Heparin Microislands in Microporous Annealed Particle Scaffolds for Accelerated Diabetic Wound Healing

Mimicking growth factor-extracellular matrix interactions for promoting cell migration is a powerful technique to improve tissue integration with biomaterial scaffolds for the regeneration of damaged tissues. This is attempted by scaffold-mediated controlled delivery of exogenous growth factors; however, the predetermined nature of this delivery can limit the scaffold's ability to meet each wound's unique spatiotemporal regenerative needs and presents translational hurdles. To address this limitation, a new approach to growth factor organization is presented that incorporates heparin microislands (mu Islands), which are spatially isolated heparin-containing microparticles that can reorganize and protect endogenous local growth factors via heterogeneous sequestration at the microscale in vitro and result in functional improvements in wound healing. More specifically, the heparin mu Islands are incorporated within microporous annealed particle scaffolds, which allows facile tuning of microenvironment heterogeneity through ratiometric mixing of microparticle sub-populations. In this manuscript, the ability of heparin mu Islands to heterogeneously sequester applied growth factor and control downstream cell migration in vitro is demonstrated. Further, their ability to significantly improve wound healing outcomes (epidermal regeneration and re-vascularization) in a diabetic wound model relative to two clinically relevant controls is presented.

Automated summary

By incorporating heparin microislands to reorganize and protect endogenous local growth factors at the microscale, a new approach to growth factor organization has been shown to significantly improve wound healing outcomes. This method allows for the tuning of microenvironment heterogeneity and control of cell migration in vitro.