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Structure and thermal transitions in a biomedically relevant liquid crystalline poly(ester amide)

机译:生物医学相关液晶聚(酯酰胺)中的结构和热转变

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摘要

There is still a need to develop bioresorbable polymers with high strength and high modulus for load-bearing biomedical applications. Here we investigate the liquid crystalline structural features of poly(desaminotyrosyl-tyrosine dodecyl dodecanedioate), poly(DTD DD), a new bioresorbable poly(ester amide) that is currently studied in vivo as a slow-degrading implantable biomaterial for load bearing applications. Thermally induced structural changes in poly(DTD DD) were studied using simultaneously differential scanning calorimetry (DSC) and X-ray scattering. The hexatic SmB organization of the polymer chains that exists at room temperature becomes progressively disordered upon heating, changing into a SmF phase and then into a smectic C phase at 60°C before turning into a free flowing melt at 130°C. X-ray scattering data and thermal analysis indicate the presence of a 2D ordered structure in the polymer melt. A structural model with an interesting 3-fold symmetry in the packing of the side chains around the rigid aromatic main chain, and the packing of these chains into fibrils is proposed. The liquid crystalline behavior of poly(DTD DD) makes it possible to melt process it at low temperatures without thermal degradation. This is a noteworthy advantage for the use of poly(DTD DD) as a high strength, readily processable, yet biodegradable polymer.
机译:仍需要开发具有高强度和高模量的生物可吸收聚合物,以用于承载生物医学应用。在这里,我们研究了聚(脱氨基酪氨酰基-酪氨酸十二烷基十二烷二酸酯),聚(DTD DD)的液晶结构特征,这是一种新的可生物吸收的聚(酯酰胺),目前已在体内作为一种慢速降解的可植入生物材料进行了承载研究。同时使用差示扫描量热法(DSC)和X射线散射研究了聚(DTD DD)中热诱导的结构变化。室温下存在的聚合物链的六价SmB组织在加热时逐渐变得无序,在60°C时变为SmF相,然后变为近晶C相,然后在130°C时变成自由流动的熔体。 X射线散射数据和热分析表明聚合物熔体中存在二维有序结构。提出了一种结构模型,该模型在刚性芳族主链周围的侧链堆积以及将这些链堆积成原纤维的过程中具有有趣的三折对称性。聚(DTD DD)的液晶行为使其可以在低温下熔融加工而不会发生热降解。对于使用聚(DTD DD)作为高强度,易于加工但可生物降解的聚合物,这是一个值得注意的优势。

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