Phototethering of Collagen onto Polyetheretherketone Surfaces to Enhance Osteoblastic and Endothelial Performance

Polyetheretherketone (PEEK) is a candidate material for bone implants as an alternative to metals. However, PEEK exhibits poor osseointegration and low endothelial compatibility. This study demonstrates the phototethering of collagen onto PEEK surfaces to facilitate osteoblastic and vascular endothelial performance. In particular, collagen with methacryloyl groups is covalently tethered to the PEEK surface via surface‐initiated photopolymerization. This process is simpler than the conventional method of collagen‐tethering and can be extended to the surface‐patterning treatment of collagen. The collagen is confirmed to be tethered to the PEEK surface using attenuated total reflection Fourier transform infrared measurements, bicinchoninic acid assays, and atomic force microscopic observations. When human bone marrow‐derived mesenchymal stem cells (HbmMSCs) are cultured on collagen‐tethered PEEK (COL‐PEEK) surfaces, the cells favorably adhere and proliferate. After inducing osteogenic differentiation, the cells on the COL‐PEEK surfaces show higher expression levels of osteoblast‐related genes and mineralization than those on the PEEK surface. Moreover, the tethering of collagen greatly improves endothelial proliferation. The COL‐PEEK surfaces promotes endothelial networking in coculture with HbmMSCs. These results suggest that COL‐PEEK is highly compatible with both osteoblasts and vascular endothelial cells. COL‐PEEK is a promising implant that induces osteogenesis and angiogenesis to repair bone tissues. Collagen with methacryloyl groups is tethered to a polyetheretherketone (PEEK) surface via surface‐initiated photopolymerization using PEEK. This method is simple and promising as a phototethering technique for collagen without any pretreatment of PEEK surfaces or the addition of condensing or initiating agents. Collagen‐tethered PEEK promotes the osteoblastic differentiation of mesenchymal stem cells and the networking of vascular endothelial cells.