Wound healing, especially for diabetic
wounds, is a lengthy and complicated process involving interactions and responses at the
protein, cell, and tissue levels. Loading of
growth factors into a
hydrogel to construct a sustained-release system is considered a promising approach to improve wound healing. The present study investigates the effect of thermosensitive
heparin-
poloxamer (HP)
hydrogel-encapsulated recombinant human
fibroblast growth factor 21 (rhFGF21) on wound healing in mice with
streptozotocin-induced
diabetes mellitus. First, we studied the in vitro release of rhFGF21 from the rhFGF21-HP coacervate. The results showed that HP might control the release of rhFGF21. Next, we examined the effect of rhFGF21-HP on skin wound healing in diabetic mice. Our data showed that rhFGF21-HP significantly improved
wound closure; promoted granulation,
collagen deposition, and re-epithelialization; and enhanced the expression of CD31. Moreover, rhFGF21-HP had obvious advantages in diabetic wound healing. Therefore, the results suggest that the rhFGF21-HP
hydrogel polymer plays an important role in skin wound healing. This work provides a suitable sustained-release delivery system that can continuously release rhFGF21 and presents a promising therapeutic strategy for wound healing in patients with diabetes.-Liu, H., Zhao, Y., Zou, Y., Huang, W., Zhu, L., Liu, F., Wang, D., Guo, K., Hu, J., Chen, J., Ye, L., Li, X., Lin, L.
Heparin-
poloxamer hydrogel-encapsulated rhFGF21 enhances wound healing in diabetic mice.