TY - JOUR
T1 - Cell proliferation on titania layer with in vitro apatite forming ability
AU - Yabe, S.
AU - Tsuru, K.
AU - Hayakawa, S.
AU - Osaka, A.
AU - Yoshida, Y.
AU - Suzuki, K.
AU - Kuboki, T.
PY - 2007
Y1 - 2007
N2 - Titania layer was fabricated on the titanium substrates with chemical treatment with 20ml or 40ml of hydrogen peroxide solution and subsequent heat treatment at 400°C, coded as CHT20 and CHT40, respectively. CHT20 spontaneously deposited apatite on the surface in a simulated body fluid (SBF), while CHT40 did not. TF-XRD patterns showed that the diffraction intensity of anatase of CHT20 was higher than that of CHT40. It was suggested that the thicker titania layer indicated in vitro apatite forming ability. The cell proliferation of CHT20 and CHT40 were lower than NT and HT. Since the surface of titania layers became hydrophobic after autoclaving, we can suppose that the cell proliferation on CHT20 and CHT40 were lower than NT and HT due to their surface hydrophobicity.
AB - Titania layer was fabricated on the titanium substrates with chemical treatment with 20ml or 40ml of hydrogen peroxide solution and subsequent heat treatment at 400°C, coded as CHT20 and CHT40, respectively. CHT20 spontaneously deposited apatite on the surface in a simulated body fluid (SBF), while CHT40 did not. TF-XRD patterns showed that the diffraction intensity of anatase of CHT20 was higher than that of CHT40. It was suggested that the thicker titania layer indicated in vitro apatite forming ability. The cell proliferation of CHT20 and CHT40 were lower than NT and HT. Since the surface of titania layers became hydrophobic after autoclaving, we can suppose that the cell proliferation on CHT20 and CHT40 were lower than NT and HT due to their surface hydrophobicity.
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U2 - 10.4028/0-87849-422-7.131
DO - 10.4028/0-87849-422-7.131
M3 - Article
AN - SCOPUS:33846313603
SN - 1013-9826
VL - 330-332 I
SP - 131
EP - 134
JO - Key Engineering Materials
JF - Key Engineering Materials
ER -