All Stories

  1. Quantitative Contribution of Six Major Transporters to the Hepatic Uptake of Drugs: “SLC-Phenotyping” Using Primary Human Hepatocytes
  2. Organic Anion Transporter 2–Mediated Hepatic Uptake Contributes to the Clearance of High-Permeability–Low-Molecular-Weight Acid and Zwitterion Drugs: Evaluation Using 25 Drugs
  3. Simultaneous Assessment of Transporter-Mediated Drug–Drug Interactions Using a Probe Drug Cocktail in Cynomolgus Monkey
  4. Navigating Transporter Sciences in Pharmacokinetics Characterization Using the Extended Clearance Classification System
  5. Comparison of Proteomic Quantification Approaches for Hepatic Drug Transporters: Multiplexed Global Quantitation Correlates with Targeted Proteomic Quantitation
  6. Organic Anion Transporter 2 Mediates Hepatic Uptake of Tolbutamide, a CYP2C9 Probe Drug
  7. Molecular properties associated with transporter-mediated drug disposition
  8. Transporter-Mediated Disposition, Clinical Pharmacokinetics and Cholestatic Potential of Glyburide and Its Primary Active Metabolites
  9. Leveraging of Rifampicin-Dosed Cynomolgus Monkeys to Identify Bile Acid 3-O-Sulfate Conjugates as Potential Novel Biomarkers for Organic Anion-Transporting Polypeptides
  10. Hepatobiliary Clearance Prediction: Species Scaling From Monkey, Dog, and Rat, and In Vitro–In Vivo Extrapolation of Sandwich-Cultured Human Hepatocytes Using 17 Drugs
  11. Reliable Rate Measurements for Active and Passive Hepatic Uptake Using Plated Human Hepatocytes
  12. Quantitative Prediction of Human Renal Clearance and Drug-Drug Interactions of Organic Anion Transporter Substrates Using In Vitro Transport Data: A Relative Activity Factor Approach
  13. IVIVE of drug transporters and addressing challenges
  14. Unbound tissue exposure (Kpuu) of oatps substrates in the cynomolgus monkey
  15. Projecting ADME Behavior and Drug-Drug Interactions in Early Discovery and Development: Application of the Extended Clearance Classification System
  16. Evaluation and Quantitative Prediction of Renal Transporter-Mediated Drug-Drug Interactions
  17. Transporter-Enzyme Interplay: Deconvoluting Effects of Hepatic Transporters and Enzymes on Drug Disposition Using Static and Dynamic Mechanistic Models
  18. Hepatic Disposition of Gemfibrozil and Its Major Metabolite Gemfibrozil 1-O-β-Glucuronide
  19. Predicting Clearance Mechanism in Drug Discovery: Extended Clearance Classification System (ECCS)
  20. Quantitative Rationalization of Gemfibrozil Drug Interactions: Consideration of Transporters-Enzyme Interplay and the Role of Circulating Metabolite Gemfibrozil 1-O-β-Glucuronide
  21. Dealing with the complex drug-drug interactions: Towards mechanistic models
  22. Transporters in Drug Discovery
  23. Prediction of Pharmacokinetics and Drug–Drug Interactions When Hepatic Transporters are Involved
  24. In vitroandin vivoapproaches to characterize transporter-mediated disposition in drug discovery
  25. Clearance Mechanism Assignment and Total Clearance Prediction in Human Based upon in Silico Models
  26. Mechanism-Based Pharmacokinetic Modeling to Evaluate Transporter-Enzyme Interplay in Drug Interactions and Pharmacogenetics of Glyburide
  27. Quantitative Prediction of Renal Transporter-Mediated Clinical Drug–Drug Interactions
  28. Quantitative assessment of the contribution of sodium-dependent taurocholate co-transporting polypeptide (NTCP) to the hepatic uptake of rosuvastatin, pitavastatin and fluvastatin
  29. Development and evaluation of novel solid nanodispersion system for oral delivery of poorly water-soluble drugs
  30. Intestinal Targeting of Drugs: Rational Design Approaches and Challenges
  31. High Specificity in Response of the Sodium-Dependent Multivitamin Transporter to Derivatives of Pantothenic Acid
  32. Response to the Comment on the Article “Physiologically Based Modeling of Pravastatin Transporter-Mediated Hepatobiliary Disposition and Drug-Drug Interactions”
  33. Model-based approaches to predict drug–drug interactions associated with hepatic uptake transporters: preclinical, clinical and beyond
  34. Mechanistic Modeling to Predict the Transporter- and Enzyme-Mediated Drug-Drug Interactions of Repaglinide
  35. Pharmacokinetics and Toxicokinetics in Drug Discovery and Development
  36. Physiologically Based Modeling of Pravastatin Transporter-Mediated Hepatobiliary Disposition and Drug-Drug Interactions
  37. Preclinical Pharmacokinetics: Industrial Perspective
  38. pH-Dependent Solubility and Permeability Criteria for Provisional Biopharmaceutics Classification (BCS and BDDCS) in Early Drug Discovery
  39. Impact of drug transporter pharmacogenomics on pharmacokinetic and pharmacodynamic variability – considerations for drug development
  40. Oral Absorption, Intestinal Metabolism and Human Oral Bioavailability
  41. Optimizing PK properties of cyclic peptides: the effect of side chain substitutions on permeability and clearance
  42. Development of a new permeability assay using low‐efflux MDCKII cells
  43. Full efficacy with no CNS side-effects: unachievable panacea or reality? DMPK considerations in design of drugs with limited brain penetration
  44. pH-Sensitive Interaction of HMG-CoA Reductase Inhibitors (Statins) with Organic Anion Transporting Polypeptide 2B1
  45. Targeting Intestinal Transporters for Optimizing Oral Drug Absorption
  46. Editorial [Hot topic: Role of Intestinal Transporters and Metabolism in the Oral Absorption of Drugs and Prodrugs (Guest Editor: Manthena V. Varma)]
  47. Renal clearance in drug discovery and development: molecular descriptors, drug transporters and disease state
  48. The Intestinal Absorption of a Prodrug of the mGlu2/3 Receptor Agonist LY354740 is Mediated by PEPT1: In Situ Rat Intestinal Perfusion Studies
  49. Physicochemical Space for Optimum Oral Bioavailability: Contribution of Human Intestinal Absorption and First-Pass Elimination
  50. Physicochemical Determinants of Human Renal Clearance
  51. In Vivo Dissolution: Predominant Factor Affecting the Bioavailability of Rifampicin in its Solid Oral Dosage Forms
  52. Functional role of P-glycoprotein in limiting peroral drug absorption: optimizing drug delivery
  53. Feasibility studies on division of fixed dose combinations of anti-tubercular drugs: an improvement in the tuberculosis therapy
  54. pH-dependent functional activity of P-glycoprotein in limiting intestinal absorption of protic drugs: Kinetic analysis of quinidine efflux in situ
  55. In situ and in vivo efficacy of peroral absorption enhancers in rats and correlation to in vitro mechanistic studies
  56. Relationship between lipophilicity of BCS class III and IV drugs and the functional activity of peroral absorption enhancers
  57. Absorption enhancement, mechanistic and toxicity studies of medium chain fatty acids, cyclodextrins and bile salts as peroral absorption enhancers
  58. Prediction of in vivo intestinal absorption enhancement on P-glycoprotein inhibition, from rat in situ permeability
  59. Enhanced oral paclitaxel absorption with vitamin E-TPGS: Effect on solubility and permeability in vitro, in situ and in vivo
  60. Influence of micro-environmental pH on the gel layer behavior and release of a basic drug from various hydrophilic matrices
  61. Functional Role of P-Glycoprotein in Limiting Intestinal Absorption of Drugs:  Contribution of Passive Permeability to P-Glycoprotein Mediated Efflux Transport
  62. pH-dependent functional activity of P-glycoprotein in limiting intestinal absorption of protic drugs
  63. Rapid and selective UV spectrophotometric and RP-HPLC methods for dissolution studies of oxybutynin immediate-release and controlled-release formulations
  64. Biopharmaceutic Classification System: A Scientific Framework for Pharmacokinetic Optimization in Drug Research
  65. RP-HPLC method and its validation for the determination of naloxone from a novel transdermal formulation
  66. Factors Affecting Mechanism and Kinetics of Drug Release from Matrix-Based Oral Controlled Drug Delivery Systems
  67. Chapter 9. Mechanistic Modelling to Predict Transporter-mediated Drug Disposition and Drug–Drug Interactions