Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
about
Design and evaluation of self-microemulsifying drug delivery system (SMEDDS) of tacrolimusRole of Components in the Formation of Self-microemulsifying Drug Delivery SystemsInvestigations of a novel self-emulsifying osmotic pump tablet containing carvedilol.Development of silymarin self-microemulsifying drug delivery system with enhanced oral bioavailabilitySelf-nanoemulsifying drug delivery system of cefpodoxime proxetil containing tocopherol polyethylene glycol succinate.Design and evaluation of a self-microemulsifying drug delivery system for apigenin.Preparation and evaluation of SEDDS and SMEDDS containing carvedilol.Preparation and evaluation of self-microemulsifying drug delivery systems (SMEDDS) containing atorvastatin.Application of mixture experimental design to simvastatin apparent solubility predictions in the microemulsifion formed by self-microemulsifying.Clinical studies with oral lipid based formulations of poorly soluble compoundsPreparation and evaluation of self-microemulsifying drug delivery system containing vinpocetine.Paclitaxel in self-micro emulsifying formulations: oral bioavailability study in mice.Fabrication of lipidic nanocarriers of loratadine for facilitated intestinal permeation using multivariate design approach.Interest of multifunctional lipid excipients: case of Gelucire 44/14.A novel self-microemulsifying formulation of paclitaxel for oral administration to patients with advanced cancer.Development of self-nanoemulsifying drug delivery systems for the enhancement of solubility and oral bioavailability of fenofibrate, a poorly water-soluble drug.Microemulsions as novel drug carriers: the formation, stability, applications and toxicity.Preparation and evaluation of self-nanoemulsifying tablets of carvedilol.Self-microemulsifying drug-delivery system for improved oral bioavailability of 20(S)-25-methoxyl-dammarane-3β, 12β, 20-triol: preparation and evaluation.New perspectives on lipid and surfactant based drug delivery systems for oral delivery of poorly soluble drugs.Self-nanoemulsifying drug delivery systems: formulation insights, applications and advances.Role of excipients in successful development of self-emulsifying/microemulsifying drug delivery system (SEDDS/SMEDDS).Isoflavones: estrogenic activity, biological effect and bioavailability.Formulation strategies for drug delivery of tacrolimus: An overview.Formulation strategies to improve the bioavailability of poorly absorbed drugs with special emphasis on self-emulsifying systems.Enhancing the buccal mucosal delivery of peptide and protein therapeutics.Self-nano-emulsifying drug delivery systems: an update of the biopharmaceutical aspects.Self-assembled structures formed during lipid digestion: characterization and implications for oral lipid-based drug delivery systems.Transdermal solid delivery of epigallocatechin-3-gallate using self-double-emulsifying drug delivery system as vehicle: Formulation, evaluation and vesicle-skin interaction.Novel dietary lipid-based self-nanoemulsifying drug delivery systems of paclitaxel with p-gp inhibitor: implications on cytotoxicity and biopharmaceutical performance.Self-Microemulsifying Drug Delivery Systems: An Attractive Strategy for Enhanced Therapeutic Profile.Development and evaluation of self-microemulsifying liquid and granule formulations of Brucea javanica oil.Preparation and bioavailability assessment of SMEDDS containing valsartan.Solid self-microemulsifying formulation for candesartan cilexetil.Formulation studies of InhA inhibitors and combination therapy to improve efficacy against Mycobacterium tuberculosis.Structural aspects of digestion of medium chain triglycerides studied in real time using sSAXS and Cryo-TEM.Design of lipid-based formulations for oral administration of poorly water-soluble drug fenofibrate: effects of digestion.Rice germ oil as multifunctional excipient in preparation of self-microemulsifying drug delivery system (SMEDDS) of tacrolimus.Design and evaluation of self-nanoemulsifying pellets of repaglinide.The studies of phase equilibria and efficiency assessment for self-emulsifying lipid-based formulations.
P2860
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P2860
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
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
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
@ast
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
@en
type
label
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
@ast
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
@en
prefLabel
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
@ast
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
@en
P1476
Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs.
@en
P2093
P304
P356
10.1016/S0939-6411(00)00089-8
P407
P577
2000-07-01T00:00:00Z