Literature DB >> 9725467

Preparation and dissolution rate of gliquidone-PVP K30 solid dispersions.

P Martnez1, M M Goñi, R G Cantera, C Martin, C Dios-Viéitez, C Martínez-Ohárriz.   

Abstract

Solid dispersions of gliquidone in PVP K30 were prepared by the solvent method. These dispersions were characterized using X-ray diffraction. In comparison with the drug alone, the physical mixtures and even more the solid dispersions showed an increase in the dissolution rate. Moreover these solid dispersions were stable during storage.

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Year:  1998        PMID: 9725467     DOI: 10.1007/BF03189325

Source DB:  PubMed          Journal:  Eur J Drug Metab Pharmacokinet        ISSN: 0378-7966            Impact factor:   2.441


  5 in total

1.  Biopharmaceutical aspects of the tolbutamide-beta-cyclodextrin inclusion compound.

Authors:  J L Vila-Jato; J Blanco; J J Torres
Journal:  Farmaco Prat       Date:  1988-02

2.  Inclusion complex of acetohexamide with beta-cyclodextrin and its hypoglycemic activity in rabbit.

Authors:  K Uekama; N Matsuo; F Hirayama; T Yamaguchi; Y Imamura; H Ichibagase
Journal:  Chem Pharm Bull (Tokyo)       Date:  1979-02       Impact factor: 1.645

Review 3.  Pharmaceutical applications of solid dispersion systems.

Authors:  W L Chiou; S Riegelman
Journal:  J Pharm Sci       Date:  1971-09       Impact factor: 3.534

4.  Combined water-soluble carriers for coprecipitates of tolbutamide.

Authors:  M J Miralles; J W McGinty; A Martin
Journal:  J Pharm Sci       Date:  1982-03       Impact factor: 3.534

5.  Improved holder for intrinsic dissolution rate studies.

Authors:  J Wood; J Syarto; H Letterman
Journal:  J Pharm Sci       Date:  1965-07       Impact factor: 3.534

  5 in total

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