Poly (Betulinic Acid) Nanoparticles Loaded with bFGF Improve Functional Recovery After Spinal Cord Injury.
Xianghang ChenBeini WangYongxiu ZhouXuejuan WuAnyu DuAbdullah Al MamunYitie XuShuangshuang WangChang JiangLing XieKailiang ZhouSiwang HuZhou-Guang WangPublished in: Advanced healthcare materials (2024)
Oxidative stress (OS) is one of the crucial molecular events of secondary spinal cord injury (SCI). Basic fibroblast growth factor (bFGF) is a multipotent cell growth factor with an anti-oxidant effect. However, bFGF has a short half-life in vivo, which limits its therapeutic application. Biodegradable polymers with excellent biocompatibility have been recently applied in SCI. The negative aspect is that polymers cannot provide a significant therapeutic effect. Betulinic acid (BA), a natural anti-inflammatory compound, has been polymerized into poly (betulinic acid) (PBA) to serve as a drug carrier for bFGF. This study explores the therapeutic effects and underlying molecular mechanisms of PBA nanoparticles (NPs) loaded with bFGF (PBA-bFGF NPs) in SCI. Results show that PBA-bFGF NPs produce remarkable biocompatibility in vivo and in vitro. The results also demonstrate that local delivery of PBA-bFGF NPs enhances motor function recovery, inhibits OS, mitigates neuroinflammation, and alleviates neuronal apoptosis following SCI. Furthermore, the results indicate that local delivery of PBA-bFGF NPs activates the nuclear factor erythroid 2-related factor 2 (Nrf-2) signaling pathway following SCI. In summary, results suggest that local delivery of PBA-bFGF NPs delivers potential therapeutic advantages in the treatment and management of SCI.
Keyphrases
- spinal cord injury
- oxidative stress
- growth factor
- drug delivery
- nuclear factor
- signaling pathway
- spinal cord
- neuropathic pain
- anti inflammatory
- oxide nanoparticles
- dna damage
- traumatic brain injury
- cell proliferation
- immune response
- induced apoptosis
- emergency department
- lipopolysaccharide induced
- endoplasmic reticulum stress
- bone marrow
- inflammatory response
- pi k akt
- subarachnoid hemorrhage
- blood brain barrier
- lps induced
- replacement therapy