用作生物医学设备的聚(左旋-右旋乳酸)/聚乙二醇混合物的化学处理及物理化学和机械特性分析

V. Amaral, Juliana Souza, Thais Alves, F. Batain, Kessi Crescencio, Daniel Komatsu, Marco Chaud
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摘要

对聚合物混合物进行化学处理是为生物医学应用设计具有新特性的材料的一种有前途的替代方法。这项工作旨在生产聚乙二醇(PEG400 或 PEG4000)与聚(L-co-D,L 乳酸)/PLDLA 的聚合物混合物,并确定其生物医学用途的特性。混合物采用浇铸法制备。通过傅立叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、机械性能(穿孔、回弹性、弹性模量、塑性变形、拉伸强度和粘附性)和体外生物降解研究进行了表征。傅立叶变换红外光谱和 DSC 得出的结果表明,产生聚合物混合物的化学作用是通过氢键和/或偶极-偶极相互作用进行的。在混合物中使用 PEG400 或 PEG4000 时,化学作用产生的化合物亲水性更强,重排方式也不同。机械测试表明,材料的抗性发生了变化,突出显示了 PLDLA/PEG400 的塑性变形指数值,这种结构的可塑性比 PLDLA/PEG4000 提高了 111 倍。在生物崩解研究中,120 小时后,观察到 PLDLA/PEG4000 的质量损失更大(68.82 ± 1.46%)。水解崩解不影响 pH 值,研究期间 pH 值保持在 7.34 和 7.41 之间。总之,这些混合物可为生产具有支持组织再生特性的生物相容性生物医学设备提供宝贵的特性,其中塑性变形问题与 PEG 在体内溶解后形成的孔隙是必要的。
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Chemical Processing and Physical-Chemical and Mechanical Characterizations of Poly (L-co-D, L lactic acid)/Polyethylene Glycol Mixtures for Application as a Biomedical Device
The chemical processing of polymeric mixtures is a promising alternative for designing materials with new characteristics for biomedical applications. This work proposed to produce and characterize polymeric mixtures obtained using polyethylene glycol (PEG400 or PEG4000) with poly (L-co-D, L lactic acid)/PLDLA for biomedical use. The mixtures were prepared by the casting method. Characterizations were performed by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), mechanical properties (perforation, resilience, elastic modulus, plastic deformation, tensile strength and mucoadhesion) and in vitro biodisintegration studies. The results obtained by FTIR and DSC suggest that the chemical interactions that generate the mixtures between the polymers occurred through hydrogen bonds and/or dipole-dipole interactions. Chemical interactions created compounds that were more hydrophilic and had different rearrangements when using PEG400 or PEG4000 in the mixture. The mechanical tests showed changes in the resistance of the materials, highlighting the exponential value of plastic deformation of PLDLA/PEG400, significantly increasing the plasticity of this structure by 111-fold about PLDLA/PEG4000. In the biodisintegration study, after 120 hours, greater mass loss was observed for PLDLA/PEG4000 (68.82 ± 1.46%). Hydrolytic disintegration did not influence pH values, which remained between 7.34 and 7.41 during the study. In conclusion, these mixtures can provide valuable characteristics to produce a biocompatible biomedical device with properties to support tissue regeneration, where the issue of plastic deformation is necessary in collaboration with the formation of pores, after PEG dissolution in vivo .
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