Literature DB >> 10071817

Thermal behavior and dissolution properties of naproxen from binary and ternary solid dispersions.

P Mura, M T Faucci, A Manderioli, G Bramanti, P Parrini.   

Abstract

Solid dispersions of 10% w/w naproxen (NAP) in poly(ethylene glycol) (PEG) (4000, 6000, or 20,000) as a carrier with or without incorporation of anionic (sodium dodecyl sulfate; SDS) or nonionic (Tween 80; Tw80) surfactant were prepared by the melting method. Physicochemical characteristics were determined by differential scanning calorimetry (DSC) and X-ray diffraction analysis. The results of dissolution studies showed that drug dissolution properties were better from ternary systems than from binary systems since in the former the wetting and solubilizing effects of surfactant and polymer were additive. No influence of the PEG molecular weight was found. The best performance given by anionic surfactant has been attributed to several factors, such as higher hydrophilicity, better solubilizing power, and most facile interaction with both drug and PEG. No important changes in solid-state characteristics or in drug dissolution properties were found after 30 months storage for dispersions with or without surfactant. Only a slight decrease in initial drug dissolution rate was observed at the highest concentration (10% w/w) of SDS.

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Year:  1999        PMID: 10071817     DOI: 10.1081/ddc-100102169

Source DB:  PubMed          Journal:  Drug Dev Ind Pharm        ISSN: 0363-9045            Impact factor:   3.225


  4 in total

1.  Dissolution improvement of high drug-loaded solid dispersion.

Authors:  Siriporn Okonogi; Satit Puttipipatkhachorn
Journal:  AAPS PharmSciTech       Date:  2006-06-02       Impact factor: 3.246

2.  Influence of Low-Molecular-Weight Excipients on the Phase Behavior of PVPVA64 Amorphous Solid Dispersions.

Authors:  Kristin Lehmkemper; Samuel O Kyeremateng; Matthias Degenhardt; Gabriele Sadowski
Journal:  Pharm Res       Date:  2018-01-05       Impact factor: 4.200

3.  A Novel Approach for Analyzing the Dissolution Mechanism of Solid Dispersions.

Authors:  Yuanhui Ji; Raphael Paus; Anke Prudic; Christian Lübbert; Gabriele Sadowski
Journal:  Pharm Res       Date:  2015-02-27       Impact factor: 4.200

4.  Co-solvent evaporation method for enhancement of solubility and dissolution rate of poorly aqueous soluble drug simvastatin: in vitro-in vivo evaluation.

Authors:  Priyanka Pandya; Surendra Gattani; Pankaj Jain; Lokesh Khirwal; Sanjay Surana
Journal:  AAPS PharmSciTech       Date:  2008-12-31       Impact factor: 3.246

  4 in total

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