4.7 Article

Preparation and characterization of vanillin-crosslinked chitosan therapeutic bioactive microcarriers

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ELSEVIER
DOI: 10.1016/j.ijbiomac.2015.05.037

Keywords

Vanillin-crosslinked chitosan microspheres; Drug delivery; Biocompatibility

Funding

  1. China NSFC [31370971]
  2. Sichuan project [2012FZ0125]
  3. Chengdu project [12DXYB145JH-005]

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Chitosan microspheres with diameter of 14.3-48.5 mu m were prepared by emulsion method and using natural vanillin as cross-linking agent. The surface morphology and microstructure of the microspheres were characterized by scanning electron microscopy, X-ray diffraction and Fourier-transform infrared spectroscopy, etc. The hollow microspheres showed a well-defined spherical shape with median diameter of 30.3 mu m and possessed a uniform surface with micro-wrinkles, which is in favor of the drug release. Interpenetrating network cross-linking mechanism might result from the Schiff base reaction and the acetalization of hydroxyl and carbonyl between chitosan and vanillin. Berberine, as a model drug, was loaded in the microspheres and released in a sustainable manner. The drug loading ratio could change from 9.16% to 29.70% corresponding to the entrapment efficiency of 91.61% to 74.25%. In vitro cell culture study using MG63 cells and in vivo implantation clearly showed that the microspheres could provide favorable cell attachment and biocompatibility. The results confirm that the drug-loaded vanillin-crosslinked chitosan microspheres could be a worthy candidate either as carriers of drugs and cells, or as therapeutic matrix for bone repair and regeneration. (C) 2015 Elsevier B.V. All rights reserved.

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