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Development and Biocompatibility of Collagen-Based Composites Enriched with Nanoparticles of Strontium Containing Mesoporous Glass

机译:含锶中孔玻璃纳米粒子的胶原基复合材料的开发及其生物相容性

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摘要

In the last years bone tissue engineering has been increasingly indicated as a valid solution to meet the challenging requirements for a healthy bone regeneration in case of bone loss or fracture. In such a context, bioactive glasses have already proved their great potential in promoting the regeneration of new bone tissue due to their high bioactivity. In addition, their composition and structure enable us to incorporate and subsequently release therapeutic ions such as strontium, enhancing the osteogenic properties of the material. The incorporation of these inorganic systems in polymeric matrices enables the formulation of composite systems suitable for the design of bone scaffolds or delivery platforms. Among the natural polymers, type I collagen represents the main organic phase of bone and thus is a good candidate to develop biomimetic bioactive systems for bone tissue regeneration. However, alongside the specific composition and structure, the key factor in the design of new biosystems is creating a suitable interaction with cells and the host tissue. In this scenario, the presented study aimed at combining nano-sized mesoporous bioactive glasses produced by means of a sol–gel route with type I collagen in order to develop a bioactive hybrid formulation suitable for bone tissue engineering applications. The designed system has been fully characterized in terms of physico-chemical and morphological analyses and the ability to release Sr ions has been studied observing a more sustained profile in presence of the collagenous matrix. With the aim to improve the mechanical and thermal stability of the resulting hybrid system, a chemical crosslinking approach using 4-star poly (ethylene glycol) ether tetrasuccinimidyl glutarate (4-StarPEG) has been explored. The biocompatibility of both non-crosslinked and 4-StarPEG crosslinked systems was evaluated by in vitro tests with human osteoblast-like MG-63 cells. Collected results confirmed the high biocompatibility of composites, showing a good viability and adhesion of cells when cultured onto the biomaterial samples.
机译:在过去的几年中,越来越多地表明骨组织工程是一种有效的解决方案,可以满足在骨丢失或骨折的情况下健康骨骼再生的挑战性要求。在这种情况下,生物活性玻璃由于具有很高的生物活性,因此已经证明其在促进新骨组织再生方面具有巨大潜力。此外,它们的成分和结构使我们能够掺入并随后释放治疗性离子(例如锶),从而增强材料的成骨特性。将这些无机系统掺入聚合物基质中,就可以配制适合设计骨支架或输送平台的复合系统。在天然聚合物中,I型胶原蛋白代表骨骼的主要有机相,因此是开发仿生生物活性系统用于骨骼组织再生的良好候选者。但是,除了特定的组成和结构外,新生物系统设计中的关键因素还包括与细胞和宿主组织建立适当的相互作用。在这种情况下,本研究旨在将通过溶胶-凝胶途径生产的纳米级中孔生物活性玻璃与I型胶原蛋白相结合,以开发适用于骨组织工程应用的生物活性混合制剂。设计的系统已通过物理化学和形态学分析得到充分表征,并且已经研究了释放Sr离子的能力,并观察到存在胶原基质的情况下具有更持久的特性。为了改善所得混合体系的机械和热稳定性,已探索了使用4-星聚(乙二醇)醚戊二酰亚胺基戊二酸酯(4-StarPEG)的化学交联方法。非交联的和4-StarPEG交联的系统的生物相容性通过人类成骨细胞样MG-63细胞的体外测试进行评估。收集的结果证实了复合材料的高生物相容性,当培养到生物材料样品上时显示出良好的生存力和细胞粘附性。

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