Abstract
Calcium phosphate (CaP) was formed on glutamic acid-modified nickel-free high-nitrogen stainless steel (HNS) by a chemical solution deposition method in neutral/alkaline solution. Modification of glutamic acid on the surface of HNS was performed using trisuccinimidyl citrate (TSC) as a linker. The glutamic acid-derived carboxyl groups introduced on HNS initiated rapid nucleation of CaP during each treatment at pH 7.3 or 8.9. X-ray diffraction analysis and Fourier transform infrared spectra showed each CaP deposited on glutamic acid-immobilized HNS after 24 hrs was identified as low-crystallinity calcium-deficient carbonate-containing hydroxyapatite (HAp). A significant difference in the microstructure between the two pH values was observed; HAp deposited at pH 7.3 was composed of plate-like crystals, whereas that at pH 8.9 was chestnut-like crystals. Therefore, the pH value of the solution played an effective role in controlling the microstructure of HAp deposited on glutamic acid-immobilized HNS.
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