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Floating Microspheres for Famotidine Release

The document summarizes a study that prepared floating microspheres using famotidine (FM) as a model drug. The microspheres were made using solvent evaporation with acrycoat S100 and cellulose acetate polymers. The microspheres were characterized based on their size, morphology, drug release kinetics, and effects of preparation parameters. The microspheres exhibited prolonged drug release over 18 hours and floating for over 12 hours. Higher polymer concentration increased microsphere size and decreased drug release rate. Stirring rate during preparation did not significantly affect drug release. In vitro studies showed diffusion-controlled drug release from the microspheres.

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5 views2 pages

Floating Microspheres for Famotidine Release

The document summarizes a study that prepared floating microspheres using famotidine (FM) as a model drug. The microspheres were made using solvent evaporation with acrycoat S100 and cellulose acetate polymers. The microspheres were characterized based on their size, morphology, drug release kinetics, and effects of preparation parameters. The microspheres exhibited prolonged drug release over 18 hours and floating for over 12 hours. Higher polymer concentration increased microsphere size and decreased drug release rate. Stirring rate during preparation did not significantly affect drug release. In vitro studies showed diffusion-controlled drug release from the microspheres.

Uploaded by

nenavathkumar
Copyright
© Attribution Non-Commercial (BY-NC)
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd

Abstract  

The present study involves preparation and evaluation of floating microspheres using
famotidine (FM) as a model drug for prolongation of the gastric retention time. The
microspheres were prepared by the solvent evaporation method using different
polymers, i.e. acrycoat S100 and cellulose acetate. The size or average diameter
(d avg ) and surface morphology of the prepared microspheres were recognized and
characterized by the optical and scanning electron microscopic methods,
respectively. In vitro drug release studies were performed and the drug release
kinetics were evaluated using the linear regression method. Effects of the stirring
rate during preparation, polymer concentration on the size of the microspheres and
drug release were also observed. The prepared microspheres exhibited prolonged
drug release (18 h) and remained buoyant for more than 12 h. The mean particle
size increased and the drug release rate decreased at a higher polymer
concentration. No significant effect of the stirring rate during preparation on drug
release was observed. In vitro studies demonstrated a diffusion-controlled drug
release from the microspheres. The objective of the present study was to develop
floating microspheres of FM in order to achieve an extended retention in the upper
gastrointestinal tract, which may result in enhanced absorption and thereby improved
bioavailability. The prepared microspheres were evaluated for particle size, in
vitro release and buoyancy and incorporation efficiency. The effect of various
formulation variables on the size and drug release was investigated. In vitro drug
release studies were performed and the drug release kinetics were evaluated using
the linear regression method. FM was obtained as a gift sample from Intas
Pharmaceuticals, Ahmedabad, India. Polyvinyl alcohol was obtained from S.D. Fine
Chemicals Ltd., Mumbai, India. Dichloromethane, acrycoat S100, cellulose acetate
and Tween 80 were obtained from Central Drug House (P) Ltd., Delhi, India. All
other chemicals/reagents used were of analytical grade. A UV/visible
spectrophotometer was used for drug analysis. Experimental results were expressed
as mean ΁ SD. Chi-square test and one-way analysis of variance (ANOVA) were
applied to check significant differences in drug release from different formulations.
Differences were considered to be statistically significant at P = 3.23, DF = 1, i.e. P <
0.05. The prepared floating microspheres exhibited prolonged drug release, i.e. <18
h, and the floating time was <12 h in 0.1 N HCl. The mean particle size of the
prepared floating microspheres increased but the drug release rate from the
microspheric-coated layer decreased as the polymer concentration increased. No
significant effect of the stirring rate during preparation on drug release was
observed. In vitro data obtained for floating microspheres of FM showed excellent
floatability, good buoyancy and prolonged drug release. Microspheres of different
size and drug content could be obtained by varying the formulation variables.
Diffusion was found to be the main release mechanism. Thus, the prepared floating
microspheres may prove to be potential candidates for multiple-unit delivery devices
adaptable to any intragastric condition.

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