Clinical Engineering, Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, UK.
Biomaterials. 2013 Dec;34(37):9352-64. doi: 10.1016/j.biomaterials.2013.08.044. Epub 2013 Sep 14.
The enrichment of substrates/surfaces with selected functional groups, methyl (-CH3), allyl amine (-NH2), allyl alcohol (-OH) and acrylic acid (-COOH), can be used to trigger mesenchymal stem (MSC) cell differentiation into specified lineages, minimising the need for exogenous biological supplementation. We present the successful translation of this research phenomenon to an injectable two phase injectable PLGA system, utilising plasma techniques, for the repair of bone defects. Modified microspheres were characterised using water contact angel (WCA), X-ray Photon Spectroscopy (XPS) and scanning electron microscopy (SEM). When cultured in contact with MSCs in vitro, the ability of the modified particles, within the 2 phase system, to induce differentiation was characterised using quantitative assays for cell viability and histological analysis for key markers of differentiation throughout the entirety of the three dimensional scaffold. Biological analysis proved that selected modified microspheres have the ability to induce MSC osteogenic (-NH2 modified scaffolds) and chondrogenic (-OH modified scaffolds) differentiation throughout the entirety of the formed scaffold. Therefore optimised plasma modification of microspheres is an effective tool for the production of injectable systems for the repair of bone and cartilage defects.
可以通过选择具有特定功能基团(甲基(-CH3)、烯丙胺(-NH2)、烯丙醇(-OH)和丙烯酸(-COOH))的基底/表面来富集,以触发间充质干细胞(MSC)分化为特定谱系,从而最大程度减少对外源性生物补充的需求。我们成功地将这一研究现象转化为可注射的两相可注射 PLGA 系统,利用等离子体技术修复骨缺损。使用水接触角(WCA)、X 射线光电子能谱(XPS)和扫描电子显微镜(SEM)对改性微球进行了表征。在体外与 MSC 共培养时,通过定量细胞活力测定和组织学分析整个三维支架中分化的关键标志物,对 2 相体系中改性颗粒诱导分化的能力进行了表征。生物学分析证明,选定的改性微球具有诱导 MSC 成骨(-NH2 改性支架)和软骨分化(-OH 改性支架)的能力,贯穿整个形成的支架。因此,优化的微球等离子体改性是生产用于修复骨和软骨缺损的可注射系统的有效工具。