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Silicone Implant Coated with Tranilast-Loaded Polymer in a Pattern for Fibrosis Suppression

机译:有机硅植入物涂覆有曲尼司特的聚合物以抑制纤维化的方式

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摘要

Pathologic fibrosis around silicone implants is problematic, and thus, these implants have been coated with a mixture of a biocompatible polymer and antifibrotic drug for sustained drug release to prevent fibrosis. However, a coating applied over an entire surface would be subject to mechanical instability as the implant would be severely crumpled for implant insertion. Therefore, in this work, we proposed localized, patterned coating dots, each composed of poly(lactic-co-glycolic acid) (PLGA) and tranilast, to be applied on the surface of silicone implants. The drug loaded in the pattern-coated implant herein was well retained after a cyclic tensile test. Due to the presence of PLGA in each coating dot, the tranilast could be released in a sustained manner for more than 14 days. When implanted in a subcutaneous pocket in living rats for 12 weeks, compared with the intact implant, the pattern-coated implant showed a decreased capsule thickness and collagen density, as well as less transforming growth factor-β (TGF-β) expression and fewer fibroblasts; importantly, these changes were similar between the surfaces with and without the coating dots. Therefore, we conclude that the pattern-coating strategy proposed in this study can still effectively prevent fibrosis by maintaining the physical stability of the coatings.
机译:有机硅植入物周围的病理性纤维化是有问题的,因此,这些植入物已涂有生物相容性聚合物和抗纤维化药物的混合物,以持续释放药物以防止纤维化。然而,由于植入物将被严重弄皱以插入植入物,因此施加在整个表面上的涂层将遭受机械不稳定。因此,在这项工作中,我们提出了局部图案化的涂层点,分别由聚乳酸-乙醇酸(PLGA)和曲尼司特组成,用于有机硅植入物的表面。在循环拉伸试验后,负载在本文的图案涂覆的植入物中的药物被很好地保留。由于每个涂布点中均存在PLGA,曲尼司特可以持续释放14天以上。与完整的植入物相比,当将其植入活体大鼠的皮下口袋中12周时,图案涂层的植入物显示出减小的胶囊厚度和胶原蛋白密度,以及更少的转化生长因子-β(TGF-β)表达和更少成纤维细胞重要的是,这些变化在有涂层点和没有涂层点的表面之间是相似的。因此,我们得出结论,本研究中提出的图案涂层策略仍可以通过保持涂层的物理稳定性来有效防止纤维化。

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