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通过配体连接的梳状聚乙二醇对聚对苯二甲酸乙二酯进行表面修饰以增强内皮化。

Surface tailoring of poly(ethylene terephthalate) via ligand-tethered comb-like PEG to enhance endothelialization.

作者信息

Li Xiaolin, Ji Jian, Pu Ming, Wang Xiaoli, Shen Jiacong

机构信息

Department of Polymer Science, Zhejiang University, Hangzhou 310027, China.

出版信息

J Mater Sci Mater Med. 2008 Jan;19(1):291-9. doi: 10.1007/s10856-006-0110-1. Epub 2007 Jun 28.

Abstract

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.

摘要

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。

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