机构地区:[1]中国医科大学口腔医学院正畸科,辽宁省沈阳市110002 [2]中国医科大学口腔医学院口腔材料教研室,辽宁省沈阳市110002
出 处:《中国组织工程研究与临床康复》2009年第34期6645-6649,共5页Journal of Clinical Rehabilitative Tissue Engineering Research
基 金:辽宁省自然科学基金资助项目(20082088)~~
摘 要:背景:对镍钛形状记忆合金进行表面改性可以减少镍离子的析出,达到提高生物相容性的目的。目的:在镍钛形状记忆合金表面制备氧化涂层,评价表面氧化镍钛形状记忆合金对细胞毒性的影响。设计、时间及地点:材料-细胞学体外实验,于2008-11/12在中国医科大学口腔医学院中心实验室完成。材料:L-929细胞由中国医科大学中心实验室提供。镍钛形状记忆合金板材为北京有研亿金新材料股份有限公司产品。方法:将镍钛形状记忆合金板材制备成半径10mm、厚度3mm的圆形合金试件,分为2组:氧化组合金表面进行氧化处理,即酸洗,丙酮中超声波清洗,空气干燥,在沸腾的H2O2溶液中氧化2h,取出后去离子水超声波清洗;非氧化组合金表面不进行氧化处理。合金浸提液的制备按2组合金试件表面积与培养液之比为3cm2/mL加入RPMI-1640培养液,置于37℃培养箱内96h,微孔滤膜除菌后备用。并设立阳性对照组,加入6.4%苯酚培养液;空白对照组,加入1640培养液。主要观察指标:倒置相差显微镜观察L-929细胞在合金浸提液中的生长情况,通过MTT试验得出细胞在培养第24,48h的吸光度值,对表面氧化镍钛形状记忆合金做出细胞毒性评价。结果:①培养24h,阳性对照组细胞形态异常;氧化组、非氧化组、空白对照组细胞贴壁生长状态良好。培养48h,阳性对照组许多细胞呈中毒形态;氧化组、空白对照组细胞形态正常,生长旺盛;非氧化组少量细胞核固缩。②与空白对照组比较,随培养时间延长氧化组、非氧化组吸光度值均相应增加(P<0.05),且氧化组增加幅度高于非氧化组(P<0.05)。氧化组合金在培养24,48h时细胞毒性均为0级,表现出轻微的细胞毒性;非氧化组合金培养24h时细胞毒性为0级,48h时细胞毒性为1级,表现出较明显的细胞毒性;空白对照组无细胞毒性。结论:镍钛形状记忆合金经过表面氧化处理后细胞毒�BACKGROUND: Surface modification on nickel-titanium shape memory alloy (NiTi-SMA) may reduce separation of nickel ions so as to enhance the biocompatibility. OBJECTIVE: To evaluate the cytotoxicity of NiTi-SMA with surface oxidation. DESIGN, TIME AND SETTING: An in vitro study based on materials and cytology level was performed at Central Laboratory, School of Stomatology, China Medical University from November to December 2008. MATERIALS: L-929 cells were provided by Central Laboratory of China Medical University, and NiTi-SMA was provided by Grikin Advanced Materials Co., Ltd., Beijing. METHODS: NiTi-SMA was made into round samples with radius 10 mm and thickness 3 mm which were divided into oxidation group and non-oxidation group. Samples in the oxidation group were ultrasonically rinsed with acetone, dried in the air, oxidated in boiling H202 for 2 hours, and ultrasonically cleaned with deionized water; while, the samples in the non-oxidation group were not treated with any materials. Alloy leaching liquor was prepared with RPMI-1640 culture media according to the ratio between surface area and volume of culture solution (3 cm2/mL). The leaching liquor was maintained in incubator at 37 ~C for 96 hours, and then degerming was performed using microporous membrane. 6.4% phenol was added, which was considered as the positive control group, and 1640 culture media was considered as the blank control group. MAIN OUTCOME MEASURES: Growth of L-929 cells was observed under inverted phase contrast microscope; absorbance of cells cultured for 24 and 48 hours was detected using MTT test; cytotexicity of NiTi-SMA with surface oxidation was evaluated. RESULTS: (1) At 24 hours after culture, cells in the positive control group was abnormal; while, cells in the oxidation, non-oxidation, and blank control groups well adherent-grew. At 48 hours after culture, cytotoxicity was detected out in the positive control group; cells in the oxidation, non-oxidation, and blank control groups were normal and grew
分 类 号:R318[医药卫生—生物医学工程]
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