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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

机译:壳聚糖支架将溶菌酶掺入通过仿生途径生产的CaP涂层中:将自调控降解系统与原位孔形成相结合的组织工程学新概念

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摘要

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, and 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.
机译:这项研究描述了一种具有创新性的自调节降解材料,该材料具有逐步的原位成孔能力,可用于骨组织工程应用。该方法基于将溶菌酶掺入磷酸钙(CaP)涂层中,该涂层通过仿生涂层技术在壳聚糖支架的表面制备,目的是控制其降解速率并随后形成孔。但是,由于溶菌酶具有抗菌特性,因此这些涂层可以充当其持续释放的载体,从而防止植入时的感染。为了证明原位孔形成的概念,将包被的支架(有和没有溶菌酶)在两种不同的溶液中以不同的pH值进行孵育,以模拟正常的生理条件(pH 7.4)和炎症反应(pH 5)。随时间监测支架的重量损失和形态。在pH 7.4时,支架比在pH 5时更稳定。在pH 5孵育的支架显示其初始重量迅速降低,并且扫描电子显微镜成像显示出高度多孔的结构。此外,对掺入的溶菌酶活性的评估表明,该酶能够水解细菌细胞壁的肽聚糖(通过光密度随时间的降低而检测到),表明该酶掺入CaP后仍保持活性。涂层。

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