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Natural and synthetic polymer-based hybrid materials for tissue regeneration

机译:用于组织再生的天然和合成聚合物基混合材料

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摘要

The world’s population is aging and cases of debilitating degenerative diseases are increasing. Bone is the second most transplanted tissue after blood but natural bone grafts are in short supply. Bioglass, which is a particular composition of bioactive glass, stimulates more bone repair than other synthetic bone grafts. However, it is brittle so cannot be used in cyclically loaded sites. A promising solution is the use of hybrid materials that can potentially combine the toughness of polymers with the stiffness and bioactivity of the glass through interpenetrating inorganic-organic networks. Hybrids have the unique feature of tuneable mechanical properties and degradation rates. In this thesis, two very different polymers were investigated as the organic component of hybrids; chitosan and poly(2-hydroxyethyl methacrylate-co-(3-trimethoxysilane)propyl methacrylate). The natural polymer chitosan was incorporated into the silica sol-gel process to produce hybrids and scaffolds were fabricated using freeze drying and foaming techniques. The chemical, morphological, mechanical and degradation properties of the scaffolds were studied. In order to covalently bond the organic and inorganic components, the chitosan was functionalised with an alkoxysilane crosslinker, 3-glycidoxypropyl trimethoxysilane. Using NMR and FTIR, the functionalisation reaction and side-reactions were characterised, discovering that the reaction was only 20% efficient at all pH values. To avoid the inefficient functionalisation reactions and concerns over the reproducibility of natural polymers, the synthetic co-polymer poly(2-hydroxyethyl methacrylate-co-(3-trimethoxysilane)propyl methacrylate) was synthesised by controlled polymerisation techniques (ATRP and ARGET ATRP) and typical free radical polymerisation (FRP). ATRP gave good control over molecular weight distributions, but the copper catalyst had serious implications on the chemical and architectural structure of the polymers. An NMR kinetics study was used to identify alternative polymerisation routes that could avoid the problems associated with the copper catalyst. The polymers were introduced into the sol-gel process to produce entirely synthetic hybrids with non-brittle (tough) behaviour and dissolution rates controlled by the polymer composition. The hybrids also exhibited hydroxyapatite precipitation in simulated body fluid, indicative of potential bioactivity in vivo. Hence, the aim of producing non-brittle, bioactive materials with controllable degradation rates was achieved.
机译:世界人口正在老龄化,令人衰弱的退化性疾病的病例正在增加。骨骼是仅次于血液的第二大移植组织,但天然骨移植物供不应求。生物玻璃是生物活性玻璃的特殊成分,它比其他合成骨移植物刺激的骨修复更多。但是,它很脆,因此不能在周期性加载的站点中使用。一种有前途的解决方案是使用混合材料,该材料可以通过相互渗透的无机有机网络将聚合物的韧性与玻璃的刚度和生物活性相结合。混合动力车具有可调节机械性能和降解速率的独特功能。本文研究了两种截然不同的聚合物作为杂化物的有机组分。壳聚糖和聚(甲基丙烯酸2-羟乙酯-共-(3-三甲氧基硅烷)甲基丙烯酸丙酯)。将天然聚合物壳聚糖掺入二氧化硅溶胶-凝胶工艺中以生产杂化物,并使用冷冻干燥和发泡技术制造支架。研究了支架的化学,形态,机械和降解特性。为了使有机和无机组分共价键合,壳聚糖用烷氧基硅烷交联剂3-环氧丙氧基丙基三甲氧基硅烷官能化。使用NMR和FTIR,对官能化反应和副反应进行了表征,发现该反应在所有pH值下的效率仅为20%。为避免低效的官能化反应和对天然聚合物重现性的担忧,通过控制聚合技术(ATRP和ARGET ATRP)合成了甲基丙烯酸2-羟乙酯-甲基丙烯酸3-(三甲氧基硅烷)丙酯的共聚物典型的自由基聚合(FRP)。 ATRP可以很好地控制分子量分布,但是铜催化剂对聚合物的化学和建筑结构有严重影响。 NMR动力学研究用于确定可避免与铜催化剂相关的问题的替代聚合路线。将聚合物引入溶胶-凝胶工艺中,以生产具有非脆性(韧性)行为和由聚合物组成控制的溶解速率的完全合成的杂化物。杂种还显示出模拟体液中的羟基磷灰石沉淀,表明体内潜在的生物活性。因此,达到了生产具有可控降解速率的非脆性生物活性材料的目的。

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    Connell Louise Stephanie;

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