Review Article

Synthesis and Toxicity of Graphene Oxide Nanoparticles: A Literature Review of In Vitro and In Vivo Studies

Table 1

In vitro cytotoxicity of GO.

Dose of GO (μg/mL)Cell lineDiameter (nm)Time (h)Toxic effectReference

3.125-200Human erythrocytes
Human skin fibroblasts CRL-2522
342-76524Hemolytic activity, ROS generation, LDH release, decreased cell viability[86]
5-100Human fibroblast cells1 (height)24Dose-dependent cytotoxicity, apoptosis[79]
50–100Mouse CT26 colon carcinoma cellThickness: <2
Lateral size: 450
18Triggered autophagy, enhances cell death[96]
100-500MDA-MB-231156.448Dose-dependent cytotoxicity; DNA damage, cell cycle arrest, apoptosis[77]
0–80HeLa cellsSize distribution: in PBS, in FBS24Released LDH, increased MDA and ROS generation, decreased SOD, reduction of cell viability[97]
20Macrophage cell J774A.1
THP-1 cells
HEK293 cells
MEL cells
HUT102 cells
Smaller-sized GO: 50-350
Intermediate-sized GO: 350-750
Larger-sized GO: 750-1300
1-24Size-dependent M1 induction of macrophages, proinflammatory responses[98]
10-200Human lung epithelial A549 cellsThickness of 0.9
Lateral size: s-GO,
m-GO,
l-GO,
24Dose-dependent oxidative stress, cell viability decreased at high concentration[80]
7.8, 15.6, 31.2, 62.5, and 125MCF-7, HUVEC, KMBC/71 cells1004-24 hSignificant alterations in the expression level of miR-21, miR-29a, Bax, Bcl2, and PTEN genes after treatment in all three cells
Alteration in mitochondrial activity at cellular level
[99]
50Embryonic stem cell- (ESC-) derived cellsThickness 1.324 hNo significant difference between the level of apoptosis of GO-treated hRPE cells and untreated hRPE controls[100]