A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs.
about
Porous magnesium aluminometasilicate tablets as carrier of a cyclosporine self-emulsifying formulation.Absorption enhancement of adefovir dipivoxil by incorporating MCT and ethyl oleate complex oil phase in emulsion.Solid self-nanoemulsifying cyclosporin A pellets prepared by fluid-bed coating: preparation, characterization and in vitro redispersibility.Potentials of proniosomes for improving the oral bioavailability of poorly water-soluble drugs.Development and evaluation of a solid self-nanoemulsifying drug delivery system for loratadin by extrusion-spheronizationFormulation of nimodipine nanocrystals for oral administration.Microemulsions as drug delivery systems to improve the solubility and the bioavailability of poorly water-soluble drugs.Self-nanoemulsifying drug delivery systems: formulation insights, applications and advances.Lipid-based oral multiparticulate formulations - advantages, technological advances and industrial applications.Transforming lipid-based oral drug delivery systems into solid dosage forms: an overview of solid carriers, physicochemical properties, and biopharmaceutical performance.Formulation strategies to improve the bioavailability of poorly absorbed drugs with special emphasis on self-emulsifying systems.Self-microemulsifying drug delivery system (SMEDDS)--challenges and road ahead.Preclinical formulations: insight, strategies, and practical considerations.Physical stabilization of low-molecular-weight amorphous drugs in the solid state: a material science approach.Oral bioavailability: issues and solutions via nanoformulations.First in man bioavailability and tolerability studies of a silica-lipid hybrid (Lipoceramic) formulation: a Phase I study with ibuprofen.Controversies with self-emulsifying drug delivery system from pharmacokinetic point of view.Development of a solid self-microemulsifying drug delivery system (SMEDDS) for solubility enhancement of naproxen.Development, characterisation and evaluation of supersaturated triglyceride free drug delivery (s-TFDDS) of lornoxicam.Novel Solid Self-Nanoemulsifying Drug Delivery System (S-SNEDDS) for Oral Delivery of Olmesartan Medoxomil: Design, Formulation, Pharmacokinetic and Bioavailability Evaluation.A comparison between use of spray and freeze drying techniques for preparation of solid self-microemulsifying formulation of valsartan and in vitro and in vivo evaluation.Optimization, ex vivo permeation, and stability study of lipid nanocarrier loaded gelatin capsules for treatment of intermittent claudication.Development of Solid SEDDS, V: Compaction and Drug Release Properties of Tablets Prepared by Adsorbing Lipid-Based Formulations onto Neusilin® US2.Nebulized oil-in-water nanoemulsion mists for pulmonary delivery: development, physico-chemical characterization and in vitro evaluation.Enhanced oral bioavailability of etodolac by self-emulsifying systems: in-vitro and in-vivo evaluation.Calcium Alginate-Neusilin US2 Nanocomposite Microbeads for Oral Sustained Drug Delivery of Poor Water Soluble Drug Aceclofenac Sodium.Self-emulsifying drug delivery system and the applications in herbal drugs.Development of novel amisulpride-loaded solid self-nanoemulsifying tablets: preparation and pharmacokinetic evaluation in rabbits.Antimalarial solid self-emulsifying system for oral use: in vitro investigation.Development and Evaluation of Liquid and Solid Self-Emulsifying Drug Delivery Systems for Atorvastatin.In vitro digestion of the self-emulsifying lipid excipient Labrasol(®) by gastrointestinal lipases and influence of its colloidal structure on lipolysis rate.Design and development of SMEDDS for colon-specific drug delivery.Development of novel flurbiprofen-loaded solid self-microemulsifying drug delivery system using gelatin as solid carrier.Quality by design approach for oral bioavailability enhancement of irbesartan by self-nanoemulsifying tablets.Improvement of the bioavailability and glycaemic metabolism of cinnamon oil in rats by liquid loadable tablets.Preparation and Evaluation of Solid-Self-Emulsifying Drug Delivery System Containing Paclitaxel for Lymphatic DeliveryPreparation and Evaluation of Emamectin Benzoate Solid Microemulsion
P2860
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P2860
A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs.
description
2008 nî lūn-bûn
@nan
2008 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
A new solid self-microemulsify ...... of poorly water soluble drugs.
@ast
A new solid self-microemulsify ...... of poorly water soluble drugs.
@en
A new solid self-microemulsify ...... of poorly water soluble drugs.
@nl
type
label
A new solid self-microemulsify ...... of poorly water soluble drugs.
@ast
A new solid self-microemulsify ...... of poorly water soluble drugs.
@en
A new solid self-microemulsify ...... of poorly water soluble drugs.
@nl
prefLabel
A new solid self-microemulsify ...... of poorly water soluble drugs.
@ast
A new solid self-microemulsify ...... of poorly water soluble drugs.
@en
A new solid self-microemulsify ...... of poorly water soluble drugs.
@nl
P2093
P1476
A new solid self-microemulsify ...... of poorly water soluble drugs.
@en
P2093
Jiangling Wan
Xiangliang Yang
P304
P356
10.1016/J.EJPB.2008.05.001
P407
P577
2008-05-17T00:00:00Z