Keywords: تعامل دارو و دارو; Stroke; Antiepileptic drugs; Drug-drug interaction; Statins; Calcium channel blockers; Anticoagulants; AED; antiepileptic drug; EIAED; enzyme-inducer AED; NEIAED; non-EIAED; CCB; calcium-channel blocker; NOAC; non-vitamin K antagonist oral anticoagulant;
مقالات ISI تعامل دارو و دارو (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: تعامل دارو و دارو; Therapeutic drug monitoring; Venlafaxine; Quetiapine; Drug-drug interaction; CYP3A4;
Keywords: تعامل دارو و دارو; Integrated action crossing; Machine learning; Drug-drug interaction; Non-communicable disease;
Keywords: تعامل دارو و دارو; Valsartan; Population pharmacokinetics; Drug-drug interaction; Fixed-dose combination; NONMEM;
Keywords: تعامل دارو و دارو; ADAM; advanced dissolution, absorption, and metabolism; AED; antiepileptic drug; AUC; area-under-the-curve; B/P; blood to plasma ratio; BID; twice daily; BMI; body mass index; CBZ; carbamazepine; CLint; intrinsic clearance; CLR; renal clearance; CL; clear
Keywords: تعامل دارو و دارو; Rhein; Rhein acyl glucuronide; Methotrexate; Organic anion transporter; Drug-drug interaction; AUC; area under the plasma time-concentration curve; ES; estrone sulfate; HBSS; Hank's balanced salt solution; HEK293; human embryonic kidney 293; IS; internal
Keywords: تعامل دارو و دارو; Drug-drug interaction; Functional similarity; Interaction prediction; Computational pharmacology;
Keywords: تعامل دارو و دارو; plasma protein binding; fraction unbound; drug-drug interaction; AUC; area under the curve; AUCR; area under the curve ratio; AAG; alpha 1-acid glycoprotein; CYP; cytochrome P450; BSA; bovine serum albumin; CRO; contract research organization; CV; coeffic
Keywords: تعامل دارو و دارو; BSA; bovine serum albumin; CYP; cytochrome P450; DDI; drug-drug interaction; DME; drug metabolizing enzyme; GST; glutathione-S-transferase; HLM; human liver microsomes; HSA; human serum albumin; NAT; N-acetyltransferase; NSAID; non-steroidal anti-inflamma
Keywords: تعامل دارو و دارو; Drug-drug interaction; Adverse drug reaction; Causality; Association rule;
Effect of Panax notoginseng saponins on the pharmacokinetics of aspirin in rats
Keywords: تعامل دارو و دارو; Aspirin; Panax notoginseng saponins; Drug-drug interaction; Pharmacokinetic; Transport;
Keywords: تعامل دارو و دارو; physiologically based pharmacokinetic modeling; drug interactions; Monte Carlo; in vitro-in vivo correlations (IVIVC); nonlinear regression; biliary excretion; biliary recycling; hepatic metabolism; hepatic transport; AUC; area under the curve of concen
Keywords: تعامل دارو و دارو; structure property relationships; molecular modeling; organic anion-transporting polypeptide transporters; drug interactions; 2D; two dimensional; 3D; three dimensional; DDI; drug-drug interaction; HEK cells; human embryonic kidney cells; IC50; inhibition
Keywords: تعامل دارو و دارو; Micropatterned fibrous mats; Hepatocyte coculture; Hepatocyte spheroid; Drug metabolism; Drug-drug interaction
Keywords: تعامل دارو و دارو; drug-drug interaction; pharmacodynamics; pharmacokinetics; selexipag; warfarin;
Keywords: تعامل دارو و دارو; AAV; Adeno associated virus; ABC; ATP-binding cassette; ACMG; American College Medical Genetics; AH; Ancestral Haplotype; ASL; airway surface liquid; ATP; Adenosine triphosphate; cas; CRISPR associated; CF; Cystic fibrosis; CFTR; Cystic Fibrosis Transmemb
Keywords: تعامل دارو و دارو; Drug-drug interaction; Erlotinib; Phenytoin;
Keywords: تعامل دارو و دارو; drug-drug interaction; finasteride; healthy subjects; pharmacokinetics; tamsulosin hydrochloride;
Identification of second-generation P2X3 antagonists for treatment of pain
Keywords: تعامل دارو و دارو; P2X3; Pain; UGT1A1; Drug-drug interaction; Purinergic receptor;
Inhibition of CYP3A by Antimalarial Piperaquine and Its Metabolites in Human Liver Microsomes With IVIV Extrapolation
Keywords: تعامل دارو و دارو; piperaquine; CYP inhibition; drug-drug interaction;
Co-administration with simvastatin or lovastatin alters the pharmacokinetic profile of sinomenine in rats through cytochrome P450-mediated pathways
Keywords: تعامل دارو و دارو; RA; rheumatoid arthritis; CV; cardiovascular; CYP enzyme; cytochrome P450 enzyme; DDI; drug-drug interaction; RLMs; rat liver microsomes; IS; internal standard; Sinomenine (PubChem CID: 5459308); Simvastatin (PubChem CID: 54454); Lovastatin (PubChem CID:
Effect of aspirin on the pharmacokinetics and absorption of panax notoginseng saponins
Keywords: تعامل دارو و دارو; Panax notoginseng saponins; Aspirin; Drug-drug interaction; Pharmacokinetic; Transport;
Celecoxib is a substrate of CYP2D6: Impact on celecoxib metabolism in individuals with CYP2C9*3 variants
Keywords: تعامل دارو و دارو; Celecoxib; CYP2C9; CYP2D6; Drug-drug interaction; Genetic polymorphism; Hydroxy celecoxib;
Modulation of the interaction between human P450 3A4 and B. megaterium reductase via engineered loops
Keywords: تعامل دارو و دارو; Cytochrome P450 3A4; Chimeric enzymes; Molecular lego; Drug-drug interaction;
A Physiologically Based Pharmacokinetic Modeling Approach to Predict Drug-Drug Interactions of Buprenorphine After Subcutaneous Administration of CAM2038 With Perpetrators of CYP3A4
Keywords: تعامل دارو و دارو; buprenorphine; drug-drug interaction; physiologically based pharmacokinetics; ketoconazole; rifampin;
Repeated administration of Sailuotong, a fixed combination of Panax ginseng, Ginkgo biloba, and Crocus sativus extracts for vascular dementia, alters CYP450 activities in rats
Keywords: تعامل دارو و دارو; Sailuotong; Panax ginseng; Ginkgo biloba; Crocus sativus; CYP450; Herb-drug interaction; Abbreviation: SLT; Sailuotong; VD; vascular dementia; TCM; traditional Chinese medicines; DDI; drug-drug interaction; CYP450; cytochrome P450; SPE; solid phase extrac
OAT1 and OAT3 also mediate the drug-drug interaction between piperacillin and tazobactam
Keywords: تعامل دارو و دارو; Piperacillin/tazobactam; Beta-lactamase inhibitor; Transporter; Organic anion transporters; Drug-drug interaction; Kidney;
LC-MS/MS assay for assessing medical adherence in patients under warfarin maintenance therapy
Keywords: تعامل دارو و دارو; Warfarin dose adjustment; Therapeutic drug monitoring; Drug-drug interaction; Patient compliance;
Ribociclib shows potential for pharmacokinetic drug-drug interactions being a substrate of ABCB1 and potent inhibitor of ABCB1, ABCG2 and CYP450 isoforms in vitro
Keywords: تعامل دارو و دارو; 95%CI; 95% confidential interval; AB; apical-to-basolateral; ABC; ATP-binding cassette; Abcb1; canine P-glycoprotein; ABCB1; human P-glycoprotein; ABCC1; multidrug resistance-associated protein 1; ABCG2; breast cancer resistance protein; BA; basolateral-t
Characterization of CYP2C Induction in Cryopreserved Human Hepatocytes and Its Application in the Prediction of the Clinical Consequences of the Induction
Keywords: تعامل دارو و دارو; cytochrome P450; mathematical models; hepatocytes; drug-drug interaction; induction; CAR; constitutive androstane receptor; CITIO; 6-(4-clorophenyl) imidazo[2,1-b][1,3]thiazole-5-carbaldehyde O-(3,4-dichlorobenzyl)oxime; P450; cytochrome P450; DDI; drug-d
The inhibitory effects of eighteen front-line antibiotics on the substrate uptake mediated by human Organic anion/cation transporters, Organic anion transporting polypeptides and Oligopeptide transporters in in vitro models
Keywords: تعامل دارو و دارو; SLCs; Solute Carrier transporters; CCK-8; Cholecystokinin octapeptide; ES; estrone-3-sulfate; PAH; 4-aminohippuric acid; MPPÂ +; Â methyl-4-phenylpyridinium acetate; Gly-Sar; glycyl-sarcosine; MTX; methotrexate; Front-line antibiotics; Organic anion/catio
Cell cultures in drug discovery and development: The need of reliable in vitro-in vivo extrapolation for pharmacodynamics and pharmacokinetics assessment
Keywords: تعامل دارو و دارو; 3Rs; Reduction, Replacement, Refinement; PBPK; physiologically based pharmacokinetic; 2D; two-dimensional; 3D; three-dimensional; HTS; high-throughput screening; IVIVE; in vitro-in vivo extrapolation; ADME; absorption, distribution, metabolism and excreti
Imaging techniques to study drug transporter function in vivo
Keywords: تعامل دارو و دارو; ABC; ATP-binding cassette; AD; Alzheimer's disease; ADME; absorption, distribution, metabolism and elimination; ATP; adenosine triphosphate; AUC; area under the curve; BBB; blood-brain barrier; BCRP; breast cancer resistance protein; BPND; non-displaceabl
Association of CYP2B6 gene polymorphisms and anti-tuberculosis drug-induced hepatotoxicity in a Chinese population
Keywords: تعامل دارو و دارو; TB; tuberculosis; ADR; adverse drug reaction; ATDH; Anti-TB drug-induced hepatotoxicity; DDI; drug-drug interaction; HIV; human immunodeficiency virus; NAT2; N-acetyltransferase 2; CYP; cytochrome P450; GST; glutathione S-transferase; ALT; alanine aminotr
Prediction of renal transporter-mediated drug-drug interactions for a drug which is an OAT substrate and inhibitor using PBPK modelling
Keywords: تعامل دارو و دارو; AUC; area under the curve; DDI; drug-drug interaction; fu; fraction unbound; IC50; inhibition constant; IV; intravenous; IVIVE; in vitro/in vivo extrapolation; Ki; inhibition constant; OAT; organic anion transporter; PBPK; physiologically based pharmacoki
In vitro to in vivo extrapolation of the complex drug-drug interaction of bupropion and its metabolites with CYP2D6; simultaneous reversible inhibition and CYP2D6 downregulation
Keywords: تعامل دارو و دارو; Drug-drug interactions; CYP2D6; Bupropion; Enzyme regulation; In vitro to in vivo extrapolation; AUC; area under plasma concentration time curve; CYP; cytochrome P450; DDI; drug-drug interaction; fm; fraction metabolized; IVIVE; in vitro to in vivo extrap
Studies of CDK 8/19 inhibitors: Discovery of novel and selective CDK8/19 dual inhibitors and elimination of their CYP3A4 time-dependent inhibition potential
Keywords: تعامل دارو و دارو; ADME; absorption, distribution, metabolism, and excretion; AML; acute myelogenous leukemia; AUC; area under the blood concentration time curve; b.i.d.; twice a day; CDK; Cyclin-dependent kinase; CLtotal; clearance; Cmax; maximum drug concentration; CRC; c
Effects of 6-paradol, an unsaturated ketone from gingers, on cytochrome P450-mediated drug metabolism
Keywords: تعامل دارو و دارو; 6-Paradol; Unsaturated ketone; Ginger; CYP inhibition; Drug-drug interaction;
Evaluation of Drug-Drug Interaction Potential Between Sacubitril/Valsartan (LCZ696) and Statins Using a Physiologically Based Pharmacokinetic Model
Keywords: تعامل دارو و دارو; physiologically based pharmacokinetic modeling; transporters; statin; absorption; organic anion-transporting polypeptide; drug-drug interaction; AUC; area under the plasma concentration-time curve; Cmax; maximum plasma concentration; CLint,T; transporter-
Current In Vitro Methods to Determine Hepatic Kpuu: A Comparison of Their Usefulness and Limitations
Keywords: تعامل دارو و دارو; active transport; passive diffusion/transport; hepatic metabolism; biliary excretion; distribution; disposition; tissue partition; protein binding; hepatocytes; human liver microsomes; ABT; 1-aminobenzotriazole; AFE; average fold error; CLint; intrinsic c
Simulations of Cytochrome P450 3A4-Mediated Drug-Drug Interactions by Simple Two-Compartment Model-Assisted Static Method
Keywords: تعامل دارو و دارو; bioavailability; cytochrome P450; drug interaction; dynamic simulation; first pass metabolism; hepatic clearance; intestinal metabolism; pharmacokinetics; simulations; parallel tube model; Ae (Ae,oral); dose fractions of urinary excreted unchanged drug af
Pretreatment With Rifampicin and Tyrosine Kinase Inhibitor Dasatinib Potentiates the Inhibitory Effects Toward OATP1B1- and OATP1B3-Mediated Transport
Keywords: تعامل دارو و دارو; drug transport; drug interactions; organic anion-transporting polypeptide transporters; hepatocytes; hepatic transport; pharmacokinetics; physiologically based pharmacokinetic modeling; AUC; area under the plasma concentration-time curve; CsA; cyclosporin
IMI - oral biopharmaceutics tools project - evaluation of bottom-up PBPK prediction success part 1: Characterisation of the OrBiTo database of compounds
Keywords: تعامل دارو و دارو; API; active pharmaceutical ingredient; AUC; area under the curve; BCS; biopharmaceutics classification system; BP; blood-to-plasma ratio; Cmax; maximum concentration; CL; clearance; Do; dose number according to BCS; DDI; drug-drug interaction; EFPIA; Euro
Quantitative Analyses of the Influence of Parameters Governing Rate-Determining Process of Hepatic Elimination of Drugs on the Magnitudes of Drug-Drug Interactions via Hepatic OATPs and CYP3A Using Physiologically Based Pharmacokinetic Models
Keywords: تعامل دارو و دارو; cytochrome P450; drug interaction; hepatic clearance; mathematical model; organic anion-transporting polypeptide transporters; pharmacokinetics; AUC; area under the plasma concentration-time curve; CL; clearance; CLint,all; overall hepatic intrinsic cle
Phase 1b Study of Abiraterone Acetate Plus Prednisone and Docetaxel in Patients with Metastatic Castration-resistant Prostate Cancer
Keywords: تعامل دارو و دارو; Abiraterone acetate; Androgen receptor; Docetaxel; Combination; Drug-drug interaction; Metastatic castration-resistant prostate cancer; Pharmacokinetics; Safety; Toxicity;
Imaging the impact of cyclosporin A and dipyridamole on P-glycoprotein (ABCB1) function at the blood-brain barrier: A [11C]-N-desmethyl-loperamide PET study in nonhuman primates
Keywords: تعامل دارو و دارو; Drug-drug interaction; Stress-test; BBB; Positron emission tomography; Radiochemistry;
Clinical Exposure Boost Predictions by Integrating Cytochrome P450 3A4-Humanized Mouse Studies With PBPK Modeling
Keywords: تعامل دارو و دارو; clinical pharmacokinetics; CYP enzymes; drug interaction; drug metabolizing enzymes; elimination; hepatic clearance; interspecies scaling; physiologically based pharmacokinetic modeling; preclinical pharmacokinetics; simulations; AUC; area under the plasm
Coupling Data Mining and Laboratory Experiments to Discover Drug Interactions Causing QT Prolongation
Keywords: تعامل دارو و دارو; data mining; data science; drug-drug interaction; long QT syndrome; APD70; action potential duration at 70% of repolarization; DDI; drug-drug interaction; ECG; electrocardiogram; EHR; electronic health records; FAERS; Food and Drug Administration adverse
Simultaneous determination of itraconazole, hydroxy itraconazole, keto itraconazole and N-desalkyl itraconazole concentration in human plasma using liquid chromatography with tandem mass spectrometry
Keywords: تعامل دارو و دارو; LC-MS; Human plasma; Itraconazole; Hydroxy itraconazole; Keto itraconazole; N-desalkyl itraconazole; Drug-drug interaction;
Characterization of Long-Lasting Oatp Inhibition by Typical Inhibitor Cyclosporine A and In Vitro-In Vivo Discrepancy in Its Drug Interaction Potential in Rats
Keywords: تعامل دارو و دارو; drug interactions; in vitro/in vivo correlations; pharmacokinetics; protein binding; transporters; CYP enzymes; hepatocytes; organic anion-transporting polypeptide transporters; multidrug resistance transporters; solute transporters; ABT; 1-aminobenzotr