by 14C-ADME studies in humans and monkeys after administration of two radiolab1
Adenovirus vector-based vaccine for infectious diseases1
Substrate recognition of renally eliminated angiotensin II receptor blockers by organic anion transporter 41
Systematic identification and characterization of cynomolgus macaque solute carrier transporters1
Adeno-associated virus-mediated knockdown demonstrates the major role of hepatic Bcrp in the overall disposition of the active metabolite of the tyrosine kinase inhibitor regorafenib in mice1
Development of a fluorescent-labeled trapping reagent to evaluate the risk posed by acyl-CoA conjugates1
Constitutive androstane receptor-responsive elements for mouse Cyp1a2 transcriptional activation induced by constitutive androstane receptor ligands1
Quantitative prediction of transporter-mediated drug-drug interactions using the mechanistic static pharmacokinetic (MSPK) model1
Involvement of multiple cytochrome P450 isoenzymes in drug interactions between ritonavir and direct oral anticoagulants1
Functional characteristics of equilibrative nucleoside transporter 2 (ENT2/SLC29A2) for the transport of urate as a newly identified substrate1
Double Trap Interface: A novel gas interface for high throughput analysis of biomedical samples by AMS1
Analysis of inhibition kinetics of three beverage ingredients, bergamottin, dihydroxybergamottin and resveratrol, on CYP2C9 activity1
Carboxylesterase-2 plays a critical role in dabigatran etexilate active metabolite formation1
Effect of antibiotic-administration period on hepatic bile acid profile and expression of pharmacokinetic-related proteins in mouse liver, kidney, and brain capillaries1
A systematic study to evaluate the safety of ticagrelor combined with aspirin in the treatment of PCI patients in Chinese population: A single nucleotide polymorphisms study1
Quantitative and targeted proteomics-based identification and validation of drug efficacy biomarkers1
Pharmacogenomics research and its clinical implementation in Thailand: Lessons learned from the resource-limited settings1
Population pharmacokinetic analysis of sirolimus in Japanese pediatric and adult subjects receiving tablet or granule formulations1
Identification of miRNAs that regulate human CYP2B6 expression1
Functional role of serine 318 of the proton-coupled folate transporter in methotrexate transport1
Quantitation and characterization of glucosylsphingosine in cerebrospinal fluid (CSF), plasma, and brain of monkey model with Gaucher disease1
Genetic variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects identified by phenotyping for trimethylaminuria and found in a database of genome resources1
Investigating catechin-mediated effects on drug solubility as a mechanism underlying a green tea-raloxifene pharmcokinetic interaction0
Development of a novel in silico classification model to assess reactive metabolite formation in cysteine trapping assay and investigation of important substructures0
Development of a high throughput screen for cytochrome P450-ligand binding assays0
In vitro evaluation of PROTAC® degrader ARV-766 for cytochrome P450- and transporter-mediated drug-drug interaction0
Impact of donor diversity on phase I and phase II activities in cryopreserved human hepatocytes and human liver microsomes0
Preferential meropenem absorption activated by 1α,25-dihydroxyvitamin D3 and shared with foscarnet, a phosphate transporter substrate, in the rat ileum0
Determination of metabolic pathways of phosphatidylcholine and lysophosphatidylcholine using a stable isotope tracer in hepatocarcinoma cell lines0
Is CYP3A4 induction a good indicator for CYP2CS in cryopreserved human hepatocytes?0
Extrapolation of physiologically based pharmacokinetic model for tacrolimus from renal to liver transplant patients0
Metabolism of non-steroidal anti-inflammatory drugs (NSAIDs) by Streptomyces griseolus CYP105A1 and its variants0
In silico approach shows good predictability for free fraction in plasma and volume of distribution in human for drugs subjected to lysosomal trapping0
Clotrimazole is a potent and selective UGT2B4 chemical inhibitor0
Identification of biomarkers to diagnose diseases and find adverse drug reactions by metabolomics0
Phosphate buffer interferes dissolution of prazosin hydrochloride in compendial dissolution testing0
CYP46A1 inhibition and activation: an in vitro high throughput screening assay to assess possible drug interactions using FDA approved chemical library0
High hepatic and plasma exposures of atorvastatin in subjects harboring impaired cytochrome P450 3A4∗16 modeled after virtual administrations and possibly associated with statin intolerance found in t0
Validation of a genotyping technique for a surrogate marker of HLA-B58:01 for allopurinol-induced Stevens–Johnson syndrome and toxic epidermal necrolysis in the Japanese population0
Population pharmacokinetics of esaxerenone, a novel non-steroidal mineralocorticoid receptor blocker, in patients with essential hypertension, patients with diabetic nephropathy, and healthy volunteer0
Inhibiting uptake activity of organic anion transporter 2 by bile acids0
Method development to correct tissue concentrations for residual blood: Application to drug distribution in brain tumors0
Construction of a fused grid-based CYP2C19-Template system and the application0
Development of a HRMS-MS method for measuring plasma 4Β-hydroxycholesterol, an endogenous biomarker of CYP3A activity, in monkeys treated with CYP3A modulators0
The mass balance recovery, absorption, metabolism, and excretion of [14C]-orvepitant in healthy male subjects after oral dosing: clinical conduct & mass balance0
Investigation of the learning process of diverse compound structures by chemical language models toward toxicity prediction0
Predicting drug metabolism and pharmacokinetics features of in-house compounds by a hybrid machine-learning model0
Identification and characterisation of a novel amino acid conjugate; ergothioneine conjugate of raloxifene through in vitro and in vivo studies0
Acetaminophen-induced liver injury and the microbiome0
An in vitro microphysiological model of subcutaneous delivery0
Urinary metabolic markers reflect on hepatic, not intestinal, CYP3A activity in healthy subjects0
Update on next generation sequencing of pharmacokinetics-related genes: Development of the PKseq panel, a platform for amplicon sequencing of drug-metabolizing enzyme and drug transporter genes0
Effect of substrate concentration on reactive metabolite assessment in drug discovery research0
Preface: In silico technologies to facilitate drug development0
Increasing the therapeutic index of ADCs with payload binding selectivity enhancers0
Delivery of small interfering RNAs by nanovesicles for cancer therapy0
Effects of steric hindrance and electron density of ester prodrugs on controlling the metabolic activation by human carboxylesterase0
Designing novel RNA medicines for the brain0
Genetic variation present in the CYP3A4 gene in Ni-Vanuatu and Kenyan populations in malaria endemicity0
Global expansion of microphysiological systems (MPS) and Japan's initiatives: Innovation in pharmaceutical development and path to regulatory acceptance0
Practical use of mechanistic modeling to discern real word complex drug interactions0
Use of human liver microsomes to assess flavin-containing monooxygenase (FMO) metabolism in vitro0
The mass balance, recovery, absorption, metabolism, and excretion of [14C]-orvepitant in healthy male subjects after oral dosing: metabolite characterisation0
Identification and characterization of erlotinib as a potent mechanism-based inactivator of human aldehyde oxidase0
Investigating protein-mediated uptake drug-drug interactions using F-methotrexate as a substrate for OATP1B1 transporter0
Comparison of human biopsy-derived and human iPS cell-derived intestinal organoids established from a single individual0
Hepatocyte CEBPA restricts the progression of liver fibrosis0
An overview of selected topics in the clinical pharmacology and translation of in vivo CRISPR-based therapies0
Establishment of endogenous canine MUC1 knock-out MDCKII cells using CRISPR-Cas9 and evaluation of drug permeation0
Intestinal microbiota-mediated biotransformations alter the pharmacokinetics of the major metabolites of azathioprine in rats after oral administration0
The distribution of perfluorooctanesulfonate (PFOS) into the liver is not dependent on fatty acid binding protein (FABP)0
LC-MS for identifying changes (or lack of it) in ADME across different cohorts0
A model-based pharmacokinetic assessment of drug–drug interaction between tacrolimus and nirmatrelvir/ritonavir in a kidney transplant patient with COVID-190
Food effects on oral drug absorption: Recent advances in understanding mechanisms and quantitative prediction0
Metabolic pathways of aschantin in human liver preparations0
Air–liquid interface culture and modified culture medium promote the differentiation of human induced pluripotent stem cells into intestinal epithelial cells0
Rifampin- and silymarin-mediated pharmcokinetic interactions of pitavastatin, pravastatin, coproporphyrin I, and coproporphyrin III in a transgenic OATP1B mouse model0
Practical QSP application from the preclinical phase to enhance the probability of clinical success: Insights from case studies in oncology0
Quantitative estimation of fraction metabolized via CYP3A for low turnover compounds, using hepatocyte co-culture system0
Challenges associated with the biomarker-informed PBPK modeling of renal transporter-mediated drug interactions0
Plausible drug interaction between cyclophosphamide and voriconazole via inhibition of CYP2B60
Systematic investigation of the metabolism of cannabinoids by human cytochrome p450s0
Method development and optimization for detecting mRNAS of drug metabolizing enzymes and transporters in exosomes derived from human blood0
Experimental validation of the reliability of dilution method for plasma protein binding assay in human plasma using 12 commercial compounds0
Downregulated expression of organic anion transporting polypeptide (Oatp) 2b1 in the small intestine of rats with acute kidney injury0
Strategies for DDI risk assessment between novel oncology agents and combination generic standard of care (SOC) agents0
Risk of pharmacokinetic drug-drug interactions with novel drugs approved by the US FDA in 2022: a detailed review of DDI data from NDA documentation0
Novel approach to determine plasma protein binding for labile compounds using equilibrium dialysis0
Physiological effects of food ingredients on intestinal epithelial cell function0
Protein-bound uremic toxin clearance as biomarkers of kidney tubular function in diabetic kidney disease0
Improvement of transdermal absorption rate by nonthermal biocompatible atmospheric pressure plasma0
Toxicity of trimethoprim and sulfamethoxazole0
Evaluation of CYP450 activity in HLM bound to magnetizable beads0
Therapeutic application of sequence-specific binding molecules for novel genome editing tools0
Establishment of human intestinal organoids derived from commercially available cryopreserved intestinal epithelium and evaluation for pharmacokinetic study0
Metabolism and excretion of therapeutic peptides: current industry practices and recommendations0
Publisher's note0
Projections for future challenges and opportunities for pharmacokineticists0
Exosomes: Breast cancer-derived extracellular vesicles; recent key findings and technologies in disease progression, diagnostics, and cancer targeting0
Oligonucleotide delivery to antigen presenting cells by using schizophyllan0
Effects of valproate, an HDAC inhibitor, on the expression of folate carriers and folate metabolism-related genes in the placenta of rats0
Drug metabolism by the human gut microbiome0
Liver targeted therapy: What mist and DDI data mean for efficacy0
Effects of acid and lactone forms of statins on S-warfarin 7-hydroxylation catalyzed by human liver microsomes and recombinant CYP2C9 variants (CYP2C9.1 and CYP2C9.3)0
Phenolsulfonphthalein as a surrogate substrate to assess altered function of the prostaglandin transporter SLCO2A10
Interactions of sutezolid and its active metabolite with human transporters0
Clinical DDI trial design and impact on product labels0
Substrate inhibition potential of arachidonic acid on 14,15-epoxidation, a biological drug developmental target, mediated by recombinant human cytochrome P450 2J2 and 2C8 enzymes0
Rare but impaired flavin-containing monooxygenase 3 (FMO3) variants reported in a recently updated Japanese mega-databank of genome resources0
In vitro evaluation of metabolism- and transporter-based drug interactions with sunscreen active ingredients0
Inhibition of cytochrome P450 3A4 enzyme activity by alkaloid psilocin from magic mushrooms: potential for drug interactions0
Impacts of SNPs on adverse events and trough concentration of imatinib in patients with gastrointestinal stromal tumors0
Physiologically based pharmacokinetic (PBPK) model that describes enhanced FcRn-dependent distribution of monoclonal antibodies (mAbs) by pI-engineering in mice0
Translational PK/PD of the targeted radioligand therapy pluvicto0
Omics analyses and their application for the discovery of biomarkers reflecting drug efficacy and adverse reaction0
Roles of human cytochrome P450 3A4/5 in dexamethasone 6β-hydroxylation mediated by liver microsomes and humanized liver in chimeric mice metabolically suppressed with azamulin0
In vitro metabolic stability and in vivo phaarmacokinetic behavior of panobinostat in mouse models for the treatment of CNS tumors0
N-nitrosamine safety assessments - Current challenges0
Novel coc-based liver tissue chip for predictive pharmacokinetic and toxicology applications0
Epicatechin gallate and epigallocatechin gallate are potent inhibitors of human arylacetamide deacetylase0
Recent studies on metabolism, DNA adducts, and biomarkers of tobacco carcinogens0
Pharmacology and translational aspects0
A synthetic G protein-coupled receptor 40 agonist GW9508 mitigates airway inflammation and mucus secretion in allergic asthma0
Multivalent cation and polycation polymer preparations influence pharmacokinetics of dolutegravir via chelation-type drug interactions0
Comparative analysis of microcystin toxicity in 2D and 3D cultured primary human hepatocytes0
Issues in assessing tissue: Plasma partition coefficients (KP) in PBPK models0
Development of quantitative translational model of neutropenia using nonclinical animal data and physiological parameters0
A family study of compound variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects found by urinary phenotyping for trimethylaminuria0
Assessing complex drug-drug interactions using the truvivotm hepatocyte model0
The utility of CYP3A activity endogenous markers for evaluating drug-drug interaction between sildenafil and CYP3A inhibitors in healthy subjects0
Black ginger extract and its active compound, 5,7-dimethoxyflavone, increase intestinal drug absorption via efflux drug transporter inhibitions0
Assessment of the clinical pharmacokinetic interaction potential mediated So-Cheong-Ryong-Tang on a cocktail of anti-inflammatory and anti-biotic drugs, established by physiologically based pharmacoki0
Evaluation and prediction of oral drug absorption and bioequivalence with food-druginteraction0
Effect of obesity on pharmacokinetics of transdermal fentanyl: Single-center retrospective study and animal study0
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