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Injectable deferoxamine nanoparticles loaded chitosan-hyaluronic acid coacervate hydrogel for therapeutic angiogenesis.
S, Vignesh; A, Sivashanmugam; Annapoorna, Mohandas; R, Janarthanan; Subramania, Iyer; Shantikumar V, Nair; R, Jayakumar.
Affiliation
  • S V; Centre for Nanosciences and Molecular Medicine, Amrita University, Kochi 682041, India.
  • A S; Centre for Nanosciences and Molecular Medicine, Amrita University, Kochi 682041, India.
  • Annapoorna M; Centre for Nanosciences and Molecular Medicine, Amrita University, Kochi 682041, India.
  • R J; Department of Plastic and Reconstructive Surgery, Amrita Institute of Medical Sciences and Research Centre, Amrita University, Kochi 682041, India.
  • Subramania I; Department of Plastic and Reconstructive Surgery, Amrita Institute of Medical Sciences and Research Centre, Amrita University, Kochi 682041, India.
  • Shantikumar V N; Centre for Nanosciences and Molecular Medicine, Amrita University, Kochi 682041, India.
  • R J; Centre for Nanosciences and Molecular Medicine, Amrita University, Kochi 682041, India. Electronic address: jayakumar77@yahoo.com.
Colloids Surf B Biointerfaces ; 161: 129-138, 2018 Jan 01.
Article in En | MEDLINE | ID: mdl-29055865
In this study, an injectable chitosan-hyaluronic acid (CS-HA) based hydrogel was designed incorporating pro-angiogenic molecule, deferoxamine loaded PLGA nanoparticles (DFO NPs), for enhancing angiogenesis. DFO-NPs were prepared by double emulsion solvent diffusion technique and characterized for their physicochemical properties. The DLS and SEM analysis showed an average particle size of 220±71nm with spherical morphology and the encapsulation efficiency was found to be 30±5%. An ECM mimicking chitosan-hyaluronic acid (CS-HA) coacervate hydrogel was prepared. Both free DFO and DFO NPs were entrapped into the prepared CS-HA composite hydrogel. The hydrogels were characterized by SEM, FTIR and Rheology. Addition of DFO NPs did not affect the injectablility and flowability of developed hydrogels. In vitro DFO release from the prepared composite hydrogels showed controlled release over a period of 10days. Both the hydrogel systems showed excellent cyto-compatability and good cell proliferation for rASCs as well as HUVECs. The DFO and DFO NPs loaded composite hydrogels revealed effective tube formation in comparison with control hydrogels without DFO and DFO NPs. The in vivo angiogenic evaluation of the free DFO and DFO NPs (0.025%w/w) loaded composite hydrogels were studied by injecting the developed hydrogel subcutaneously into mice for 2-4 weeks. The DFO NPs loaded composite hydrogel had enhanced neovascularization when compared to control gels. Thus, the developed DFO NPs loaded composite hydrogel could potentially be used for therapeutic angiogenesis.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neovascularization, Physiologic / Hydrogel, Polyethylene Glycol Dimethacrylate / Deferoxamine / Chitosan / Nanoparticles / Hyaluronic Acid Limits: Animals / Humans Language: En Journal: Colloids Surf B Biointerfaces Journal subject: QUIMICA Year: 2018 Document type: Article Affiliation country: India Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neovascularization, Physiologic / Hydrogel, Polyethylene Glycol Dimethacrylate / Deferoxamine / Chitosan / Nanoparticles / Hyaluronic Acid Limits: Animals / Humans Language: En Journal: Colloids Surf B Biointerfaces Journal subject: QUIMICA Year: 2018 Document type: Article Affiliation country: India Country of publication: Netherlands