| Literature DB >> 26572479 |
Giovanna Rassu1, Andrea Salis1, Elena Piera Porcu2, Paolo Giunchedi1, Marta Roldo3, Elisabetta Gavini4.
Abstract
Recently, the potential application of deferoxamine (DFO) in several iron dysregulation diseases has been highlighted. However, DFO presents significant limitations in clinical use due to its poor absorption in the gut and very short plasma half-life. To overcome these problems, the feasibility of chitosan/alginate hydrogels as prolonged delivery systems of DFO was investigated. Hydrogel alone or co-formulated with poly(D,L-lactide-co-glycolide) microspheres were prepared and studied in vitro. The influence of the preparation methods on the performance of composite hydrogels on controlled DFO release was explored. Spray-dried microspheres based on poly(D,L-lactide-co-glycolide) were able to encapsulate DFO, a highly water soluble drug. Nevertheless, only the composite hydrogels managed to provide sustained drug release. The inclusion of microspheres into pre-formed chitosan/alginate hydrogel provided the most efficient delivery system; the drug released from microspheres is strongly entrapped in the hydrogel network and slowly released by diffusion.Entities:
Keywords: Alginate; Chitosan; Chitosan (PubChem CID: 21896651); Composite hydrogel; Deferoxamine; Deferoxamine mesylate (PubChem CID: 62881); Iron dysregulation diseases; PLGA microparticles; Poly(d,l-lactide-co-glycolide) (PubChem CID: 23111554); Sodium alginate (PubChem CID: 6850754)
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Year: 2015 PMID: 26572479 DOI: 10.1016/j.carbpol.2015.10.048
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381