摘要
In this study, lysine was introduced into the surface of apatite-wollastonite glass ceramic （AW-GC） to improve its cytocompatibility by two steps reaction procedure. Firstly, lysine connected to N-β-（aminoethyl）-y-aminopropyl trimethoxy silane （A-1120） by covalent binding of amide group. Secondly, the lysine-functionalized A-1120 was deposited on the surface of AW-GC through a silanization reaction involving a covalent attachment. FTIR spectra indicated that lysine had been immobilized onto the surface of AW-GC successfully. Bioactivity of the surface modified AW-GC was investigated by simulated body fluid （SBF）, and the in vitro cytocompatibility was evaluated by coculturing with human osteosarcoma cell MG63. The results showed that the process of hydroxyapatite layer formed on the modified material was similar to AW-GC while the mode of hydroxyapatite deposition was changed. The growth of MG63 cells showed that modifying the AW-GC surface with lysine enhances the cell adhesion and proliferation.
In this study, lysine was introduced into the surface of apatite-wollastonite glass ceramic （AW-GC） to improve its cytocompatibility by two steps reaction procedure. Firstly, lysine connected to N-β-（aminoethyl）-y-aminopropyl trimethoxy silane （A-1120） by covalent binding of amide group. Secondly, the lysine-functionalized A-1120 was deposited on the surface of AW-GC through a silanization reaction involving a covalent attachment. FTIR spectra indicated that lysine had been immobilized onto the surface of AW-GC successfully. Bioactivity of the surface modified AW-GC was investigated by simulated body fluid （SBF）, and the in vitro cytocompatibility was evaluated by coculturing with human osteosarcoma cell MG63. The results showed that the process of hydroxyapatite layer formed on the modified material was similar to AW-GC while the mode of hydroxyapatite deposition was changed. The growth of MG63 cells showed that modifying the AW-GC surface with lysine enhances the cell adhesion and proliferation.
