School of Engineering and Applied Science, Aston Research Centre for Healthy Ageing, Aston University, Birmingham B4 7ET, UK.
Philos Trans A Math Phys Eng Sci. 2012 Mar 28;370(1963):1422-43. doi: 10.1098/rsta.2011.0308.
Bone is the second most widely transplanted tissue after blood. Synthetic alternatives are needed that can reduce the need for transplants and regenerate bone by acting as active temporary templates for bone growth. Bioactive glasses are one of the most promising bone replacement/regeneration materials because they bond to existing bone, are degradable and stimulate new bone growth by the action of their dissolution products on cells. Sol-gel-derived bioactive glasses can be foamed to produce interconnected macropores suitable for tissue ingrowth, particularly cell migration and vascularization and cell penetration. The scaffolds fulfil many of the criteria of an ideal synthetic bone graft, but are not suitable for all bone defect sites because they are brittle. One strategy for improving toughness of the scaffolds without losing their other beneficial properties is to synthesize inorganic/organic hybrids. These hybrids have polymers introduced into the sol-gel process so that the organic and inorganic components interact at the molecular level, providing control over mechanical properties and degradation rates. However, a full understanding of how each feature or property of the glass and hybrid scaffolds affects cellular response is needed to optimize the materials and ensure long-term success and clinical products. This review focuses on the techniques that have been developed for characterizing the hierarchical structures of sol-gel glasses and hybrids, from atomic-scale amorphous networks, through the covalent bonding between components in hybrids and nanoporosity, to quantifying open macroporous networks of the scaffolds. Methods for non-destructive in situ monitoring of degradation and bioactivity mechanisms of the materials are also included.
骨骼是仅次于血液的第二大广泛移植组织。需要合成替代品,以减少移植的需求,并通过充当骨骼生长的活性临时模板来再生骨骼。生物活性玻璃是最有前途的骨替代/再生材料之一,因为它们与现有骨骼结合,可降解,并通过其溶解产物对细胞的作用刺激新的骨骼生长。溶胶-凝胶衍生的生物活性玻璃可以发泡以产生适合组织内生长的互连大孔,特别是细胞迁移和血管化和细胞穿透。这些支架满足理想合成骨移植物的许多标准,但并不适用于所有骨缺损部位,因为它们易碎。提高支架韧性而不失去其他有益特性的一种策略是合成无机/有机杂化材料。这些杂化物将聚合物引入溶胶-凝胶过程中,使有机和无机成分在分子水平上相互作用,从而控制机械性能和降解速率。然而,需要充分了解玻璃和杂化支架的每个特征或特性如何影响细胞反应,以优化材料并确保长期成功和临床产品。本综述重点介绍了用于表征溶胶-凝胶玻璃和杂化物的分层结构的技术,从原子尺度的无定形网络,到杂化物中组件之间的共价键合和纳米孔隙率,再到支架的开放式大孔网络的定量。还包括用于非破坏性原位监测材料降解和生物活性机制的方法。