Elastic porous microspheres/extracellular matrix hydrogel injectable composites releasing dual bio-factors enable tissue regeneration.
Yi LiSiyang LiuJingjing ZhangYumeng WangHongjiang LuYuexi ZhangGuangzhou SongFanhua NiuYufan ShenAdam C MidgleyWen LiDe-Ling KongDe Ling KongPublished in: Nature communications (2024)
Injectable biomaterials have garnered increasing attention for their potential and beneficial applications in minimally invasive surgical procedures and tissue regeneration. Extracellular matrix (ECM) hydrogels and porous synthetic polymer microspheres can be prepared for injectable administration to achieve in situ tissue regeneration. However, the rapid degradation of ECM hydrogels and the poor injectability and biological inertness of most polymeric microspheres limit their pro-regenerative capabilities. Here, we develop a biomaterial system consisting of elastic porous poly(l-lactide-co-ε-caprolactone) (PLCL) microspheres mixed with ECM hydrogels as injectable composites with interleukin-4 (IL-4) and insulin-like growth factor-1 (IGF-1) dual-release functionality. The developed multifunctional composites have favorable injectability and biocompatibility, and regulate the behavior of macrophages and myogenic cells following injection into muscle tissue. The elicited promotive effects on tissue regeneration are evidenced by enhanced neomusle formation, vascularization, and neuralization at 2-months post-implantation in a male rat model of volumetric muscle loss. Our developed system provides a promising strategy for engineering bioactive injectable composites that demonstrates desirable properties for clinical use and holds translational potential for application as a minimally invasive and pro-regenerative implant material in multiple types of surgical procedures.
Keyphrases
- tissue engineering
- extracellular matrix
- stem cells
- minimally invasive
- drug delivery
- skeletal muscle
- hyaluronic acid
- reduced graphene oxide
- wound healing
- molecularly imprinted
- working memory
- cancer therapy
- cell proliferation
- drug release
- signaling pathway
- oxidative stress
- binding protein
- cell cycle arrest
- risk assessment