Apatite-forming ability of vinylphosphonic acid-based copolymer in simulated body fluid: effects of phosphate group content
- 256 Downloads
Phosphate groups on materials surfaces are known to contribute to apatite formation upon exposure of the materials in simulated body fluid and improved affinity of the materials for osteoblast-like cells. Typically, polymers containing phosphate groups are organic matrices consisting of apatite–polymer composites prepared by biomimetic process using simulated body fluid. Ca2+ incorporation into the polymer accelerates apatite formation in simulated body fluid owing because of increase in the supersaturation degree, with respect to apatite in simulated body fluid, owing to Ca2+ release from the polymer. However, the effects of phosphate content on the Ca2+ release and apatite-forming abilities of copolymers in simulated body fluid are rather elusive. In this study, a phosphate-containing copolymer prepared from vinylphosphonic acid, 2-hydroxyethyl methacrylate, and triethylene glycol dimethacrylate was examined. The release of Ca2+ in Tris-NaCl buffer and simulated body fluid increased as the additive amount of vinylphosphonic acid increased. However, apatite formation was suppressed as the phosphate groups content increased despite the enhanced release of Ca2+ from the polymer. This phenomenon was reflected by changes in the surface zeta potential. Thus, it was concluded that the apatite-forming ability of vinylphosphonic acid-2-hydroxyethyl methacrylate-triethylene glycol dimethacrylate copolymer treated with CaCl2 solution was governed by surface state rather than Ca2+ release in simulated body fluid.
Compliance with ethical standards
Conflict of interest
The authors declare that they have no conflict of interest.
- 23.Garrett Q, Laycock B, Garrett RW. Hydrogel lens monomer constituents modulate protein sorption. Invest Ophthalmol Vis Sci. 2000;41:1687–95.Google Scholar
- 25.Neuman W, Neuman M. The chemical dynamics of bone mineral. Chicago: University of Chicago Press; 1958.Google Scholar