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Evaluation of process parameters involved in chitosan microsphere preparation by the o/w/o multiple emulsion method
F Pavanetto1, P Perugini, B Conti
1Department of Pharmaceutical Chemistry, University of Pavia, Italy.
Journal of Microencapsulation
|November 1, 1996
Summary
This study prepared hydrophobic drug-loaded microspheres using a multiple emulsion technique with chitosan. Key variables like acetic acid concentration and drug-polymer ratio influenced microsphere characteristics and drug content.
Area of Science:
- Biopolymer science
- Materials science
- Pharmaceutical technology
Background:
- Chitosans are versatile biopolymers with significant potential in medical and pharmaceutical applications.
- Developing effective drug delivery systems for hydrophobic drugs remains a challenge in pharmaceutical science.
Purpose of the Study:
- To prepare hydrophobic drug-loaded microspheres using an oil-in-water-in-oil (o/w/o) multiple emulsion technique.
- To investigate the impact of critical process variables on microsphere characteristics and drug encapsulation efficiency.
Main Methods:
- Utilized an o/w/o multiple emulsion technique for microsphere preparation.
- Employed two chitosans with varying molecular weights and deacetylation degrees.
- Investigated the effects of acetic acid concentration and drug-polymer ratio using ketoprofen as a model hydrophobic drug.
Main Results:
- The multiple emulsion method successfully produced well-formed chitosan microspheres with good yields.
- Acetic acid concentration in chitosan solutions significantly affected microsphere particle size and drug content.
- The lowest theoretical drug-to-chitosan ratio resulted in the highest drug encapsulation efficiencies.
Conclusions:
- The o/w/o multiple emulsion technique is a viable method for producing hydrophobic drug-loaded chitosan microspheres.
- Process parameters, specifically acetic acid concentration and drug-polymer ratio, are critical for controlling microsphere properties.
- Optimizing the drug-polymer ratio is essential for maximizing drug encapsulation efficiency in these chitosan-based delivery systems.