
NSF Org: |
TI Translational Impacts |
Recipient: |
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Initial Amendment Date: | May 22, 2007 |
Latest Amendment Date: | November 30, 2007 |
Award Number: | 0712489 |
Award Instrument: | Standard Grant |
Program Manager: |
Gregory T. Baxter
TI Translational Impacts TIP Directorate for Technology, Innovation, and Partnerships |
Start Date: | July 1, 2007 |
End Date: | June 30, 2008 (Estimated) |
Total Intended Award Amount: | $0.00 |
Total Awarded Amount to Date: | $150,000.00 |
Funds Obligated to Date: |
FY 2008 = $50,000.00 |
History of Investigator: |
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Recipient Sponsored Research Office: |
PO Box 415 Hattiesburg MS US 39403-0000 (601)467-9418 |
Sponsor Congressional District: |
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Primary Place of Performance: |
PO Box 415 Hattiesburg MS US 39403-0000 |
Primary Place of
Performance Congressional District: |
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Unique Entity Identifier (UEI): |
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Parent UEI: |
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NSF Program(s): | SBIR Phase I |
Primary Program Source: |
01000809DB NSF RESEARCH & RELATED ACTIVIT |
Program Reference Code(s): |
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Program Element Code(s): |
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Award Agency Code: | 4900 |
Fund Agency Code: | 4900 |
Assistance Listing Number(s): | 47.084 |
ABSTRACT
This Small Business Innovation Research (SBIR) Phase I research research project aims to develop a polymer system for drug eluting coronary stents (DES). The material is expected to provide higher drug loading with a controlled drug release profile, as well as tunable mechanical properties over the lifetime of the stent. This will be accomplished using block terpolymers of specific composition to which drug molecules will be covalently attached.
Recent advances in DES technology have increased the success rate of CHD treatment; however, restenosis (re-blockage of the artery through the stent) occurs in 10% of the implanted stents. Also currently available drug eluting coatings deliver the bulk of the loaded drug within the first 48 hours of stent placement, with little to no delivery after 30 days. Thus a new type of stent that can overcome the limitations of current stents would be of significant value.
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