Table 3.
Type of NPs | Size | Drug loaded/synergy | Effects |
---|---|---|---|
ZnO NPs | 60–95 nm spherical | — | Mitigated the diabetic complications [104] |
ZnO NPs | ∼20 nm spherical | — | A significant decrease in fasting blood glucose and increase in high-density lipoprotein levels [105] |
ZnO NPs | 10–30 nm | Thiamine | ZnO NPs in combination with thiamine-improved diabetes therapy [106] |
ZnO NPs | — | — | ZnO NPs effectively reversed diabetes-induced pancreatic injury [107] |
ZnO-RSW NPs | ∼20 nm | Conjugated red sandalwood (RSW) | ZnO-RSW NPs showed excellent activity against the crude murine pancreatic glucosidase as compared to the individual ZnO NPs and the RSW extract [103] |
ZnO NPs | — | — | ZnO NPs acted as a potent antidiabetic agent evidenced by improved glucose disposal, insulin levels, and zinc status in diabetic rats [100] |
ZnO NPs | ∼10 nm | — | ZnO NPs presented pleiotropic antidiabetic effects via improved insulin signaling, enhanced glucose uptake, decreased hepatic glucose output, decreased lipolysis, and enhanced pancreatic beta cell mass [108] |
ZnO NPs, CeO2 NPs, Ag NPs | ZnO NPs: 55 nm, CeO2 NPs: 54 nm, Ag NPs: 22.5 nm | — | ZnO NPs and Ag NPs had more potent antihyperglycemic activity than CeO2 NPs [109] |
ZnO NPs | Spherical: 96–115 nm; hexagonal: 57 ± 0.3 nm | — | ZnO NPs displayed better antidiabetic potential (IC50: 66.78 μg/mL) than ZnNO3 (IC50: 91.33 μg/mL) in terms of the α-amylase inhibition activity [26] |
ZnO NPs | — | Vildagliptin | ZnO NPs and vildagliptin have synergistic effects on the therapy of type-2 diabetes [110] |
ZnO NPs | 10–15 nm spherical | — | ZnO NPs could improve glucose tolerance and higher serum insulin and reduce blood glucose, nonesterified fatty acids, and triglycerides [101] |