Wu Feng, Li Jingan, Zhang Kun, He Zikun, Yang Ping, Zou Dan, Huang Nan
Key Lab. for Advanced Technologies of Materials, Ministry of Education, School of Material Science and Engineering, Southwest Jiaotong University , Chengdu 610031, PR China.
School of Life Science, Zhengzhou University , 100 Science Road, Zhengzhou 450001, PR China.
ACS Appl Mater Interfaces. 2016 Jan 13;8(1):109-21. doi: 10.1021/acsami.5b07427. Epub 2015 Dec 22.
Surface modification by conjugating biomolecules has been widely proved to enhance biocompatibility of cardiovascular implanted devices. Here, we aimed at developing a multifunctional surface that not only provides good hemocompatibility but also functions well in inducing desirable vascular cell-material interaction. In the present work, the multicoatings of hyaluronic acid (HA) and dopamine (PDA) were prepared onto 316L stainless steel (316L SS) via chemical conjugation (Michael addition, Schiff base reaction, and electrostatic adsorption). The results of platelet adhesion and activation and the whole blood tests indicated that the HA/PDA coatings obtained better hemocompatibility compared with the bare 316L SS and HA or PDA immobilized on 316L SS. The HA/PDA coatings also inhibited the proliferation of smooth muscle cells and adhesion/activation of macrophages effectively, whereas not all the HA/PDA coatings improved surface endothelialization rapidly and the effects of the multifunctional coatings on endothelial cell growth depend on the HA amounts (1.0, 2.0, and 5.0 mg/mL, labeled as PDA-HA-1, PDA-HA-2, and PDA-HA-5 respectively). Herein the PDA-HA-1 and PDA-HA-2 coatings were found to improve endothelial cell adhesion and proliferation significantly. The tissue compatibility of the HA/PDA coatings also depends on the HA amounts, and the PDA-HA-2 coating was proved to cause milder in vivo tissue response. Additionally, the mechanism of the HA molecular weight change and in vivo tissue response was also explored. These results effectively suggested that the HA/PDA coating might be promising when serving as a cardiovascular implanted device coating.
通过结合生物分子进行表面修饰已被广泛证明可增强心血管植入装置的生物相容性。在此,我们旨在开发一种多功能表面,它不仅能提供良好的血液相容性,还能在诱导理想的血管细胞与材料相互作用方面发挥良好作用。在本研究中,通过化学共轭(迈克尔加成、席夫碱反应和静电吸附)在316L不锈钢(316L SS)上制备了透明质酸(HA)和多巴胺(PDA)的多层涂层。血小板粘附和活化以及全血测试结果表明,与裸露的316L SS以及固定在316L SS上的HA或PDA相比,HA/PDA涂层具有更好的血液相容性。HA/PDA涂层还能有效抑制平滑肌细胞的增殖以及巨噬细胞的粘附/活化,然而并非所有的HA/PDA涂层都能迅速改善表面内皮化,多功能涂层对内皮细胞生长的影响取决于HA的用量(1.0、2.0和5.0 mg/mL,分别标记为PDA-HA-1、PDA-HA-2和PDA-HA-5)。在此发现,PDA-HA-1和PDA-HA-2涂层能显著改善内皮细胞的粘附和增殖。HA/PDA涂层的组织相容性也取决于HA的用量,并且已证明PDA-HA-2涂层在体内引起的组织反应更轻微。此外,还探讨了HA分子量变化和体内组织反应的机制。这些结果有力地表明,HA/PDA涂层作为心血管植入装置涂层可能具有广阔前景。