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成品生物陶瓷腻子修复水泥 iRoot BP Plus 与原代人成骨细胞的细胞相容性。

Cytocompatibility of the ready-to-use bioceramic putty repair cement iRoot BP Plus with primary human osteoblasts.

机构信息

Department of Endodontics, School of Dentistry, Grande Rio University (UNIGRANRIO), Rio de Janeiro, Brazil.

出版信息

Int Endod J. 2012 Jun;45(6):508-13. doi: 10.1111/j.1365-2591.2011.02003.x. Epub 2012 Feb 25.

DOI:10.1111/j.1365-2591.2011.02003.x
PMID:22364572
Abstract

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 3 mm 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 48 h. 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 48 h 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.

摘要

目的

验证 iRoot BP Plus(iRoot)的体外细胞相容性,并与 White ProRoot MTA(MTA)进行比较。

方法

使用后退扩孔技术对 36 个人上颌中切牙根管进行预备。在根尖 3mm 处垂直于根的长轴进行切割,并用超声器械和带连续冲洗水的金刚石倒刺根尖预备器制备根尖腔,制备标准化的根管。然后,用 iRoot 或 MTA 填充根尖腔,并将每个根尖暴露于细胞培养基中 24 或 48 小时。将人成骨细胞暴露于由此获得的提取物中,并进行多参数细胞活力测定,评估线粒体活性、膜完整性和细胞密度。通过单向方差分析对结果进行分析,并通过 Duncan 后检验进行补充(P<0.05)。

结果

暴露于 MTA 的细胞显示出与未处理细胞(阴性对照)相似的细胞相容性模式,在两个实验时间点(P>0.05)。然而,在暴露 48 小时后,iRoot 的活力明显低于 MTA 和对照组(P<0.001)。然而,iRoot 并未引起严重的细胞毒性作用,因为在大多数测试中,细胞活力仍高于对照组的 70%。

结论

iRoot 和 MTA 具有生物相容性,不会引起严重的细胞毒性作用。

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