Interindividual variability in metformin pharmacokinetics in pediatric patients. Pediatric Research. 2026.
Protein Abundance of Hydrolytic Drug Metabolizing Enzymes in Different Tissues and across Species. Journal of Medicinal Chemistry. 2026.
Characterization of Lysosomal Hydrolases and Transporters and Their Age-Dependent Variability: Relevance to Drug Metabolism and Transport of Small Molecule and Biologic Drugs. Clinical Pharmacology and Therapeutics. 2026.
Predicting Pharmacokinetic Variability and Drug Interaction Risk Using Omics-Based Biomarkers. Clinical and Translational Science. 2026; 19(5):e70591.
Metabolite Panel for Estimation of Glomerular Filtration Rate (Abstract ID: 226554) Journal of Pharmacology and Experimental Therapeutics. 2026; 393(5):104160.
Proteomic Characterization of Human Kinases Across Tissue Types: Implications for Kinase Activated Drugs (Abstract ID: 225691) Journal of Pharmacology and Experimental Therapeutics. 2026; 393(5):104195.
Integrating renal transporter biomarkers into drug development: Discovery, clinical assessment, and precision medicine. Drug Metabolism and Pharmacokinetics. 2026; 67:101515.
Population Physiologically-Based Pharmacokinetic Modeling to Determine Ontogeny: A Quantitative Clinical Pharmacology Example in Pediatric Rare Disease. CPT: Pharmacometrics and Systems Pharmacology. 2026; 15(2):e70174.
Pharmacogenetic hSLCO1B1*14-Guided Dosing of Methotrexate in Transgenic Arthritic Mice Normalizes Exposure and Response. Clinical and Translational Science. 2026; 19(1):e70449.
Placental proteomic signatures of preterm birth, gestational age, and birthweight. BMC Pregnancy and Childbirth. 2025; 26(1):50.
Promise of Quantitative Proteomics in the Qualification of New Approach Methodologies. Clinical Pharmacology and Therapeutics. 2025; 118(6):1273-1275.
Confounding Effect of Hepatic Carboxylesterase 1 (CES1) Variability on Clopidogrel Oxidation. Molecular Pharmaceutics. 2025; 22(12):7359-7370.
Protein Abundance of Clinically Relevant Drug-Metabolizing Hydrolases in Human Liver and Intestine by Targeted versus Global Proteomics Approaches: A Comparative Study. Journal of Proteome Research. 2025; 24(11):5683-5695.
From Discovery to Translation: Endogenous Substrates of OAT1 and OAT3 as Clinical Biomarkers for Renal Secretory Function. Clinical Pharmacology and Therapeutics. 2025; 118(3):693-704.
Inter-individual variability, differential tissue abundance, and sub-cellular localization of human aldo-keto reductases (AKRs) and hydroxy-steroid dehydrogenases (HSDs). Biochemical Pharmacology. 2025; 239:117044.
Curcumin enhances the oral bioavailability of testosterone by inhibiting its intestinal metabolism. Drug Metabolism And Disposition. 2025; 53(9):100144.
Quantitative Contributions of Hepatic and Renal Organic Cation Transporters to the Clinical Pharmacokinetic Cimetidine-Metformin Interaction. Clinical Pharmacology and Therapeutics. 2025; 118(2):343-354.
Pentagalloyl glucose inhibits monosodium urate-induced inflammation and NLRP3 inflammasome formation via TAK1. American Journal of Physiology - Cell Physiology. 2025; 329(2):C500-C512.
Extending Investigations of miR-126-5p on the Regulation of CYP2A6, the Major Nicotine-Inactivating Enzyme. Pharmacology Research & Perspectives. 2025; 13(4):e70149.
Characterization of organic anion transporting polypeptide (OATP)1B1 and OATP1B3 humanized rat as a translational model to study the pharmacokinetics of OATP1B substrate drugs. Drug Metabolism And Disposition. 2025; 53(7):100101.
A new naphthalene-based fluorogenic substrate for cytochrome P450 4A11. Biochemical Journal. 2025; 482(12):839-857.
Protein abundance of hydrolytic drug metabolizing enzymes in different tissues and across species. Drug Metabolism and Pharmacokinetics. 2025; 61:101350.
Characterization of age-dependent abundance of drug transporter proteins and conjugating enzymes in human hepatocytes: Implication for pediatric drug dosing. Drug Metabolism and Pharmacokinetics. 2025; 61:101453.
Identification and validation of selective endogenous substrates of organic anion transporter 1 (OAT1) versus OAT3 using metabolomics and in-vitro mechanistic studies. Drug Metabolism and Pharmacokinetics. 2025; 61:101454.
The ontogeny and inter-individual variability of hydrolytic drug-metabolizing enzymes in human liver. Drug Metabolism and Pharmacokinetics. 2025; 61:101127.
Development of human glucuronide atlas and its application for identifying endogenous UGT substrates by a novel metabolomic-based DMET biomarker discovery (MDBD) approach. Drug Metabolism and Pharmacokinetics. 2025; 61:101301.
Integrating intestinal physiology and drug metabolism, disposition, and interactions through PBPK modeling. Drug Metabolism and Pharmacokinetics. 2025; 61:101072.
Influence of locally bioavailable herbal components on the regulation of gut homoeostatis via expression of intestinal drug metabolizing enzymes and transporters in irinotecan-induced intestinal injury model. Drug Metabolism and Pharmacokinetics. 2025; 61:101335.
Organic cation transporters 2: Structure, regulation, functions, and clinical implications. Drug Metabolism And Disposition. 2025; 53(3):100044.
Identification of Potential Pre-Dose Endogenous Metabolic Features Associated with Metformin Plasma Exposure in Healthy Adults and Pediatric Patients (Abstract ID: 167055) Journal of Pharmacology and Experimental Therapeutics. 2025; 392(3):101700.
Confounding Effect of Phenol Red on OAT- and OATP-Mediated Transporter Assays: Implications for Accuracy and Translatability of In Vitro Data (Abstract ID: 168143) Journal of Pharmacology and Experimental Therapeutics. 2025; 392(3):101704.
Diclofenac Glucuronidation and Oxidation Are Inhibited by Curcumin Standard and Supplements (Abstract ID: 167709) Journal of Pharmacology and Experimental Therapeutics. 2025; 392(3):101701.
Investigation of Interindividual Variability of Drug Metabolizing Kinases in Human Hepatocytes: Influence of Age, Sex, and Race (Abstract ID: 161579) Journal of Pharmacology and Experimental Therapeutics. 2025; 392(3):101673.
Identification of Potential Endogenous Substrates of Cytochrome P450 Enzymes Using an Optimized Metabolomics-Based Approach (Abstract ID: 161986) Journal of Pharmacology and Experimental Therapeutics. 2025; 392(3):101676.
Effects of Chronic Alcohol Intake on the Composition of the Ensemble of Drug-Metabolizing Enzymes and Transporters in the Human Liver. Journal of Xenobiotics. 2025; 15(1).
Is N1-Methylnicotinamide a Good Organic Cation Transporter 2 (OCT2) Biomarker? Metabolites. 2025; 15(2).
A transcriptomic comparison of in vitro models of the human placenta. Placenta. 2025; 159:52-61.
Editorial: Diverse functions of drug transporters. Frontiers in Pharmacology. 2025; 16:1697775.
Evaluation of the Drug-Drug Interaction Potential of Cannabidiol Against UGT2B7-Mediated Morphine Metabolism Using Physiologically Based Pharmacokinetic Modeling. Pharmaceutics. 2024; 16(12).
Developmental Expression of Drug Transporters and Conjugating Enzymes Involved in Enterohepatic Recycling: Implication for Pediatric Drug Dosing. Clinical Pharmacology and Therapeutics. 2024; 116(6):1615-1626.
Non-additivity of the functional properties of individual P450 species and its manifestation in the effects of alcohol consumption on the metabolism of ketamine and amitriptyline. Biochemical Pharmacology. 2024; 230(Pt 1):116569.
Age-Dependent Changes in Cytochrome P450 Abundance and Composition in Human Liver. Drug Metabolism And Disposition. 2024; 52(12):1363-1372.
Quantitative Proteomics for Translational Pharmacology and Precision Medicine: State of The Art and Future Outlook. Drug Metabolism And Disposition. 2024; 52(11):1208-1216.
Differential Tissue Abundance of Membrane-Bound Drug Metabolizing Enzymes and Transporter Proteins by Global Proteomics. Drug Metabolism And Disposition. 2024; 52(11):1152-1160.
Age-Dependent Abundance of CYP450 Enzymes Involved in Metronidazole Metabolism: Application to Pediatric PBPK Modeling. Clinical Pharmacology and Therapeutics. 2024; 116(4):1090-1099.
Microcystin-LR activates serine/threonine kinases and alters the phosphoproteome in human HepaRG cells. Toxicon. 2024; 249:108072.
Transcriptomic comparison of in vitro models of the human placenta. Placenta. 2024; 154:e22.
Identification of the Biotransformation Pathways of a Potential Oral Male Contraceptive, 11β-Methyl-19-Nortestosterone (11β-MNT) and Its Prodrugs: An In Vitro Study Highlights the Contribution of Polymorphic Intestinal UGT2B17. Pharmaceutics. 2024; 16(8).
Comparison of Relative Activity versus Relative Expression Factors (RAF versus REF) in Predicting Glucuronidation Mediated Drug Clearance Using Recombinant UGTs. Pharmaceutical Research. 2024; 41(8):1621-1630.
Sex and the Kidney Drug-Metabolizing Enzymes and Transporters: Are Preclinical Drug Disposition Data Translatable to Humans? Clinical Pharmacology and Therapeutics. 2024; 116(1):235-246.
Ontogeny of Human Liver Aldehyde Oxidase: Developmental Changes and Implications for Drug Metabolism. Molecular Pharmaceutics. 2024; 21(6):2740-2750.
Biotransformation Pathways of 11β-Methyl-19-Nortestosterone and Its Prodrugs: Mechanistic In vitro Studies Unveils Involvement of Polymorphic Intestinal UGT2B17. Journal of Pharmacology and Experimental Therapeutics. 2024; 389:38.
Predicting contributions of hepatic and renal organic cation transporters to the clinical pharmacokinetic cimetidine-metformin interaction using a mechanistic PBPK model. Journal of Pharmacology and Experimental Therapeutics. 2024; 389:442.
Interplay of Alcohol Intake, Smoking, and Sex on the Protein Abundance of Hepatic Drug Metabolizing Enzymes and Transporters in Humans. Journal of Pharmacology and Experimental Therapeutics. 2024; 389:237.
Non-additivity of the functional properties of P450 enzymes in the human drug-metabolizing ensemble revealed in a study with a series of individual microsomal preparations. Journal of Pharmacology and Experimental Therapeutics. 2024; 389:40.
De Novo Identification and Validation of Human Endogenous Biomarkers of Renal Organic Anion Transporters for Predicting Interindividual Variability. Journal of Pharmacology and Experimental Therapeutics. 2024; 389:433-434.
Deconvoluting the Global Metabolomic Changes Caused by a Complex Clinical Pharmacokinetic Cimetidine-Metformin Interaction Involving Organic Cation Transporters. Journal of Pharmacology and Experimental Therapeutics. 2024; 389:233.
Quantitative Proteomics of Human Urine-Isolated Extracellular Vesicles Reveals Significant and Reproducible Enrichment of EV Markers and Renal Drug-Interacting Proteins. Journal of Pharmacology and Experimental Therapeutics. 2024; 389:437.
Microcystin-LR activates MAPKs and alters the phosphoproteome in human HepaRG cells. Journal of Pharmacology and Experimental Therapeutics. 2024; 389:18.
Novel metabolomics approach to identify biomarkers of organic anion renal transporters. Drug Metabolism and Pharmacokinetics. 2024; 55:100805.
What is new in LC-MS proteomics: Techniques and applications in IVIVE and precision medicine. Drug Metabolism and Pharmacokinetics. 2024; 55:100563.
Promiscuity and quantitative contribution of UGT2B17 in drug and steroid metabolism determined by experimental and computational approaches. Drug Metabolism and Pharmacokinetics. 2024; 55:100955.
Relative expression versus activity factor (ref vs. raf) to estimate fractional contribution of individual UGT isoforms (FGLUC) in drug glucuronidation. Drug Metabolism and Pharmacokinetics. 2024; 55:100811.
Quantitative proteomics identifies significant changes in the abundance and composition of hepatic drug metabolizing enzymes in heavy alcohol drinkers. Drug Metabolism and Pharmacokinetics. 2024; 55:100926.
Can LS180 cells predict metabolism and drug-drug interaction potential of UGT2B17 substrates? Drug Metabolism and Pharmacokinetics. 2024; 55:100917.
Cytochrome P450 Family 4F2 and 4F11 Haplotype Mapping and Association with Hepatic Gene Expression and Vitamin K Hydroxylation Activity. ACS Pharmacology and Translational Science. 2024; 7(3):716-732.
Global Proteomics Analysis of Lysophosphatidic Acid Signaling in PC-3 Human Prostate Cancer Cells: Role of CCN1. International Journal of Molecular Sciences. 2024; 25(4).
Promiscuity and Quantitative Contribution of UGT2B17 in Drug and Steroid Metabolism Determined by Experimental and Computational Approaches. Journal of Chemical Information and Modeling. 2024; 64(2):483-498.
Effect of Cimetidine on Metformin Pharmacokinetics and Endogenous Metabolite Levels in Rats. Drug Metabolism And Disposition. 2024; 52(2):86-94.
Chapter 8 Application of in vitro models for pediatric translational research. In: Essentials of Translational Pediatric Drug Development. Elsevier; 2024:155-188.
Characterization of Gla proteoforms and non-Gla peptides of gamma carboxylated proteins: Application to quantification of prothrombin proteoforms in human plasma. Analytica Chimica Acta. 2023; 1284:341972.
Analysis of the interplay of physiological response to food intake and drug properties in food-drug interactions. Drug Metabolism and Pharmacokinetics. 2023; 53:100518.
Effect of probenecid on blood levels and renal elimination of furosemide and endogenous compounds in rats: Discovery of putative organic anion transporter biomarkers. Biochemical Pharmacology. 2023; 218:115867.
The Plasma Membrane Monoamine Transporter is Highly Expressed in Neuroblastoma and Functions as an mIBG Transporter. Journal of Pharmacology and Experimental Therapeutics. 2023; 387(3):239-248.
Innovations, Opportunities, and Challenges for Predicting Alteration in Drug-Metabolizing Enzyme and Transporter Activity in Specific Populations. Drug Metabolism And Disposition. 2023; 51(12):1547-1550.
Experimental pharmacology in precision medicine. Pharmacology Research & Perspectives. 2023; 11(6):e01147.
Impact of CYP2C:TG Haplotype on CYP2C19 Substrates Clearance In Vivo, Protein Content, and In Vitro Activity. Clinical Pharmacology and Therapeutics. 2023; 114(5):1033-1042.
Dissecting Parameters Contributing to the Underprediction of Aldehyde Oxidase-Mediated Metabolic Clearance of Drugs. Drug Metabolism And Disposition. 2023; 51(10):1362-1371.
Characterization of Xenobiotic and Steroid Disposition Potential of Human Placental Tissue and Cell Lines (BeWo, JEG-3, JAR, and HTR-8/SVneo) by Quantitative Proteomics. Drug Metabolism And Disposition. 2023; 51(8):1053-1063.
High-Throughput Assay of Cytochrome P450-Dependent Drug Demethylation Reactions and Its Use to Re-Evaluate the Pathways of Ketamine Metabolism. Biology. 2023; 12(8).
Involvement of the p38/MK2 Pathway in MCLR Hepatotoxicity Revealed through MAPK Pharmacological Inhibition and Phosphoproteomics in HepaRG Cells. International Journal of Molecular Sciences. 2023; 24(13).
Intestinal Metabolism of Diclofenac by Polymorphic UGT2B17 Correlates with its Highly Variable Pharmacokinetics and Safety across Populations. Clinical Pharmacology and Therapeutics. 2023; 114(1):161-172.
High-Resolution Mass Spectrometry Coupled with XCMS Online for High-throughput Detection and Identification of Drug Metabolites. Journal of Pharmacology and Experimental Therapeutics. 2023; 385:182.
Identification of Putative Novel Biomarkers of Organic Anion Transporter 1 and 3 for the Prediction of Transporter-Mediated Drug-Drug Interactions. Journal of Pharmacology and Experimental Therapeutics. 2023; 385:187-188.
Identification of endogenous biomarkers of renal organic cation transporters in rats by global metabolomics analysis. Journal of Pharmacology and Experimental Therapeutics. 2023; 385:577.
Relevance of Human Aldoketoreductases and Microbial β-Glucuronidases in Testosterone Disposition. Drug Metabolism And Disposition. 2023; 51(4):427-435.
Quantitative Characterization of Clinically Relevant Drug-Metabolizing Enzymes and Transporters in Rat Liver and Intestinal Segments for Applications in PBPK Modeling. Molecular Pharmaceutics. 2023; 20(3):1737-1749.
Quantification of Accurate Composition and Total Abundance of Homologous Proteins by Conserved-Plus-Surrogate Peptide Approach: Quantification of UDP Glucuronosyltransferases in Human Tissues. Drug Metabolism And Disposition. 2023; 51(3):285-292.
Interplay of Breast Cancer Resistance Protein (Bcrp/Abcg2), Sex, and Fed State in Oral Pharmacokinetic Variability of Furosemide in Rats. Pharmaceutics. 2023; 15(2).
An optimized proteomics-based approach to estimate blood contamination and cellular heterogeneity of frozen placental tissue. Placenta. 2023; 131:111-118.
Dimethandrolone, a Potential Male Contraceptive Pill, is Primarily Metabolized by the Highly Polymorphic UDP-Glucuronosyltransferase 2B17 Enzyme in Human Intestine and Liver. Drug Metabolism And Disposition. 2022; 50(12):1493-1500.
Cardiac Disease Alters Myocardial Tissue Levels of Epoxyeicosatrienoic Acids and Key Proteins Involved in Their Biosynthesis and Degradation. International Journal of Molecular Sciences. 2022; 23(20).
Differential proteomics analysis of JEG-3 and JAR placental cell models and the effect of androgen treatment. Journal of Steroid Biochemistry and Molecular Biology. 2022; 222:106138.
Clinical Implications of Altered Drug Transporter Abundance/Function and PBPK Modeling in Specific Populations: An ITC Perspective. Clinical Pharmacology and Therapeutics. 2022; 112(3):501-526.
Can analysis of serum androgens aid in the diagnosis of polycystic ovary syndrome (PCOS) in adolescents? Expert Review of Endocrinology and Metabolism. 2022; 17(5):375-381.
Quantitative Proteomics in Translational Absorption, Distribution, Metabolism, and Excretion and Precision Medicine. Pharmacological Reviews. 2022; 74(3):769-796.
A Tribute to Professor Saranjit Singh - A Critical Thinker, Innovator, Mentor, and Educator. Journal of Pharmaceutical Sciences. 2022; 111(5):1224-1231.
The disposition of polychlorinated biphenyls (PCBs) differs between germ-free and conventional mice. Environmental Toxicology and Pharmacology. 2022; 92:103854.
Assessing the Effect of Organic Anion Transporter Inhibition on Circulating Pyridoxic Acid, an Endogenous Transporter Biomarker, using Physiologically‐based Pharmacokinetic Modeling. The FASEB Journal. 2022; 36(S1).
Proteomics‐informed physiologically‐based pharmacokinetic (PBPK) modeling revealed differential effects of UGT2B17 variability on the pharmacokinetics of diclofenac following intravenous and oral administration. The FASEB Journal. 2022; 36(S1).
Effect of di‐ethylhexyl phthalate (DEHP) on androgen related proteins in JEG‐3 placental cells. The FASEB Journal. 2022; 36(S1).
Poor and variable oral bioavailability of dimethandrolone (DMA), an investigational male hormonal contraceptive, is likely associated with UGT2B17 mediated first‐pass metabolism. The FASEB Journal. 2022; 36(S1).
Effect of acetaminophen treatment on endocrine pathways in placenta: Proteomics investigation in JEG‐3 cell model. The FASEB Journal. 2022; 36(S1).
Exploration of the Plausible Mechanism of Ethambutol Induced Ocular Toxicity by Using Proteomics Informed Physiologically Based Pharmacokinetic (PBPK) Modeling. Pharmaceutical Research. 2022; 39(4):677-689.
Comparison of Tissue Abundance of Non-Cytochrome P450 Drug-Metabolizing Enzymes by Quantitative Proteomics between Humans and Laboratory Animal Species. Drug Metabolism And Disposition. 2022; 50(3):197-203.
Interindividual Variability and Differential Tissue Abundance of Mitochondrial Amidoxime Reducing Component Enzymes in Humans. Drug Metabolism And Disposition. 2022; 50(3):191-196.
Exploring the Interactome of Cytochrome P450 2E1 in Human Liver Microsomes with Chemical Crosslinking Mass Spectrometry. Biomolecules. 2022; 12(2).
Ontogeny of Scaling Factors for Pediatric Physiology-Based Pharmacokinetic Modeling and Simulation: Microsomal Protein Per Gram of Liver. Drug Metabolism And Disposition. 2022; 50(1):24-32.
Functional characterization of novel rare CYP2A6 variants and potential implications for clinical outcomes. Clinical and Translational Science. 2022; 15(1):204-220.