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 Nov;279(Pt 1):135166. doi: 10.1016/j.ijbiomac.2024.135166. Epub 2024 Aug 29.
Although significant progress in developing biodegradable magnesium alloy materials in cardiovascular stents has been achieved recently, they still face challenges such as rapid in vivo corrosion degradation, inferior blood compatibility, and limited re-endothelialization after the implantation. Hydrogel coating that can catalyze the liberation of gas signal molecules offers a good solution to alleviate the corrosion rate and enhance the biocompatibility of magnesium and its alloys. In this study, based on alkaline heat treatment and construction of polydopamine coating on the surface of magnesium alloy, sodium alginate/carboxymethyl chitosan (SA/CMCS) gel was simultaneously covalently grafted onto the surface to build a natural polymer hydrogel coating, and selenocystamine (SeCA) and CO release molecules (CORM-401) were respectively immobilized on the surface of the hydrogel coating to ameliorate the anticoagulant performance and accelerate endothelial cells (ECs) growth by catalyzing the release of endogenous gas signal molecules (NO or CO). The findings verified that the as-prepared hydrogel coating can catalyze the liberation of CO or NO and significantly improve the corrosion resistance of magnesium alloy. At the same time, owing to the excellent hydrophilicity of the hydrogel coating, the good anticoagulant property of sodium alginate, and the ability of CMCS to promote the ECs growth, the modified magnesium alloy could significantly improve the albumin adsorption while preventing the adsorption of fibrinogen, hence significantly augmenting the anticoagulant properties and promoting the ECs growth. Under the catalytic release of NO or CO, the released gas molecules further enhanced hemocompatibility and promoted endothelial cell (EC) growth and the expression of vascular endothelial growth factor (VEGF) and NO of ECs. Therefore, the bioactive coatings that can catalyze the release of NO or CO have potential applications in constructing surface bioactive coatings for magnesium alloy materials used for intravascular stents.
尽管最近在心血管支架用可生物降解镁合金材料的开发方面取得了重大进展,但它们仍然面临着体内腐蚀降解迅速、血液相容性差以及植入后再内皮化有限等挑战。能够催化气体信号分子释放的水凝胶涂层为缓解镁及其合金的腐蚀速率和增强其生物相容性提供了很好的解决方案。在这项研究中,基于镁合金表面的碱性热处理和聚多巴胺涂层的构建,同时将海藻酸钠/羧甲基壳聚糖(SA/CMCS)凝胶共价接枝到表面上,构建了天然聚合物水凝胶涂层,并分别将硒半胱氨酸(SeCA)和 CO 释放分子(CORM-401)固定在水凝胶涂层的表面,通过催化内源性气体信号分子(NO 或 CO)的释放来改善抗凝血性能并加速内皮细胞(ECs)的生长。研究结果证实,所制备的水凝胶涂层可以催化 CO 或 NO 的释放,显著提高镁合金的耐腐蚀性。同时,由于水凝胶涂层具有优异的亲水性、海藻酸钠的良好抗凝血性以及 CMCS 促进 ECs 生长的能力,改性镁合金可以显著提高白蛋白的吸附能力,同时阻止纤维蛋白原的吸附,从而显著提高抗凝血性能并促进 ECs 的生长。在 NO 或 CO 的催化释放下,释放的气体分子进一步增强了血液相容性,并促进了内皮细胞(EC)的生长以及血管内皮生长因子(VEGF)和 ECs 中 NO 的表达。因此,能够催化释放 NO 或 CO 的生物活性涂层在构建用于血管内支架的镁合金材料表面生物活性涂层方面具有潜在的应用。