School of Medical and Health Engineering, Institute of Biomedical Engineering and Health Sciences, Changzhou University, Changzhou 213164, China.
The Affiliated Huai'an Hospital of Xuzhou Medical University, Huai'an 223003, China.
Int J Biol Macromol. 2024 Jun;271(Pt 2):132487. doi: 10.1016/j.ijbiomac.2024.132487. Epub 2024 May 18.
Due to its biofunctions similar to NO, the CO gas signaling molecule has gradually shown great potential in cardiovascular biomaterials for regulating the in vivo performances after the implantation and has received increasing attention. To construct a bioactive surface with CO-releasing properties on the surface of magnesium-based alloy to augment the anticorrosion and biocompatibility, graphene oxide (GO) was firstly modified using carboxymethyl chitosan (CS), and then CO-releasing molecules (CORM401) were introduced to synthesize a novel biocompatible nanomaterial (GOCS-CO) that can release CO in the physiological environments. The GOCS-CO was further immobilized on the magnesium alloy surface modified by polydopamine coating with Zn (PDA/Zn) to create a bioactive surface capable of releasing CO in the physiological environment. The outcomes showed that the CO-releasing coating can not only significantly enhance the anticorrosion and abate the corrosion degradation rate of the magnesium alloy in a simulated physiological environment, but also endow it with good hydrophilicity and a certain ability to adsorb albumin selectively. Owing to the significant enhancement of anticorrosion and hydrophilicity, coupled with the bioactivity of GOCS, the modified sample not only showed excellent ability to prevent platelet adhesion and activation and reduce hemolysis rate but also can promote endothelial cell (EC) adhesion, proliferation as well as the expression of nitric oxide (NO) and vascular endothelial growth factor (VEGF). In the case of CO release, the hemocompatibility and EC growth behaviors were further significantly improved, suggesting that CO molecules released from the surface can significantly improve the hemocompatibility and EC growth. Consequently, the present study provides a novel surface modification method that can simultaneously augment the anticorrosion and biocompatibility of magnesium-based alloys, which will strongly promote the research and application of CO-releasing bioactive coatings for surface functionalization of cardiovascular biomaterials and devices.
由于其类似 NO 的生物功能,CO 气体信号分子在调节植入后体内性能的心血管生物材料中逐渐显示出巨大的潜力,受到越来越多的关注。为了在镁基合金表面构建具有 CO 释放性能的生物活性表面,以提高其耐腐蚀性和生物相容性,首先用羧甲基壳聚糖(CS)对氧化石墨烯(GO)进行修饰,然后引入 CO 释放分子(CORM401)合成一种新型生物相容性纳米材料(GOCS-CO),可在生理环境中释放 CO。将 GOCS-CO 进一步固定在多巴胺涂层修饰的锌修饰的镁合金表面(PDA/Zn)上,以创建可在生理环境中释放 CO 的生物活性表面。结果表明,CO 释放涂层不仅可以显著提高镁合金在模拟生理环境中的耐腐蚀性并降低其腐蚀降解速率,还赋予其良好的亲水性和一定的选择性吸附白蛋白的能力。由于耐腐蚀性和亲水性的显著提高,再加上 GOCS 的生物活性,改性后的样品不仅表现出优异的抑制血小板黏附和激活以及降低溶血率的能力,还能促进内皮细胞(EC)黏附、增殖以及一氧化氮(NO)和血管内皮生长因子(VEGF)的表达。在 CO 释放的情况下,血液相容性和 EC 生长行为得到进一步显著改善,表明表面释放的 CO 分子可显著提高血液相容性和 EC 生长。因此,本研究提供了一种同时提高镁基合金耐腐蚀性和生物相容性的新型表面改性方法,这将有力地促进 CO 释放生物活性涂层在心血管生物材料和器件表面功能化方面的研究和应用。