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. 2022 Jun 16;23(12):6724. doi: 10.3390/ijms23126724

Table 1.

Overview of recent toxicity studies of ZnO NPs with different models.

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]