Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract.
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Surface tension in human pathophysiology and its application as a medical diagnostic toolEnhancement of Loperamide Dissolution Rate by Liquisolid Compact TechniqueMechanistic approaches to predicting oral drug absorption.Insulin-loaded nanoparticles based on N-trimethyl chitosan: in vitro (Caco-2 model) and ex vivo (excised rat jejunum, duodenum, and ileum) evaluation of penetration enhancement properties.Understanding peroral absorption: regulatory aspects and contemporary approaches to tackling solubility and permeability hurdlesRavuconazole self-emulsifying delivery system: in vitro activity against Trypanosoma cruzi amastigotes and in vivo toxicity.Absorption Study of Genistein Using Solid Lipid Microparticles and Nanoparticles: Control of Oral Bioavailability by Particle SizesThe use of biorelevant dissolution media to forecast the in vivo performance of a drug.Nanomedicine in GIA novel domperidone hydrogel: preparation, characterization, pharmacokinetic, and pharmacodynamic properties.Recent advances in lipid nanoparticle formulations with solid matrix for oral drug delivery.Effect of ingested lipids on drug dissolution and release with concurrent digestion: a modeling approach.Liquisolid Tablets for Dissolution Enhancement of a Hypolipidemic Drug.Styrene maleic acid micelles as a nanocarrier system for oral anticancer drug delivery - dual uptake through enterocytes and M-cells.Superiority of liquid crystalline cubic nanocarriers as hormonal transdermal vehicle: comparative human skin permeation-supported evidence.Development and Evaluation of Novel Self-Nanoemulsifying Drug Delivery Systems Based on a Homolipid from Capra hircus and Its Admixtures with Melon Oil for the Delivery of IndomethacinControlled Drug Delivery: Historical perspective for the next generation.Supercritical fluid technology for enhanced drug delivery.Influence of simulated gastrointestinal conditions on particle-induced cytotoxicity and interleukin-8 regulation in differentiated and undifferentiated Caco-2 cells.Recent progress in the computational prediction of aqueous solubility and absorption.Release mechanisms for polyelectrolyte capsules.Prediction of human pharmacokinetics--gastrointestinal absorption.Impact of physiological, physicochemical and biopharmaceutical factors in absorption and metabolism mechanisms on the drug oral bioavailability of rats and humans.In vitro models for processes involved in intestinal absorption.Development of self-nanoemulsifying drug delivery systems for the enhancement of solubility and oral bioavailability of fenofibrate, a poorly water-soluble drug.Drug nanoparticles: formulating poorly water-soluble compounds.Polymeric micelles and alternative nanonized delivery vehicles for poorly soluble drugs.Styrene maleic acid-encapsulated paclitaxel micelles: antitumor activity and toxicity studies following oral administration in a murine orthotopic colon cancer model.Development of prednisone:polyethylene glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters.The pros and cons of polyelectrolyte capsules in drug delivery.Population Pharmacokinetic Modeling To Estimate the Contributions of Genetic and Nongenetic Factors to Efavirenz Disposition.A biorelevant dissolution stress test device - background and experiences.Advances in gastro retentive drug-delivery systems.Solid dispersions, part I: recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs.Models for oral uptake of nanoparticles in consumer products.Crystalline nanosuspensions as potential toxicology and clinical oral formulations for BCS II/IV compounds.Inorganic matrices: an answer to low drug solubility problem.In vitro-in vivo extrapolation (IVIVE) for predicting human intestinal absorption and first-pass elimination of drugs: principles and applications.Advances in dissolution instrumentation and their practical applications.Microenvironmental pH-modification to improve dissolution behavior and oral absorption for drugs with pH-dependent solubility.
P2860
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P2860
Influence of physicochemical properties on dissolution of drugs in the gastrointestinal tract.
description
2001 nî lūn-bûn
@nan
2001 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մարտին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Influence of physicochemical p ...... in the gastrointestinal tract.
@ast
Influence of physicochemical p ...... in the gastrointestinal tract.
@en
Influence of physicochemical p ...... in the gastrointestinal tract.
@nl
type
label
Influence of physicochemical p ...... in the gastrointestinal tract.
@ast
Influence of physicochemical p ...... in the gastrointestinal tract.
@en
Influence of physicochemical p ...... in the gastrointestinal tract.
@nl
prefLabel
Influence of physicochemical p ...... in the gastrointestinal tract.
@ast
Influence of physicochemical p ...... in the gastrointestinal tract.
@en
Influence of physicochemical p ...... in the gastrointestinal tract.
@nl
P1476
Influence of physicochemical p ...... in the gastrointestinal tract.
@en
P2093
J B Dressman
P356
10.1016/S0169-409X(00)00130-7
P407
P577
2001-03-01T00:00:00Z