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SBIR-STTR Award
4
Nitric oxide releasing ultra-slippery antibacterial surfaces for indwelling catheter applications
Award last edited on: 5/16/2023
Sponsored Program
SBIR
Awarding Agency
NIH : CDC
Total Award Amount
$1,148,399
Award Phase
2
Solicitation Topic Code
NCEZID-020-PHS2019
Principal Investigator
Sean Hopkins
Company Information
inNOveta Biomedical LLC
220 Riverbend Road
Athens, GA 30602
(702) 343-4130
N/A
N/A
Location:
Single
Congr. District:
10
County:
Clarke
Phase I
Contract Number:
75DS30119P06553
Start Date:
00/00/00
Completed:
00/00/00
Phase I year
2019
Phase I Amount
$150,000
Although decades of research have been done to develop the ideal blood contacting catheters there still remains no long term solution that prevents infection and thrombosis As antibiotic resistant bacteria become more prevalent the traditional methods of treatment become more obsolete The proposed research is to combine the long term antibacterial efficacy of a silicone rubber S nitrosothiol based nitric oxide NO donor in combination with the liquid infusion of silicone oil to provide an ultra slippery interface to prevent bacteria and protein adhesion The fabricated catheters will be tested for cytotoxic effects against human cell lines to ensure it is safe for commercial use The antibacterial effectiveness of the catheters will be tested against two of the most common bacteria related to catheter infection methicillin resistant Staphlococcus aureus MRSA and Pseudomonas aeruginosa using a CDC biofilm reactor over a d period Our central hypothesis is that this combined NO liquid infused surface will have enhanced biocompatible properties by reducing the formation of biofilms through preventing bacteria adhesion while simultaneously improving its hemocompatible properties by reducing protein adsorption
Phase II
Contract Number:
75D30120C09815
Start Date:
00/00/00
Completed:
00/00/00
Phase II year
2020
Phase II Amount
$998,399
The objective of this potential project is to combine the long-term antibacterial efficacy of a silicone rubber, S-nitrosothiol based nitric oxide (NO) donor in combination with the liquid-infusion of silicone oil to provide an ultra-slippery interface to prevent bacterial and protein adhesion that can be used on indwelling urinary or intravascular catheters to prevent or significantly reduce biofilm formation by organisms known to cause healthcare-associated infections. The overall goal of Phase II is to provide data and specifications necessary to obtain initial 510(k) clearance and initiate clinical use of the NO generating SNAP catheter for reduced thrombosis and infection within one year of the completion of Phase II activities.
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