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负载金的氧化铈纳米颗粒的细胞毒性和抗菌活性

Cytotoxicity and antibacterial activity of gold-supported cerium oxide nanoparticles.

作者信息

Babu K Suresh, Anandkumar M, Tsai T Y, Kao T H, Inbaraj B Stephen, Chen B H

机构信息

Centre for Nano Sciences and Technology, Madanjeet School of Green Energy Technologies, Pondicherry University, Kalapet, India.

Department of Food Science, Fu Jen University, Taipei, Taiwan.

出版信息

Int J Nanomedicine. 2014 Nov 27;9:5515-31. doi: 10.2147/IJN.S70087. eCollection 2014.

Abstract

BACKGROUND

Cerium oxide nanoparticles (CeO2) have been shown to be a novel therapeutic in many biomedical applications. Gold (Au) nanoparticles have also attracted widespread interest due to their chemical stability and unique optical properties. Thus, decorating Au on CeO2 nanoparticles would have potential for exploitation in the biomedical field.

METHODS

In the present work, CeO2 nanoparticles synthesized by a chemical combustion method were supported with 3.5% Au (Au/CeO2) by a deposition-precipitation method. The as-synthesized Au, CeO2, and Au/CeO2 nanoparticles were evaluated for antibacterial activity and cytotoxicity in RAW 264.7 normal cells and A549 lung cancer cells.

RESULTS

The as-synthesized nanoparticles were characterized by X-ray diffraction, scanning and transmission electron microscopy, and ultraviolet-visible measurements. The X-ray diffraction study confirmed the formation of cubic fluorite-structured CeO2 nanoparticles with a size of 10 nm. All synthesized nanoparticles were nontoxic towards RAW 264.7 cells at doses of 0-1,000 μM except for Au at >100 μM. For A549 cancer cells, Au/CeO2 had the highest inhibitory effect, followed by both Au and CeO2 which showed a similar effect at 500 and 1,000 μM. Initial binding of nanoparticles occurred through localized positively charged sites in A549 cells as shown by a shift in zeta potential from positive to negative after 24 hours of incubation. A dose-dependent elevation in reactive oxygen species indicated that the pro-oxidant activity of the nanoparticles was responsible for their cytotoxicity towards A549 cells. In addition, cellular uptake seen on transmission electron microscopic images indicated predominant localization of nanoparticles in the cytoplasmic matrix and mitochondrial damage due to oxidative stress. With regard to antibacterial activity, both types of nanoparticles had the strongest inhibitory effect on Bacillus subtilis in monoculture systems, followed by Salmonella enteritidis, Escherichia coli, and Staphylococcus aureus, while, in coculture tests with Lactobacillus plantarum, S. aureus was inhibited to a greater extent than the other bacteria.

CONCLUSION

Gold-supported CeO2 nanoparticles may be a potential nanomaterial for in vivo application owing to their biocompatible and antibacterial properties.

摘要

背景

氧化铈纳米颗粒(CeO₂)已被证明在许多生物医学应用中是一种新型治疗剂。金(Au)纳米颗粒因其化学稳定性和独特的光学性质也引起了广泛关注。因此,在CeO₂纳米颗粒上修饰金在生物医学领域具有开发潜力。

方法

在本研究中,通过化学燃烧法合成的CeO₂纳米颗粒采用沉积沉淀法负载3.5%的金(Au/CeO₂)。对合成的金、CeO₂和Au/CeO₂纳米颗粒在RAW 264.7正常细胞和A549肺癌细胞中的抗菌活性和细胞毒性进行了评估。

结果

通过X射线衍射、扫描和透射电子显微镜以及紫外可见测量对合成的纳米颗粒进行了表征。X射线衍射研究证实形成了尺寸为10nm的立方萤石结构CeO₂纳米颗粒。除了浓度大于100μM的金之外,所有合成的纳米颗粒在0 - 1000μM剂量下对RAW 264.7细胞均无毒性。对于A549癌细胞,Au/CeO₂具有最高的抑制作用,其次是金和CeO₂,它们在500和1000μM时显示出相似的效果。纳米颗粒的初始结合通过A549细胞中的局部带正电位点发生,孵育24小时后zeta电位从正变为负表明了这一点。活性氧的剂量依赖性升高表明纳米颗粒的促氧化活性是其对A549细胞细胞毒性的原因。此外,透射电子显微镜图像上看到的细胞摄取表明纳米颗粒主要定位于细胞质基质中,并且由于氧化应激导致线粒体损伤。关于抗菌活性,两种类型的纳米颗粒在单培养系统中对枯草芽孢杆菌的抑制作用最强,其次是肠炎沙门氏菌、大肠杆菌和金黄色葡萄球菌,而在与植物乳杆菌的共培养试验中,金黄色葡萄球菌比其他细菌受到更大程度的抑制。

结论

负载金的CeO₂纳米颗粒因其生物相容性和抗菌特性可能是一种潜在的体内应用纳米材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e14/4251533/3c80f290391e/ijn-9-5515Fig1.jpg

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