摘要
Spinal cord injury (SCI) causes severe neurological deficits and remains difficult to treat with current strategies such as surgical decompression or corticosteroids, which offer limited benefits. Hydrogels represent a promising alternative because they provide structural support and serve as therapeutic carriers. Quaternized chitosan (QCS), a derivative of chitosan, shows improved solubility and anti-inflammatory properties but lacks crosslinking ability and degrades rapidly, restricting its application in SCI. To overcome these limitations, we introduced methacrylate groups into QCS (QCS-MA), enabling photo-crosslinking, faster gelation, and enhanced mechanical stability while preserving bioactivity. QCS-MA was blended with type I collagen to form an interpenetrating hydrogel (QCS-MA/COL) through hydrogen bonding, then loaded with progranulin (PGRN), a multifunctional growth factor known to promote neuronal survival and modulate immune responses. The resulting PGRN@QCS-MA/COL hydrogel displayed favorable mechanical properties, injectability, and biocompatibility, while inducing macrophage polarization toward a reparative M2 phenotype. In a mouse SCI model, it significantly improved motor recovery, reduced lesion cavity formation, attenuated chronic inflammation, and enhanced axonal and neural regeneration. These findings highlight the potential of QCS-MA as a tunable immunomodulatory delivery platform, synergizing with PGRN and collagen to provide a biomimetic strategy for neural repair.
危险品化学品经营许可证(带存储)