Studies of the interaction of graphene oxide (GO) with endothelial cells under static and flow conditions

IF 4.2 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
B. Dabrowski, G. Ulanowicz, Z. Brzozka, A. Zuchowska
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引用次数: 0

Abstract

Graphene oxide, due to its unique properties, has several potential applications in biomedicine, especially as a drug carrier. Despite emerging studies on its cytotoxicity and uptake into cells, there are still gaps in knowledge on this area. When analyzing the internalization of nanomaterials, many different factors must be considered, including particle size, surface modifications, and interactions with biological fluids that can change their properties. In the present study, we evaluated the effects of graphene oxide fractions in different sizes and samples incubated in human serum on endothelial cells (HUVECs). In addition, the study was conducted in both macroscale and microscale using Cell-on-a-Chip technology to better replicate in vivo conditions. Our findings indicate that samples incubated with serum reduce the efficiency of fraction uptake into cells. It was also observed that the uptake efficiency of graphene oxide (GO) fractions is higher in the microscale (in more real to in vivo environment) compared to the macroscale. Our research has shown that in order to determine the correct interaction of new materials into mammalian cells, it is necessary to take into account many different biochemical and physical factors.

研究氧化石墨烯 (GO) 在静态和流动条件下与内皮细胞的相互作用。
氧化石墨烯因其独特的性能,在生物医学领域有多种潜在应用,尤其是作为药物载体。尽管有关氧化石墨烯的细胞毒性和细胞吸收的研究不断涌现,但这方面的知识仍然存在空白。在分析纳米材料的内化时,必须考虑许多不同的因素,包括粒度、表面修饰以及与生物液体的相互作用,这些都会改变纳米材料的特性。在本研究中,我们评估了不同大小的氧化石墨烯馏分和在人血清中培养的样品对内皮细胞(HUVECs)的影响。此外,为了更好地复制体内条件,本研究还利用细胞芯片技术在宏观和微观尺度上进行了研究。我们的研究结果表明,用血清培养的样品会降低馏分被细胞吸收的效率。我们还观察到,与宏观尺度相比,氧化石墨烯(GO)馏分在微观尺度(更真实的体内环境)下的吸收效率更高。我们的研究表明,为了确定新材料与哺乳动物细胞的正确相互作用,有必要考虑许多不同的生物化学和物理因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.00
自引率
4.70%
发文量
185
审稿时长
34 days
期刊介绍: Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man. Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals. In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.
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