SBIR/STTR Research Award

A new biomarker for diabetic foot ulcers

Award identifier 06be78c703331c2af928a2d468b3c7c59ab39338ddf46b19bbfb33695bbde873Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$280,702

Program and phase

SBIR · Phase I

Award year

2015

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Noveratech L.L.C.
Proposal award date
2015-02-09
Contract end date
2016-08-08
UEI
DHTASEX58M16
Solicitation number
PA14-058
Topic code
100

Research abstract

DESCRIPTION provided by applicant This proposal is submitted in response to the new NIDDK announcement PA calling for development of methodologies or biomarkers to help understand the pathophysiology of T D type diabetes T D complications An estimated of the million diabetic patients in this country will develop diabetic foot ulcers DFU at some point in their lives DFU is the leading cause of non traumatic lower extremity amputations caused by non healing wounds Despite thousands of dressing products developed to treat chronic wounds none has proven effective for DFU As stated in the RFA a significant obstacle for progress in developing drugs for diabetic complications is the paucity of biomarkers and surrogate endpoints for measuring the initiation progression and response to treatments of diabetic complications Although many factors are involved in non healing DFU tissue ischemia is known to be a major factor contributing to poor wound healing Ischemia may not be the initiating factor for DFU because most ulcers start from a combination of neuropathy pressure loading and or trauma However tissue ischemia is the main cause that hinders healing Providing oxygen to chronic ulcers has not obtained stable results This is because oxygen is only one of the ingredients required for HEP production The specific aim of this phase I proposal is to explore the possibility of using high energy phosphate HEP contents as a biomarker to predict the progression and recurrence of diabetic ulcers We plan to use a diabetic animal wound model with and without ischemia to test the changes of HEP in these wounds along with the expression of several key factors known to be critical to wound healing such as vascular endothelial growth factors cytokines macrophages collagens and angiogenesis and correlated them to obtain a preliminary picture of the relationship between these factors and the haling of diabetic wounds The result may provide a preliminary indication whether the change of HEP content alone or along with other key factors will be better used to predict the likelihood of healing This is a difficult job but we already have a proof of concept PUBLIC HEALTH RELEVANCE A significant obstacle for progress in developing drugs for diabetic complications is the paucity of biomarkers and surrogate endpoints to measure the initiation progress and response to treatments for diabetic foot ulcers despite decades of research We have found that tissue high energy phosphate contents are severely reduced in human diabetic wounds and supplementation of high energy phosphate to diabetic wounds in animals resulted in enhanced healing along with up regulation of growth factors cytokines angiogenesis and macrophage accumulation and proliferation This phase I proposal will explore the possibility of using tissue high energy phosphate as a biomarker to predict the likelihood of healing along with the expression of growth factors cytokines macrophages and angiogenesis Our goal is to develop a biomarker which is low cost easy to use and accurate for diabetic foot ulcers

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

7 SBIR/STTR records share this UEI (2012–2022). Reported award amounts total $4,704,588. Reported amounts are not federal obligations.

Phases: Phase I, Phase II – Direct to Phase II, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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