SBIR-STTR Award

Antiatherogenic Properties of tert-Butylhydroquinone
Award last edited on: 4/1/19

Sponsored Program
STTR
Awarding Agency
NIH : NHLBI
Total Award Amount
$100,000
Award Phase
1
Solicitation Topic Code
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Principal Investigator
William L Stone

Company Information

Bioinventions LLC

2109 West Market Street Suite 120
Johnson City, TN 37604
   (423) 439-8762
   N/A
   N/A

Research Institution

East Tennessee State University

Phase I

Contract Number: 1R41HL076925-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2004
Phase I Amount
$100,000
Atherosclerosis is the underlying cause of most cardiovascular disease and considerable evidence supports the role of hypercholesterolemia as a risk factor for this disease. In preliminary work, we found that tertiary-butyl hydroquinone (TBHQ), at a dose lower than approved for human use, was effective in reducing plasma levels of both total cholesterol and triglycerides in a rat model. TBHQ is phenolic antioxidant commonly used as a food preservative. A patent, "Method for Reducing Blood Cholesterol and/or Blood Triglycerides," was subsequently obtained. The long-term objective of this research proposal is to determine the antiatherogenic potential of TBHQ and advance its commercial development. Our specific aims are to test the efficacy of TBHQ in: (1) reducing aortic atherosclerosis; (2) lowering plasma lipid levels; (3) promoting a less atherogenic lipoprotein profile and; (4) reducing plasma levels of C-reactive protein (CRP). Elevated levels of CRP are a risk factor for cardiovascular disease. In our phase I experiments, we will use the apoE knockout (apoE-/-) mouse model since it has been extensively used to study the antiatherogenic potential of other phenolic antioxidants. Our preliminary market analysis suggests that TBHQ could have a potential market of $100 million per year as a lipid-lowering agent. Commercial development should be accelerated since NIH has already conducted extensive toxicological studies with TBHQ.

Thesaurus Terms:
antiatherogenic agent, cardiovascular disorder chemotherapy, cardiovascular pharmacology, drug design /synthesis /production, drug screening /evaluation, hydroquinone, nonhuman therapy evaluation acute phase protein, aorta disorder, atherosclerosis, cardiovascular disorder risk, cholesterol, disease /disorder model, lipid metabolism, protein localization, protein metabolism, triglyceride computer program /software, dietary lipid, genetically modified animal, laboratory mouse, statistics /biometry

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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