Zinc is an essential trace element with stimulatory effects on bone formati
on. Therefore, zinc was doped into beta-tricalcium phosphate to develop zin
c-releasing biomaterials to promote bone formation. The zinc-doped beta-tri
calcium phosphate, beta-tricalcium phosphate, and hydroxyapatite powders we
re mixed at a (Ca+Zn)/P molar ratio of 1.60, followed by sintering into a d
ense body at 1100 degrees C for 1 h. The sintered body was a composite cera
mic consisting of zinc-doped beta-tricalcium phosphate and hydroxyapatite p
hases. The composite ceramic contained zinc oxide when the zinc content was
higher than 1.20 wt %. The composite ceramic released zinc under pseudophy
siological conditions. However, the release of calcium and phosphate decrea
sed with an increase in zinc content in a range higher than 0.12 wt t % owi
ng to a decrease in solubility of the zinc-doped beta-tricalcium phosphate
phase. Proliferation of osteoblastic MC3T3-E1 cells was significantly incre
ased on the composite ceramic with a zinc content from 0.6 to 1.20 wt %, co
mpared with those without zinc. When the zinc content was higher than 1.20
wt %, release of zinc from the zinc oxide caused cytotoxicity. Therefore, t
he zinc content of the composite ceramic must be <1.20 wt %. (C) 2000 John
Wiley & Sons, Inc.