Hydrolysis and cytocompatibility of zinc-containing α-tricalcium phosphate powder

被引:19
作者
Sogo, Y
Ito, A
Kamo, M
Sakurai, T
Onuma, K
Ichinose, N
Otsuka, M
LeGeros, RZ
机构
[1] Natl Inst Adv Ind Sci & Technol, Inst Human Sci & Biomed Engn, Tsukuba, Ibaraki 3058566, Japan
[2] Waseda Univ, Sch Sci & Engn, Dept Mat Sci & Engn, Shinjuku Ku, Tokyo 1698555, Japan
[3] Kobe Pharmaceut Univ, Kobe, Hyogo 6588558, Japan
[4] NYU, Coll Dent, Dept Biomat, New York, NY 10010 USA
来源
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS | 2004年 / 24卷 / 6-8期
关键词
zinc; alpha-tricalcium phosphate; cytocompatibility; hydrolysis;
D O I
10.1016/j.msec.2004.08.016
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Zinc is an essential trace element with stimulatory effects on bone formation in vitro and in vivo. In order to apply zinc-containing alpha-tricalcium phosphate (alphaZnTCP) to alphaTCP-based calcium phosphate cement, alphaZnTCP powders containing various amounts of zinc were prepared and the optimum zinc content was examined from the viewpoints of hydrolysis property and cytocompatibility. Single-phase alphaZnTCP containing zinc from 0.00 to 1.26 wt.% was obtained by heating zinc-containing beta-tricalcium phosphate at 1450 degreesC. At a zinc content of 0.11 wt.%, there was no significant difference in the amount of calcium-deficient low-crystalline apatite formed by hydrolysis between pure alphaTCP and alphaZnTCP. The hydrolysis of alphaZnTCP was significantly retarded by incorporating zinc at or more than 0.26 wt.% due to the inhibitory effect of zinc on the crystal growth of apatite. The MC3T3-E1 cell densities cultured with pure alphaTCP and 0.11 Zn wt.% alphaZnTCP powders showed no significant difference in the range of powder dose from 10 to 1000 mug mL(-1). The result indicated that the cytocompatibility of pure alphaTCP powder was comparable to that of alphaZnTCP at the zinc content of 0.11 wt.%. Therefore, the optimum zinc content of alphaZnTCP powder is less than 0.26 wt.%, and preferably at or less than 0.11 wt.% to apply to an alphaTCP-based calcium phosphate cement. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:709 / 715
页数:7
相关论文
共 25 条
[1]  
[Anonymous], WHO TECH REP SER
[2]   INTERLAYERING OF CRYSTALLINE OCTACALCIUM PHOSPHATE AND HYDROXYLAPATITE [J].
BROWN, WE ;
SCHROEDER, LW ;
FERRIS, JS .
JOURNAL OF PHYSICAL CHEMISTRY, 1979, 83 (11) :1385-1388
[3]   SKELETAL REPAIR BY IN-SITU FORMATION OF THE MINERAL PHASE OF BONE [J].
CONSTANTZ, BR ;
ISON, IC ;
FULMER, MT ;
POSER, RD ;
SMITH, ST ;
VANWAGONER, M ;
ROSS, J ;
GOLDSTEIN, SA ;
JUPITER, JB ;
ROSENTHAL, DI .
SCIENCE, 1995, 267 (5205) :1796-1799
[4]   TOXICITY OF HYDROXYAPATITE INVITRO - THE EFFECT OF PARTICLE-SIZE [J].
EVANS, EJ .
BIOMATERIALS, 1991, 12 (06) :574-576
[5]  
HURLEY LS, 1969, P SOC EXP BIOL MED, V130, P856, DOI 10.3181/00379727-130-33672
[6]  
Ito A, 2000, J BIOMED MATER RES, V50, P178, DOI 10.1002/(SICI)1097-4636(200005)50:2<178::AID-JBM12>3.3.CO
[7]  
2-X
[8]   Resorbability and solubility of zinc-containing tricalcium phosphate [J].
Ito, A ;
Kawamura, H ;
Miyakawa, S ;
Layrolle, P ;
Kanzaki, N ;
Treboux, G ;
Onuma, K ;
Tsutsumi, S .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 60 (02) :224-231
[9]   Zinc-releasing calcium phosphate for stimulating bone formation [J].
Ito, A ;
Kawamura, H ;
Otsuka, M ;
Ikeuchi, M ;
Ohgushi, H ;
Ishikawa, K ;
Onuma, K ;
Kanzaki, N ;
Sogo, Y ;
Ichinose, N .
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS, 2002, 22 (01) :21-25
[10]   Inhibitory effect of magnesium and zinc on crystallization kinetics of hydroxyapatite (0001) face [J].
Kanzaki, N ;
Onuma, K ;
Treboux, G ;
Tsutsumi, S ;
Ito, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (17) :4189-4194