Synthesis and cell adhesive properties of linear and cyclic RGD functionalized polynorbornene thin films
Described herein is the efficient synthesis and evaluation of bioactive arginine-glycine-aspartic acid (RGD) functionalized polynorbornene-based materials for cell adhesion and spreading. Polynorbornenes containing either linear or cyclic RGD peptides were synthesized by ring-opening metathesis po...
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Main Authors: | , , , , , , |
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Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2013
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Online Access: | https://hdl.handle.net/10356/85266 http://hdl.handle.net/10220/12839 |
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Institution: | Nanyang Technological University |
Language: | English |
Summary: | Described herein is the efficient synthesis and evaluation of bioactive arginine-glycine-aspartic acid (RGD)
functionalized polynorbornene-based materials for cell adhesion and spreading. Polynorbornenes containing either linear or
cyclic RGD peptides were synthesized by ring-opening metathesis polymerization (ROMP) using the well-defined ruthenium
initiator [(H2IMes)(pyr)2(Cl)2RuCHPh]. The random copolymerization of three separate norbornene monomers allowed for
the incorporation of water-soluble polyethylene glycol (PEG) moieties, RGD cell recognition motifs, and primary amines for
postpolymerization cross-linking. Following polymer synthesis, thin-film hydrogels were formed by cross-linking with
bis(sulfosuccinimidyl) suberate (BS3), and the ability of these materials to support human umbilical vein endothelial cell
(HUVEC) adhesion and spreading was evaluated and quantified. When compared to control polymers containing either no
peptide or a scrambled RDG peptide, polymers with linear or cyclic RGD at varying concentrations displayed excellent cell
adhesive properties in both serum-supplemented and serum-free media. Polymers with cyclic RGD side chains maintained cell
adhesion and exhibited comparable integrin binding at a 100-fold lower concentration than those carrying linear RGD peptides.
The precise control of monomer incorporation enabled by ROMP allows for quantification of the impact of RGD structure and
concentration on cell adhesion and spreading. The results presented here will serve to guide future efforts for the design of RGD
functionalized materials with applications in surgery, tissue engineering, and regenerative medicine. |
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