Hu Mengyue, Peng Xu, Shi Shubin, Wan Chang, Cheng Can, Lei Ningning, Yu Xixun
College of Polymer Science and Engineering, Sichuan University, Chengdu 610065, P. R. China.
Experimental and Research Animal Institute, Sichuan University, Chengdu 610065, P. R. China.
J Mater Chem B. 2022 Oct 19;10(40):8218-8234. doi: 10.1039/d2tb01704k.
Clinically frequently-used glutaraldehyde (GA)-crosslinked bioprosthetic valve leaflets (BVLs) are still curbed by acute thrombosis, malignant immunoreaction, calcification, and poor durability. In this study, an anticoagulant heparin-like biomacromolecule, sulfonated, oxidized pectin (SAP) with a dialdehyde structure was first obtained by modifying citrus pectin with sulfonation of 3-amino-1-propane sulfonic acid and then oxidating with periodate. Notably, a novel crosslinking approach was established by doubly crosslinking BVLs with SAP and the nature-derived crosslinking agent quercetin (Que), which play a synergistic role in both crosslinking and bioactivity. The double crosslinked BVLs also presented enhanced mechanical properties and enzymatic degradation resistance owing to the double crosslinking networks formed CN bonds and hydrogen bonds, respectively, and good HUVEC-cytocompatibility. The and assay manifested that the double-crosslinked BVLs had excellent anticoagulant and antithrombotic properties, owing to the introduction of SAP. The subcutaneous implantation also demonstrated that the obtained BVLs showed a reduced inflammatory response and great resistance to calcification, which is attributed to quercetin with multiple physiological activities and depletion of aldehyde groups by hydroxyl aldehyde reaction. With excellent stability, hemocompatibility, anti-inflammatory, anti-calcification, and pro-endothelialization properties, the obtained double-crosslinked BVLs, SAP + Que-PP, would have great potential to substitute the current clinical GA-crosslinked BVLs.
临床上常用的戊二醛(GA)交联生物人工心脏瓣膜小叶(BVLs)仍受到急性血栓形成、恶性免疫反应、钙化和耐久性差等问题的限制。在本研究中,首先通过用3-氨基-1-丙烷磺酸磺化柑橘果胶,然后用过碘酸盐氧化,得到了一种具有双醛结构的抗凝肝素样生物大分子——磺化氧化果胶(SAP)。值得注意的是,建立了一种新的交联方法,即通过将BVLs与SAP和天然衍生的交联剂槲皮素(Que)进行双重交联,二者在交联和生物活性方面发挥协同作用。由于分别形成了CN键和氢键的双重交联网络,双重交联的BVLs还表现出增强的机械性能和抗酶降解性,以及良好的人脐静脉内皮细胞(HUVEC)细胞相容性。 分析表明,由于引入了SAP,双重交联的BVLs具有优异的抗凝和抗血栓性能。皮下植入实验也表明,所获得的BVLs表现出炎症反应减轻和对钙化的高度抗性,这归因于具有多种生理活性的槲皮素以及通过羟醛反应消耗醛基。所获得的双重交联BVLs,即SAP + Que-PP,具有优异的稳定性、血液相容性、抗炎、抗钙化和促内皮化性能,有很大的潜力替代目前临床使用的GA交联BVLs。