Graduate student, Department of Prosthodontics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul, Republic of Korea.
Clinical Instructor, Department of Prosthodontics, Seoul National University Dental Hospital, Seoul, Republic of Korea.
J Prosthet Dent. 2023 Dec;130(6):936.e1-936.e9. doi: 10.1016/j.prosdent.2023.09.014. Epub 2023 Oct 5.
Selecting the sterilization method is important because sterilization can alter the surface chemistry of implant materials, including zirconia, and influence their cellular biocompatibility. Studies on the biological effects of sterilization on implant materials are lacking.
The purpose of this in vitro study was to evaluate the biocompatibility of gamma-ray irradiated 3 mol% yttria-stabilized tetragonal zirconia polycrystal (3Y-TZP) compared with unirradiated titanium, 3Y-TZP, and pure gold.
Disk-shaped specimens each of commercially pure grade 4 titanium, 3Y-TZP, gamma-rayed 3Y-TZP, and pure gold were prepared and evaluated for osteogenic potential by using a clonal murine cell line of immature osteoblasts derived from mice (MC3T3-E1 cells). The surface topography (n=3), chemical analysis of the disks (n=3), and cell morphology cultured on these surfaces were examined using scanning electron microscopy, confocal laser scanning microscopy, and energy dispersive spectroscopy. Cellular biocompatibility was analyzed for 1 and 3 days after seeding. Cell adhesion and spreading were evaluated using confocal laser scanning microscopy (n=3). Cell proliferation was evaluated using methyl thiazolyl tetrazolium assay (n=3). Kruskal-Wallis and Bonferroni corrections were used to evaluate the statistical significance of the intergroup differences (α=.05).
Gamma-ray sterilization of 3Y-TZP showed significantly higher surface roughness compared with titanium and gold (P<.002). On day 1, the proliferation and adhesion of MC3T3-E1 cells cultured on gamma-rayed 3Y-TZP were significantly higher than those cultured on gold (P<.05); however, cell spreading was significantly lower than that of titanium on days 1 and 3 (P<.05). On day 3, cell proliferation of gamma-rayed 3Y-TZP was significantly lower than that of unirradiated 3Y-TZP (P<.05). Cell adhesion of gamma-rayed 3Y-TZP was slightly lower than that of zirconia and titanium but without significant difference (P>.05).
Gamma-rayed zirconia exhibited increased surface roughness compared with titanium and significantly decreased bioactivity compared with titanium and zirconia. The use of gamma-ray sterilization on zirconia is not promising regarding biocompatibility, and the effect of this sterilization method on implant materials warrants further investigation.
选择合适的灭菌方法很重要,因为灭菌会改变植入材料(包括氧化锆)的表面化学性质,并影响其细胞生物相容性。目前缺乏关于灭菌对植入材料生物学影响的研究。
本体外研究的目的是评估与未辐照的钛、3Y-TZP 和纯金相比,γ射线辐照的 3mol%氧化钇稳定四方氧化锆多晶(3Y-TZP)的生物相容性。
制备商用纯 4 级钛、3Y-TZP、γ射线辐照 3Y-TZP 和纯金的圆盘状试件,并使用源自小鼠的未成熟成骨细胞的克隆鼠骨肉瘤细胞系(MC3T3-E1 细胞)评估其成骨潜力。使用扫描电子显微镜、共聚焦激光扫描显微镜和能量色散光谱法检查试件的表面形貌(n=3)、试件的表面化学分析(n=3)和在这些表面上培养的细胞形态。在接种后 1 天和 3 天分析细胞的生物相容性。使用共聚焦激光扫描显微镜评估细胞黏附(n=3)和细胞铺展。使用噻唑蓝比色法评估细胞增殖(n=3)。使用 Kruskal-Wallis 和 Bonferroni 校正法评估组间差异的统计学意义(α=.05)。
与钛和金相比,3Y-TZP 的γ射线灭菌显示出明显更高的表面粗糙度(P<.002)。在第 1 天,在γ射线辐照的 3Y-TZP 上培养的 MC3T3-E1 细胞的增殖和黏附明显高于金上培养的细胞(P<.05);然而,在第 1 天和第 3 天,细胞铺展明显低于钛(P<.05)。在第 3 天,γ射线辐照的 3Y-TZP 的细胞增殖明显低于未辐照的 3Y-TZP(P<.05)。γ射线辐照的 3Y-TZP 的细胞黏附略低于氧化锆和钛,但无统计学差异(P>.05)。
与钛相比,γ射线辐照的氧化锆表现出更高的表面粗糙度,与钛和氧化锆相比,其生物活性明显降低。γ 射线灭菌在生物相容性方面对氧化锆的应用前景并不乐观,这种灭菌方法对植入材料的影响需要进一步研究。