Table 2.
Nanomedicines | Motor function recovery | Therapeutic effects | Advantages/disadvantages | Refs. |
---|---|---|---|---|
Glutathione | Improve significantly | Antioxidant | Reduces inflammation; very low bioavailability | [29] |
Methylprednisolone | Improve significantly | Immunosuppressant | Reduces inflammation; water-sodium retention, susceptible to infection | [6, 30] |
Hydralazine | Improve significantly | Antioxidant | Reduces inflammation; short half-life and long-term toxicity | [31] |
NT3-Chitosan | Improve significantly | Anti-infection, neuroprotection | Regeneration; difficult to be dissolved in human fluid | [32] |
CeO2-PCL | Improve in vitro biocompatibility and auto-recovery abilities | Delivered a bone regeneration drug | Increases biocompatibility of the drug; not available for injection and the in vivo effects are unknown | [33] |
Se-CQDs | Improve significantly after 8 weeks | Reduced the inflammation, astrogliosis, and apoptosis induced by secondary injury | Remarkable protective effect for nerves; not cost-effective, toxic concern | [34] |
R-DHLA-AuNCs-Zn | Improve significantly after 7 days | Immunosuppressant | Reduces inflammation, anti-apoptosis, anti-oxidant, injectable, low toxicity, cost-effective, simple preparation | Current work |
NT3, neurotrophin3; CeO2-PCL (CeO2 particles assembled onto poly (∊ -caprolactone) (PCL)) Se-CODS (Selenium-Doped Carbon Quantum Dots)