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Sterilizing Medical Equipment With One Atmosphere Uniform Glow Discharge Plasma

Award Information
Agency: Environmental Protection Agency
Branch: N/A
Contract: EP-D-04-029
Agency Tracking Number: EP-D-04-029
Amount: $69,941.00
Phase: Phase I
Program: SBIR
Solicitation Topic Code: N/A
Solicitation Number: N/A
Solicitation Year: N/A
Award Year: 2004
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
934 Corridor Park Blvd.
Knoxville, TN 37932
United States
DUNS: 158986732
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 Kimberley Kelly-Wittenberg
 President & Chief Executive Officer
 (856) 777-3776
Business Contact
 Kimberley Kelly-Wittenberg
Title: President & Chief Executive Officer
Phone: (856) 777-3776
Research Institution

The goal of this Phase I research project is to investigate the feasibility and commercial potential of using the One Atmosphere Uniform Glow Discharge Plasma (OAUGDPTM) as a low-temperature sterilization process for medical equipment. Current sterilization technologies that pose a risk to health care workers and the environment are being phased out of use (e.g., ethylene oxide sterilization). This heightens the need to develop innovative environmentally and employee friendly technologies. The OAUGDP patented technology has been shown to be effective at sterilizing/decontaminating a number of surfaces for applications in biological/chemical decontamination, improving indoor air quality, blood products, and food. Furthermore, OAUGDP does not require consumables to operate nor does it generate waste or harmful byproducts.

To demonstrate proof of concept, Atmospheric Glow Technologies will address the following goals:

¿ Fabricate an OAUGDP prototype that will sterilize contaminated medical equipment.

¿ Inoculate stainless steel surgical instruments with microorganisms and assess the OAUGDP exposure time necessary to sterilize the device in the presence or absence of organic debris.

¿ Inoculate common sensitive medical equipment with microorganisms and assess the plasma exposure time necessary to sterilize the device in the presence or absence of organic debris.

¿ Evaluate any potential surface modifications or effect on functionality occurring as a result of OAUGDP exposure through microscopic and analytical techniques.

¿ Prepare a final report and the Phase II proposal.

* Information listed above is at the time of submission. *

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