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Polymer Crosslinking: a new Strategy to Enhance Mechanical Properties and Structural Stability of Bioactive Glasses

机译:聚合物交联:提高生物活性玻璃机械性能和结构稳定性的新策略

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The organic-inorganic hybrids fabricated by the sol-gel method are intrinsically bioactive materials with extensive applications in bone tissue engineering. The brittleness and limited water uptake capacity of these monoliths, however, restrict their applications for engineering the soft tissues and their interfaces with bone. To address these challenges, we developed a unique method in which polymer crosslinking was used to cease the over-condensation of a bioactive glass component and eradicate the formation of brittle structure.udIn this study, an organosilane-functionalized gelatin methacrylate was covalently bonded to a bioactive glass during the sol-gel process, and the condensation of silica networks was controlled by polymer-crosslinking. The physicochemical properties and mechanical strength of these hybrid hydrogels were then tuned by the incorporation of secondary crosslinking agents such as poly(ethylene glycol diacrylate). The resulting elastic hydrogels displayed tuneable compressive modulus in the range of 42 kPa to 530 kPa. The swelling behaviours of these hybrids and their structural integrities were also favourable for tissue engineering applications. Moreover, these hybrid hydrogels kept their structures for more than 28 days in simulated body fluid. The bioactivity of the constructs due to the presence of silica networks were confirmed by detecting nearly 2-fold increase in the alkaline phosphatase activity of the cultured bone progenitor cells on these hybrid hydrogels within 28 days of in vitro culture. Within the same period, in vivo studies on mice subcutaneous model showed that the hybrid hydrogels were highly biocompatible and well-tolerated. udIn summary, the bioactivity of the constructs, their tuneable physicochemical properties, the outstanding biocompatibility, and biodegradability of the hybrid hydrogels showed the high potential of the developed technique for fabrication of constructs for a variety of soft and hard tissue regeneration.
机译:通过溶胶-凝胶法制备的有机-无机杂化物是固有的生物活性材料,在骨组织工程中具有广泛的应用。但是,这些整料的脆性和有限的吸水能力限制了它​​们在工程化软组织及其与骨骼的界面方面的应用。为了解决这些挑战,我们开发了一种独特的方法,其中使用聚合物交联来终止生物活性玻璃组分的过度冷凝并消除脆性结构的形成。 ud在这项研究中,有机硅烷官能化的甲基丙烯酸明胶被共价键合到溶胶-凝胶过程中产生生物活性玻璃,而二氧化硅网络的缩合则通过聚合物交联来控制。这些杂化水凝胶的理化性质和机械强度随后通过掺入第二交联剂(如聚乙二醇二丙烯酸酯)进行调节。所得的弹性水凝胶显示出可调节的压缩模量,范围为42 kPa至530 kPa。这些杂种的溶胀行为及其结构完整性也有利于组织工程应用。此外,这些混合水凝胶在模拟体液中保持其结构超过28天。通过检测在体外培养的28天内这些杂交水凝胶上培养的骨祖细胞的碱性磷酸酶活性增加了近2倍,证实了由于存在二氧化硅网络而导致的构建体的生物活性。在同一时期内,对小鼠皮下模型的体内研究表明,杂化水凝胶具有高度的生物相容性和良好的耐受性。总而言之,构建体的生物活性,其可调节的理化特性,出色的生物相容性和杂化水凝胶的生物降解性表明,开发的技术可用于制造各种软硬组织再生的构建体,具有很高的潜力。

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    Negahi Shirazi Ali;

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  • 年度 2015
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