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一种用于生物医学应用的获取纳米尺寸氧化石墨烯的新方法。

A New Approach to Obtaining Nano-Sized Graphene Oxide for Biomedical Applications.

作者信息

Bolibok Paulina, Szymczak Bartosz, Roszek Katarzyna, Terzyk Artur P, Wiśniewski Marek

机构信息

Physicochemistry of Carbon Materials Research Group, Faculty of Chemistry, Nicolaus Copernicus University in Toruń, Gagarina 7, 87-100 Toruń, Poland.

Department of Biochemistry, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University in Toruń, Lwowska 1, 87-100 Toruń, Poland.

出版信息

Materials (Basel). 2021 Mar 10;14(6):1327. doi: 10.3390/ma14061327.

Abstract

Graphene oxide (GO) is one of the most exciting and widely used materials. A new method of nanographene oxide (n-GO) formation is presented. The described unique sequence of ultrasonication in dimethyl sulfoxide solution allows us to obtain different sizes of n-GO sheets by controlling the timing of the cutting and re-aggregation processes. The obtained n-GO exhibits only minor spectral changes, mainly due to the formation of S-containing surface groups; thus, it can be concluded that the material is not reduced during the process. Maintaining the initial oxygen functionalities together with the required nano-size (down to 200 nm) and high homogeneity are beneficial for extensive applications of n-GO. Moreover, we prove that the obtained material is evidently biocompatible. The calculated half-maximal effective concentration (EC50) increases by 5-fold, i.e., from 50 to 250 µg/mL, when GO is converted to n-GO. As a consequence, the new n-GO neither disturbs blood flow even in the narrowest capillaries nor triggers a toxic influence in surrounding cells. Thus, it can be a serious candidate for drugs and biomolecule carriers administered systemically.

摘要

氧化石墨烯(GO)是最令人兴奋且应用广泛的材料之一。本文提出了一种生成纳米氧化石墨烯(n-GO)的新方法。所描述的在二甲基亚砜溶液中独特的超声处理顺序,使我们能够通过控制切割和重新聚集过程的时间来获得不同尺寸的n-GO片层。所获得的n-GO仅表现出微小的光谱变化,主要是由于含硫表面基团的形成;因此,可以得出结论,该材料在过程中未被还原。保持初始的氧官能团以及所需的纳米尺寸(低至200 nm)和高均匀性有利于n-GO的广泛应用。此外,我们证明所获得的材料具有明显的生物相容性。当GO转化为n-GO时,计算得出的半数最大效应浓度(EC50)增加了5倍,即从50 μg/mL增加到250 μg/mL。因此,新的n-GO即使在最狭窄的毛细血管中也不会干扰血流,也不会对周围细胞产生毒性影响。因此,它可能是全身给药的药物和生物分子载体的有力候选者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eea/8000960/9cdc952dc33b/materials-14-01327-g001.jpg

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