4.6 Article

Biofunctionalization of a Clickable Organic Layer Photochemically Grafted on Titanium Substrates

Journal

LANGMUIR
Volume 27, Issue 8, Pages 4848-4856

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/la104853t

Keywords

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Funding

  1. Alliance for NanoHealth [W81XWH-09-2-0139]
  2. NSF [DMR-0706627]
  3. NIH [R21HD058985, R21EY018303]
  4. The Welch Foundation [E-1498]
  5. Texas Center for Superconductivity at the University of Houston

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We have developed a general method combining photochemical grafting and copper-catalyzed click chemistry for biofunctionalization of titanium substrates. The UV-activated grafting of an alpha,omega-alkenyne onto TiO2/Ti substrates provided a clickable thin film platform. The selective attachment of the vinyl end of the molecule to the surface was achieved by masking the alkynyl end with a trimethylgermanyl (TMG) protecting group. Subsequently, various oligo(ethylene glycol) (OEG) derivatives terminated with an azido group were attached to the TMG-alkynyl modified titanium surface via a one-pot deprotection/click reaction. The films were characterized by X-ray photoelectron spectroscopy (XPS), contact angle goniometry, ellipsometry, and atomic force microscopy (AFM). We showed that the titanium surface presenting click-immobilized OEG substantially suppressed the nonspecific attachment of protein and cells as compared to the unmodified titanium substrate. Furthermore, glycine-arginine-glycine-aspartate (GRGD), a cell adhesion peptide, was coimmobilized with OEG on the platform. We demonstrated that the resultant GRGD-presenting thin film on Ti substrates can promote the specific adhesion and spreading of AsPC-1 cells.

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