Influence of drug polarity upon the solid-state structure and release properties of self-emulsifying drug delivery systems in relation with water affinity.

No abstract is available for this paper.

• Publication year

  2009

• Venue

  Colloids and Surfaces B: Biointerfaces

• Publication date

  2009-06-01

• Fields of study

  Medicine, Materials Science, Chemistry

• Identifiers
  DOI 10.1016/j.colsurfb.2009.01.008PMID 19203864
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Oral lipid-based formulations.

  2007cited by this paper
• Influence of wettability and surface activity on release behavior of hydrophilic substances from lipid matrices.

  2007cited by this paper
• Importance of Surface Tension Characterization for Food, Pharmaceutical and Packaging Products: A Review

  2006cited by this paper
• Formulation of poorly water-soluble drugs for oral administration: physicochemical and physiological issues and the lipid formulation classification system.

  2006cited by this paper
• Wetting properties at the surface of iota-carrageenan-based edible films.

  2006cited by this paper
• Influence of cryogenic grinding on properties of a self-emulsifying formulation.

  2004cited by this paper
• Solubilization behavior of poorly soluble drugs with combined use of Gelucire 44/14 and cosolvent.

  2004cited by this paper
• Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs.

  2004cited by this paper
• Impact et étalement de micro-gouttes sur des substrats solides

  2003cited by this paper
• An investigation into the structure and bioavailability of alpha-tocopherol dispersions in Gelucire 44/14.

  2003cited by this paper
• Enhanced bioavailability of piroxicam using Gelucire 44/14 and labrasol: in vitro and in vivo evaluation.

  2003cited by this paper
• The influence of drug incorporation on the structure and release properties of solid dispersions in lipid matrices.

  2003cited by this paper
• The mechanisms of drug release from solid dispersions in water-soluble polymers.

  2002cited by this paper
• Preparation and in vitro characterization of a eutectic based semisolid self-nanoemulsified drug delivery system (SNEDDS) of ubiquinone: mechanism and progress of emulsion formation.

  2002cited by this paper
• Abstract of "ANALYSIS OF IMPACT OF DROPLETS ON HORIZONTAL SURFACES"

  2000cited by this paper
• Melt extrusion--an alternative method for enhancing the dissolution rate of 17beta-estradiol hemihydrate.

  2000cited by this paper
• Effect of the wettability characteristics of polyethylene glycol derivatives on the drug release of wax matrices.

  2000cited by this paper
• Enhanced absorption of indomethacin after oral or rectal administration of a self-emulsifying system containing indomethacin to rats.

  2000cited by this paper
• A New Method for Dissolution Studies of Lipid-Filled Capsules Employing Nifedipine as a Model Drug

  1999cited by this paper
• Powder dynamic contact angle data in the pharmaceutical industry.

  1999cited by this paper
• WETTABILITY OF DRUG LOADED POLYMER MATRICES

  1998cited by this paper
• Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine

  1998cited by this paper
• A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in Vitro Drug Product Dissolution and in Vivo Bioavailability

  1995cited by this paper

• Development of Gel-in-Oil Emulsions for Khellin Topical Delivery

  2020cites this paper
• Fat content and storage conditions are key factors on the partitioning and activity of carvacrol in antimicrobial packaging

  2020cites this paper
• Sistemas de entrega de fármacos autoemulsificables: una plataforma de desarrollo alternativa para la industria farmacéutica colombiana

  2019cites this paper
• Dissolution and bioavailability enhancement of Atorvastatin: Gelucire semi-solid binary system

  2018cites this paper
• Development of rectal self-emulsifying suspension of a moisture-labile water-soluble drug.

  2018cites this paper
• Evolution of the Microstructure of Sustained-release Matrix Tablets during Dissolution and Storage

  2018cites this paper
• Development and evaluation of self-nanoemulsifying drug delivery systems for oral delivery of indomethacin

  2018cites this paper
• Self-emulsifying delivery systems: one step ahead in improving solubility of poorly soluble drugs

  2017cites this paper
• Size characterization of commercial micelles and microemulsions by Taylor dispersion analysis.

  2015cites this paper
• Preparation and study of naproxen in silica and lipid/polymer hybrid composites

  2014cites this paper
• Polyoxylglycerides and glycerides: effects of manufacturing parameters on API stability, excipient functionality and processing.

  2014cites this paper
• A Gelucire 44/14 and labrasol based solid self emulsifying drug delivery system: formulation and evaluation

  2013cites this paper
• Evaluation of lipid-based formulations of poorly water-soluble drugs in the gastro-intestinal tract using in vitro tests

  2011cites this paper
• Lauroyl polyoxylglycerides, functionalized coconut oil, enhancing the bioavailability of poorly soluble active substances

  2009influential citation
• Self-emulsifying drug delivery systems (SEDDS): formulation development, characterization, and applications.

  2009cites this paper