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 2020-10-01 to 2024-10-01.)
ArticleCitations
Difference in the lipid nanoparticle technology employed in three approved siRNA (Patisiran) and mRNA (COVID-19 vaccine) drugs148
Adenovirus vector-based vaccine for infectious diseases71
Recent advances in lipid nanoparticles for delivery of nucleic acid, mRNA, and gene editing-based therapeutics43
Identification of biomarkers to diagnose diseases and find adverse drug reactions by metabolomics41
Quantitative and targeted proteomics-based identification and validation of drug efficacy biomarkers21
Current progress in identifying endogenous biomarker candidates for drug transporter phenotyping and their potential application to drug development21
An improved TK-NOG mouse as a novel platform for humanized liver that overcomes limitations in both male and female animals20
Pharmacogenomics research and its clinical implementation in Thailand: Lessons learned from the resource-limited settings20
Classification of drugs for evaluating drug interaction in drug development and clinical management18
Suppressive effect of quercetin against bleomycin-induced epithelial-mesenchymal transition in alveolar epithelial cells16
Characterization of covalent binding of tyrosine kinase inhibitors to plasma proteins15
Exosomes: Breast cancer-derived extracellular vesicles; recent key findings and technologies in disease progression, diagnostics, and cancer targeting13
Transport via Niemann-Pick C1 Like 1 contributes to the intestinal absorption of ubiquinone13
Cytochrome P450-dependent drug oxidation activities and their expression levels in liver microsomes of chimeric TK-NOG mice with humanized livers12
Delivery of small interfering RNAs by nanovesicles for cancer therapy12
Genetic variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects identified by phenotyping for trimethylaminuria and found in a database of genome resources11
Feature importance of machine learning prediction models shows structurally active part and important physicochemical features in drug design11
Species difference in brain penetration of P-gp and BCRP substrates among monkey, dog and mouse11
Food effects on gastrointestinal physiology and drug absorption10
The utility of CYP3A activity endogenous markers for evaluating drug-drug interaction between sildenafil and CYP3A inhibitors in healthy subjects10
Post-transcriptional regulation of OATP2B1 transporter by a microRNA, miR-2410
A physiologically based pharmacokinetic/pharmacodynamic modeling approach for drug-drug interaction evaluation of warfarin enantiomers with sorafenib10
Development of template systems for ligand interactions of CYP3A5 and CYP3A7 and their distinctions from CYP3A4 template9
Recent progress in the use of microRNAs as biomarkers for drug-induced toxicities in contrast to traditional biomarkers: A comparative review9
Application of comprehensive lipidomics to biomarker research on adverse drug reactions8
Dual kinetics of OATP2B1: Inhibitory potency and pH-dependence of OATP2B1 inhibitors8
Comparison of the inhibitory effects of azole antifungals on cytochrome P450 3A4 genetic variants8
Oxidative metabolism and pharmacokinetics of the EGFR inhibitor BIBX1382 in chimeric NOG-TKm30 mice transplanted with human hepatocytes8
Quantitative analysis of mRNA expression levels of aldo-keto reductase and short-chain dehydrogenase/reductase isoforms in human livers8
WDR23 regulates the expression of Nrf2-driven drug-metabolizing enzymes8
Synthetic molecule libraries for nucleic acid delivery: Design parameters in cationic/ionizable lipids and polymers8
Applications of a grid-based CYP3A4 Template system to understand the interacting mechanisms of large-size ligands; part 4 of CYP3A4 Template study7
Differences in transport function of the human and rat orthologue of the Organic Anion Transporting Polypeptide 2B1 (OATP2B1)7
Refined CYP2E1∗ Template∗∗ system to decipher the ligand-interactions7
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 t7
A series of simple detection systems for genetic variants of flavin-containing monooxygenase 3 (FMO3) with impaired function in Japanese subjects7
Associations of HLA and drug-metabolizing enzyme genes in co-trimoxazole-induced severe cutaneous adverse reactions7
Mathematical modeling analysis of hepatic uric acid disposition using human sandwich-cultured hepatocytes7
Visualisation of real-time oral biodistribution of fluorescent labeled self-microemulsifying drug delivery system of olmesartan medoxomil using optical imaging method6
A model-based pharmacokinetic assessment of drug–drug interaction between tacrolimus and nirmatrelvir/ritonavir in a kidney transplant patient with COVID-196
BTK-inhibitor drug covalent binding to lysine in human serum albumin using LC-MS/MS6
Diclofenac potentiates the antitumor effect of cisplatin in a xenograft mouse model transplanted with cisplatin-resistant cells without enhancing cisplatin-induced nephrotoxicity6
Establishment of MDR1-knockout human enteroids for pharmaceutical application6
Effects of steric hindrance and electron density of ester prodrugs on controlling the metabolic activation by human carboxylesterase6
Gene and oligonucleotide delivery via micro- and nanobubbles by ultrasound exposure6
A UPLC-MS/MS method reveals the pharmacokinetics and metabolism characteristics of kaempferol in rats under hypoxia6
Plausible drug interaction between cyclophosphamide and voriconazole via inhibition of CYP2B66
Urinary metabolic markers reflect on hepatic, not intestinal, CYP3A activity in healthy subjects5
Epicatechin gallate and epigallocatechin gallate are potent inhibitors of human arylacetamide deacetylase5
Physiologically based pharmacokinetic modeling of altered tizanidine systemic exposure by CYP1A2 modulation: Impact of drug-drug interactions and cigarette consumption5
In vivo drug interactions of itopride and trimethylamine mediated by flavin-containing monooxygenase 3 in humanized-liver mice5
Inhibiting uptake activity of organic anion transporter 2 by bile acids5
Multivalent cation and polycation polymer preparations influence pharmacokinetics of dolutegravir via chelation-type drug interactions5
Intestinal microbiota-mediated biotransformations alter the pharmacokinetics of the major metabolites of azathioprine in rats after oral administration5
Bioavailability of tetracyclines is substantially increased by administration of cyclosporine A, a non-specific efflux-pump blocker5
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 alprazolam5
A family study of compound variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects found by urinary phenotyping for trimethylaminuria5
Predicting drug metabolism and pharmacokinetics features of in-house compounds by a hybrid machine-learning model5
Development of fluorescent-labeled trapping reagents based on cysteine to detect soft and hard electrophilic reactive metabolites5
Inhibitory effects of non-steroidal anti-inflammatory drugs on human liver microsomal morphine glucuronidation: Implications for drug-drug interaction liability5
Further survey of genetic variants of flavin-containing monooxygenase 3 (FMO3) in Japanese subjects found in an updated database of genome resources and identified by phenotyping for trimethylaminuria4
Comparison of the inhibitory properties of the fruit component naringenin and its glycosides against OATP1A2 genetic variants4
Comparative single dose pharmacokinetics and metabolism of racemic primaquine and its enantiomers in human volunteers4
Imaging Mass Spectrometry (IMS) for drug discovery and development survey: Results on methods, applications and regulatory compliance4
Clinical evaluation of [18F]pitavastatin for quantitative analysis of hepatobiliary transporter activity4
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)4
6-Hydroxyindole is an endogenous long-lasting OATP1B1 inhibitor elevated in renal failure patients4
Downregulated expression of organic anion transporting polypeptide (Oatp) 2b1 in the small intestine of rats with acute kidney injury4
Synthesis and evaluation of tofacitinib analogs designed to mitigate metabolic activation4
Investigation of the arcane inhibition of human organic anion transporter 3 by benzofuran antiarrhythmic agents4
Double Trap Interface: A novel gas interface for high throughput analysis of biomedical samples by AMS4
Synthetic mRNA for ex vivo therapeutic applications4
Impacts of SNPs on adverse events and trough concentration of imatinib in patients with gastrointestinal stromal tumors4
Black ginger extract and its active compound, 5,7-dimethoxyflavone, increase intestinal drug absorption via efflux drug transporter inhibitions4
Oligonucleotide delivery to antigen presenting cells by using schizophyllan4
The association between SLC16A11 haplotype and lipid metabolism in Japanese patients with type 2 diabetes4
Simplified daptomycin dosing regimen for adult patients with methicillin-resistant Staphylococcus aureus infections based on population pharmacokinetic analysis4
Identification of miRNAs that regulate human CYP2B6 expression4
Assessing cytochrome P450-based drug-drug interactions with hemoglobin-vesicles, an artificial red blood cell preparation, in healthy rats4
Utility of Göttingen minipigs for the prediction of human pharmacokinetic profiles after intravenous drug administration4
Comparison of human biopsy-derived and human iPS cell-derived intestinal organoids established from a single individual4
Molecular cloning, sequence analysis, and tissue distribution of marmoset monoamine oxidases A and B3
Roles of human cytochrome P450 3A4/5 in dexamethasone 6β-hydroxylation mediated by liver microsomes and humanized liver in chimeric mice metabolically suppressed with azamulin3
Generation of Caco-2 cells with predictable metabolism by CYP3A4, UGT1A1 and CES using the PITCh system3
Construction of a fused grid-based template system of CYP2C9 and its application3
Disposition of E-selectin-targeting liposomes in tumor spheroids with a perfusable vascular network3
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
Trimethylamine N-oxygenation in cynomolgus macaques genotyped for flavin-containing monooxygenase 3 (FMO3)3
Pharmacokinetics of genistein distribution in blood and retinas of diabetic and non-diabetic rats3
Therapeutic application of sequence-specific binding molecules for novel genome editing tools3
Human plasma concentration-time profiles of troglitazone and troglitazone sulfate simulated by in vivo experiments with chimeric mice with humanized livers and semi-physiological pharmacokinetic model3
Inhibitory effects of type 2 diabetes serum components in P450 inhibition assays can potential diagnose asymptomatic diabetic mice3
Highly specific, quantitative polymerase chain reaction probe for the quantification of human cells in cynomolgus monkeys3
Probe drug T-1032 N-oxygenation mediated by cytochrome P450 3A5 in human hepatocytes in vitro and in humanized-liver mice in vivo3
Substrate recognition of renally eliminated angiotensin II receptor blockers by organic anion transporter 43
Different substrate elimination rates of model drugs pH-dependently mediated by flavin-containing monooxygenases and cytochromes P450 in human liver microsomes3
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 genes3
Construction of a fused grid-based CYP2C19-Template system and the application3
Effect of deuteration on the single dose pharmacokinetic properties and postoperative analgesic activity of methadone3
Pharmacokinetic/pharmacodynamic modeling of roxadustat's effect on LDL cholesterol in patients in Japan with dialysis-dependent chronic kidney disease and anemia3
Investigation of the role and quantitative impact of breast cancer resistance protein on drug distribution into brain and CSF in rats3
Analysis of inhibition kinetics of three beverage ingredients, bergamottin, dihydroxybergamottin and resveratrol, on CYP2C9 activity3
Carboxylesterase-2 plays a critical role in dabigatran etexilate active metabolite formation3
Evaluation of cytochrome P450-based drug metabolism in hemorrhagic shock rats that were transfused with native and an artificial red blood cell preparation, Hemoglobin-vesicles3
Adenosine deaminases acting on RNA modulate the expression of the human pregnane X receptor3
Extrapolation of physiologically based pharmacokinetic model for tacrolimus from renal to liver transplant patients3
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 population2
Effects of valproate, an HDAC inhibitor, on the expression of folate carriers and folate metabolism-related genes in the placenta of rats2
Phosphate buffer interferes dissolution of prazosin hydrochloride in compendial dissolution testing2
Establishment of human intestinal organoids derived from commercially available cryopreserved intestinal epithelium and evaluation for pharmacokinetic study2
Reduced theophylline clearance due to hepatic congestion secondary to right heart failure - A population pharmacokinetic study2
New in vitro screening system to detect drug-induced liver injury using a culture plate with low drug sorption and high oxygen permeability2
In vitro metabolism of the new antifungal dapaconazole using liver microsomes2
Blood concentrations of tacrolimus upon conversion from rabeprazole to vonoprazan in renal transplant recipients: Correlation with cytochrome P450 gene polymorphisms2
The carboxyl-terminal di-lysine motif is essential for catalytic activity of UDP-glucuronosyltransferase 1A92
Evaluation and prediction of oral drug absorption and bioequivalence with food-druginteraction2
Phenolsulfonphthalein as a surrogate substrate to assess altered function of the prostaglandin transporter SLCO2A12
A procedure for method development and protein binding ratio as the indicator of sensitivity with anticancer agents on MALDI mass spectrometry imaging2
Estimation of absolute oral bioavailability without performing an intravenous clinical study2
Quantitative prediction of transporter-mediated drug-drug interactions using the mechanistic static pharmacokinetic (MSPK) model2
Formation of reactive metabolites of benzbromarone in humanized-liver mice2
Development of a new assay system for bladder cancer using interactions between cytochromes P450 and serum2
Apple-derived extracellular vesicles modulate the expression of human intestinal bile acid transporter ASBT/SLC10A2 via downregulation of transcription factor RARα2
Model-based assessment of pharmacokinetic changes of sunitinib, tacrolimus, and everolimus in a patient with metastatic renal cell carcinoma after renal transplantation2
Improvement of transdermal absorption rate by nonthermal biocompatible atmospheric pressure plasma2
Ilexsaponin A1: In vitro metabolites identification and evaluation of inhibitory drug-drug interactions2
NUDT15 is a key genetic factor for prediction of hematotoxicity in pediatric patients who received a standard low dosage regimen of 6-mercaptopurine2
Administration of erlotinib in apple juice overcomes decreased absorption in a rat model of gastric acid suppression2
Novel food drug interaction mechanism involving acyclovir, chitosan and endogenous mucus2
Functional characterization of human organic anion transporter 10 (OAT10/SLC22A13) as an orotate transporter2
Ataluren metabolism: Ataluren-O-1β-acyl glucuronide is a stable circulating metabolite in mouse, rat, dog and human1
CNS penetration of methotrexate and its metabolite 7-hydroxymethotrexate in mice bearing orthotopic Group 3 medulloblastoma tumors and model-based simulations for children1
Tenofovir activation is diminished in the brain and liver of creatine kinase brain-type knockout mice1
Construction of a fused grid-based CYP2C8-Template system and the application1
Metabolism of non-steroidal anti-inflammatory drugs (NSAIDs) by Streptomyces griseolus CYP105A1 and its variants1
Comparison of the transport kinetics of fexofenadine and its pH dependency among OATP1A2 genetic variants1
Biotransformation of protein degraders bavdegalutamide and XL01126 in permeabilized cryopreserved human hepatocytes1
Impact of miR-222-3p-mediated downregulation of arylacetamide deacetylase on drug hydrolysis and lipid accumulation1
Applications of model simulation in pharmacological fields and the problems of theoretical reliability1
Sodium citrate buffer improves pazopanib solubility and absorption in gastric acid-suppressed rat model1
Protection of mice against carbon tetrachloride-induced acute liver injury by endogenous and exogenous estrogens1
Transcript abundance of hepatic drug-metabolizing enzymes in two dog breeds compared with 14 species including humans1
Prediction of drug-drug interaction risk of P-glycoprotein substrate in drug discovery1
Exposure-response analysis of the efficacy and safety of esaxerenone, a novel nonsteroidal mineralocorticoid receptor blocker, in hypertensive patients with or without diabetic kidney disease1
Animal species differences in the pyridoxine transport function of SLC19A3: Absence of Slc19a3-mediated pyridoxine uptake in the rat small intestine1
In vitro inhibitory effects of components from Salvia miltiorrhiza on catalytic activity of three human Arachidonic acid ω-hydroxylases1
Simple confirmation methods for rare but impaired variants of human flavin-containing monooxygenase 3 (FMO3) found in an updated genome resource databank1
Molecular cloning and tissue distribution of marmoset thiopurine S-methyltransferase1
Drug transporters are implicated in the diffusion of tacrolimus into the T lymphocyte in kidney and liver transplant recipients: Genetic, mRNA, protein expression, and functionality1
Inhibitory effects of indoxyl sulfate and creatinine on the renal transport of meropenem and biapenem in rats1
Population pharmacokinetics of esaxerenone, a novel non-steroidal mineralocorticoid receptor blocker, in patients with essential hypertension, patients with diabetic nephropathy, and healthy volunteer1
Cross-species drug metabolism and impact of metabolic stability testing under anaerobic condition on predicting pharmacokinetics of keto-enol containing compound in humans1
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
Ferulic acid prevents Diosbulbin B-induced liver injury by inhibiting covalent modifications on proteins1
Involvement of multiple cytochrome P450 isoenzymes in drug interactions between ritonavir and direct oral anticoagulants1
In vitro demonstration of antedrug mechanism of a pharmacokinetic booster to improve CYP3A4 substrates by CYP3A4-mediated metabolism inhibition0
Modern pediatric drug development: Practical case examples and regulatory outcomes from novel applications of modelling0
Effect of antibiotic-administration period on hepatic bile acid profile and expression of pharmacokinetic-related proteins in mouse liver, kidney, and brain capillaries0
In vivo and in vitro biotransformation of molnupiravir (MOV), An oral prodrug of the antiviral ribonucleoside analog Β-D-N4-hydroxycytidine (NHC)0
Assessing victim drug-drug interaction – Reaction phenotyping of CYP and non-CYP0
Population pharmacokinetic analysis of sirolimus in Japanese pediatric and adult subjects receiving tablet or granule formulations0
Plasma protein binding in special populations: do current PBPK models correctly account for potential changes to fraction unbound?0
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 simulation0
Latest developments in nitrosamine structure-activity relationships for carcinogenicity0
Dose optimization with population pharmacokinetics of ritonavir-boosted lopinavir for Thai people living with HIV with and without active tuberculosis0
Clinical studies on pharmacogenomics and DDIS involving drug transporters0
Deciphering the cell and zonal distribution of drug metabolizing enzymes and transporters in humans by single cell transcriptomics0
Exploration of bioactivation of a branched-chain ketoacid dehydrogenase kinase (BDK) inhibitor0
Novel multi-tissue chips for predictive pharmacokinetic studies0
Evaluation of a cost-effective in vitro human model for predicting intrinsic hepatocyte clearance of slowly metabolized compounds0
Physiologically based pharmacokinetic modeling of adeno-associated viruses and the transgene product0
Plasma protein binding of oligonucleotides using rapid agarose gel electrophoretic mobility shift assay0
Human liver chimeric mouse and trasngenic animals are useful tools for quantitatively predicting clearance and drug-drug interactions in human0
Cannabinoid-induced drug-drug interactions with hydromorphone.0
In vitro uptake of an MC3 lipid nanoparticle formulation by mice, non-human primate, and human hepatocytes and Kupffer cells0
Stereoisomer separation of drugs and biomarkers using supercritical fluid chromatography to support PK/PD studies0
From stratified dose adjustment to personalised dosing: Linking LCMS proteomics in tissues to more clinically practical liquid biopsy samples – Opportunities and challenges0
Monocarboxylate transporter 10: substrate-dependent mode of transport0
Understanding CYP3A4 and P-GP mediated drug-drug interactions through PBPK modeling - case example of pralsetinib0
Utilizing various plasma protein binding tools for free fraction determination of lipophilic and lipopeptide drugs0
Effect of linker-payload design on the PK of ADCS0
Synthesis and characterization of human metabolites of the echinocandid drug rezafungin by microbial biotransformation0
Gene and Oligonucleotide Delivery0
The effect of traditional herbal medicine on the permeability of clarithromycin and loxoprofen in CACO-2 cell model0
Application of machine learning techniques in population pharmacokinetics/pharmacodynamics modeling0
The mass balance recovery, absorption, metabolism, and excretion of [14C]-orvepitant in healthy male subjects after oral dosing: radiosynthesis of [14c]-orvepitant0
Quantitation and characterization of glucosylsphingosine in cerebrospinal fluid (CSF), plasma, and brain of monkey model with Gaucher disease0
Prediction of human clearance using human liver microsomes and hepatocytes with 455 drugs0
Successful optimization of pharmacokinetics and pharmacodynamics of oral cyclic peptide PCSK9 inhibitors0
Constitutive androstane receptor-responsive elements for mouse Cyp1a2 transcriptional activation induced by constitutive androstane receptor ligands0
Strategies for enhancing oral exposure of water-insoluble compounds0
Drug induced organ toxicity: Transporter roles and derisking approaches0
Population pharmacokinetic and exposure-response analyses of d-amphetamine after administration of lisdexamfetamine dimesylate in Japanese pediatric ADHD patients0
Characterization of plasma vonoprazan and CYP3A activity using its endogenous marker and genetic variants in patients with digestive system disorders0
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 interactions0
Novel approaches and troubleshooting for developing a high-throughput oligonucleotide LC-MS method beyond the current stage0
A novel method for predicting the unbound valproic acid concentration0
Jasmone, an essential oil component, is an antagonist of aryl hydrocarbon receptor in liver and intestinal cells0
Using quantitative systems pharmacology (QSP) models to characterize the PK of novel drug modalities0
Assessment of covalent binding body burden in Hmrel human hepatocyte co-culture model for metabollically low turnover compounds0
Lysosomal trapping measurement in multiple cell types using a high content imaging (HCI) system0
Enriching metabolite fractions for assessment of AHR activation potential: a proof of concept study0
An approach using a gamma-distributed delay model to evaluate the anticancer effect of doxorubicin-encapsulated polymeric micelles by predictive pharmacokinetic-pharmacodynamic modeling0
Can LS180 cells predict metabolism and drug-drug interaction potential of UGT2B17 substrates?0
Hepatocyte formation, reactivity, and stability differences of acyl glucuronide and acyl coenzyme a conjugates0
Pharmacokinetics of ginsenosides and effect of the lactic acid bacteria on pharmacokinetics of ginsenosides in mice and human0
This is no longer just about liver: LC-MS proteomics for organ exposure brain/kidney/gut/skin/placenta0
Evaluation of biliary excretion process of drugs and bile acids using permeation assay by a novel in vitro hepatocyte culture system (ICHEP)0
Relative expression versus activity factor (ref vs. raf) to estimate fractional contribution of individual UGT isoforms (FGLUC) in drug glucuronidation0
The characterization of the pharmacokinetic profile of anti-tumor B (ATB) in oral cancer patients0
Establishment of the relay method for low-turnover compounds in hepatocyte0
Systematic identification and characterization of cynomolgus macaque solute carrier transporters0
Metabolism of DHED in vitro and in vivo to support drug optimization0
Basic tenets for the ADME of protein therapeutics0
Prediction and validation of human hepatobiliary clearances and hepatic concentrations of transported drugs using the relative expression factor (REF) and PET imaging approaches0
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
UGT-mediated clearance IVIVE may be improved using relative activity factor approach0
DMPK perspective on quantitative model analysis for chimeric antigen receptor cell therapy: Advances and challenges0
Unveiling the intracellular journey: GOLGA8N-mediated subcellular trafficking of siRNA drugs and its implications on silencing efficacy0
Development of a fluorescent-labeled trapping reagent to evaluate the risk posed by acyl-CoA conjugates0
Optimization of methods for reducing turnaround time and compound consumptionwith echo liquid handling and automation enabling high capacity analysis for ADME screening0
Potential ADME-related issues for PROTACs0
Physiologically based pharmacokinetic modeling to predict the clinical effect of azole antifungal agents as CYP3A inhibitors on azelnidipine pharmacokinetics0
Title page0
Identification and characterization of novel metabolites of F2-isoprostanes0
Physiologically based pharmacokinetic modeling of CYP2C8 substrate rosiglitazone and its metabolite to predict metabolic drug-drug interaction0
Corrigendum to “Utility of Göttingen minipigs for the prediction of human pharmacokinetic profiles after intravenous drug administration” [Drug Metabol Pharmacokinet 41 (2021) 100408]0
Beyond non-human primates: Transgenics and PBPK models for predicting the human PK of protein therapeutics0
Comparison of clearance and metabolic pathways in suspension hepatocytes and hepatopac cultures0
Physiologically based pharmacokinetic model analysis of the inhibitory effect of vonoprazan on the metabolic activation of proguanil0
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
What is the role of CYP1A1 in drug metabolism?0
Redox metabolism in intestine and liver aggravates retronecine-type pyrrolizidine alkaloids-induced liver injury0
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
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 pharmacokinetics0
Exploring the human 3D small intestinal model (epiintestinaltm) for improved prediction of oral absorption, metabolism and complex drug-drug interactions of small molecule drugs0
Mathematical modeling of affinity design goals for CIS-binding BI-specific antibody-based molecules0
The practical impact of the FDA draft guidance on human mass balance studies – a year of client discussions0
Dynamic free fraction: concept, methodology and impact on hepatic clearance prediction using the well-stirred model0
Pharmacokinetic interaction of caffeine and theophylline in mice0
A practical approach for measuring acyl glucuronide migration half life0
Evaluation of a novel, primary human hepatocyte tri-culture model, truvivotm, for its ability to predict metabolic clearance of CYP, UGT, and AO substrates0
Verification of a physiologically based pharmacokinetic model of caffeine that incorporates mechanistic descriptors of absorption0
Enzyme induction fundamentals, assays, data interpretation and in vivo translation0
Preclinical evaluation of the potential for cytochrome P450 inhibition and induction by tucatinib0
Functional role of serine 318 of the proton-coupled folate transporter in methotrexate transport0
Development of an in vitro metabolism approach of acrylamide covalent drugs for predicting metabolism and disposition in human0
Story of maturation - Modelers vs models in the paediatric space0
The spectrum of hepatic clearance models, from old to new0
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
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