Chronic wounds disproportionately affect diabetic individuals compared to the general population. One in four diabetic individuals are predicted to develop a chronic wound during their lifetime, with a recurrence rate close to 70%. Many chronic wounds progress in severity, with 12% of recurrent chronic wounds resulting in amputation. While growth factor therapy has demonstrated a limited ability to promote wound healing, the current therapeutic modalities do not accurately recreate the natural wound healing process. The objective of this project is to develop new therapeutic wound dressings that more accurately recreate the natural wound healing dynamics seen in vivo. The central hypothesis of this proposal is that layer-by-layer (LbL) technology can be used to create stratified electrostatic assemblies that temporally modulate local cytokine levels in chronic wounds and stimulate the healing process. To test this hypothesis, Aim 1 will develop 'affinity polymers'that specifically bind cytokines to enable tuning of the temporal release profile. LbL constructs will be subsequently fabricated that possess two different therapeutic strategies: (1) the release of vascular endothelial growth factor (VEGF) followed by the release of platelet derived growth factor (PDGF) to promote angiogenesis and reepithelialization, and (2) the sustained release of CX3CL1 to recruit therapeutic cells to the wound bed. In vitro characterization will be used to optimize the cytokine loading, release profile, and biological activity of the dressings. Following dressing development, Aim 2 will examine the ability of temporally modulated cytokine delivery to promote wound healing in a diabetic mouse model. Collectively, these aims will uncover new insights into the ability to promote chronic wound healing via the synergistic signaling that arise from coordinated cytokine delivery. This work will subsequently lay the foundation for developing a new clinical strategy for treating patients suffering from chronic wounds.

Public Health Relevance

The proposed research will develop a new therapeutic bandage that mimics key biological traits from normal wound healing. For the millions of patients that develop non-healing chronic wounds each year, such as diabetic foot ulcers, this research will yield a new wound dressing that promotes normal wound healing.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32DK097858-01A1
Application #
8526170
Study Section
Special Emphasis Panel (ZDK1-GRB-R (J1))
Program Officer
Castle, Arthur
Project Start
2013-02-01
Project End
2015-01-31
Budget Start
2013-02-01
Budget End
2014-01-31
Support Year
1
Fiscal Year
2013
Total Cost
$49,214
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Castleberry, Steven A; Almquist, Benjamin D; Li, Wei et al. (2016) Self-Assembled Wound Dressings Silence MMP-9 and Improve Diabetic Wound Healing In Vivo. Adv Mater 28:1809-17
Almquist, Benjamin D; Castleberry, Steven A; Sun, Julia B et al. (2015) Combination Growth Factor Therapy via Electrostatically Assembled Wound Dressings Improves Diabetic Ulcer Healing In Vivo. Adv Healthc Mater 4:2090-2099