首页> 外文期刊>Frontiers in Physics >Synthesis, Characterization and 3D Micro-Structuring via 2-Photon Polymerization of Poly(glycerol sebacate)-Methacrylatea??An Elastomeric Degradable Polymer
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Synthesis, Characterization and 3D Micro-Structuring via 2-Photon Polymerization of Poly(glycerol sebacate)-Methacrylatea??An Elastomeric Degradable Polymer

机译:聚癸二酸甘油酯-甲基丙烯酸甲酯的2-光子聚合合成,表征及3D微结构-弹性可降解聚合物

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Poly(glycerol sebacate) (PGS) has been utilised in numerous biomaterial applications over recent years. This elastomeric and rapidly degradable polymer is cytocompatible and suited to various applications in soft tissue engineering and drug delivery. Although PGS is simple to synthesise as an insoluble prepolymer, it requires the application of high temperatures for extended periods of time to produce an insoluble matrix. This places limitations on the processing capabilities of PGS and its possible applications. Here, we present a photocurable form of PGS with improved processing capabilities: PGS-methacrylate (PGS-M). By methacrylating the secondary hydroxyl groups of the glycerol units in the PGS prepolymer chains, the material was rendered photocurable and, in combination with a photoinitiator, crosslinked rapidly on exposure to UV light at ambient temperatures. The polymera??s molecular weight and the degree of methacrylation could be controlled independently and the mechanical properties of the crosslinked material tailored. The polymer also displayed rapid degradation under physiological conditions and cytocompatibility with various primary cell types. As a demonstration of the processing capabilities of PGS-M, µm scale 3D scaffold structures were fabricated using 2-photon polymerisation and used for 3D cell culture. The tunable properties of PGS-M coupled with its enhanced processing capabilities make the polymer an attractive potential biomaterial for various future applications.
机译:聚癸二酸甘油酯(PGS)近年来已在许多生物材料应用中得到利用。这种弹性体和可快速降解的聚合物具有细胞相容性,适用于软组织工程和药物输送中的各种应用。尽管PGS易于合成为不溶性预聚物,但它需要长时间应用高温才能产生不溶性基质。这限制了PGS及其可能的应用程序的处理能力。在这里,我们介绍了具有改进的处理能力的PGS的可光固化形式:PGS-甲基丙烯酸酯(PGS-M)。通过对PGS预聚物链中甘油单元的仲羟基进行甲基丙烯酸酯化处理,使该材料变得可光固化,并与光引发剂结合,在环境温度下暴露于UV光下迅速交联。聚合物的分子量和甲基丙烯酸化程度可以独立控制,并且可以调整交联材料的机械性能。该聚合物还显示出在生理条件下的快速降解以及与各种原代细胞类型的细胞相容性。为了证明PGS-M的处理能力,使用2光子聚合技术制作了微米级的3D支架结构,并将其用于3D细胞培养。 PGS-M的可调节特性及其增强的加工能力使该聚合物成为未来各种应用的有吸引力的潜在生物材料。

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