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锐钛矿型和金红石型TiO₂薄膜对CHO-K1细胞的体外细胞毒性评价

Cytotoxicity Evaluation of Anatase and Rutile TiO₂ Thin Films on CHO-K1 Cells in Vitro.

作者信息

Cervantes Blanca, López-Huerta Francisco, Vega Rosario, Hernández-Torres Julián, García-González Leandro, Salceda Emilio, Herrera-May Agustín L, Soto Enrique

机构信息

Instituto de Fisiología, Benemérita Universidad Autónoma de Puebla, 14 sur 6301, Col. San Manuel, 72570 Puebla, Mexico.

Instituto de Investigaciones Biomédicas "Alberto Sols", Consejo Superior de Investigaciones Científicas-Universidad Autónoma de Madrid, Arturo Duperier, 4, 28029 Madrid, Spain.

出版信息

Materials (Basel). 2016 Jul 26;9(8):619. doi: 10.3390/ma9080619.

Abstract

Cytotoxicity of titanium dioxide (TiO₂) thin films on Chinese hamster ovary (CHO-K1) cells was evaluated after 24, 48 and 72 h of culture. The TiO₂ thin films were deposited using direct current magnetron sputtering. These films were post-deposition annealed at different temperatures (300, 500 and 800 °C) toward the anatase to rutile phase transformation. The root-mean-square (RMS) surface roughness of TiO₂ films went from 2.8 to 8.08 nm when the annealing temperature was increased from 300 to 800 °C. Field emission scanning electron microscopy (FESEM) results showed that the TiO₂ films' thickness values fell within the nanometer range (290-310 nm). Based on the results of the tetrazolium dye and trypan blue assays, we found that TiO₂ thin films showed no cytotoxicity after the aforementioned culture times at which cell viability was greater than 98%. Independently of the annealing temperature of the TiO₂ thin films, the number of CHO-K1 cells on the control substrate and on all TiO₂ thin films was greater after 48 or 72 h than it was after 24 h; the highest cell survival rate was observed in TiO₂ films annealed at 800 °C. These results indicate that TiO₂ thin films do not affect mitochondrial function and proliferation of CHO-K1 cells, and back up the use of TiO₂ thin films in biomedical science.

摘要

在培养24、48和72小时后,评估了二氧化钛(TiO₂)薄膜对中国仓鼠卵巢(CHO-K1)细胞的细胞毒性。TiO₂薄膜采用直流磁控溅射沉积。这些薄膜在不同温度(300、500和800°C)下进行沉积后退火,以促进锐钛矿相向金红石相的转变。当退火温度从300°C提高到800°C时,TiO₂薄膜的均方根(RMS)表面粗糙度从2.8纳米增加到8.08纳米。场发射扫描电子显微镜(FESEM)结果表明,TiO₂薄膜的厚度值在纳米范围内(290 - 310纳米)。基于四唑盐染料和台盼蓝试验的结果,我们发现,在上述培养时间后,TiO₂薄膜没有显示出细胞毒性,此时细胞活力大于98%。无论TiO₂薄膜的退火温度如何,在48或72小时后,对照基质和所有TiO₂薄膜上的CHO-K1细胞数量都比24小时后更多;在800°C退火的TiO₂薄膜中观察到最高的细胞存活率。这些结果表明,TiO₂薄膜不会影响CHO-K1细胞的线粒体功能和增殖,并支持了TiO₂薄膜在生物医学科学中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6e0/5509025/d33a119713ef/materials-09-00619-g001.jpg

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