Journal
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY
Volume 22, Issue 7, Pages 860-870Publisher
TAYLOR & FRANCIS LTD
DOI: 10.3109/10837450.2015.1108982
Keywords
Biodegradable; box-Benkehn design; drug delivery; fingolimod; poly (3-hydroxybutyrate-co-hydroxyvalerate)
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Funding
- Tehran University of Medical Sciences [21609]
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This study was focused on the fabrication, statistical optimization and in vitro characterization of poly (hydroxybutyrate-co-hydroxyvalerate) (PHBV) nanoparticles loaded with fingolimod. PHBV-based fingolimod nanoparticles were prepared by single and double evaporation methods; the incorporation efficiency of fingolimod was higher with the single emulsion evaporation method in the nanosize range particles. Fingolimod HCL was neutralized with NaOH in order to slow down the release of the highly soluble fingolimod. The encapsulation efficiency of neutralized fingolimod was much higher (53-73%) due to the insoluble form of the drug used in encapsulation. It was found that the amount of fingolimod, concentration of PHBV and polyvinyl alcohol (PVA) would influence the encapsulation efficiency significantly. The effect of these parameters on the Particle size, PdI, loading capacity and loading efficacy was studied. The optimum conditions were 1.32% PHBV, 0.42% PVA and 5mg fingolimod. The average size of optimized nanoparticles which measured with the aid of the Box-Behnken experimental design was 250nm and entrapment efficiency of 73(%). Drug-release from the nanospheres over a four-week period has shown a characteristic triphasic release pattern with an initial burst effect.
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