Literature DB >> 11404040

A comparison of alternative polymer excipients and processing methods for making solid dispersions of a poorly water soluble drug.

E Broman1, C Khoo, L S Taylor.   

Abstract

Solid dispersions were prepared with the extremely poorly water soluble drug, probucol and the water soluble polymers, polyvinyl pyrrolidone (PVP), polyacrylic acid (PAA) or polyethylene oxide (PEO) and blends of these polymers. The solid dispersions were prepared either by the solvent evaporation method, or by compression moulding into films. The materials were characterised by a combination of thermal analysis and FT-Raman spectroscopy. The physical state of the drug was observed to be dependent on the carrier, thus the PVP solid dispersions contained amorphous probucol, whilst the PAA and PEO systems contained the crystalline polymorph II. The method of production was not found to greatly influence the state of the drug in the solid dispersion. The greatest extent of release into solution was observed for the binary blend of drug and PEO, and the blending of polymers was not found to have any advantageous effects in this study.

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Year:  2001        PMID: 11404040     DOI: 10.1016/s0378-5173(01)00709-8

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  17 in total

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5.  Theoretical and practical approaches for prediction of drug-polymer miscibility and solubility.

Authors:  Patrick J Marsac; Sheri L Shamblin; Lynne S Taylor
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6.  Molecular interaction among probucol/PVP/SDS multicomponent system investigated by solid-state NMR.

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Journal:  Pharm Res       Date:  2006-09-13       Impact factor: 4.200

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Journal:  Pharm Res       Date:  2006-08-23       Impact factor: 4.200

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

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Journal:  AAPS PharmSciTech       Date:  2008-12-31       Impact factor: 3.246

9.  Evaluation of drug load and polymer by using a 96-well plate vacuum dry system for amorphous solid dispersion drug delivery.

Authors:  Po-Chang Chiang; Yingqing Ran; Kang-Jye Chou; Yong Cui; Amy Sambrone; Connie Chan; Ryan Hart
Journal:  AAPS PharmSciTech       Date:  2012-05-05       Impact factor: 3.246

10.  Dissolution enhancement of glibenclamide by solid dispersion: solvent evaporation versus a supercritical fluid-based solvent -antisolvent technique.

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Journal:  Res Pharm Sci       Date:  2014 Sep-Oct
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