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. 2013 Feb 8;19(4):292–307. doi: 10.1089/ten.teb.2012.0577

Table 2.

Recent Examples of Molecules and Methods of Immobilization Used to Achieve Enhanced Endothelialization

Author Biofunctionalization molecule Immobilization method Model Effects
Shin et al.84 VEGF PDA/Dipping In vitro VEGF did not produce significantly more HUVEC adhesion than PDA alone; VEGF did support increased CD31 expression
Du et al.108 Hyaluronic acid Covalently bound In vitro Increased HUVEC attachment
Yin et al.63 Anti-CD34 3,4-dihydroxyphenyalinine and l-lysine co-polypeptide linking In vitro Attachment and growth of ECs and EPCs increased
Kuwabara et al.79 CAG peptide Mixed into PCL solution for electrospinning fibers Rat Higher rate of confluent endothelialization of grafts
De Visscher et al.43 SDF-1α Immersed in fibronectin solution, followed by SDF-1α immersion Sheep Four times higher fraction of CD34+ cells adhered; all grafts patent after 3 months
Williams et al.73 Laminin type 1 Covalently bound Rat Accelerated neovascularization and endothelialization
Zheng et al.77 Nap-FFGRGD Molecular self-assembly of a hydrogelator75 Rabbit Threefold increase in endothelial coverage; 100% patency at 2 and 4 weeks compared to 60% patency in uncoated grafts

ECs, endothelial cells; EPCs, endothelial progenitor cells; PDA, poly(dopamine), VEGF, vascular endothelial growth factor; HUVEC, human umbilical vein endothelial cells; CAG, cysteine-alanine-glycine; SDF, stromal cell-derived factor; PCL, poly(caprolactone).