4.8 Article

Chitosan scaffolds incorporating lysozyme into CaP coatings produced by a biomimetic route: A novel concept for tissue engineering combining a self-regulated degradation system with in situ pore formation

期刊

ACTA BIOMATERIALIA
卷 5, 期 9, 页码 3328-3336

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2009.05.027

关键词

Chitosan; Cap coatings; Lysozyme; Degradation; In situ pore formation

资金

  1. European NoE EXPERTISSUES [NMP3-CT-2004-500283]
  2. European STREP HIPPOCRATES [NMP3-CT-2003-505758]
  3. Portuguese Foundation for Science and Technology (FCT)

向作者/读者索取更多资源

This study describes an innovative self-regulated degrading material with gradual in situ pore formation ability for bone tissue engineering applications. This approach is based on the incorporation of the lysozyme enzyme into calcium phosphate (CaP) coatings, prepared on the surface of chitosan scaffolds by means of a biomimetic coating technique with the aim of controlling their degradation rate and subsequent formation of pores. However, because lysozyme has antibacterial properties, these coatings may act as a carrier for its sustained release, preventing infection upon implantation. In order to prove the concept of in situ pore formation, the coated scaffolds (with and without lysozyme) were incubated in two different solutions at different pH to simulate normal physiological conditions (pH 7.4) and inflammatory response (pH 5). The weight loss and morphology of the scaffolds was monitored over time. At pH 7.4, the scaffolds remained more stable than at pH 5. The scaffolds incubated at pH 5 showed a rapid decrease in their initial weight, ana scanning electron microscopy imaging revealed the formation of a highly porous structure. Furthermore, evaluation of the activity of the incorporated lysozyme revealed that the enzyme was able to hydrolyse the peptidoglycan of the bacteria cell walls (as detected by the decrease in optical density with time), indicating that the enzyme remained active after being incorporated into the CaP coating. (C) 2009 Published by Elsevier Ltd. on behalf of Acta Materialia Inc.

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