Studies on the in vitro release characteristics of ibuprofen-loaded polystyrene microparticles.

Abstract:

:Ibuprofen-loaded polystyrene microparticles were prepared by the emulsion-solvent evaporation process from an aqueous system. The effects of different parameters on the drug content and on the release of the drug from the microparticles were investigated. The drug content, in all the formulations, was less than the theoretical drug loading. The lower drug content was due to drug partitioning to the external aqueous phase during formulation. Statistical analysis revealed that the variation in the concentrations of the emulsion stabilizer and the organic disperse phase volume did not significantly alter the release of the drug. Although an increase in drug loading increased drug release from the microparticles, a biphasic linear relationship was observed between the time required for 50% drug release and the drug loading. The effect of size of the microparticles on drug release was more important for the low drug-loaded microparticles than that for the high drug-loaded microparticles. Such release behaviour from the microparticles was explained on the basis of the morphological structure of the microparticles.

journal_name

J Microencapsul

authors

Tamilvanan S,Sa B

doi

10.1080/026520400288553

subject

Has Abstract

pub_date

2000-01-01 00:00:00

pages

57-67

issue

1

eissn

0265-2048

issn

1464-5246

journal_volume

17

pub_type

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