Poly (Betulinic Acid) Nanoparticles Loaded with bFGF Improve Functional Recovery After Spinal Cord Injury

Author:

Chen Xianghang123,Wang Beini4,Zhou Yongxiu4,Wu Xuejuan4,Du Anyu4,Al Mamun Abdullah35,Xu Yitie4,Wang Shuangshuang1,Jiang Chang1,Xie Ling3,Zhou Kailiang6,Hu Siwang1,Xiao Jian146ORCID

Affiliation:

1. Department of Arthroplasty The First People's Hospital of Wenling The Affiliated Wenling Hospital of Wenzhou Medical University Taizhou Zhejiang 317500 China

2. College of Nursing Wenzhou Medical University Wenzhou Zhejiang 325000 China

3. School of Pharmaceutical Science Wenzhou Medical University Wenzhou Zhejiang 325000 China

4. Oujiang Laboratory (Zhejiang Lab for Regenerative Medicine Vision and Brain Health) School of Pharmaceutical Science Wenzhou Medical University Wenzhou Zhejiang 325000 China

5. Central Research Laboratory of The Sixth Affiliated Hospital of Wenzhou Medical University Lishui People's Hospital Lishui City Zhejiang 323000 China

6. Department of Orthopaedics The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University Wenzhou Zhejiang 325000 China

Abstract

AbstractOxidative 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.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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