Abstract
Implant failure due to poor osteogenesis and bacterial infection remains a major concern, emphasizing the importance of enhancing both the osteogenic and antibacterial activities of implants. This study focuses on using polydopamine (PDA)-bridged bone morphogenetic protein-2 (BMP2) and grafting it onto benzophenone (BP)-photoinitiated 2-methacryloyloxyethyl phosphorylcholine (MPC)-coated stainless steel (SS) to form a functionalized SS substrate (SS-BP-MPC-PDA-BMP2). The PDA bridge layer induced a greater BMP2 immobilization level (6-fold improvement), mitigated burst release, and sustained a controlled release rate (0.44 ng/cm2/day) over a ten-day period. Surface wettability (at a water contact angle of 33°) and smoothness (at a root mean square of 24 nm) were achieved in the BMP2-coated sample, with a higher antibacterial fouling efficacy (41%) against Staphylococcus aureus(S. aureus) than the pristine SS and MPC-functionalized substrate (13–34%). Finally, this PDA-BMP2-modified SS prevented biofilm formation onto the surface and demonstrated the highest preosteoblast cell (MC3T3-E1 cell) metabolic activity (100–110% of the control value), with excellent proliferation behavior among the tested samples. The developed protocol is promising for implant material modification, particularly for orthopedic and dental applications.
| Original language | English |
|---|---|
| Pages (from-to) | 652-662 |
| Number of pages | 11 |
| Journal | ACS Omega |
| Volume | 11 |
| Issue number | 1 |
| DOIs | |
| State | Published - 13 01 2026 |
Bibliographical note
Publisher Copyright:© 2025 The Authors. Published by American Chemical Society
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