Zhou Jinsheng, Huang Zixiang, Sun Yugui, Cui Mengmeng, Luo Zhongkuan, Yu Bin, Zou Xianghui, Hu Huiyuan
College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, 518000, China; Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, 518000, China; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, 521041, China.
College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen, 518000, China.
Colloids Surf B Biointerfaces. 2021 Jul;203:111718. doi: 10.1016/j.colsurfb.2021.111718. Epub 2021 Mar 23.
An innovative g-CN catalyzed surface-initiated photo atom transfer radical polymerization (SI-photoATRP) has been developed to construct MEDSAH zwitterionic polymer brushes on PVA hydrogel surface. g-CN catalyzed SI-photoATRP is temporal and spatial control. As a heterogeneous reaction system, it can solve the catalyst residues problem. After grafting with MEDSAH, surface chemical composition and morphology of PVA-g-pMEDSAH hydrogel confirmed that MEDSAH was successfully grafted onto PVA hydrogel. Thermal property of PVA-g-pMEDSAH hydrogel decreased and hydrophilicity increased. No statistically significant differences between PVA and PVA-g-pMEDSAH were observed on mechanical properties. Cytotoxicity in vitro of PVA-g-pMEDSAH hydrogel could be considered as no cytotoxicity for L929 and NDHF cells. The antifouling properties of PVA-g-pMEDSAH hydrogel were significantly improved due to the enhancement of the surface hydration and steric repulsion effects caused by pMEDSAH polymer brushes. In addition, g-CN is easier to modify to enhance the photocatalyst property. Thus, the heterogeneous reaction system of g-CN catalyzed SI-photoATRP has huge potential applied in biomaterials surface modification.
一种创新的g-CN催化表面引发光原子转移自由基聚合(SI-光引发原子转移自由基聚合)已被开发出来,用于在聚乙烯醇(PVA)水凝胶表面构建MEDSAH两性离子聚合物刷。g-CN催化的SI-光引发原子转移自由基聚合具有时间和空间可控性。作为一种非均相反应体系,它可以解决催化剂残留问题。用MEDSAH接枝后,PVA-g-pMEDSAH水凝胶的表面化学成分和形态证实MEDSAH已成功接枝到PVA水凝胶上。PVA-g-pMEDSAH水凝胶的热性能下降,亲水性增加。在机械性能方面,未观察到PVA和PVA-g-pMEDSAH之间有统计学上的显著差异。PVA-g-pMEDSAH水凝胶在体外对L929和NDHF细胞的细胞毒性可被认为无细胞毒性。由于pMEDSAH聚合物刷引起的表面水合作用和空间排斥效应的增强,PVA-g-pMEDSAH水凝胶的抗污性能得到显著改善。此外,g-CN更容易改性以增强光催化剂性能。因此,g-CN催化的SI-光引发原子转移自由基聚合的非均相反应体系在生物材料表面改性方面具有巨大的应用潜力。