Improving drug solubility for oral delivery using solid dispersions.
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Revealing facts behind spray dried solid dispersion technology used for solubility enhancementPolymorph Impact on the Bioavailability and Stability of Poorly Soluble DrugsDevelopment of micro-fibrous solid dispersions of poorly water-soluble drugs in sucrose using temperature-controlled centrifugal spinningPharmaceutical Cocrystals: Regulatory and Strategic Aspects, Design and DevelopmentA Novel Diphenylthiosemicarbazide Is a Potential Insulin Secretagogue for Anti-Diabetic AgenImproved dissolution and anti-inflammatory activity of ibuprofen-polyethylene glycol 8000 solid dispersion systemsMicroemulsions for oral administration and their therapeutic applicationsStability and Biological Activity Evaluation of Chlorantraniliprole Solid Nanodispersions Prepared by High Pressure HomogenizationEvaluation of Stability and Biological Activity of Solid Nanodispersion of Lambda-Cyhalothrin.Modulating Drug Release and Enhancing the Oral Bioavailability of Torcetrapib with Solid Lipid Dispersion Formulations.Downscaling drug nanosuspension production: processing aspects and physicochemical characterization.Evaluation of colloidal solid dispersions: physiochemical considerations and in vitro release profileAcyclic CB[n]-type molecular containers: effect of solubilizing group on their function as solubilizing excipients.Valproic acid-hydrophilic cyclodextrin complexes and valproic acid-solid dispersions: evaluation of their potential pharmaceutical use.New metastable form of glibenclamide prepared by redispersion from ternary solid dispersions containing polyvinylpyrrolidone-K30 and sodium lauryl sulfate.Investigating the Dissolution Performance of Amorphous Solid Dispersions Using Magnetic Resonance Imaging and Proton NMR.Acyclic Cucurbit[n]uril-Type Molecular Containers: Influence of Linker Length on Their Function as Solubilizing Agents.Characterization, Molecular Docking, and In Vitro Dissolution Studies of Solid Dispersions of 20(S)-Protopanaxadiol.Novel oral fast-disintegrating drug delivery devices with predefined inner structure fabricated by Three-Dimensional Printing.Enhanced bioavailability of apigenin via preparation of a carbon nanopowder solid dispersion.In-situ freeze-drying - forming amorphous solids directly within capsules: An investigation of dissolution enhancement for a poorly soluble drug.Design and mechanism of on-off pulsed drug release using nonenteric polymeric systems via pH modulation.An optimized commercially feasible milling technique for molecular encapsulation of meloxicam in β-cyclodextrin.Supersaturated dissolution data and their interpretation: the TPGS-carbamazepine model case.Electrospun solid dispersions of Maraviroc for rapid intravaginal preexposure prophylaxis of HIVEnhanced dissolution and stability of Tanshinone IIA base by solid dispersion system with nano-hydroxyapatiteEnhancing the bioavailability of magnolol in rabbits using melting solid dispersion with polyvinylpyrrolidone.In vitro and in vivo evaluation of amorphous solid dispersions generated by different bench-scale processes, using griseofulvin as a model compound.Acyclic cucurbit[n]uril-type molecular containers: influence of aromatic walls on their function as solubilizing excipients for insoluble drugs.Development of a mini-tablet of co-grinded prednisone-Neusilin complex for pediatric useNovel patchouli alcohol ternary solid dispersion pellets prepared by poloxamersImpact of polymer conformation on the crystal growth inhibition of a poorly water-soluble drug in aqueous solutionPreparation and pharmacokinetics evaluation of oral self-emulsifying system for poorly water-soluble drug Lornoxicam.Enhanced oral bioavailability of fenofibrate using polymeric nanoparticulated systems: physicochemical characterization and in vivo investigation.Acyclic cucurbit[n]uril-type molecular containers: influence of glycoluril oligomer length on their function as solubilizing agents.Molecular interaction studies of amorphous solid dispersions of the antimelanoma agent betulinic acidCoating solid dispersions on microneedles via a molten dip-coating method: development and in vitro evaluation for transdermal delivery of a water-insoluble drug.Amphotericin B delivery from bone cement increases with porosity but strength decreasesOne Polymorph and Various Morphologies of Phenytoin at a Silica Surface Due to Preparation KineticsSynthesis of a Disulfonated Derivative of Cucurbit[7]uril and Investigations of its Ability to Solubilize Insoluble Drugs.
P2860
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P2860
Improving drug solubility for oral delivery using solid dispersions.
description
2000 nî lūn-bûn
@nan
2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Improving drug solubility for oral delivery using solid dispersions.
@ast
Improving drug solubility for oral delivery using solid dispersions.
@en
type
label
Improving drug solubility for oral delivery using solid dispersions.
@ast
Improving drug solubility for oral delivery using solid dispersions.
@en
prefLabel
Improving drug solubility for oral delivery using solid dispersions.
@ast
Improving drug solubility for oral delivery using solid dispersions.
@en
P1476
Improving drug solubility for oral delivery using solid dispersions.
@en
P2093
P356
10.1016/S0939-6411(00)00076-X
P407
P577
2000-07-01T00:00:00Z