首页> 外文期刊>International endodontic journal >Cytocompatibility of the ready-to-use bioceramic putty repair cement iRoot BP Plus with primary human osteoblasts
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Cytocompatibility of the ready-to-use bioceramic putty repair cement iRoot BP Plus with primary human osteoblasts

机译:即用型生物陶瓷油灰修补水泥iRoot BP Plus与人类原代成骨细胞的细胞相容性

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Aim To verify the in vitro cytocompatibility of iRoot BP Plus (iRoot) and to compare it with White ProRoot MTA (MTA). Methodology Thirty-six human maxillary incisor root canals were prepared using a step-back flaring technique. The apical 3mm was resected perpendicular to the long axis at the roots, and root-end cavities were prepared with the aid of an ultrasonic device plus a diamond retrotip with continuous irrigation using water, producing standardized preparations. After that, the root-end cavities were filled with iRoot or MTA, and each root was exposed to cell culture media for 24 or 48h. Human osteoblast cells were exposed to the extracts thus obtained, and a multiparametric cell viability assay was performed, evaluating mitochondrial activity, membrane integrity and cell density. The results were analysed by one-way analysis of variance, complemented with the Duncan post-test (P<0.05). Results Cells exposed to MTA revealed a cytocompatibility pattern similar to the untreated cells (negative control), at both experimental times (P>0.05). iRoot, however, promoted a significantly poorer viability than MTA and the control, after 48h of exposure (P<0.001). Nevertheless, iRoot did not induce critical cytotoxic effects because cell viability remained higher than 70% of the control group in most tests performed. Conclusion iRoot and MTA were biocompatible and did not induce critical cytotoxic effects.
机译:目的验证iRoot BP Plus(iRoot)的体外细胞相容性,并将其与White ProRoot MTA(MTA)进行比较。方法学使用后退扩口技术制备了36条人类上颌切牙的根管。根部垂直于长轴切下根尖3mm,并借助超声仪加金刚石逆磨尖并用水连续冲洗制备根端腔,以制备标准制剂。之后,用iRoot或MTA填充根端腔,并将每个根暴露于细胞培养基24或48h。将人成骨细胞暴露于如此获得的提取物中,并进行多参数细胞生存力测定,评估线粒体活性,膜完整性和细胞密度。通过单因素方差分析对结果进行分析,并辅以Duncan后检验(P <0.05)。结果暴露于MTA的细胞在两个实验时间均显示出与未处理细胞(阴性对照)相似的细胞相容性模式(P> 0.05)。但是,暴露48小时后,iRoot的存活力明显比MTA和对照差(P <0.001)。尽管如此,iRoot并未诱导关键的细胞毒性作用,因为在大多数执行的测试中,细胞活力仍高于对照组的70%。结论iRoot和MTA具有生物相容性,不会引起关键的细胞毒性作用。

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