TY - JOUR
T1 - Direct covalent attachment of silver nanoparticles on radical-rich plasma polymer films for antibacterial applications
AU - Akhavan, Behnam
AU - Bakhshandeh, Sadra
AU - Najafi-Ashtiani, Hamed
AU - Fluit, Ad C.
AU - Boel, Edwin
AU - Vogely, Charles
AU - Van Der Wal, Bart C.H.
AU - Zadpoor, Amir A.
AU - Weinans, Harrie
AU - Hennink, Wim E.
AU - Bilek, Marcela M.
AU - Amin Yavari, Saber
N1 - Funding Information:
The research for this paper was financially supported by the University of Sydney – Utrecht University Partnership Collaboration Award, grant no. CB.842300.3.50.029.
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - Prevention and treatment of biomaterial-associated infections (BAI) are imperative requirements for the effective and long-lasting function of orthopedic implants. Surface-functionalization of these materials with antibacterial agents, such as antibiotics, nanoparticles and peptides, is a promising approach to combat BAI. The well-known silver nanoparticles (AgNPs) in particular, although benefiting from strong and broad-range antibacterial efficiency, have been frequently associated with mammalian cell toxicity when physically adsorbed on biomaterials. The majority of irreversible immobilization techniques employed to fabricate AgNP-functionalized surfaces are based on wet-chemistry methods. However, these methods are typically substrate-dependent, complex, and time-consuming. Here we present a simple and dry strategy for the development of polymeric coatings used as platforms for the direct, linker-free covalent attachment of AgNPs onto solid surfaces using ion-assisted plasma polymerization. The resulting coating not only exhibits long-term antibiofilm efficiency against adherent Staphylococcus aureus (S. aureus), but also enhances osteoblast adhesion and proliferation. High resolution X-ray photoelectron spectroscopy (XPS), before and after sodium dodecyl sulfate (SDS) washing, confirms covalent bonding. The development of such silver-functionalized surfaces through a simple, plasma-based process holds great promise for the fabrication of implantable devices with improved tissue-implant integration and reduced biomaterial associated infections.
AB - Prevention and treatment of biomaterial-associated infections (BAI) are imperative requirements for the effective and long-lasting function of orthopedic implants. Surface-functionalization of these materials with antibacterial agents, such as antibiotics, nanoparticles and peptides, is a promising approach to combat BAI. The well-known silver nanoparticles (AgNPs) in particular, although benefiting from strong and broad-range antibacterial efficiency, have been frequently associated with mammalian cell toxicity when physically adsorbed on biomaterials. The majority of irreversible immobilization techniques employed to fabricate AgNP-functionalized surfaces are based on wet-chemistry methods. However, these methods are typically substrate-dependent, complex, and time-consuming. Here we present a simple and dry strategy for the development of polymeric coatings used as platforms for the direct, linker-free covalent attachment of AgNPs onto solid surfaces using ion-assisted plasma polymerization. The resulting coating not only exhibits long-term antibiofilm efficiency against adherent Staphylococcus aureus (S. aureus), but also enhances osteoblast adhesion and proliferation. High resolution X-ray photoelectron spectroscopy (XPS), before and after sodium dodecyl sulfate (SDS) washing, confirms covalent bonding. The development of such silver-functionalized surfaces through a simple, plasma-based process holds great promise for the fabrication of implantable devices with improved tissue-implant integration and reduced biomaterial associated infections.
UR - http://www.scopus.com/inward/record.url?scp=85054130953&partnerID=8YFLogxK
U2 - 10.1039/c8tb01363b
DO - 10.1039/c8tb01363b
M3 - Article
AN - SCOPUS:85054130953
SN - 2050-7518
VL - 6
SP - 5845
EP - 5853
JO - Journal of Materials Chemistry B
JF - Journal of Materials Chemistry B
IS - 37
ER -