Table 1.
ZnO NPs Dosage | Toxicity Classification | Species/Cell Type | Exposure/Assay | Observations | Ref. |
---|---|---|---|---|---|
0.05, 0.2 mg/kg | Acute toxicity | Mice | Single intravenous exposure | Accumulation to spleen, liver and lungs; increase of 8-OHdG. LD50: 0.3 mg/kg | [5] |
9.38, 18.75, 37.50, 75.00, 150.00 mg/kg | Acute toxicity | Mice | Intraperitoneal injection for 5 d and 10 d | Histopathological damage to kidneys, spleen, heart, and brain; effects on hematological and biochemical parameters. LD50: 299.9 mg/kg | [6] |
31.25, 125, 500 mg/kg | Subchronic toxicity | Rat | Oral gavage for 90 d | Inflammatory damage to stomach, pancreas, eye, prostate gland tissues. | [7] |
2000 mg/kg | Teratogenicity | Rat | Oral gavage | Fetal malformation, skeletal dysplasia and spinal insufficiency. | [8] |
0.245, 245.26 mg/kg | Mutagenicity | Chicks | Intraperitoneal injection for 2 d | Induction of micronucleus, binucleus and heteromorphus in erythrocytes. | [9] |
1 µg/mL | Carcinogenic risk | Mice embryonic fibroblasts |
Exposure for 2 and 12 weeks | Upregulation of the early biomarkers of carcinogenesis, MTH1. | [10] |
10 mg/kg | Nephrotoxicity | Mice | Single intraperitoneal injection | Renal tubule and glomerulus damage, increase of serum creatinine and blood urea nitrogen; HIF-1α-mediated apoptosis and autophagy. | [11] |
600, 1000 mg/kg | Cardiotoxicity | Rat | Oral gavage for 5 d | Increase of troponin-T, creatine kinase-MB, myoglobin, TNF-α, IL-6, cardiac calcium concentration, DNA damage and Caspase-3 activity. | [12] |
5.6 mg/kg | Neurotoxicity | Mice | Intraperitoneal injection 3 times per week for 28 d | Damage to blood brain barrier; disorder of nerve cell arrangement; neuronal degeneration; nistenite loss. | [13] |
350 mg/kg | Immunotoxicity | Rat | Oral gavage for 28 d | Increase of MDA, IL-1β, TNF-α, TLR4 and TLR6; increase of apoptotic bodies and tingible body macrophages; appearance of abnormal thymocytes; | [14] |
100 mg/kg | Reproductive toxicity | Mice | Oral gavage for 3 d | Induction of oxidative stress and apoptosis; weight loss of male mice testicular; activation of Shh pathway in ovaries; Caspase-related uteri injury. | [15] |