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    eBook

    Contributors: Gonzalez-Alvarez, Maria Isabel, Dahan, Arik

    Subject Terms: bioequivalence, Biopharmaceutics Classification System, in vitro, dissolution test, pravastatin, oral absorption, in silico modeling, GastroPlus, Phoenix WinNonlin, pharmacokinetics, clinical studies, ibuprofen, manometry, gastrointestinal, mechanistic modeling, PBPK, PBBM, disintegration, dissolution, enteric-coated, ICH, quality control, regional intestinal permeability, permeation enhancers, absorption-modifying excipients, oral peptide delivery, intestinal perfusion, pharmaceutical development, controlled release drug product, biopharmaceutics classification system, drug solubility, drug permeability, location-dependent absorption, segregated flow intestinal model (SFM), traditional model (TM), route-dependent intestinal metabolism, first-pass effect, drug-drug interactions, DDI, in vitro in vivo extrapolations, IVIVE, zero-order absorption, first-order absorption, combined zero- and first-order absorption, transit compartment absorption model, in situ perfusion, microdevices, shape, mucoadhesion, colon absorption, nutrient digestion, nutrient absorption, gastrointestinal hormone, postprandial glycaemia, energy intake, region of the gut, obesity, type 2 diabetes, Franz–PAMPA, BCS drugs, biomimetic membrane, Franz cell, passive drug transport, BCS class IV drugs, segmental-dependent intestinal permeability, intestinal absorption, oral drug delivery, biopharmaceutics, physiologically-based pharmacokinetic (PBPK) modeling, furosemide, intestinal permeability, human colon carcinoma cell layer (Caco-2), hierarchical support vector regression (HSVR), drug absorption, drug solubility/dissolution, regional/segmental-dependent permeability and absorption, Medicine and Nursing, Manufacturing industries

    File Description: image/jpeg

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    eBook

    Contributors: Song, Im-Sook

    Subject Terms: tofacitinib, dose-dependent pharmacokinetics, hepatic and intestinal first-pass effect, rats, catalposide, in vitro human metabolism, UDP-glucuronosyltransferase, sulfotransferase, carboxylesterase, celecoxib, drug–drug interaction, fluorescence, HPLC, metabolism, repaglinide, HSG4112, anti-obesity agent, stereoselectivity, pharmacokinetics, compound K, protopanaxadiol (PPD), biliary excretion, intestinal metabolism, Carthamus tinctorius extract, notoginseng total saponins, comparative pharmacokinetic study, large volume direct injection, compatibility mechanism, mertansine, human hepatocytes, cytochrome P450, UDP-glucuronosyltransferases, sodium-glucose cotransporter 2 (SGLT2) inhibitors, DWP16001, kidney distribution, inhibition mode, diabetes, transporter-enzyme interplay, influx transporter, efflux transporter, physiologically based pharmacokinetic model, cytochrome P450 enzymes, tiropramide, healthy Korean subjects, modeling, population pharmacokinetic, quercetin, breast cancer resistance protein, inhibitor, prazosin, sulfasalazine, kinetic analysis, food–drug interactions, Caco-2, EpiIntestinal, first-pass, P-gp, BCRP, drug transporter, CYP3A4, oral availability, automatization, drug absorption, drug dosing, head-and-neck cancer, real-time measurements, taxanes, tissue engineering, UHPLC-MS/MS, metformin, verapamil, drug interaction, organic cation transporter 2, renal excretion, acute renal failure, gentamicin, cisplatin, hepatic CYP3A1(23), creatinine clearance, renal clearance, nonrenal clearance, Medicine and Nursing, Manufacturing industries

    File Description: image/jpeg

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    Academic Journal

    Contributors: Konvalinka, Jan [Academy of Sciences of the Czech Republic (ASCR), Prague (Czech Republic). Gilead Sciences and IOCB Research Centre. Inst. of Organic Chemistry and Biochemistry; Charles Univ., Prague (Czech Republic). Dept. of Biochemistry]

    Source: Journal of Biological Chemistry; 290; 18

    File Description: Medium: ED; Size: p. 11321-11336

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