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Cellulose acetate microspheres prepared by o/w emulsification and solvent evaporation method
K S Soppimath1, A R Kulkarni, T M Aminabhavi
1Department of Chemistry, Polymer Research Group, Karnatak University, Dharwad 580 003, India.
Journal of Microencapsulation
|November 7, 2001
Summary
This study developed cellulose acetate microspheres for drug delivery using emulsification and solvent evaporation. Optimized parameters yielded high encapsulation efficiencies and controlled, non-Fickian drug release kinetics.
Area of Science:
- Materials Science
- Pharmaceutical Sciences
- Chemical Engineering
Background:
- Cellulose acetate microspheres are promising for drug delivery applications.
- Controlled release formulations require precise control over microsphere properties.
- Emulsification and solvent evaporation are key methods for microsphere fabrication.
Purpose of the Study:
- To develop and characterize cellulose acetate microspheres using the o/w emulsification and solvent evaporation method.
- To investigate the influence of process parameters on microsphere characteristics.
- To optimize the formulation for desired drug loading and release profiles.
Main Methods:
- Microsphere fabrication via oil-in-water (o/w) emulsification and solvent evaporation.
- Utilized polyvinyl alcohol as an emulsifying agent.
- Employed a 3^3 randomized full factorial design for parameter optimization.
- Analyzed particle size, drug loading capacity, and release kinetics.
Main Results:
- Achieved spherical microspheres with smooth surfaces and high encapsulation efficiencies (73-98%).
- Acetone in the oil phase significantly reduced particle size.
- Observed slow, non-Fickian drug release up to approximately 8 hours.
- Statistical analysis identified solvent composition and emulsifying agent concentration as key factors influencing drug release.
Conclusions:
- The developed cellulose acetate microspheres demonstrate potential for controlled drug delivery.
- Process parameters, particularly solvent composition and emulsifier concentration, significantly impact microsphere properties and drug release.
- Further optimization can tailor microsphere characteristics for specific pharmaceutical applications.