Center of Interventional Radiology and Vascular Surgery, Department of Radiology, Cultivation and Construction Site of the State Key Laboratory of Intelligent Imaging and Interventional Medicine, Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Medical School, Southeast University, Nanjing, Jiangsu Province, People's Republic of China.
Department of Biochemistry and Molecular Biology, Medical School, Southeast University, Nanjing, Jiangsu Province, People's Republic of China.
Int J Nanomedicine. 2024 Jun 4;19:5157-5172. doi: 10.2147/IJN.S462691. eCollection 2024.
Poly-L-lactic acid (PLLA) stents have broad application prospects in the treatment of cardiovascular diseases due to their excellent mechanical properties and biodegradability. However, foreign body reactions caused by stent implantation remain a bottleneck that limits the clinical application of PLLA stents. To solve this problem, the biocompatibility of PLLA stents must be urgently improved. Albumin, the most abundant inert protein in the blood, possesses the ability to modify the surface of biomaterials, mitigating foreign body reactions-a phenomenon described as the "stealth effect". In recent years, a strategy based on albumin camouflage has become a focal point in nanomedicine delivery and tissue engineering research. Therefore, albumin surface modification is anticipated to enhance the surface biological characteristics required for vascular stents. However, the therapeutic applicability of this modification has not been fully explored.
Herein, a bionic albumin (PDA-BSA) coating was constructed on the surface of PLLA by a mussel-inspired surface modification technique using polydopamine (PDA) to enhance the immobilization of bovine serum albumin (BSA).
Surface characterization revealed that the PDA-BSA coating was successfully constructed on the surface of PLLA materials, significantly improving their hydrophilicity. Furthermore, in vivo and in vitro studies demonstrated that this PDA-BSA coating enhanced the anticoagulant properties and pro-endothelialization effects of the PLLA material surface while inhibiting the inflammatory response and neointimal hyperplasia at the implantation site.
These findings suggest that the PDA-BSA coating provides a multifunctional biointerface for PLLA stent materials, markedly improving their biocompatibility. Further research into the diverse applications of this coating in vascular implants is warranted.
聚左旋乳酸(PLLA)支架由于其优异的机械性能和生物降解性,在心血管疾病的治疗中有广泛的应用前景。然而,支架植入引起的异物反应仍然是限制 PLLA 支架临床应用的瓶颈。为了解决这个问题,迫切需要提高 PLLA 支架的生物相容性。白蛋白是血液中最丰富的惰性蛋白,具有修饰生物材料表面的能力,减轻异物反应——这种现象被描述为“隐身效应”。近年来,基于白蛋白伪装的策略已成为纳米医学输送和组织工程研究的焦点。因此,白蛋白表面修饰有望增强血管支架所需的表面生物特性。然而,这种修饰的治疗适用性尚未得到充分探索。
在此,通过贻贝启发的表面改性技术,利用聚多巴胺(PDA)在 PLLA 表面构建仿生白蛋白(PDA-BSA)涂层,以增强牛血清白蛋白(BSA)的固定化。
表面特性分析表明,成功地在 PLLA 材料表面构建了 PDA-BSA 涂层,显著提高了其亲水性。此外,体内和体外研究表明,这种 PDA-BSA 涂层增强了 PLLA 材料表面的抗凝血性能和促进内皮化作用,同时抑制了植入部位的炎症反应和新生内膜增生。
这些发现表明,PDA-BSA 涂层为 PLLA 支架材料提供了多功能的生物界面,显著提高了其生物相容性。进一步研究这种涂层在血管植入物中的多种应用是必要的。