4.5 Article

Cytocompatibility of Ti3C2TX MXene with Red Blood Cells and Human Umbilical Vein Endothelial Cells and the Underlying Mechanisms

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CHEMICAL RESEARCH IN TOXICOLOGY
卷 36, 期 3, 页码 347-359

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AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrestox.2c00154

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2D nanomaterials, including Ti3C2Tx MXene, have been widely used in biomedical applications due to their biocompatibility. In this study, the cytocompatibility of Ti3C2Tx was studied with red blood cells (RBCs) and human umbilical vein endothelial cells (HUVECs), and it was found that Ti3C2Tx exhibited excellent compatibility with both cell lines.
Two-dimensional (2D) nanomaterials have been widely used in biomedical applications because of their biocompatibility. Considering the high risk of exposure of the circulatory system to Ti3C2Tx, we studied the cytocompatibility of Ti3C2Tx MXene with red blood cells (RBCs) and human umbilical vein endothelial cells (HUVECs) and showed that Ti3C2Tx had excellent compatibility with the two cell lines. Ti3C2Tx at a concentration as high as 200 mu g/mL caused a negligible percent hemolysis of 0.8%. By contrast, at the same treatment concentration, graphene oxide (GO) caused a high percent hemolysis of 50.8%. Scanning electron microscopy revealed that RBC structures remained intact in the Ti3C2Tx treatment group, whereas those in the GO group completely deformed, sunk, and shrunk, which resulted in the release of cell contents. This difference can be largely ascribed to the distinct surficial properties of the two nanosheets. In specific, the fully covered surface-terminating -O and -OH groups leading to Ti3C2Tx had a very hydrophilic surface, thereby hindering its penetration into the highly hydrophobic interior of the cell membrane. However, the strong direct van der Waals attractions coordinated with hydrophobic interactions between the unoxidized regions of GO and the lipid hydrophobic tails can still damage the integrity of the cell membranes. In addition, the sharp and keen-edged corners of GO may also facilitate its relatively strong cell membrane damage effects than Ti3C2Tx. Thus, the excellent cell membrane compatibility of Ti3C2Tx nanosheets and their ultraweak capacity to provoke excessive ROS generation endowed them with much better compatibility with HUVECs than GO nanosheets. These results indicate that Ti3C2Tx has much better cytocompatibility than GO and provide a valuable reference for the future biomedical applications of Ti3C2Tx.

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