Development of a Field-Ready Antimicrobial Wound Dressing for the Treatment of Vesicant Burns

Award Information
Agency: Department of Defense
Branch: Office for Chemical and Biological Defense
Contract: W81XWH-07-C-0063
Agency Tracking Number: C071-113-0151
Amount: $99,623.00
Phase: Phase I
Program: SBIR
Awards Year: 2007
Solitcitation Year: 2007
Solitcitation Topic Code: CBD07-113
Solitcitation Number: 2007.1
Small Business Information
505 S. Rosa Road, Suite 169, Madison, WI, 53704
Duns: 160392168
Hubzone Owned: N
Woman Owned: Y
Socially and Economically Disadvantaged: N
Principal Investigator
 Barry Steiglitz
 Molecular Biology Scientist
 (608) 441-2750
Business Contact
 Robert Barnard
Title: Vice President and Treasurer
Phone: (608) 441-2750
Research Institution
Cutaneous wounds, such as those resulting from vesicant exposure and thermal injuries, provide an ideal environment for bacterial growth and the complications stemming from wound sepsis. The availability of ready-to-use, antimicrobial skin substitutes that are readily deployed in the field would provide immediate wound closure and reduce the incidence of infection in these wounds. To address these needs, Stratatech Corporation is developing a field-ready, tissue engineered antimicrobial therapeutic called EpiReadyDefense™ for treatment of vesicant, thermal and traumatic cutaneous injuries. This product is designed to contain elevated levels of naturally-occurring antimicrobial peptides in the context of a fully-stratified skin substitute that is ready to use and stable at ambient temperatures. During Phase I of the project, procedures will be developed to format Stratatech’s existing antimicrobial skin substitute for ambient storage. Efforts will focus on preserving tissue architecture and strength, as well as maintaining the antimicrobial properties required in the final product. In Phase II, the antimicrobial properties of EpiReadyDefense™ will be determined in an established animal model of burn wound infection. Phase II studies will also include preclinical safety studies that will be required to support ultimate clinical evaluation and approval of EpiReadyDefense™ tissue.

* information listed above is at the time of submission.

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