Abstract
Zirconium tetra(tert-butoxide) reacts with surface amide groups of polyamide nylon 6/6 to give (η2-amidate)zirconium complexes in high yield. These surface complexes react to bond the cell-adhesive peptide arginine-glycine-aspartic acid (RGD) to the polymer surface. A surface loading of 0.18 nmol/cm2 of RGD is achieved, which is 20-1000 times higher than previously reported attainable on natural or synthetic polymers by other strategies. Approximately 40% of the nylon surface is covered by the RGD, which gives a surface that is both stable to hydrolysis and highly active for cell adhesion and spreading in vitro.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 93-97 |
| Number of pages | 5 |
| Journal | Journal of the American Chemical Society |
| Volume | 129 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 10 2007 |
All Science Journal Classification (ASJC) codes
- Catalysis
- General Chemistry
- Biochemistry
- Colloid and Surface Chemistry