From: Advances in the application of Mxene nanoparticles in wound healing
MXenes | Type of Cells | Dose | Toxicity Effects | Reference |
---|---|---|---|---|
Ti3C2Tx | A549, MRC-5, A375, HaCaT cells | 0-500 µg mL− 1, 24 h | Concentration dependent cytotoxicity. Toxic effects were higher against cancerous cells in comparison to normal ones. | [50] |
Ti2NTx | MCF-7, A365, MCF-10 A, HaCaT cells | 62.5–500 µg mL− 1 ,24 h | Higher toxicity to cancer cell lines than normal cell lines | [65] |
Ti3C2Tx | Human umbilical vein dothelial cells (HUVECs) | 100 and 500 µgmL− 1,48 h | No obvious acute cytotoxicity. | [68] |
Ti3C2Tx | neural stem cells (NSCs) and NSCs-derived differentiated cells | 12.5–100 µg mL− 1, 24 h | At 25 µg mL− 1, Ti3C2Tx nanosheets caused significant cytotoxicity to NSCs. | [66] |
Ti3C2Tx | human mesenchymal stem cells (hMSCs) | 0-100 µg mL− 1, 7 days | > 50 µg mL− 1, obvious cytotoxicity was shown | [67] |
Nb2CTx | Breast 4T1, glioma U87 cancer cel | 0–200 µg mL− 1, 24 h | 200µgmL− 1, no significant cytotoiccity, exposed to NIR, cancer cells were inhibited | [27] |