TY - JOUR
T1 - Surface reactivity of octacalcium phosphate-derived fluoride-containing apatite in the presence of polyols and fluoride
AU - Tsutsui, Sei
AU - Anada, Takahisa
AU - Shiwaku, Yukari
AU - Tsuchiya, Kaori
AU - Yamazaki, Hajime
AU - Suzuki, Osamu
N1 - Funding Information:
This study was supported in part by Grants-in-aid (25670829, 15K15720, and 17K19740) from the Ministry of Education, Science, Sports and Culture of Japan (MEXT) and a Joint Research Program with Kao Corporation. We are grateful to Drs. Yoshitaka Yano and Atsushi Yamagishi of Kao Corporation for their critical and essential advises to form the plan of the present study from the view point of biomineralization.
Publisher Copyright:
© 2017 Wiley Periodicals, Inc.
PY - 2018/8
Y1 - 2018/8
N2 - The present study was designed to characterize co-precipitated fluoridated apatitic materials from octacalcium phosphate (OCP) precursor and to investigate their surface reactions with polyols including glycerol in the presence of fluoride ions. Laboratory-synthesized fluoridated apatite crystals (LS-FA) were obtained in a solution containing fluoride (F) from 25 to 500 ppm. LS-FAs and commercially available fluoroapatite (FA) and hydroxyapatite (HA) were characterized by physical techniques, such as X-ray diffraction. LS-FA obtained in the presence of 100 ppmF (100 ppm-LS-FA) had an apatitic structure, but its solubility was close to HA in a culture medium (α-MEM) despite the fact it contains over 3 wt % of F. 100 ppm-LS-FA, FA, and HA were then subjected to the human serum albumin (HSA) adsorption test at pH 7.4 (in a 150 mM Tris–HCl buffer) and the dissolution and re-mineralization experiments in the presence of xylitol, D-sorbitol, or glycerol, and F under acidic and neutral conditions. Adsorption affinity of HSA was estimated as highest for FA and lowest for LS-FA. LS-FA, FA, and HA were immersed in a lactic acid solution with the polyols and/or F ion-containing solution up to 200 ppm to analyze the dissolution behavior. LS-FA had the highest dissolution tendency in the conditions examined. Glycerol enhanced the dissolution of phosphate from apatite crystals in particular from LS-FA. The results suggest that the apatite crystals, obtained through the hydrolysis of OCP in the presence of F, provide a more reactive surface than FA or HA under physiological environments.
AB - The present study was designed to characterize co-precipitated fluoridated apatitic materials from octacalcium phosphate (OCP) precursor and to investigate their surface reactions with polyols including glycerol in the presence of fluoride ions. Laboratory-synthesized fluoridated apatite crystals (LS-FA) were obtained in a solution containing fluoride (F) from 25 to 500 ppm. LS-FAs and commercially available fluoroapatite (FA) and hydroxyapatite (HA) were characterized by physical techniques, such as X-ray diffraction. LS-FA obtained in the presence of 100 ppmF (100 ppm-LS-FA) had an apatitic structure, but its solubility was close to HA in a culture medium (α-MEM) despite the fact it contains over 3 wt % of F. 100 ppm-LS-FA, FA, and HA were then subjected to the human serum albumin (HSA) adsorption test at pH 7.4 (in a 150 mM Tris–HCl buffer) and the dissolution and re-mineralization experiments in the presence of xylitol, D-sorbitol, or glycerol, and F under acidic and neutral conditions. Adsorption affinity of HSA was estimated as highest for FA and lowest for LS-FA. LS-FA, FA, and HA were immersed in a lactic acid solution with the polyols and/or F ion-containing solution up to 200 ppm to analyze the dissolution behavior. LS-FA had the highest dissolution tendency in the conditions examined. Glycerol enhanced the dissolution of phosphate from apatite crystals in particular from LS-FA. The results suggest that the apatite crystals, obtained through the hydrolysis of OCP in the presence of F, provide a more reactive surface than FA or HA under physiological environments.
UR - http://www.scopus.com/inward/record.url?scp=85052577210&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85052577210&partnerID=8YFLogxK
U2 - 10.1002/jbm.b.34026
DO - 10.1002/jbm.b.34026
M3 - Article
C2 - 29076293
AN - SCOPUS:85052577210
SN - 1552-4973
VL - 106
SP - 2235
EP - 2244
JO - Journal of Biomedical Materials Research - Part B Applied Biomaterials
JF - Journal of Biomedical Materials Research - Part B Applied Biomaterials
IS - 6
ER -