Estimating drug solubility in the gastrointestinal tract.
about
Statistical comparison of dissolution profiles to predict the bioequivalence of extended release formulations.The use of betaine HCl to enhance dasatinib absorption in healthy volunteers with rabeprazole-induced hypochlorhydria.The role of turmerones on curcumin transportation and P-glycoprotein activities in intestinal Caco-2 cells.Application of prodrugs to inflammatory diseases of the gut.Predicting pharmacokinetics of drugs using physiologically based modeling--application to food effectsPopulation-based mechanistic prediction of oral drug absorptionReview: physical chemistry of solid dispersions.Gastric emptying of non-disintegrating solid drug delivery systems in fasted state: relevance to drug dissolution.Biomagnetic methods: technologies applied to pharmaceutical research.Biorelevant in-vitro performance testing of orally administered dosage forms.Critical gases for critical issues: CO2 technologies for oral drug delivery.Polymeric micelles for oral drug administration enabling locoregional and systemic treatments.Computational-Regulatory Developments in the Prediction of Oral Drug Absorption.Release characteristics of quetiapine fumarate extended release tablets under biorelevant stress test conditions.The In Vitro Lipolysis of Lipid-Based Drug Delivery Systems: A Newly Identified Relationship between Drug Release and Liquid Crystalline Phase.Statistical investigation of simulated fed intestinal media composition on the equilibrium solubility of oral drugsProduction of advanced solid dispersions for enhanced bioavailability of itraconazole using KinetiSol Dispersing.Simulated food effects on drug release from ethylcellulose: PVA-PEG graft copolymer-coated pellets.Establishment of in vitro-in vivo equivalence of highly variable drugs - a generic product development perspective.Understanding pharmacokinetic food effects using molecular dynamics simulation coupled with physiologically based pharmacokinetic modeling.Prediction of Phase I single-dose pharmacokinetics using recombinant cytochromes P450 and physiologically based modelling.Statistical investigation of the full concentration range of fasted and fed simulated intestinal fluid on the equilibrium solubility of oral drugs.Dual Level Statistical Investigation of Equilibrium Solubility in Simulated Fasted and Fed Intestinal Fluid.The role of particle size of glyburide crystals in improving its oral absorption.Predicting Oral Drug Absorption: Mini Review on Physiologically-Based Pharmacokinetic Models.The apparent solubilizing capacity of simulated intestinal fluids for poorly water-soluble drugs.Structure-Activity Relationships of the Main Bioactive Constituents of Euodia rutaecarpa on Aryl Hydrocarbon Receptor Activation and Associated Bile Acid Homeostasis.Cocrystal of Ibuprofen⁻Nicotinamide: Solid-State Characterization and In Vivo Analgesic Activity Evaluation.
P2860
Q33803999-65E174DD-FF59-4BB8-B36A-E651374E2127Q35318395-CAFDFC6B-BF7D-408C-A4E7-A2D2C66155F5Q35765642-079A1B3E-CF8C-4FD2-81A4-26F1FC76C40DQ37096512-073FCC23-6665-4631-A163-0D235AEA5817Q37149095-A144CB9A-0835-4ED2-8120-6CA4F09C22DCQ37214520-2647378E-C68B-4BC9-9C17-224F0E41D874Q37643840-24C42F28-A230-4BF6-A31E-7FA130D472B6Q37768454-99AC3092-FEE1-420E-840B-0B9C55F693CDQ37800414-7C2441F9-4736-44F3-9237-96E820531DA9Q38017705-5477B3AA-6629-4415-BC5A-87CFD2FE7F08Q38183855-FEDB119E-0385-44C5-AC65-55DEEFEA7E07Q38250152-8D4D553B-00C8-49DF-BB1A-BE01E01847DCQ38910818-72ED4B0E-0577-4AA7-A0DD-B90155EF84DEQ41904421-B53BABFE-4F75-4176-A1C1-6E117FAB81D6Q42178278-67B0FEB8-8FC6-448F-8970-893A961EBE0EQ42321064-5C980020-5338-49A5-802A-D024F477ADBBQ43119931-67527DDF-7384-409C-A151-AD2A4EAABD2BQ43277956-76A6FCA8-00F5-4C1B-B004-C3EFF6EA8BE9Q44912878-896793D8-F764-492E-8104-FE3D8B33E679Q45667088-E5F7508E-E7C2-47A3-8E91-0144519E7AB9Q46183071-10A55C07-3FF9-453A-AAB2-3736E80BC152Q47139757-24A6D1B1-10D7-44A4-974A-C9D1BEFA2853Q47145238-6B73EC5E-2BA7-4AAB-B197-1E12BBFE5BC3Q47224401-80B915E3-C615-479D-820F-0847CC3316D6Q47338381-1DD9B4D6-04A5-49C8-A5D6-C165E88BCC3EQ51405119-4A648B2B-3F83-45B9-9FE2-F6DBF2F65979Q52691794-D8AC94B0-706E-41D1-9B6F-3B13C992F1B3Q55424195-39DD7E5A-B36E-40BC-A41D-9B4207198696
P2860
Estimating drug solubility in the gastrointestinal tract.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Estimating drug solubility in the gastrointestinal tract.
@en
type
label
Estimating drug solubility in the gastrointestinal tract.
@en
prefLabel
Estimating drug solubility in the gastrointestinal tract.
@en
P2093
P1476
Estimating drug solubility in the gastrointestinal tract.
@en
P2093
P304
P356
10.1016/J.ADDR.2007.05.009
P407
P577
2007-05-29T00:00:00Z