SBIR/STTR Research Award

Cell Sprayer for Chronic Wound Therapy

Award identifier e159d3c6f88694ae12b5aa7d47c7269f3b74034c80e7a9fc36a392fed6578605Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$99,615

Program and phase

STTR · Phase I

Award year

2009

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
PLUROGEN THERAPEUTICS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2009-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Chronic wounds, such as diabetic wounds, are a major global health and economic burden. In the United States alone, 10.8 million chronic wounds occur every year (de Zoysa et al., 2005) which is estimated to cost over 15 billion annually in the U.S. (Farley, 2005). Currently, the diabetes population in the United States is 20.8 million adults and children (American Diabetes Association), and at any given time, approximately 6% or 1.2 million diabetic patients have a chronic wound (de Zoysa et al., 2005). These wounds are typically characterized as very difficult to heal and may result in amputation. In the recent past, various biological wound therapies ( advanced wound therapeutics ) have become available to the clinician. However, from a clinical standpoint, these products have not been universally embraced--mechanisms are not clearly understood, efficacy not always predictable or reproducible, and treatment guidelines are undefined. A collaborative team of investigators from the University of Virginia and Plurogen Therapeutics, Inc is developing a transformative cell-based therapy for healing chronic diabetic wounds. The new therapy, termed CEAL therapy, is based on the use of autologous human stem cells harvested during liposuction procedures (hASCs), which are formulated into self-adherent 3-dimensional multi-cell aggregates (SNiMs). CEAL therapy has proven both safe and effective in drastically accelerating the healing of diabetic wounds in a pre-clinical model. The next step toward commercialization of this novel wound healing therapy is testing in patients, but before this can be accomplished, a controlled method for delivering CEAL therapy must be developed and tested for feasibility. To this end, we propose the following specific aims in Phase I of STTR funding: Aim 1) Perform in vitro feasibilty tests of a 1st Generation CEAL Sprayer and optimize/re-design the device to meet eight well-defined engineering design specifications, and Aim 2) Perform in vivo feasibility tests of the CEAL Sprayer in a mouse model of diabetes-induced delayed wound healing. hASCs have a number of attributes that make them an appealing and unique therapeutic strategy for tissue regeneration and healing of chronic wounds, and CEAL therapy offers significant potential advantages related to cost-efficient commercialization, therapeutic efficacy, and end-user appeal. The proposed work will significantly advance this promising new therapy for a global health problem toward clinical use. PUBLIC HEALTH RELEVANCE: Chronic diabetic wounds are widespread among the global and aging population, and current treatments are inadequate. We have developed a novel cell-based therapy that utilizes a patient's own adipose (fat) tissue that demonstrates safety and efficacy in a pre-clinical small animal model of diabetic skin wounds. The goal of the proposed work is to develop a medical device/system that effectively and efficiently delivers adipose- derived cells to open wounds using an aerosolized spray-on mechanism.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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