Using thermal diffusivity as a cytotoxic evaluation tool for silica nanoparticles

IF 2.5 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY
Libertad Juárez-Santacruz, José Luis Jiménez-Pérez, Angel Netzahual-Lopantzi
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Abstract

Silicon dioxide nanoparticles are receiving increasing attention due to their new properties and wide applications. The aim of this study was to investigate the cytotoxic potential of 300 nm SiO2 nanospheres on erythrocytes using thermal diffusivity values. Cytotoxicity was correlated with thermal diffusivity of the hemolysates; thermal values ​​were from 10.00 ± 0.40 × 10− 4 cm2/s to 12.20 ± 0.07 × 10− 4 cm2/s. The concentrations tested were 50, 100, 200, 400 and 800 µg/ml of silica nanoparticles. To evaluate cytotoxicity, human erythrocytes were obtained. Hemolytic damage in red blood cells had an exponential behavior dependent on the concentration of SiO2 nanostructures. The use of concentrations of 800 µg/ml exceeds the limit of compatibility for human red blood cells. Antioxidant enzyme quantification assays were also performed in which a dose-dependent depletion of catalase activity levels and an increase in glutathione S-transferase was observed. Therefore, oxidative stress was suggested as a mechanism of toxicity in erythrocytes.

Abstract Image

利用热扩散率评估二氧化硅纳米粒子的细胞毒性
二氧化硅纳米粒子因其新特性和广泛应用而受到越来越多的关注。本研究旨在利用热扩散值研究 300 纳米二氧化硅纳米球对红细胞的细胞毒性潜力。细胞毒性与溶血的热扩散率相关;热扩散率值从 10.00 ± 0.40 × 10- 4 cm2/s 到 12.20 ± 0.07 × 10- 4 cm2/s。测试的二氧化硅纳米颗粒浓度分别为 50、100、200、400 和 800 微克/毫升。为了评估细胞毒性,我们采集了人类红细胞。红细胞的溶血损伤与二氧化硅纳米结构的浓度呈指数关系。使用 800 µg/ml 的浓度超过了人体红细胞的相容性极限。此外,还进行了抗氧化酶定量测定,结果表明过氧化氢酶活性水平呈剂量依赖性下降,谷胱甘肽 S 转移酶水平上升。因此,氧化应激被认为是红细胞中毒的一种机制。
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来源期刊
Applied Physics A
Applied Physics A 工程技术-材料科学:综合
CiteScore
4.80
自引率
7.40%
发文量
964
审稿时长
38 days
期刊介绍: Applied Physics A publishes experimental and theoretical investigations in applied physics as regular articles, rapid communications, and invited papers. The distinguished 30-member Board of Editors reflects the interdisciplinary approach of the journal and ensures the highest quality of peer review.
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