Literature DB >> 8445510

Formulation and evaluation of vinylpyrrolidone/vinylacetate copolymer microspheres with griseofulvin.

D Vojnovic1, F Rubessa, M Bogataj, A Mrhar.   

Abstract

Regular spherical microspheres of 220-260 microns average size have been prepared from vinylpyrrolidone/vinylacetate copolymer using a solvent evaporation method. Griseofulvin has been incorporated into these microspheres and its physical characterization has been carried out by differential scanning calorimetry (DSC), X-ray diffractometry and X-ray photoelectron spectroscopy. An increase of solubility was observed only with the 1:3 drug/polymer microspheres and the comparison of the dissolution profiles of microspheres with pure griseofulvin resulted in an enhancing effect. Furthermore the release rate of griseofulvin, incorporated into the microspheres, was shown to be biphasic and dependent upon the penetration of water into the microspheres, hydration and dissolution of the polymer and finally dissolution of the drug.

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Year:  1993        PMID: 8445510     DOI: 10.3109/02652049309015315

Source DB:  PubMed          Journal:  J Microencapsul        ISSN: 0265-2048            Impact factor:   3.142


  2 in total

1.  Formulation of controlled release microspheres containing nicardipine: the role of pharmacokinetic modeling and computer simulation.

Authors:  A Mrhar; M Bogataj; I Grabnar; R Karba
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1999 Jan-Mar       Impact factor: 2.569

2.  Influence of the Encapsulation Efficiency and Size of Liposome on the Oral Bioavailability of Griseofulvin-Loaded Liposomes.

Authors:  Sandy Gim Ming Ong; Long Chiau Ming; Kah Seng Lee; Kah Hay Yuen
Journal:  Pharmaceutics       Date:  2016-08-26       Impact factor: 6.321

  2 in total

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