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'Ultramixing': A Simple and Effective Method To Obtain Controlled and Stable Dispersions of Graphene Oxide in Cell Culture Media

机译:“UltraMixing”:一种在细胞培养基中获得石墨烯的控制和稳定分散体的简单有效方法

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The last decade has seen an increase in the application of graphene oxide (GO) in the biomedical field. GO has been successfully exploited for its ability to deliver many kinds of drugs into target cells. However, GO toxicity assessment is still controversial. Several studies have demonstrated that GO protein coating is crucial to alleviate the material's toxicity. Besides, coronation leads to the formation of big agglomerates, reducing the cellular uptake of the material and thus its therapeutic efficiency. In this work, we propose a simple and efficient method based on rapid (ultra-turrax, UT) mixing to control protein corona formation. Using the UT protocol, we were able to reduce GO agglomeration in the presence of proteins and obtain stable GO dispersions in cell culture media. By labelling GO with luminescent nanoparticles (quantum dots), we studied the GO internalization kinetic and efficiency. Comparing the "classic" and UT protocols, we found that the latter allows faster and more efficient internalization both in macrophages and HeLa cells without affecting cell viability. We believe that the use of UT protocol will be interesting and suitable for the preparation of next-generation GO-based drug-delivery platforms.
机译:过去十年已经看到石墨烯氧化物(GO)在生物医学领域的应用增加。已经成功地利用了将多种药物交给目标细胞的能力。然而,Go毒性评估仍然存在争议。几项研究表明,去蛋白质涂料至关重要,以减轻材料的毒性至关重要。此外,加冕导致大聚体的形成,降低了材料的细胞吸收,从而降低了其治疗效率。在这项工作中,我们提出了一种基于Rapid(Ultra-Turrax,UT)混合来控制蛋白质电晕形成的简单有效的方法。使用UT协议,我们能够在蛋白质存在下降低凝聚,并在细胞培养基中获得稳定的去分散体。通过用发光纳米颗粒(量子点)来标记,我们研究了Go Internalization动力学和效率。比较“经典”和UT协议,我们发现后者允许在巨噬细胞和HELA细胞中更快,更有效地内化,而不会影响细胞活力。我们认为,使用UT协议将是有趣的,适合编制下一代基于GO的药物交付平台。

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