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多聚多巴胺介导的多种生物活性分子固定化用于功能性血管移植物材料的开发。

Polydopamine-mediated immobilization of multiple bioactive molecules for the development of functional vascular graft materials.

机构信息

Department of Bioengineering, College of Engineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791, Republic of Korea.

出版信息

Biomaterials. 2012 Nov;33(33):8343-52. doi: 10.1016/j.biomaterials.2012.08.011. Epub 2012 Aug 20.

Abstract

In this study, we introduced a simple method for polydopamine-mediated immobilization of dual bioactive factors for the preparation of functionalized vascular graft materials. Polydopamine was deposited on elastic and biodegradable poly(lactic acid-co-ɛ-caprolactone) (PLCL) films, and a cell adhesive RGD-containing peptide and basic fibroblast growth factor were subsequently immobilized by simple dipping. We used an enzyme-linked immunosorbent assay and fluorescamine assay to confirm that we had stably immobilized bioactive molecules on the polydopamine-coated PLCL film in a reaction time-dependent manner. When human umbilical vein endothelial cells (HUVEC) were cultured on the prepared substrates, the number of adherent cells and proliferation of HUVEC for up to 14 days were greatest on the film immobilized with dual factors. On the other hand, the film immobilized with RGD peptide exhibited the highest migration speed compared to the other groups. The expression of cluster of differentiation 31 and von Willebrand factor, which indicates maturation of endothelial cells, was highly stimulated in the dual factor-immobilized group, and passively adsorbed factors showed a negligible effect. The immobilization of bioactive molecules inspired by polydopamine was successful, and adhesion, migration, proliferation and differentiation of HUVEC were synergistically accelerated by the presence of multiple signaling factors. Collectively, our results have demonstrated that a simple coating with polydopamine enables the immobilization of multiple bioactive molecules for preparation of polymeric functionalized vascular graft materials.

摘要

在这项研究中,我们介绍了一种简单的方法,用于通过聚多巴胺介导的双重生物活性因子固定化来制备功能化的血管移植物材料。聚多巴胺沉积在弹性和可生物降解的聚(丙交酯-共-ε-己内酯)(PLCL)薄膜上,随后通过简单的浸渍将细胞黏附性含有 RGD 的肽和碱性成纤维细胞生长因子固定化。我们使用酶联免疫吸附测定和荧光胺测定证实,我们以时间依赖的方式将生物活性分子稳定地固定在聚多巴胺涂覆的 PLCL 薄膜上。当人脐静脉内皮细胞(HUVEC)在制备的基板上培养时,在固定有双重因子的薄膜上培养的细胞黏附数量和 HUVEC 的增殖最多可达 14 天。另一方面,与其他组相比,固定有 RGD 肽的薄膜表现出最高的迁移速度。CD31 和血管性血友病因子的表达,表明内皮细胞的成熟,在双重因子固定化组中被高度刺激,而被动吸附的因子则几乎没有效果。聚多巴胺诱导的生物活性分子的固定化是成功的,并且多种信号因子的存在协同加速了 HUVEC 的黏附、迁移、增殖和分化。总的来说,我们的结果表明,简单的聚多巴胺涂层能够固定多种生物活性分子,用于制备聚合物功能化的血管移植物材料。

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