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Modulated in Vitro Biocompatibility of a Unique Cross-Linked Salicylic Acid-Poly(epsilon-caprolactone)-Based Biodegradable Polymer

机译:独特的交联的水杨酸-聚(ε-己内酯)为基础的可生物降解聚合物的体外调制生物相容性

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Herein, we report the development of a unique architecture by chemically cross-linking salicylic acid (SA)-based poly(anhydride ester) onto a biodegradable amine-functionalized poly(caprolactone) (PCL), using lactic acid as a spacer. The ester and amide linkages in the SA PCL polymer, synthesized through melt condensation, were confirmed by NMR and FT-IR spectroscopic techniques. The enzymatic and nonenzymatic hydrolytic degradation profile exhibited linear degradation kinetics over an extended time period (>5 weeks). The compatibility and growth of C2C12 myoblast cells were found to be significantly improved on the fast-degrading SA PCL substrates compared to those over neat PCL and amine-functionalized PCL. Further, the decreased red blood cell damage, illustrated by 0.39% hemolysis activity and a minimal number of platelet adhesion on a SA PCL polymeric surface confirmed good hemocompatibility of the as-synthesized polymer. Together with a moderate bactericidal property, the spectrum of properties of this novel polymer can be attributed to the synergistic effect of the presence of chemical moieties of SA and amine groups in PCL. In summary, it is considered that a SA PCL-based cross-linked composite can be utilized as a new biodegradable polymer.
机译:在这里,我们报告了通过使用乳酸作为间隔基,将基于水杨酸(SA)的聚(酸酐酯)化学交联到可生物降解的胺官能化的聚己内酯(PCL)上的独特体系结构的开发。通过熔融缩合合成的SA PCL聚合物中的酯键和酰胺键已通过NMR和FT-IR光谱技术证实。酶促和非酶促水解降解曲线在延长的时间段(> 5周)内表现出线性降解动力学。与纯PCL和胺官能化PCL相比,在快速降解的SA PCL基质上,C2C12成肌细胞的相容性和生长得到了显着改善。此外,由0.39%的溶血活性和在SA PCL聚合物表面上的血小板粘附的最小数量所说明的减少的红细胞损伤证实了所合成的聚合物具有良好的血液相容性。加上适度的杀菌性能,这种新型聚合物的性能谱可归因于PCL中SA和胺基化学部分的协同作用。总之,认为可以将基于SA PCL的交联复合材料用作新的可生物降解的聚合物。

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