The purpose of this study was to research the osseointegration in the interface of dental gold alloy. Some investigator presented that gold was biologically safe but occurred fibrous integration on implant interface. We used 4 different gold composition implant to investigate the osseointegration on implant interface. Osseointegration occurred on the all implant interface. We thought that osseointegration depended not only on gold composition but also on precious metal composition such as platinum or silver. If we use precious metal implant, it might reduce the Galvanic current and chemical corrosion which were occurred between titanium implant and percious metal suprastructure. We recommend that precious metal implant was superior to non-precious metal implant without financial problem.

Cell adhesion is used as a parameter to evaluate the biocompatibility of dental implant and also affected by the surface form of dental implant. Most study have showed different cell reaction by the composition and the surface morphology of implant. Therefore it is thought that the osteoblastic activity would be affected by the surface roughness and composition of implants. This study was performed to evaluate the biological activity and morphological change of normal human osteoblastic cells(NHost) depending on the variations of implant surfaces. We used grade 2 titanium disks which were being air-blasted with TiO2 50 ㎛, 110 ㎛, 250 ㎛ powder by 3psi compressed air and non-blasted as control. We evaluated and compared morphologic change, adhesion assay, and Ca, P, ALP concentration of NHost in vitro. The obtained results were as follows. 1. In the growth curve, although the growth of experimental groups were lower than that of the group of NHost only, there was no significant difference between each groups. 2. Inverted microscopic findings showed NHosts in early stage of each group were adherant perpendicular to the titanium disk and the multilayered NHosts were attached with various directions after 4 weeks. 3. Scanning electron microscopic(SEM) features showed that NHosts in all groups seemed to be attached multilayered and connected with each process after 2 weeks. 4. NHosts' processes were found by the SEM after one day culture. The cell adhesion of experiment group was higher than that of control group. 110 ㎛(the 3rd group) showed prominant process of NHost on the titanium disk surface. 5. Although the concentrations of Ca, P and ALP were gradually reduced, ANOVA analysis of each groups were partially different, and ANOVA analysis of 4th group were significantly different with others. From the aboving results, NHosts cultured on the titanium disks showed similar morphological change and cell proliferation. There were partially differences in each group except the 4th group, and the 4th group were significantly different with other's in biological activity. We thought that biological activity and adhesion of NHost cell on titanium had been affected by the variation of the titanium surface roughness.

Hydroxyapatite(HA) has been widely used as bone substitutes to rehabilitate bone loss area by new bone formation. But there were some problem of bone formation around HAs due to a little space between HAs embedded in bone loss area. The purpose of this study was to observe morphologically new bone formation around HAs mixed with PLGA block (5.5㎜ in diameter, 4 mm in depth) in Newzealand white rabbit tibia. Before 1 week of sacrification, Alizarin red was injected intraperitoneally into rabbit. At 3 day, 1, 2, 4, 10, 18, 32 weeks, bones with HA as control group(CG)and HA mixed with PLGA block as experimental group (EG)were fixed with 10 % neutral formalin, dehydrated, and embedded with Spurr low viscosity resin. After the specimens were cut by 500 ㎛ with slow diamond wheel saw, these were coated with carbon and examined by REM, LSM and qualifative analysis of calcium and phosphorous deposition were done with EPMA. The obtained results were as follows. 1. Both group showed scattered HA around compact bone under REM and little AZ labelled bone under LSM at 3 days. 2. Both group showed active AZ labelled bone, while EG showed higher Ca(calcium) and P(phosphate) deposition than that of CG at 1 wk. 3. There was decreased AZ labelled bone of both group under LSM. REM of EG showed HA associated with new bone from compact bone, while EPMA features showed similar to Ca and P deposition at 1 wk and EG showed higher than that of CG. 4. REM features of both group showed resorbed HA associated with new bone. There was decreased AZ labelled bone of both group under LSM. EPMA features showed higher Ca and P deposition at 4 wks than that of 2 wks. 5. New bone of both group was well demarcated from compact bone under REM at 10 wks. LSM features showed various AZ labelled bone, but weak AZ labelled than that of CG. 6. LSM features of 14 wks showed discontinuous AZ labelled on osteon formation. EPMA of both group showed increased Ca deposition, while there was higher Ca deposition of EG and similar P deposition to CG. 7. REM featureless of 18 wks in EG showed similar gray color to compact bone. LSM features showed osteon formation with little concentric lamellars. EPMA of both group showed increased Ca deposition, while there was higher Ca and P deposition of EG. 8. New bone was ill demarcated from compact bone and increased otseon formation of REM features at 32 wks. There was little AZ labelled bone. EPMA features showed higher Ca and P deposition of EG than that of compact bone. From the aboving results, there was early active AZ labelled bone of both group within 1-2 weeks and since 18 weeks new bone with active osteon formation was poorly demarcated from compact bone. Calcium deposition of EG was early increased than that of CG deposition since 4 weeks after experiments. It was suggested that EG showed active and rapid new bone formation and similar bone mineralization of compact bone