Keywords: محاسباتی ADME; absorption; computational ADME; efflux pumps; in vitro models; organic cation transporters; P-glycoprotein; peptide transporters; pulmonary delivery/absorption; ABC transporters; organic anion-transporting polypeptide transporters; BAL; bronchoalveolar l
مقالات ISI محاسباتی ADME (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: محاسباتی ADME; in silico modeling; QSAR; transporters; computational ADME; high-throughput technologies; AUC; area under the curve; BCRP; breast cancer resistance protein; DDI; drug-drug interaction; fup; protein unbound fraction in plasma; ITC; International Transpor
Keywords: محاسباتی ADME; Solubility; High throughput technologies; Analytical chemistry; Computational ADME; In silico modeling; Computer aided drug design; ROC curve analysis;
Keywords: محاسباتی ADME; ADME; blood-brain barrier; computational ADME; drug transport; unbound brain-to-plasma concentration ratio; machine learning; in silico modeling;
Keywords: محاسباتی ADME; oxytetracycline; physiologically based pharmacokinetic (PBPK) modeling; dogs; tetracycline antibiotics; Food Animal Residue Avoidance Databank (FARAD); computational ADME; mathematical model; pharmacokinetics; in silico modeling; disposition;
Keywords: محاسباتی ADME; tissue partition; physicochemical properties; population pharmacokinetic/pharmacodynaMic Models; drug transport; active transport; QSPR; Monte Carlo; in silico Modeling; computational ADME; computational biology;
In Silico Prediction of hPXR Activators Using Structure-Based Pharmacophore Modeling
Keywords: محاسباتی ADME; PXR; cytochrome P450; computational ADME; induction; in silico modeling; molecular modeling;
Ion-Pairing Contribution to the Liposomal Transport of Topotecan as Revealed by Mechanistic Modeling
Keywords: محاسباتی ADME; structure-transport relationship; zwitterion; passive diffusion/transport; nanoparticles; mathematical model; liposomes; ion-pairing; controlled release; computational ADME; cancer;
Three-Dimensional Quantitative Structure-Activity Relationship Analysis for Human Pregnane X Receptor for the Prediction of CYP3A4 Induction in Human Hepatocytes: Structure-Based Comparative Molecular Field Analysis
Keywords: محاسباتی ADME; computational ADME; structure activity relationship (SAR); protein structure; QSAR; molecular modeling;
Hepatocyte Composition-Based Model as a Mechanistic Tool for Predicting the Cell Suspension: Aqueous Phase Partition Coefficient of Drugs in In Vitro Metabolic Studies
Keywords: محاسباتی ADME; distribution; hepatocytes; liver; metabolism; metabolic clearance; unbound fraction; computational ADME; in vitro-in vivo extrapolation; IVIVE; pharmacokinetics; PBPK modeling;
Toward a new paradigm for the efficient in vitro–in vivo extrapolation of metabolic clearance in humans from hepatocyte data
Keywords: محاسباتی ADME; hepatocytes; intrinsic clearance; unbound fraction; computational ADME; in vitro–in vivo extrapolation; in vitro–in vivo correlation; IVIVE; pharmacokinetics; physiologically based pharmacokinetics; PBPK modeling
In Vitro-In Vivo Extrapolation of Clearance: Modeling Hepatic Metabolic Clearance of Highly Bound Drugs and Comparative Assessment with Existing Calculation Methods
Keywords: محاسباتی ADME; disposition; microsomes; hepatic clearance; metabolic clearance; unbound fraction; computational ADME; in vitro-in vivo extrapolation; IVIVE; pharmacokinetics; PBPK modeling;
Prediction of Steady-State Volume of Distribution of Acidic Drugs by Quantitative Structure-Pharmacokinetics Relationships
Keywords: محاسباتی ADME; computational ADME; distribution; in silico modeling; multivariate analysis; pharmacokinetics; QSPR; steady-state volume of distribution (VDss);
Evolution of a Detailed Physiological Model to Simulate the Gastrointestinal Transit and Absorption Process in Humans, Part II: Extension to Describe Performance of Solid Dosage Forms
Keywords: محاسباتی ADME; modeling; simulation; prediction; gastrointestinal tract; absorption; dosage forms; pharmacokinetics; PBPK; dissolution; Computational ADME;
Quantitative structure-plasma protein binding relationships of acidic drugs
Keywords: محاسباتی ADME; protein binding; plasma protein binding (PPB); computational ADME; QSAR; fraction of unbound drug (fu); fu prediction; acidic drugs; complexation; drug design;
Comparative Assessment of In Vitro-In Vivo Extrapolation Methods used for Predicting Hepatic Metabolic Clearance of Drugs
Keywords: محاسباتی ADME; disposition; microsomes; clearance; unbound fraction; computational ADME; in vitro-in vivo extrapolation; in vitro-in vivo correlation; IVIVE; pharmacokinetics; PBPK modeling;
An Integrated Pharmacokinetic Model for the Influence of CYP3A4 Expression on the In Vivo Disposition of Lopinavir and Its Modulation by Ritonavir
Keywords: محاسباتی ADME; drug metabolizing enzymes; drug interactions; ADME; bioavailability; computational ADME; cytochrome P450;
QSAR Analysis of Blood-Brain Distribution: The Influence of Plasma and Brain Tissue Binding
Keywords: محاسباتی ADME; QSAR; in silico modeling; nonlinear regression; computational ADME; blood-brain barrier; CNS; passive diffusion; drug transport; plasma protein binding; tissue binding;
PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 4: Prediction of plasma concentration-time profiles in human from in vivo preclinical data by using the Wajima approach
Keywords: محاسباتی ADME; computational ADME; absorption; clearance; disposition; distribution; firstâtimeâinâhuman; allometry; QSAR; PBPK; pharmacokinetics;
PhRMA CPCDC initiative on predictive models of human pharmacokinetics, part 2: Comparative assessment of prediction methods of human volume of distribution
Keywords: محاسباتی ADME; volume of distribution at steady state; pharmacokinetics; protein binding; computational ADME; first-time-in-human; in vitro models; distribution; allometry;
Microsome composition-based model as a mechanistic tool to predict nonspecific binding of drugs in liver microsomes
Keywords: محاسباتی ADME; distribution; microsomes; clearance; metabolism; metabolic clearance; unbound fraction; computational ADME; in vitro-in vivo extrapolation; IVIVE; pharmacokinetics; PBPK modeling;
Evolution of a detailed physiological model to simulate the gastrointestinal transit and absorption process in humans, Part 1: Oral solutions
Keywords: محاسباتی ADME; modeling; simulation; prediction; gastrointestinal tract; absorption; pharmacokinetics; PBPK; computational ADME; mathematical models; oral absorption;
PhRMA CPCDC Initiative on Predictive Models of Human Pharmacokinetics, Part 1: Goals, Properties of the Phrma Dataset, and Comparison with Literature Datasets
Keywords: محاسباتی ADME; allometry; bioavailability; clearance; computational ADME; first-in-human; pharmacokinetics; oral absorption; PhRMA; PBPK; volume of distribution;
PHRMA CPCDC initiative on predictive models of human pharmacokinetics, part 5: Prediction of plasma concentration-time profiles in human by using the physiologicallyâbased pharmacokinetic modeling approach
Keywords: محاسباتی ADME; animal alternative; computational ADME; drug discovery; drug development; absorption; distribution; disposition; in vitro-in vivo correlation; pharmacokinetics; PBPK modeling;
Analysis of Nifedipine Absorption from Soft Gelatin Capsules Using PBPK Modeling and Biorelevant Dissolution Testing
Keywords: محاسباتی ADME; absorption; biorelevant media; computational ADME; dissolution; nifedipine; PBPK modeling; pharmacokinetics; PK-Sim; precipitation; solubility;
The Development and Validation of a Computational Model to Predict Rat Liver Microsomal Clearance
Keywords: محاسباتی ADME; clearance; computational ADME; QSAR; metabolism; in silico; modeling;
Ionization-Specific Prediction of Blood-Brain Permeability
Keywords: محاسباتی ADME; QSAR; in silico modeling; nonlinear regression; computational ADME; blood-brain barrier; drug transport; passive diffusion; permeability;
Prediction of Drug Tissue to Plasma Concentration Ratios Using a Measured Volume of Distribution in Combination With Lipophilicity
Keywords: محاسباتی ADME; physiochemical properties; tissue partition; computational ADME; pharmacokinetics; physiological model; distribution; preclinical pharmacokinetics; log P; clinical pharmacokinetics; ADME;
Pharmacokinetics in Drug Discovery
Keywords: محاسباتی ADME; absorption; toxicology; structure-activity relatioship (SAR); population pharmacokinetics; pharmacokinetic/pharmacodynamic models; computational ADME; biophysical models; biopharmaceutics classification system (BCS); bioequivalence; ADME;
Circulatory Transport and Capillary-Tissue Exchange as Determinants of the Distribution Kinetics of Inulin and Antipyrine in Dog
Keywords: محاسباتی ADME; computational ADME; nonlinear regression; pharmacokinetics; permeability; distributed model; blood flow; distribution; mathematical model; diffusion;
Quantitative structure–pharmacokinetic relationships for drug clearance by using statistical learning methods
Keywords: محاسباتی ADME; Clearance; Consensus models; Computational ADME; General regression neural network; k-nearest neighbour; QSAR; Support vector regression
Quantitative Structure-Pharmacokinetic Relationships for Drug Distribution Properties by Using General Regression Neural Network
Keywords: محاسباتی ADME; blood-brain barrier; computational ADME; distribution; general regression neural network; human serum albumin binding; milk-plasma distribution; pharmacokinetics;
Extrapolation of human pharmacokinetic parameters from rat, dog, and monkey data: Molecular properties associated with extrapolative success or failure
Keywords: محاسباتی ADME; clearance; distribution; preclinical pharmacokinetics; computational ADME; physicochemical properties; mean residence time;
An Evaluation of the Utility of Physiologically Based Models of Pharmacokinetics in Early Drug Discovery
Keywords: محاسباتی ADME; pharmacokinetics; physiological model; simulations; computational ADME; absorption; GastroPlus; drug discovery;