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Preparation of sustained-release composite coating formed by dexamethasone and oxidated sodium alginate

机译:地塞米松与氧化海藻酸钠形成缓释复合涂层的制备

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摘要

Inflammatory reaction and thrombosis are the unsolved main problems of non-coated biomaterials applied in cardiac surgery. In the present study, a series of sustained composite coating was prepared and characterized, such as in the chemical modification of polyvinyl chloride (PVC) for applications in cardiac surgery and the assessment of the biological property of modified PVC. The composite coatings were mainly formed by dexamethasone (DXM) and oxidated sodium alginate (OSA) through ionic and covalent bond methods. The biocompatibility and hemocompatibility of the coating surface were evaluated. Scanning electron microscopy analysis of the surface morphologies of the thrombus and platelets revealed that DXM-OSA coating improved the antithrombogenicity and biocompatibility of PVC circuits, which were essential for cardiac pulmonary bypass surgery. Evaluation of in vitro release revealed that the DXM on group PPC was gradually released in 8 h. Thus, DXM that covalently combined on the PVC surface showed sustained release. By contrast, DXM on groups PPI and PPD was quickly or shortly released, suggesting that groups PPI and PPD did not have sustained-release property. Overall, results indicated that the DXM-OSA composite coating may be a promising coating for the sustained delivery of DXM.
机译:炎症反应和血栓形成是心脏外科手术中使用的非涂层生物材料尚未解决的主要问题。在本研究中,制备并表征了一系列连续复合涂层,例如用于心脏外科手术的聚氯乙烯(PVC)的化学改性以及改性PVC的生物学性能评估。复合涂层主要由地塞米松(DXM)和氧化海藻酸钠(OSA)通过离子键和共价键方法形成。评价涂层表面的生物相容性和血液相容性。扫描电子显微镜对血栓和血小板表面形态的分析表明,DXM-OSA涂层改善了PVC回路的抗血栓形成性和生物相容性,这对心脏肺部搭桥手术至关重要。体外释放的评估表明,PPC组上的DXM在8小时内逐渐释放。因此,在PVC表面上共价结合的DXM表现出持续释放。相比之下,PPI和PPD组的DXM迅速或短期释放,表明PPI和PPD组不具有持续释放的特性。总体而言,结果表明DXM-OSA复合涂层可能是DXM持续交付的有前途的涂层。

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