TY - JOUR
T1 - Labile Zn ions on octacalcium phosphate-derived Zn-containing hydroxyapatite surfaces
AU - Honda, Yoshitomo
AU - Anada, Takahisa
AU - Morimoto, Shinji
AU - Suzuki, Osamu
N1 - Funding Information:
We thank H. Kubota and A. Harada of the Tohoku University School of Dentistry and Y. Shiwaku of Tohoku University School of Dentistry, Division of Advanced Prosthetic Dentistry for cooperating Japan, for cooperating with us to prepare and measure the Zn-CaPs and hy-Zn-CaPs. This study was supported in part by Grants-in Aid ( 17076001 , 19390490 , 21659452 , 23390450 , 23659909 , and 23106010 ) from the Ministry of Education, Science, Sports and Culture of Japan
PY - 2013/5/15
Y1 - 2013/5/15
N2 - We previously synthesized and characterized zinc-containing octacalcium phosphate (OCP) and its hydrolyzed Ca-deficient hydroxyapatite (HA). In the present report, we attempted to define the state of Zn in the OCP-derived Zn-calcium phosphates (CaPs) in relation to the presence of specific amino acids. Zn-containing OCPs were prepared in solutions that included Zn ions up to a concentration of 3.5 mM, and their hydrolyzates [hydrolyzed (hy)-Zn-CaP] were obtained in hot water. The materials were characterized by x-ray diffraction and scanning electron microscopy. The concentration of Ca and Zn ions at room temperature was determined by analyzing the supernatant after incubating the materials in α-minimal essential medium (α-MEM) and HEPES buffer including cysteine, histidine, lysine, aspartic acid, and glutamic acid. Zn ions were more dissolved in α-MEM than HEPES buffer in the absence of amino acids. The inclusion of the amino acids enhanced Zn dissolution by several hundred fold, even in HEPES buffer. Among the amino acids, both cysteine and histidine enhanced the release of Zn. The effect was particularly remarkable with cysteine even in the presence of the other amino acids tested. These results indicate that Zn ions are present as a surface labile pool, which tends to be preferentially desorbed by cysteine, a ubiquitous molecule present in serum.
AB - We previously synthesized and characterized zinc-containing octacalcium phosphate (OCP) and its hydrolyzed Ca-deficient hydroxyapatite (HA). In the present report, we attempted to define the state of Zn in the OCP-derived Zn-calcium phosphates (CaPs) in relation to the presence of specific amino acids. Zn-containing OCPs were prepared in solutions that included Zn ions up to a concentration of 3.5 mM, and their hydrolyzates [hydrolyzed (hy)-Zn-CaP] were obtained in hot water. The materials were characterized by x-ray diffraction and scanning electron microscopy. The concentration of Ca and Zn ions at room temperature was determined by analyzing the supernatant after incubating the materials in α-minimal essential medium (α-MEM) and HEPES buffer including cysteine, histidine, lysine, aspartic acid, and glutamic acid. Zn ions were more dissolved in α-MEM than HEPES buffer in the absence of amino acids. The inclusion of the amino acids enhanced Zn dissolution by several hundred fold, even in HEPES buffer. Among the amino acids, both cysteine and histidine enhanced the release of Zn. The effect was particularly remarkable with cysteine even in the presence of the other amino acids tested. These results indicate that Zn ions are present as a surface labile pool, which tends to be preferentially desorbed by cysteine, a ubiquitous molecule present in serum.
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U2 - 10.1016/j.apsusc.2013.02.040
DO - 10.1016/j.apsusc.2013.02.040
M3 - Article
AN - SCOPUS:84876408157
SN - 0169-4332
VL - 273
SP - 343
EP - 348
JO - Applied Surface Science
JF - Applied Surface Science
ER -