生物陶瓷牙髓封闭剂对HepG2和V79细胞系的遗传毒性和细胞毒性评价:采用彗星和微核试验的体外研究

IF 5 3区 医学 Q1 ENGINEERING, BIOMEDICAL
Antonija Tadin, Marija Badrov, Danijela Juric Kacunic, Nada Galic, Matea Macan, Ivan Kovacic, Davor Zeljezic
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引用次数: 0

摘要

背景:本研究的主要目的是评估硅酸钙基密封剂(BioRoot RCS和MTA Fillapex)与环氧树脂基密封剂(AH Plus)的细胞毒性和遗传毒性作用。材料与方法:以HepG2和V79细胞株为实验材料,采用彗星法和微核法测定细胞毒性和遗传毒性。暴露72 h后,以两种不同浓度(3 cm2/mL和0.5 cm2/mL)对材料的洗脱液进行测试。使用Mann-Whitney和Kruskal-Wallis检验分析数据(p < 0.05)。结果:两种细胞系在较低浓度下,MTA Fillapex的彗星测定参数与阴性对照相比无显著差异(p < 0.05)。此外,在所有彗星试验参数、浓度和细胞系方面,与AH Plus相比,它的基因毒性作用显著降低(p≤0.001)。BioRoot RCS仅在较高浓度和HepG2细胞系中表现出较低的原发性DNA损伤(p≤0.001)。在两种生物陶瓷密封剂中,BioRoot RCS的尾部强度值高于MTA Fillapex (p < 0.05)。与彗星实验结果相比,BioRoot RCS与MTA Fillapex相比显著减少了HepG2细胞系的核芽和核质桥的数量,而V79细胞系仅观察到核芽的减少(p < 0.05)。与阴性对照相比,两种材料均增加了凋亡细胞数(p < 0.05)。与AH Plus相比,BioRoot RCS和MTA Fillapex显著减少微核细胞数量,增加未损伤染色质细胞数量(p < 0.05)。结论:研究结果表明,MTA Fillapex和BioRoot RCS比AH Plus具有更好的生物相容性,这证明了它们在体外具有更低的细胞毒性和基因毒性。这些结果支持在临床实践中使用硅酸钙基密封剂,强调需要进一步研究以评估其在体内的性能及其对患者安全的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Genotoxicity and Cytotoxicity of Bioceramic Endodontic Sealers in HepG2 and V79 Cell Lines: An In Vitro Study Using the Comet and Micronucleus Assays.

Background: The primary objective of this study was to evaluate the cytotoxic and genotoxic effects of calcium silicate-based sealers (BioRoot RCS and MTA Fillapex) compared to an epoxy-based sealer (AH Plus).

Materials and methods: The study was conducted in vitro with the cell lines HepG2 and V79 to evaluate cytotoxicity and genotoxicity using the comet and micronucleus assays. Eluates of the materials were tested at two different concentrations (3 cm2/mL and 0.5 cm2/mL) after an exposure time of 72 h. Data were analyzed using the Mann-Whitney and Kruskal-Wallis tests (p < 0.05).

Results: At lower concentrations in both cell lines, MTA Fillapex showed no significant difference in the measured comet assay parameters compared to the negative control (p > 0.05). In addition, it showed significantly lower genotoxic effects compared to AH Plus for all comet assay parameters, concentrations, and cell lines (p ≤ 0.001). BioRoot RCS showed lower primary DNA damage (p ≤ 0.001) than AH Plus, only at higher concentrations and in the HepG2 cell line. Concerning the two tested bioceramic sealers, BioRoot RCS showed higher tail intensity values compared to MTA Fillapex (p < 0.05). In contrast to the results of the comet assay, BioRoot RCS significantly reduced the number of nuclear buds and nucleoplasmic bridges in the HepG2 cell line compared to MTA Fillapex, whereas reduction in the V79 cell line was only observed for nuclear buds (p < 0.05). Both materials increased the number of apoptotic cells compared to the negative control (p < 0.05). In comparison to AH Plus, BioRoot RCS and MTA Fillapex significantly reduced the number of cells with micronuclei and increased the number of cells with undamaged chromatin (p < 0.05).

Conclusions: The findings suggest that MTA Fillapex and BioRoot RCS exhibit superior biocompatibility over AH Plus, as evidenced by their lower cytotoxic and genotoxic effects in vitro. These results support the use of calcium silicate-based sealers in clinical practice, highlighting the need for further studies to evaluate their performance in vivo and their implications for patient safety.

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来源期刊
Journal of Functional Biomaterials
Journal of Functional Biomaterials Engineering-Biomedical Engineering
CiteScore
4.60
自引率
4.20%
发文量
226
审稿时长
11 weeks
期刊介绍: Journal of Functional Biomaterials (JFB, ISSN 2079-4983) is an international and interdisciplinary scientific journal that publishes regular research papers (articles), reviews and short communications about applications of materials for biomedical use. JFB covers subjects from chemistry, pharmacy, biology, physics over to engineering. The journal focuses on the preparation, performance and use of functional biomaterials in biomedical devices and their behaviour in physiological environments. Our aim is to encourage scientists to publish their results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Several topical special issues will be published. Scope: adhesion, adsorption, biocompatibility, biohybrid materials, bio-inert materials, biomaterials, biomedical devices, biomimetic materials, bone repair, cardiovascular devices, ceramics, composite materials, dental implants, dental materials, drug delivery systems, functional biopolymers, glasses, hyper branched polymers, molecularly imprinted polymers (MIPs), nanomedicine, nanoparticles, nanotechnology, natural materials, self-assembly smart materials, stimuli responsive materials, surface modification, tissue devices, tissue engineering, tissue-derived materials, urological devices.
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