Dissolvable Immunomodulatory Microneedles for Treatment of Skin Wounds

Author:

Ghelich Pejman1,Samandari Mohamadmahdi1,Hassani Najafabadi Alireza1,Tanguay Adam1,Quint Jacob1ORCID,Menon Nikhil1,Ghanbariamin Delaram1,Saeedinejad Farnoosh1,Alipanah Fatemeh1,Chidambaram Ramaswamy2,Krawetz Roman34,Nuutila Kristo5,Toro Steven1,Barnum Lindsay1,Jay Gregory D.6,Schmidt Tannin A.1,Tamayol Ali1ORCID

Affiliation:

1. Department of Biomedical Engineering University of Connecticut Health Center Farmington CT 06030 USA

2. Center for Comparative Medicine University of Connecticut Health Center Farmington CT 06030 USA

3. McCaig Institute for Bone & Joint Health University of Calgary Calgary AB T2N 4Z6 Canada

4. Department of Surgery University of Calgary Calgary AB T2N 1N4 Canada

5. US Army Institute of Surgical Research Fort Sam Houston Texas 78234 USA

6. Emergency Medicine Brown University Providence RI 02908 USA

Abstract

AbstractSustained inflammation can halt or delay wound healing, and macrophages play a central role in wound healing. Inflammatory macrophages are responsible for the removal of pathogens, debris, and neutrophils, while anti‐inflammatory macrophages stimulate various regenerative processes. Recombinant human Proteoglycan 4 (rhPRG4) is shown to modulate macrophage polarization and to prevent fibrosis and scarring in ear wound healing. Here, dissolvable microneedle arrays (MNAs) carrying rhPRG4 are engineered for the treatment of skin wounds. The in vitro experiments suggest that rhPRG4 modulates the inflammatory function of bone marrow‐derived macrophages. Degradable and detachable microneedles are developed from gelatin methacryloyl (GelMA) attach to a dissolvable gelatin backing. The developed MNAs are able to deliver a high dose of rhPRG4 through the dissolution of the gelatin backing post‐injury, while the GelMA microneedles sustain rhPRG4 bioavailability over the course of treatment. In vivo results in a murine model of full‐thickness wounds with impaired healing confirm a decrease in inflammatory biomarkers such as TNF‐α and IL‐6, and an increase in angiogenesis and collagen deposition. Collectively, these results demonstrate rhPRG4‐incorporating MNA is a promising platform in skin wound healing applications.

Funder

National Institutes of Health

U.S. Department of Defense

Publisher

Wiley

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