聚醚骨架PEO-PPO对聚脲干凝胶释药行为的影响

Julia G. Vargas, H. Andrada, Bruno A. Fico, Julia M Paulino, Natália N. Silveira, R. D. dos Santos, E. F. Molina
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引用次数: 0

摘要

为了评价双氯芬酸钠负载和卸载后聚脲的结构变化和热稳定性,合成了含聚环氧聚丙烯(PPO)或聚环氧聚乙烯(PEO)的聚醚胺和六亚甲基二异氰酸酯三聚体hdi的聚脲网络。该网络的形成受溶胶-凝胶反应控制,然后用不同的技术(FTIR, XRD, TGA)对所得材料进行了表征。此外,双氯芬酸的释放量可以作为时间的函数进行调节,研究材料的吸水或溶胀能力、细胞毒性和药物释放量。因此,对PEO-或PPO-基聚醚胺(分子量相近)的亲水性进行了选择,并将其释放曲线与PEO/PPO聚脲基质的吸水性进行了相关性研究。最终可以建立双氯芬酸释放与聚脲基质性质之间的联系,例如聚合物的性质(PEO/PPO)和亲水性(吸水)。我们的目标是确定发展创新功能生物材料的挑战和机遇,用于健康应用。
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Influence of Polyether Backbone PEO–PPO on the Drug Release Behavior of Polyurea Xerogels
To evaluate possible structural changes and thermal stability of the polyurea unloaded and loaded with diclofenac sodium, polyurea networks based on polyetheramine containing polypropylene oxide (PPO) or polyethylene oxide (PEO) and hexamethylene diisocyanate trimer-HDI were synthesized. The formation of the network was controlled by sol-gel reactions, and the obtained materials were then characterized by different techniques (FTIR, XRD, TGA). Moreover, the amount of diclofenac released could be modulated as a function of time, studying the water absorption or swelling capacity, the cytotoxicity of the material and the amount of drug released. A choice was therefore made on the hydrophilicity of PEO- or PPO-based polyetheramine (with similar molecular weight), and the release profile was hereafter correlated with the water absorption by the PEO/PPO polyurea matrix. Links could finally be established between the release of diclofenac and the polyurea matrices properties, such as the nature of polymer (PEO/PPO) and the hydrophilicity (water uptake). Our objective here is to identify challenges and opportunities for the development of innovative functional biomaterials for health applications.
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