TY - JOUR
T1 - Effect of hydrogen peroxide on bovine serum albumin adsorption on Ti6Al4V alloy
T2 - A scanning Kelvin probe force microscopy study
AU - Rahimi, Ehsan
AU - Offoiach, Ruben
AU - Hosseinpour, Saman
AU - Davoodi, Ali
AU - Baert, Kitty
AU - Lutz, Alexander
AU - Terryn, Herman
AU - Lekka, Maria
AU - Fedrizzi, Lorenzo
PY - 2021/10/15
Y1 - 2021/10/15
N2 - Protein adsorption on the surface of implant materials greatly affects the performance of the implants, such as their stability as well as the release of metal ions from and the adhesion of cells to their surface. In addition, the production of extracellular H2O2 from the activation of inflammatory cells could interfere with protein–metal interactions and/or modify the conformation of adsorbed proteins. In this study, we utilised scanning Kelvin probe force microscopy (SKPFM) to visualise the impact of H2O2 on bovine serum albumin (BSA) adsorption on the positively polarised Ti6Al4V alloy in a phosphate-buffered saline (PBS) solution. We show that the negatively charged BSA adsorbs onto the surface of polished and anodically polarised Ti6Al4V in a dense layer with a continuous network-like morphology or cluster shape and reduces the variation in the total surface potential compared to that of blank Ti6Al4V. However, addition of H2O2 to the PBS solution interferes with the formation of the dense protein network, and only a thin and discontinuous protein layer adsorbs onto the surface of the Ti6Al4V alloy, lowering the total surface potential difference. The information presented in this work provides new insights into the adsorption distribution of proteins on metallic substrates in biomaterials field.
AB - Protein adsorption on the surface of implant materials greatly affects the performance of the implants, such as their stability as well as the release of metal ions from and the adhesion of cells to their surface. In addition, the production of extracellular H2O2 from the activation of inflammatory cells could interfere with protein–metal interactions and/or modify the conformation of adsorbed proteins. In this study, we utilised scanning Kelvin probe force microscopy (SKPFM) to visualise the impact of H2O2 on bovine serum albumin (BSA) adsorption on the positively polarised Ti6Al4V alloy in a phosphate-buffered saline (PBS) solution. We show that the negatively charged BSA adsorbs onto the surface of polished and anodically polarised Ti6Al4V in a dense layer with a continuous network-like morphology or cluster shape and reduces the variation in the total surface potential compared to that of blank Ti6Al4V. However, addition of H2O2 to the PBS solution interferes with the formation of the dense protein network, and only a thin and discontinuous protein layer adsorbs onto the surface of the Ti6Al4V alloy, lowering the total surface potential difference. The information presented in this work provides new insights into the adsorption distribution of proteins on metallic substrates in biomaterials field.
KW - Albumin protein
KW - Hydrogen peroxide
KW - Protein surface potential
KW - SKPFM
KW - Ti6Al4V alloy
UR - http://www.scopus.com/inward/record.url?scp=85109543887&partnerID=8YFLogxK
U2 - 10.1016/j.apsusc.2021.150364
DO - 10.1016/j.apsusc.2021.150364
M3 - Article
AN - SCOPUS:85109543887
VL - 563
JO - Applied Surface Science
JF - Applied Surface Science
SN - 0169-4332
M1 - 150364
ER -