Composite chitosan/alginate hydrogel for controlled release of deferoxamine: A system to potentially treat iron dysregulation diseases

被引:89
作者
Rassu, Giovanna [1 ]
Salis, Andrea [1 ]
Porcu, Elena Piera [2 ]
Giunchedi, Paolo [1 ]
Roldo, Marta [3 ]
Gavini, Elisabetta [1 ]
机构
[1] Univ Sassari, Dept Chem & Pharm, I-07100 Sassari, Italy
[2] Univ Pavia, Expt Med, I-27100 Pavia, Italy
[3] Univ Portsmouth, Inst Biomed & Biomol Sci, Portsmouth PO1 2DT, Hants, England
关键词
Deferoxamine; Composite hydrogel; Chitosan; Alginate; PLGA microparticles; Iron dysregulation diseases; ADVANCED HEPATOCELLULAR-CARCINOMA; DISTRACTION OSTEOGENESIS; BONE DEFECT; SKIN FLAPS; DRUG; MODEL; DESFERRIOXAMINE; MICROPARTICLES; MICROSPHERES; REGENERATION;
D O I
10.1016/j.carbpol.2015.10.048
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
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. (c) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1338 / 1347
页数:10
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