Keywords: جذب دهانی; ALT; alanine aminotransferase; ANOVA; analysis of variance; CCl4; carbon tetrachloride; COX-2; cyclooxygenase-2; DLS; dynamic light scattering; ESI; electrospray ionization; GI; gastrointestinal; 6G; 6-gingerol; 8G; 8-gingerol; GE; ginger extract; HPMC; h
مقالات ISI جذب دهانی (ترجمه نشده)
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Keywords: جذب دهانی; solubility; dissolution; permeability; oral absorption; species difference; dog; BCS; Fa; fraction of oral dose absorbed; Fah; Fa in humans; Fad; Fa in dogs; kel; elimination rate constant; Do; dose number; MAD; maximum absorbable dose; BW; body weight; F
Keywords: جذب دهانی; AUC; area under the plasma concentration-time curve; BCS; biopharmaceutics classification system; FFA; fenofibric acid; FFB; fenofibrate; HCO40; NIKKOL HCO-40; HCO60; NIKKOL HCO-60; HPLC; high performance liquid chromatography; M1944; Labrafil® M 1944CS;
Keywords: جذب دهانی; A to BA; pical to Basolateral; ANOVA; Analysis of variance; AUC; Area under the curve; B to A; Basolateral to Apical; BA; Bioavailability; CL; Clearance; CMC; Carboxymethyl cellulose; DMSO; Dimethyl sulfoxide; ER; Extraction ratio; FDA; Food and Drug Admi
Keywords: جذب دهانی; solubility; in silico modeling; micelle; oral absorption; phospholipids;
Keywords: جذب دهانی; anti-infectives; bioavailability; clinical pharmacokinetics; formulation; oral absorption; pharmacokinetics; HCV; hepatitis C virus; GT; genotype; DAA; direct-acting antiviral; RBV; ribavirin; GLE; glecaprevir; PIB; pibrentasvir; Cmax; maximum plasma conc
Keywords: جذب دهانی; Human gastric emptying; Bioavailability; Gastrointestinal mass transport model; Bioequivalence; Aspiration/motility study; Phenol red; Paromomycin; In vivo dissolution; Oral absorption; Nonabsorbable marker; Gastrointestinal;
Keywords: جذب دهانی; Oral absorption; Paediatrics; Physiologically based pharmacokinetics; Bioavailability; Absorption rate;
Keywords: جذب دهانی; dissolution; high throughput technology(s); oral absorption; Biopharmaceutics Classification System (BCS); formulation; in vitro model(s); permeation enhancers(s); solubility; supersaturation;
Keywords: جذب دهانی; clinical pharmacokinetics; distribution; hepatic clearance; in vitro-in vivo correlations (IVIVC); metabolic clearance; oral absorption; physiological model; preclinical pharmacokinetics; protein binding; simulations;
Keywords: جذب دهانی; Sex difference; Excipients; Polyoxyethylene polymers; Polyethylene glycol 400; Multi drug resistance protein 1 (MDR1; Ciclosporin A; Bioavailability; Oral absorption;
Keywords: جذب دهانی; Ion pair; Oral absorption; Partition coefficient; Alendronate; Membrane permeability; Arginine;
Keywords: جذب دهانی; in silico modeling; disposition; formulation; gastrointestinal; mathematical model; oral drug delivery; oral absorption; physiologically based pharmacokinetic modeling;
Keywords: جذب دهانی; Antiviral agents; Prodrugs; Chemical synthesis; Stability; Biodisposition; Oral absorption; Pharmacology; Toxicology;
Keywords: جذب دهانی; Oral absorption; Size effect; Silica nanoparticles; Intestinal transport; Interaction; Food component; Surface interaction;
Keywords: جذب دهانی; oral drug delivery; biopharmaceutics; clinical pharmacokinetics; gastrointestinal; oral absorption; bioequivalence; disposition;
Keywords: جذب دهانی; Pulmonary drug delivery; Large porous particles; Poly(lactic/glycolic) acid (PLGA PLA); Lung metabolism; Controlled release/delivery; Oral absorption;
Keywords: جذب دهانی; SNEDDS; Food effect; Low soluble compounds; Humans; Enabling formulations; Oral absorption; Cinnarizine
Keywords: جذب دهانی; nanotechnology; oral drug delivery; drug transport; dissolution; physical characterization; stabilization; bioavailability; oral absorption; pharmacokinetics; pharmacodynamics;
Keywords: جذب دهانی; Biopharmaceutics Classification System (BCS); bioequivalence; excipients; oral absorption; permeability; cimetidine; acyclovir; ANDA; Abbreviated New Drug Application; BCS; biopharmaceutics classification system; BE; bioequivalence; HPMC; hydroxypropyl me
Keywords: جذب دهانی; oral drug delivery; gastrointestinal transit; Biopharmaceutics Classification System; oral absorption; ADME; in vitro models; in vitro/in vivo correlations;
Keywords: جذب دهانی; pharmacokinetics; physiologically based pharmacokinetic modeling; absorption; food effects; oral absorption; particle size;
Keywords: جذب دهانی; amorphous; poorly water soluble drugs; formulation; solid dispersion; flubendazole; spray drying; ordered mesoporous silica; oral absorption; filarial disease; ACN; acetonitrile; API; active pharmaceutical ingredient; AUC; area under the curve; Cmax; maxi
Keywords: جذب دهانی; Cyclodextrins; Risk analysis; Pharmacokinetics; Modelling; Fraction absorbed; Oral absorption; Rats;
Keywords: جذب دهانی; Saquinavir; Fexofenadine; Cremophor EL; P-gp; Oral absorption
Keywords: جذب دهانی; Oral absorption; Solubility; Inter-subject variability; Humans; Gastrointestinal fluids
Keywords: جذب دهانی; Glyburide; Paroxetine; Oral absorption; Intestinal transport; Caco-2 cells; Pharmacokinetics; Organic anion transporting polypeptides
Keywords: جذب دهانی; biopharmaceutics classification system; gastrointestinal; luminal volume; oral absorption; osmolality; passive diffusion; permeability
Keywords: جذب دهانی; clinical study; microdose; cassette dose; Nonlinear pharmacokinetics; bioavailability; first-pass metabolism; dose proportionality; oral absorption
Keywords: جذب دهانی; Drug delivery; Amorphous state; Sustained release; Oral absorption; Cytotoxicity;
Keywords: جذب دهانی; Oral absorption; Insulin; Cell-penetrating peptide; Penetratin; Intermolecular interaction; Caco-2 cells;
Keywords: جذب دهانی; cocrystals; food effects; oral absorption; supersaturation; physicochemical properties; preformulation; solubility; surfactants; mathematical model; poorly water-soluble drugs;
Keywords: جذب دهانی; intestinal absorption; salt selection; bioequivalence; biopharmaceutics classification system (BCS); in silico modeling; dissolution; food effects; formulation; gastrointestinal transit; oral absorption
Keywords: جذب دهانی; ADME; bioavailability; biopharmaceutics classification system (BCS); clinical pharmacokinetics; clearance; formulation; oral absorption; physiological model; preclinical pharmacokinetics; solubility
Keywords: جذب دهانی; Solid lipid nanoparticles; Nanostructured lipid carriers; Oxyresveratrol; Oral absorption;
Keywords: جذب دهانی; Everolimus; Solid dispersion; Oral absorption; Stability; Solvent wetting technique;
Keywords: جذب دهانی; DAMPA, double artificial membrane permeation assay; DMSO, dimethylsulfoxide; D/P system, dissolution/permeation system; PAMPA, parallel artificial membrane permeation assay; PC, egg-phosphatidylcholineArtificial membrane; Permeability; Oral absorption; Hu
Keywords: جذب دهانی; Amlodipine free base; Orally disintegrating tablets; Coated dextrin microcapsules; Spray drying; Oral absorption
Keywords: جذب دهانی; absorption; tablet; bioequivalence; dissolution; formulation; gels; oral absorption; solid dosage form; solubility; surfactants;
Keywords: جذب دهانی; bioequivalence; metabolite; parent drug; pharmacokinetics; pharmacodynamics; losartan potassium; metabolism; bioavailability; oral absorption; ADME;
Keywords: جذب دهانی; dual asymmetric centrifugation; lipogelosomes; archae; imaging methods; oral absorption; proteins; liposomes; permeation enhancers;
Keywords: جذب دهانی; ADME; absorption, distribution, metabolism and excretion; A(O)EL; Acceptable (Operator) Exposure Level; BMDL; lower 95% confidence limit of the benchmark dose; HLV; Human Limit Value; MoS; Margin of Safety; NOAEL; No-Observed-Adverse-Effect-Level; OEL; Oc
Keywords: جذب دهانی; Taste masking; Biorelevant dissolution; Oral absorption; Pharmacokinetics; Biopharmaceutics; Paediatric;
Keywords: جذب دهانی; Human intestinal fluid; Simulated intestinal fluid; Oral absorption; Solubility; Jejunal solubility; Duodenal solubility;
Keywords: جذب دهانی; bioavailability; dissolution rate; excipients; formulation; oral drug delivery; oral absorption; physicochemical properties; physical stability; tablet; solid dispersion;
Keywords: جذب دهانی; alginate; formulation; drug delivery; hydrogels; gastroretention; physicochemical properties; oral absorption;
Keywords: جذب دهانی; oral absorption; simulations; drug effects; pharmacokinetics; permeability;
Keywords: جذب دهانی; BCS; Fraction absorbed; Oral absorption; Heterogeneous; Variability;
Biopharmaceutical Characterization and Oral Efficacy of a New Rapid Acting Antidepressant Ro 25-6981
Keywords: جذب دهانی; oral absorption; caco-2 cells; gastrointestinal; permeability; CYP enzymes; microsomes; in vitro models; in silico modeling; metabolism; physicochemical;
Application of an In Vitro Dissolution/Permeation System to Early Screening of Oral Formulations of Poorly Soluble, Weakly Basic Drugs Containing an Acidic pH-Modifier
Keywords: جذب دهانی; oral absorption; Biopharmaceutics Classification System (BCS); dissolution; permeability; in vitro/in vivo correlations (IVIVC);