Li Xiaolin, Ji Jian, Pu Ming, Wang Xiaoli, Shen Jiacong
Department of Polymer Science, Zhejiang University, Hangzhou 310027, China.
J Mater Sci Mater Med. 2008 Jan;19(1):291-9. doi: 10.1007/s10856-006-0110-1. Epub 2007 Jun 28.
The comb-like PEG (CPEG) end-tethered with L-lysine was explored to surface modification of PET to enhance endothelialization. The hydroxyl end groups of CPEG were oxygenated into aldehyde groups. The CPEG-CHO was grafted onto the aminolysized PET. The L-lysine was then end-tethered onto surface via the residual aldehyde groups. The surface modification was confirmed by ATR-FTIR, contact angle and XPS measurements. The endothelial cell adhesion, proliferation and viability results indicated that the PET-CPEG resisted cell adhesion and growth, where as PET-CPEG-lysine promoted cell adhesion and growth. The MTT assay and total cell protein tests indicated that the endothelial cells on PET-CPEG-lysine had high viability. Cell spread uniformly and covered completely on the PET-CPEG-lysine. The CPEG end tethered with L-lysine could regulate cell adhesion and growth and enhance surface endothelialization.
研究了用L-赖氨酸末端连接的梳状聚乙二醇(CPEG)对聚对苯二甲酸乙二酯(PET)进行表面改性以增强内皮化。将CPEG的羟基端基氧化成醛基。将CPEG-CHO接枝到氨基化的PET上。然后通过残留的醛基将L-赖氨酸末端连接到表面。通过衰减全反射傅里叶变换红外光谱(ATR-FTIR)、接触角和X射线光电子能谱(XPS)测量对表面改性进行了确认。内皮细胞黏附、增殖和活力结果表明,PET-CPEG能抵抗细胞黏附和生长,而PET-CPEG-赖氨酸则促进细胞黏附和生长。MTT法和总细胞蛋白测试表明,PET-CPEG-赖氨酸上的内皮细胞具有高活力。细胞在PET-CPEG-赖氨酸上均匀铺展并完全覆盖。用L-赖氨酸末端连接的CPEG可以调节细胞黏附和生长并增强表面内皮化。