首页> 外文期刊>Journal of Conservative Dentistry >Comparative evaluation of radiopacity and cytotoxicity of platelet-rich fibrin, platelet-rich fibrin + 50wt% nano-hydroxyapatite, platelet-rich fibrin + 50wt% dentin chips: An in vitro study
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Comparative evaluation of radiopacity and cytotoxicity of platelet-rich fibrin, platelet-rich fibrin + 50wt% nano-hydroxyapatite, platelet-rich fibrin + 50wt% dentin chips: An in vitro study

机译:富血小板纤维蛋白,富血小板纤维蛋白+ 50wt%纳米羟基磷灰石,富血小板纤维蛋白+ 50wt%牙本质芯片的放射线不透性和细胞毒性的比较评估:一项体外研究

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Aims: The aim of this study is to impart radiopacity to platelet-rich fibrin (PRF) using two different bioactive agents (nano-hydroxyapatite [nHA] and dentin chips [DC]) and to assess the cell proliferation rate induced by the modified PRF. Subjects and Materials: PRF was modified with 50wt% of nHA (G bone-SHAG31, Surgiwear Company) and 50wt% of DC. The five samples of each group (Group 1 – dentin disc, Group 2 – PRF, Group 3 – PRF + 50wt% nHA, and Group 4-PRF + 50wt% DC) were digitally radiographed together with 8-mm aluminum stepwedge using DIGORA software (for Windows 2.9.113.490). The aluminum equivalent of radiopacity of the samples was compared with the dentin disc (control). Further cytotoxicity (on L929 mouse fibroblast cell lines) among the groups was assessed using methyl thiazolyl tetrazolium assay. Statistical Analysis Used: One-way ANOVA with posthoc Tukey-honestly significant difference tests were applied to assess the significance among the various groups. Results: The mean aluminum equivalent radiopacity among each group showed statistically significant results with P 0.05. Group 3 (PRF + 50wt% nHA) can achieve an aluminum equivalent radiopacity (1.51 ± 0.089) better than Group 4 (0.97 ± 0.22 mmAl). The cell viability was 73% for all groups. Conclusions: This study found that the addition of bioactive radiopacifiers into PRF was able to impart radiopacity and these biomaterials were proved to be noncytotoxic.
机译:目的:本研究的目的是使用两种不同的生物活性剂(纳米羟基磷灰石[nHA]和牙本质芯片[DC])赋予富含血小板的纤维蛋白(PRF)射线不透性,并评估修饰的PRF诱导的细胞增殖速率。受试者和材料:用50wt%的nHA(G bone-SHAG31,Surgiwear Company)和50wt%的DC修饰PRF。使用DIGORA软件,对每组的五个样品(第1组–牙本质盘,第2组– PRF,第3组– PRF + 50wt%nHA和第4-PRF + 50wt%DC)和8毫米铝台阶楔进行数字射线照相。 (适用于Windows 2.9.113.490)。将样品的不透射线的铝当量与牙本质盘(对照)进行比较。使用甲基噻唑基四唑鎓测定法评估各组之间的进一步细胞毒性(对L929小鼠成纤维细胞系)。使用的统计分析:单因素方差分析与事后Tukey-诚实地进行显着性差异检验,以评估各组之间的显着性。结果:各组的平均铝当量射线不透性显示出统计学显着性结果,P <0.05。第3组(PRF + 50wt%nHA)的铝等效射线不透性(1.51±0.089)比第4组(0.97±0.22 mmAl)高。所有组的细胞存活率均> 73%。结论:这项研究发现,向PRF中添加生物活性不透射线剂能够赋予不透射线性,并且这些生物材料被证明具有非细胞毒性。

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