Literature DB >> 17136760

Effect of characteristics of compounds on maintenance of an amorphous state in solid dispersion with crospovidone.

Yusuke Shibata1, Makiko Fujii, Makiko Kokudai, Shinobu Noda, Hideko Okada, Masuo Kondoh, Yoshiteru Watanabe.   

Abstract

Solid dispersion (SD) of indomethacin with crospovidone (CrosPVP) shows useful characteristics for preparation of dosage forms. This study aimed to determine the types of drugs that could adopt a stable amorphous form in SD. Twenty compounds with various melting points (70-218 degrees C), molecular weights (135-504) and functional groups (amide, amino, carbonyl, hydroxyl, ketone etc.) were prepared in SD with CrosPVP. The CrosPVP SDs were prepared using a mechanical mixing and heating method. Melting point and molecular weight were found to have no influence on the ability of a compound to maintain an amorphous state in SD. All compounds containing hydrogen-bond-donor functional groups existed in an amorphous state in SD for at least 6 months. Infrared spectra suggested an interaction between the functional groups of these compounds and amide carbonyl group of CrosPVP. Compounds without hydrogen-bond-donor groups could not maintain an amorphous state and underwent recrystallization within 1 month. It was suggested that the presence of a hydrogen-bond-donor functional group in a compound is an important factor affecting the stable formation of SD with CrosPVP, which contains a hydrogen-bond acceptor.

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Year:  2007        PMID: 17136760     DOI: 10.1002/jps.20794

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  4 in total

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3.  Use of Polyvinyl Alcohol as a Solubility-Enhancing Polymer for Poorly Water Soluble Drug Delivery (Part 1).

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Journal:  AAPS PharmSciTech       Date:  2015-12-04       Impact factor: 3.246

Review 4.  Crosslinked hydrogels-a promising class of insoluble solid molecular dispersion carriers for enhancing the delivery of poorly soluble drugs.

Authors:  Dajun D Sun; Ping I Lee
Journal:  Acta Pharm Sin B       Date:  2014-01-22       Impact factor: 11.413

  4 in total

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