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纳米级化学相互作用增强了生物玻璃复合材料的物理性能。

Nanoscale chemical interaction enhances the physical properties of bioglass composites.

机构信息

School of Chemical and Biomolecular Engineering, The University of Sydney , Sydney, NSW, Australia.

出版信息

ACS Nano. 2013 Oct 22;7(10):8469-83. doi: 10.1021/nn402157n. Epub 2013 Sep 9.

Abstract

Bioglasses are favorable biomaterials for bone tissue engineering; however, their applications are limited due to their brittleness. In addition, the early failure in the interface is a common problem of composites of bioglass and a polymer with high mechanical strength. This effect is due to the phase separation, nonhomogeneous mixture, nonuniform mechanical strength, and different degradation properties of two compounds. To address these issues, in this study a nanoscale interaction between poly(methyl methacrylate) (PMMA) and bioactive glass was formed via silane coupling agent (3-trimethoxysilyl)propyl methacrylate (MPMA). A monolith was produced at optimum composition from this hybrid by the sol-gel method at 50 °C with a rapid gelation time (<50 min) that possessed superior physicochemical properties compared to pure bioglass and physical mixture. For instance, the Young's modulus of bioglass was decreased 40-fold and the dissolution rate of silica was retarded 1.5-fold by integration of PMMA. Prolonged dissolution of silica fosters bone integration due to the continuous dissolution of bioactive silica. The primary osteoblast cells were well anchored and cell migration was observed on the surface of the hybrid. The in vivo studies in mice demonstrated that the integrity of the hybrids was maintained in subcutaneous implantation. They induced mainly a mononuclear phagocytic tissue reaction with a low level of inflammation, while bioglass provoked a tissue reaction with TRAP-positive multinucleated giant cells. These results demonstrated that the presence of a nanoscale interaction between bioglass and PMMA affects the properties of bioglass and broadens its potential applications for bone replacement.

摘要

生物玻璃是用于骨组织工程的理想生物材料;然而,由于其脆性,其应用受到限制。此外,生物玻璃与具有高机械强度的聚合物复合材料的早期失效是一个常见问题。这种效应是由于两种化合物的相分离、不均匀混合、不均匀的机械强度和不同的降解特性。为了解决这些问题,本研究通过硅烷偶联剂(3-三甲氧基硅丙基甲基丙烯酸酯)(MPMA)在聚甲基丙烯酸甲酯(PMMA)和生物活性玻璃之间形成纳米级相互作用。通过溶胶-凝胶法在 50°C 下由该杂化物在最佳组成下生产出一种整体,凝胶时间快(<50 分钟),与纯生物玻璃和物理混合物相比具有优异的物理化学性能。例如,通过整合 PMMA,生物玻璃的杨氏模量降低了 40 倍,二氧化硅的溶解速率降低了 1.5 倍。由于生物活性二氧化硅的持续溶解,二氧化硅的长期溶解促进了骨整合。原代成骨细胞很好地锚定在杂化物表面,观察到细胞迁移。在小鼠体内研究表明,皮下植入时杂化物的完整性得以维持。它们主要诱导单核吞噬组织反应,炎症水平低,而生物玻璃则引发具有 TRAP 阳性多核巨细胞的组织反应。这些结果表明,生物玻璃和 PMMA 之间纳米级相互作用的存在会影响生物玻璃的性质,并拓宽其在骨替代方面的潜在应用。

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