Evaluation of a bilayered, micropatterned hydrogel dressing for full-thickness wound healing

Author:

Magin Chelsea M1,Neale Dylan B2,Drinker Michael C1,Willenberg Bradley J234,Reddy Shravanthi T1,La Perle Krista MD5,Schultz Gregory S2,Brennan Anthony B146

Affiliation:

1. Sharklet Technologies, Inc., Aurora, CO 80045, USA

2. Department of Materials Science and Engineering, University of Florida, Gainesville, FL 32611, USA

3. Department of Internal Medicine, University of Central Florida, Orlando, FL 32827, USA

4. Saisijin Biotech, LLC, Orlando, FL 32827, USA

5. Department of Veterinary Biosciences, College of Veterinary Medicine and Comparative Pathology & Mouse Phenotyping Shared Resource, Comprehensive Cancer Center The Ohio State University, Columbus, OH 43210, USA

6. J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, FL 32611, USA

Abstract

Nearly 12 million wounds are treated in emergency departments throughout the United States every year. The limitations of current treatments for complex, full-thickness wounds are the driving force for the development of new wound treatment devices that result in faster healing of both dermal and epidermal tissue. Here, a bilayered, biodegradable hydrogel dressing that uses microarchitecture to guide two key steps in the proliferative phase of wound healing, re-epithelialization, and revascularization, was evaluated in vitro in a cell migration assay and in vivo in a bipedicle ischemic rat wound model. Results indicate that the Sharklet™-micropatterned apical layer of the dressing increased artificial wound coverage by up to 64%, P = 0.024 in vitro. In vivo evaluation demonstrated that the bilayered dressing construction enhanced overall healing outcomes significantly compared to untreated wounds and that these outcomes were not significantly different from a leading clinically available wound dressing. Collectively, these results demonstrate high potential for this new dressing to effectively accelerate wound healing.

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology

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