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 2021-06-01 to 2025-06-01.)
ArticleCitations
Corrigendum to “Utility of Göttingen minipigs for the prediction of human pharmacokinetic profiles after intravenous drug administration” [Drug Metabol Pharmacokinet 41 (2021) 100408]189
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 pharmacokinetics109
The spectrum of hepatic clearance models, from old to new63
Monocarboxylate transporter 10: substrate-dependent mode of transport25
Development of an in vitro metabolism approach of acrylamide covalent drugs for predicting metabolism and disposition in human24
The mass balance recovery, absorption, metabolism, and excretion of [14C]-orvepitant in healthy male subjects after oral dosing: radiosynthesis of [14c]-orvepitant22
Beyond non-human primates: Transgenics and PBPK models for predicting the human PK of protein therapeutics17
Formation of reactive metabolites of benzbromarone in humanized-liver mice15
Clinical studies on pharmacogenomics and DDIS involving drug transporters15
Applications of model simulation in pharmacological fields and the problems of theoretical reliability15
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 simulation14
Development of a new assay system for bladder cancer using interactions between cytochromes P450 and serum14
Dual kinetics of OATP2B1: Inhibitory potency and pH-dependence of OATP2B1 inhibitors13
In vitro demonstration of antedrug mechanism of a pharmacokinetic booster to improve CYP3A4 substrates by CYP3A4-mediated metabolism inhibition12
Lysosomal trapping measurement in multiple cell types using a high content imaging (HCI) system12
Double Trap Interface: A novel gas interface for high throughput analysis of biomedical samples by AMS12
Human liver chimeric mouse and trasngenic animals are useful tools for quantitatively predicting clearance and drug-drug interactions in human11
Pharmacokinetics of ginsenosides and effect of the lactic acid bacteria on pharmacokinetics of ginsenosides in mice and human11
Strategies for enhancing oral exposure of water-insoluble compounds10
Gene and Oligonucleotide Delivery9
Mathematical modeling of affinity design goals for CIS-binding BI-specific antibody-based molecules9
Physiologically based pharmacokinetic modeling to predict the clinical effect of azole antifungal agents as CYP3A inhibitors on azelnidipine pharmacokinetics9
Enzyme induction fundamentals, assays, data interpretation and in vivo translation9
Appreciation to Reviewers9
Effect of linker-payload design on the PK of ADCS9
This is no longer just about liver: LC-MS proteomics for organ exposure brain/kidney/gut/skin/placenta8
Effect of antibiotic-administration period on hepatic bile acid profile and expression of pharmacokinetic-related proteins in mouse liver, kidney, and brain capillaries8
Pharmacokinetic interaction of caffeine and theophylline in mice8
In vitro and in vivo interactions between nicotine and the cannabis terpene limonene8
Carboxylesterase-2 plays a critical role in dabigatran etexilate active metabolite formation8
Cloning, sequence analysis, and tissue expression of marmoset paraoxonase 17
IN VITRO AND IN VIVO SYSTEMS FOR PREDICTING THE ADME OF PROTEIN THERAPEUTICS: ARE WE THERE YET?”7
Clinical studies on pharmacogenomics and DDIS involving drug transporters7
Disposition of E-selectin-targeting liposomes in tumor spheroids with a perfusable vascular network7
Strategies for de-risking n-nitrosamine impurities in APIS7
Suppression and induction of UGT by rhein and alvocidib in intestinal epithelial cells7
Use of mathematical modeling to guide out-of-the-box thinking for ADC development7
Lecture title not available7
Simple confirmation methods for rare but impaired variants of human flavin-containing monooxygenase 3 (FMO3) found in an updated genome resource databank6
Exposure to mixed microplastic particles altered the fecal microbiome and its associated predictive functional pathways in mice6
Micro-physiological system of human lung: The current status and application to drug discovery6
Effect of pregnancy-related hormones on mRNA expression of hepatic drug transporters and enzymes6
Development of physiologically-based pharmacokinetic models to predict food effects and co-administration of proton pump inhibitors on the pharmacokinetics of sonidegib and vismodegib6
Spatial mapping of gemcitabine and its pharmacologically active metabolites in tissues using MALDI mass spectrometry imaging6
A workflow for oligonucleotide metabolite identification studies6
Corrigendum to “Establishment of human intestinal organoids derived from commercially available cryopreserved intestinal epithelium and evaluation for pharmacokinetic study” [Drug Metabol Pharmacokine6
Prediction of pharmacokinetics and pharmacodynamics in human for IRAK4 targeted protein degrader6
Epicatechin gallate and epigallocatechin gallate are potent inhibitors of human arylacetamide deacetylase5
Effects of valproate, an HDAC inhibitor, on the expression of folate carriers and folate metabolism-related genes in the placenta of rats5
Opportunities for microphysiological systems from the view of Japanese industries5
Impact of donor diversity on phase I and phase II activities in cryopreserved human hepatocytes and human liver microsomes5
Mechanisms of afatinib-induced intestinal epithelial barrier dysfunction using human mini-gut model5
In vitro metabolic stability and in vivo phaarmacokinetic behavior of panobinostat in mouse models for the treatment of CNS tumors5
Use of human liver microsomes to assess flavin-containing monooxygenase (FMO) metabolism in vitro5
Therapeutic application of sequence-specific binding molecules for novel genome editing tools5
Plausible drug interaction between cyclophosphamide and voriconazole via inhibition of CYP2B65
Intestinal microbiota-mediated biotransformations alter the pharmacokinetics of the major metabolites of azathioprine in rats after oral administration5
The effect of clofazimine in modulating intracellular concentrations of remdesivir and GS-441524: A potential mechanism of enhancing antiviral effects against SARS-COV-25
Interactions of sutezolid and its active metabolite with human transporters5
Prediction of drug-drug interaction risk of P-glycoprotein substrate in drug discovery5
Oligonucleotide delivery to antigen presenting cells by using schizophyllan5
Metabolism of non-steroidal anti-inflammatory drugs (NSAIDs) by Streptomyces griseolus CYP105A1 and its variants5
Experimental validation of the reliability of dilution method for plasma protein binding assay in human plasma using 12 commercial compounds5
OCT1 transporter kinetics and long-term modulation studies in 3D cultured primary human hepatocytes5
Development of fluorescent-labeled trapping reagents based on cysteine to detect soft and hard electrophilic reactive metabolites5
Insights into drug development with quantitative systems pharmacology: A prospective case study of uncovering hyperkalemia risk in diabetic nephropathy with virtual clinical trials5
Comparative analysis of microcystin toxicity in 2D and 3D cultured primary human hepatocytes5
Increasing the therapeutic index of ADCs with payload binding selectivity enhancers4
Comparison on metabolic fate of dendrobium polysaccharides in gut microbiota fermentation process between healty and diabetic status4
Promiscuity and quantitative contribution of UGT2B17 in drug and steroid metabolism determined by experimental and computational approaches4
Assessing complex drug-drug interactions using the truvivotm hepatocyte model4
A practical approach for measuring acyl glucuronide migration half life4
Acetaminophen-induced liver injury and the microbiome4
ADME: 14C-RLY-4008 following oral administration to rats4
Stereoisomer separation of drugs and biomarkers using supercritical fluid chromatography to support PK/PD studies4
Jasmone, an essential oil component, is an antagonist of aryl hydrocarbon receptor in liver and intestinal cells4
Verification of a physiologically based pharmacokinetic model of caffeine that incorporates mechanistic descriptors of absorption4
Beyond the basics: A deep dive into parameter estimation for advanced PBPK and QSP models4
Evaluation of OSTΑ/Β transporter activity on the basal membrane of CACO-2 cell monolayers4
Substrate-dependent characteristics in the transport function of SLC19A3: examination of the aspect of its sensitivity to flavonoids4
Utility of Göttingen minipigs for the prediction of human pharmacokinetic profiles after intravenous drug administration4
Unveiling the intracellular journey: GOLGA8N-mediated subcellular trafficking of siRNA drugs and its implications on silencing efficacy4
Evaluating the impact of glycocalyx on partitioning and distribution of basic drugs4
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 radiolab3
Evaluation of a novel, primary human hepatocyte tri-culture model, truvivotm, for its ability to predict metabolic clearance of CYP, UGT, and AO substrates3
Exploration of bioactivation of a branched-chain ketoacid dehydrogenase kinase (BDK) inhibitor3
Clinical evaluation of [18F]pitavastatin for quantitative analysis of hepatobiliary transporter activity3
Understanding CYP3A4 and P-GP mediated drug-drug interactions through PBPK modeling - case example of pralsetinib3
Drug transporters are implicated in the diffusion of tacrolimus into the T lymphocyte in kidney and liver transplant recipients: Genetic, mRNA, protein expression, and functionality3
Development of template systems for ligand interactions of CYP3A5 and CYP3A7 and their distinctions from CYP3A4 template3
The effect of traditional herbal medicine on the permeability of clarithromycin and loxoprofen in CACO-2 cell model3
【Continuous exposure to therapeutic drugs doxorubicin and vincristine reduces drug efficacy through transcriptional and post-transcriptional regulation of P-glycoprotein in follicular lymphoma】3
Genetic variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects identified by phenotyping for trimethylaminuria and found in a database of genome resources3
The practical impact of the FDA draft guidance on human mass balance studies – a year of client discussions3
Preclinical evaluation of the potential for cytochrome P450 inhibition and induction by tucatinib3
Synthetic mRNA for ex vivo therapeutic applications3
What is the role of CYP1A1 in drug metabolism?3
Functional assessment of immortalized human brain microvascular endothelial cells with different passage numbers: A case study for a prospective proposal on variability management of in vitro blood-br3
Adenovirus vector-based vaccine for infectious diseases2
ADME considerations from FIH to drug approval2
CYP and UGT inhibition to assess perpetrator drug-drug interaction potential2
Pharmacokinetic properties of a truncated milk fat globule-EGF-like factor 8 in rats2
Development and application of 3D cardiac tissues derived from human pluripotent stem cells2
For hepatically cleared drugs, liver to blood KPUU at steady-state is always equal to FH , which exposes the deficiency of the present extended clearance concept equation2
Imaging Mass Spectrometry (IMS) for drug discovery and development survey: Results on methods, applications and regulatory compliance2
Transporter or membrane barriers effects on hepatic clearance (the extended clearance equation) models and the need for scaling for IVIVE2
Microbiome impacts on drug metabolism2
Reduced theophylline clearance due to hepatic congestion secondary to right heart failure - A population pharmacokinetic study2
Establishment and characterization of an in vitro model for NTCP substrate and inhibition assessment2
Difference in the lipid nanoparticle technology employed in three approved siRNA (Patisiran) and mRNA (COVID-19 vaccine) drugs2
OATP1B-mediated hepatic uptake of low-molecular weight acid compounds: assessment of HIF prolyl-hydroxylase inhibitors (DUSTATS)2
Involvement of multiple cytochrome P450 isoenzymes in drug interactions between ritonavir and direct oral anticoagulants2
Population pharmacokinetic modeling of treosulfan and rationale for dose recommendation in children treated for conditioning prior to allogeneic hematopoietic stem cell transplantation2
Elucidate the metabolism of lipidated serotonin and selected drugs by cytochrome P450 2U1 (CYP2U1) in nanodiscs2
Ferulic acid prevents Diosbulbin B-induced liver injury by inhibiting covalent modifications on proteins2
Synthetic molecule libraries for nucleic acid delivery: Design parameters in cationic/ionizable lipids and polymers2
P-GP limits rodent oral absoprtion of protacs2
Predicting drug metabolism and pharmacokinetics features of in-house compounds by a hybrid machine-learning model1
Endosomal escape for intracellular delivery of RNA therapeutics: current and future strategies1
A family study of compound variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects found by urinary phenotyping for trimethylaminuria1
LC-MS for identifying changes (or lack of it) in ADME across different cohorts1
Establishment of human intestinal organoids derived from commercially available cryopreserved intestinal epithelium and evaluation for pharmacokinetic study1
Quantitative proteomics identifies significant changes in the abundance and composition of hepatic drug metabolizing enzymes in heavy alcohol drinkers1
Comparison of the transport kinetics of fexofenadine and its pH dependency among OATP1A2 genetic variants1
Drug metabolism by the human gut microbiome1
Designing novel RNA medicines for the brain1
A live cell high content imaging assay for monitoring large molecule uptake into aproximate proximal tubule epithelial cells via megalin and cubilin1
Population pharmacokinetics of blonanserin in Japanese adolescent and adult patients with schizophrenia1
An improved TK-NOG mouse as a novel platform for humanized liver that overcomes limitations in both male and female animals1
CYP46A1 inhibition and activation: an in vitro high throughput screening assay to assess possible drug interactions using FDA approved chemical library1
Physiologically based pharmacokinetic (PBPK) model that describes enhanced FcRn-dependent distribution of monoclonal antibodies (mAbs) by pI-engineering in mice1
Oxidative metabolism and pharmacokinetics of the EGFR inhibitor BIBX1382 in chimeric NOG-TKm30 mice transplanted with human hepatocytes1
Characterization of LysoTracker Red uptake by in vitro model cells of the outer blood-retinal barrier: Implication of lysosomal trapping with cytoplasmic vacuolation and cytotoxicity1
Bringing totality-of-evidence into PBPK predictions: fraction metabolised by aldehyde oxidase1
Novel coc-based liver tissue chip for predictive pharmacokinetic and toxicology applications1
Impacts of SNPs on adverse events and trough concentration of imatinib in patients with gastrointestinal stromal tumors1
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 pharmacoki1
Validation of a modified in situ perfusion model for measuring drug intestinal excretion and evaluation of the drug-drug interactions in the intestine by I.V. administration1
Downregulated expression of organic anion transporting polypeptide (Oatp) 2b1 in the small intestine of rats with acute kidney injury1
Evaluation and prediction of oral drug absorption and bioequivalence with food-druginteraction1
Metabolic pathways of aschantin in human liver preparations1
Liver targeted therapy: What mist and DDI data mean for efficacy1
Cross-species drug metabolism and impact of metabolic stability testing under anaerobic condition on predicting pharmacokinetics of keto-enol containing compound in humans1
Impact of P-glycoprotein on intracellular drug concentration in peripheral blood mononuclear cells and K562 cells1
Translational PK/PD of the targeted radioligand therapy pluvicto1
Practical use of mechanistic modeling to discern real word complex drug interactions1
Challenges associated with the biomarker-informed PBPK modeling of renal transporter-mediated drug interactions1
Characterization of 14 pharmaceutical excipients in the CACO-2 permeability assay1
Predicting muscarinic receptor occupancy in human bladder mucosa from urinary concentrations of antimuscarinic agents for overactive bladder1
Using quantitative systems pharmacology (QSP) models to characterize the PK of novel drug modalities0
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 study0
NUDT15 is a key genetic factor for prediction of hematotoxicity in pediatric patients who received a standard low dosage regimen of 6-mercaptopurine0
Opportunities and challenges in drug development for retinal diseases0
UGT-mediated clearance IVIVE may be improved using relative activity factor approach0
Simplified daptomycin dosing regimen for adult patients with methicillin-resistant Staphylococcus aureus infections based on population pharmacokinetic analysis0
Cytochrome P450-dependent drug oxidation activities and their expression levels in liver microsomes of chimeric TK-NOG mice with humanized livers0
Characterization of plasma vonoprazan and CYP3A activity using its endogenous marker and genetic variants in patients with digestive system disorders0
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 study0
Investigating protein-mediated uptake drug-drug interactions using F-methotrexate as a substrate for OATP1B1 transporter0
Exposure-response analysis of the efficacy and safety of esaxerenone, a novel nonsteroidal mineralocorticoid receptor blocker, in hypertensive patients with or without diabetic kidney disease0
Drug metabolism: A half-century plus of progress, continued needs, and new opportunities0
Approach to de-risk structural alerts in compound progression0
In silico approach shows good predictability for free fraction in plasma and volume of distribution in human for drugs subjected to lysosomal trapping0
Investigating cross-species differences of MDR1-mediated drug transport0
Unveiling the intra-tumor fate of trastuzumab deruxtecan in a xenograft model to support its mechanism of action0
Diclofenac potentiates the antitumor effect of cisplatin in a xenograft mouse model transplanted with cisplatin-resistant cells without enhancing cisplatin-induced nephrotoxicity0
In vitro evaluation of PROTAC® degrader ARV-766 for cytochrome P450- and transporter-mediated drug-drug interaction0
Effects of steric hindrance and electron density of ester prodrugs on controlling the metabolic activation by human carboxylesterase0
14C-radiolabeled human ADME: a review of clinical microtracer mass balance data0
Animal species differences in the pyridoxine transport function of SLC19A3: Absence of Slc19a3-mediated pyridoxine uptake in the rat small intestine0
Is CYP3A4 induction a good indicator for CYP2CS in cryopreserved human hepatocytes?0
Optimization of methods for reducing turnaround time and compound consumptionwith echo liquid handling and automation enabling high capacity analysis for ADME screening0
Mechanistic pharmacokinetics & pharmacodynamics of GaINAc-siRNA0
Strategies for DDI risk assessment between novel oncology agents and combination generic standard of care (SOC) agents0
A UPLC-MS/MS method reveals the pharmacokinetics and metabolism characteristics of kaempferol in rats under hypoxia0
Novel approach to determine plasma protein binding for labile compounds using equilibrium dialysis0
Transcript abundance of hepatic drug-metabolizing enzymes in two dog breeds compared with 14 species including humans0
Encequidar is a gut-restricted P-GP specific inhibitor that boosts oral bioavailability and inhibits intestinal secretion in rats and dogs.0
Construction of a fused grid-based CYP2C19-Template system and the application0
CNS penetration of methotrexate and its metabolite 7-hydroxymethotrexate in mice bearing orthotopic Group 3 medulloblastoma tumors and model-based simulations for children0
Development of plasma stability assay for oligonucleotides0
Can prostaglandins be used as biomarkers for atypical antipsychotic mediated immune system dyregulation in zebra fish?0
Can LS180 cells predict metabolism and drug-drug interaction potential of UGT2B17 substrates?0
Quantification of fluticasone propionate in human plasma by LC–MS/MS and its application in the pharmacokinetic study of nasal spray at clinical doses0
Functional role of serine 318 of the proton-coupled folate transporter in methotrexate transport0
Successful optimization of pharmacokinetics and pharmacodynamics of oral cyclic peptide PCSK9 inhibitors0
In vitro characterization of taurine transport using the human brain microvascular endothelial cell line as a human blood-brain barrier model0
Characteristics of membrane transport, metabolism, and target protein binding of cyclic depsipeptide destruxin E in HeLa cells0
A novel method for predicting the unbound valproic acid concentration0
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 metabolism0
Probe drug T-1032 N-oxygenation mediated by cytochrome P450 3A5 in human hepatocytes in vitro and in humanized-liver mice in vivo0
Extrapolation of physiologically based pharmacokinetic model for tacrolimus from renal to liver transplant patients0
Functional characteristics of equilibrative nucleoside transporter 2 (ENT2/SLC29A2) for the transport of urate as a newly identified substrate0
The mass balance, recovery, absorption, metabolism, and excretion of [14C]-orvepitant in healthy male subjects after oral dosing: metabolite characterisation0
High-throughput assessment for drug protein binding using magnetized silica beads method in human liver microsomes0
Comprehensive in vitro evaluation of the inhibitory effects of relatively high molecular weight peptides on drug-drug interaction-associated four liver transporters and its association with physicoche0
A successful preclinical toxicology package0
Effect of substrate concentration on reactive metabolite assessment in drug discovery research0
Ilexsaponin A1: In vitro metabolites identification and evaluation of inhibitory drug-drug interactions0
Pharmacokinetics and safety of rilpivirine in healthy Japanese subjects and exploration of ethnic sensitivity of rilpivirine pharmacokinetics with physiologically based pharmacokinetic model approach0
A procedure for method development and protein binding ratio as the indicator of sensitivity with anticancer agents on MALDI mass spectrometry imaging0
Understanding mechanisms of negative food effect for voclosporin using physiologically based pharmacokinetic modeling0
Clinical DDI trial design and impact on product labels0
DMPK perspective on quantitative model analysis for chimeric antigen receptor cell therapy: Advances and challenges0
Converting suspension-type human primary hepatocytes to be plateable-type for use as an in vitro pharmacokinetics model0
In vitro liver models for toxicological research0
Assessment of covalent binding body burden in Hmrel human hepatocyte co-culture model for metabollically low turnover compounds0
Determination of metabolic pathways of phosphatidylcholine and lysophosphatidylcholine using a stable isotope tracer in hepatocarcinoma cell lines0
Pharmacokinetics of genistein distribution in blood and retinas of diabetic and non-diabetic rats0
Pharmacokinetics of perfluoroocanoic acid and perfluorohexane sulfonic acid in various rat models0
Investigation of the learning process of diverse compound structures by chemical language models toward toxicity prediction0
Inhibiting uptake activity of organic anion transporter 2 by bile acids0
Transporter activity characterization in a novel human hepatic cell-based tri-culture system0
Phenolsulfonphthalein as a surrogate substrate to assess altered function of the prostaglandin transporter SLCO2A10
Physiologically based pharmacokinetic model analysis of the inhibitory effect of vonoprazan on the metabolic activation of proguanil0
Exploring the potential of machine learning approach in predicting clinical CYP3A induction-mediated drug-drug interaction0
Delivery of small interfering RNAs by nanovesicles for cancer therapy0
Identification and characterization of novel metabolites of F2-isoprostanes0
In vitro inhibitory effects of components from Salvia miltiorrhiza on catalytic activity of three human Arachidonic acid ω-hydroxylases0
Hepatocyte formation, reactivity, and stability differences of acyl glucuronide and acyl coenzyme a conjugates0
Assessing victim drug-drug interaction – Reaction phenotyping of CYP and non-CYP0
Future direction of animal alternative/microphysiological systems in drug discovery and development0
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 mice0
Experiences in industry predicting hepatic clearance: Successes, disconnects, failures, and room for improvement0
Development of a fluorescent-labeled trapping reagent to evaluate the risk posed by acyl-CoA conjugates0
What is new in LC-MS proteomics: Techniques and applications in IVIVE and precision medicine0
Approaches to predict human PK profiles for compounds undergoing transporter mediated clearance in early drug development: From dedrick plot to PBPK modeling0
Advanced in vitro evaluation of drug-induced kidney injury using microphysiological systems in drug discovery and development0
In vitro evaluation of metabolism- and transporter-based drug interactions with sunscreen active ingredients0
Improving in vitro clearance assay performance and prediction accuracy with advanced human hepatocyte models for highly stable RO5 and BRO5 compounds0
In vitro hydrolysis of areca nut xenobiotics in human liver0
Smart compound library based on machine learning, sensing technology, and programmable logic control0
Identification and characterization of erlotinib as a potent mechanism-based inactivator of human aldehyde oxidase0
Biotransformation of protein degraders bavdegalutamide and XL01126 in permeabilized cryopreserved human hepatocytes0
Associations of HLA and drug-metabolizing enzyme genes in co-trimoxazole-induced severe cutaneous adverse reactions0
Novel metabolomics approach to identify biomarkers of organic anion renal transporters0
Inhibition of cytochrome P450 3A4 enzyme activity by alkaloid psilocin from magic mushrooms: potential for drug interactions0
The inhibitory effects of major cannabinoids and their metabolites on R- and S-oxazepam metabolism0
Bioavailability of tetracyclines is substantially increased by administration of cyclosporine A, a non-specific efflux-pump blocker0
Clotrimazole is a potent and selective UGT2B4 chemical inhibitor0
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
Development of a HRMS-MS method for measuring plasma 4Β-hydroxycholesterol, an endogenous biomarker of CYP3A activity, in monkeys treated with CYP3A modulators0
Establishment of MDR1-knockout human enteroids for pharmaceutical application0
Prevention of irinotecan-induced intestinal toxicity by locally bioavailable herbal components via maintaining gut oxidative stress homeostasis0
Genetic variation present in the CYP3A4 gene in Ni-Vanuatu and Kenyan populations in malaria endemicity0
Preferential meropenem absorption activated by 1α,25-dihydroxyvitamin D3 and shared with foscarnet, a phosphate transporter substrate, in the rat ileum0
Absorption, metabolism, and excretion of inavolisib (GDC-0077), a PI3KA inhibitor in humans0
WITHDRAWN: Drugs that induce and inhibit cytochrome P450. A study with real-world evidence0
Evaluation of a cost-effective in vitro human model for predicting intrinsic hepatocyte clearance of slowly metabolized compounds0
Development of intestinal organoids and microphysiological systems and their application to drug discovery0
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