TY - JOUR
T1 - Improvement in zirconia osseointegration by means of a biological glass coating
T2 - An in vitro and in vivo investigation
AU - Aldini, N. Nicoli
AU - Fini, M.
AU - Giavaresi, G.
AU - Torricelli, P.
AU - Martini, L.
AU - Giardino, R.
AU - Ravaglioli, A.
AU - Krajewski, A.
AU - Mazzocchi, M.
AU - Dubini, B.
AU - Ponzi-Bossi, M. G.
AU - Rustichelli, F.
AU - Stanic, V.
PY - 2002
Y1 - 2002
N2 - The biocompatibility and osseointegration of zirconia (ZrO2), either coated with RKKP bioglaze® or uncoated, were evaluated in vitro and in vivo. The in vitro test was performed in human osteoblasts, whereas maximal sensitization was performed in 23 Dunkin Hurtley guinea pigs. RKKP bioglaze-coated and uncoated (controls) ZrO2 cylinders were implanted in the distal femoral epiphyses of 14 Sprague-Dawley rats under general anesthesia, and animals were sacrificed at 30 and 60 days. Lactate dehydrogenase, alkaline phosphatase, and Thiazolyl Blue (MTT) were tested in vitro. A graded score was used for evaluating the results of the sensitization test. Histomorphometry and microhardness testing were performed to quantify the osseointegration rate, as well as bone quality around the implants. Neither in vitro cytotoxicity nor sensitization were observed. Histomorphometry demonstrated that at 30 days, the affinity index was significantly higher in coated implants than in uncoated ones (p <0.05); at 60 days, the behavior of coated implants was better than that of uncoated ones, but differences were not significant. Significant increases in bone microhardness were found at 1000 μm from the interface area for both uncoated (p <0.0005) and RKKP bioglaze®-coated (p <0.0005) ZrO2, and also within 200 μm from the interface (p = 0.014) but only for coated ZrO2. These results suggest that RKKP bioglaze®-coated ZrO2 permits biocompatible devices with improved osseointegration properties to be manufactured.
AB - The biocompatibility and osseointegration of zirconia (ZrO2), either coated with RKKP bioglaze® or uncoated, were evaluated in vitro and in vivo. The in vitro test was performed in human osteoblasts, whereas maximal sensitization was performed in 23 Dunkin Hurtley guinea pigs. RKKP bioglaze-coated and uncoated (controls) ZrO2 cylinders were implanted in the distal femoral epiphyses of 14 Sprague-Dawley rats under general anesthesia, and animals were sacrificed at 30 and 60 days. Lactate dehydrogenase, alkaline phosphatase, and Thiazolyl Blue (MTT) were tested in vitro. A graded score was used for evaluating the results of the sensitization test. Histomorphometry and microhardness testing were performed to quantify the osseointegration rate, as well as bone quality around the implants. Neither in vitro cytotoxicity nor sensitization were observed. Histomorphometry demonstrated that at 30 days, the affinity index was significantly higher in coated implants than in uncoated ones (p <0.05); at 60 days, the behavior of coated implants was better than that of uncoated ones, but differences were not significant. Significant increases in bone microhardness were found at 1000 μm from the interface area for both uncoated (p <0.0005) and RKKP bioglaze®-coated (p <0.0005) ZrO2, and also within 200 μm from the interface (p = 0.014) but only for coated ZrO2. These results suggest that RKKP bioglaze®-coated ZrO2 permits biocompatible devices with improved osseointegration properties to be manufactured.
KW - Biocompatibility osseointegration
KW - Bioglass
KW - Ceramics
KW - Zirconia
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U2 - 10.1002/jbm.10162
DO - 10.1002/jbm.10162
M3 - Article
C2 - 12007209
AN - SCOPUS:0036275289
SN - 1549-3296
VL - 61
SP - 282
EP - 289
JO - Journal of Biomedical Materials Research - Part A
JF - Journal of Biomedical Materials Research - Part A
IS - 2
ER -