초록 ▼

Sterilization methods and apparatus are effective to achieve a 6-log reduction in CFUs of industry standard bacteria and bacterial spores, i.e., B. stearothermophilus and B. subtilis spores, by subjecting sterilizable materials to a chemical additive-containing carbon dioxide sterilant fluid at or n

Sterilization methods and apparatus are effective to achieve a 6-log reduction in CFUs of industry standard bacteria and bacterial spores, i.e., B. stearothermophilus and B. subtilis spores, by subjecting sterilizable materials to a chemical additive-containing carbon dioxide sterilant fluid at or near its supercritical pressure and temperature conditions. Most preferably, the chemical additive-containing supercritical carbon dioxide sterilant fluid is agitated during sterilization, e.g., via mechanical agitation or via pressure cycling.

대표청구항 ▼

What is claimed is: 1. A sterilization method comprising: (a) bringing a material in need of sterilization into contact with a sterilant fluid comprised of carbon dioxide at supercritical pressure and temperature conditions, and a sterilization enhancing effective amount of between about 0.001% to

What is claimed is: 1. A sterilization method comprising: (a) bringing a material in need of sterilization into contact with a sterilant fluid comprised of carbon dioxide at supercritical pressure and temperature conditions, and a sterilization enhancing effective amount of between about 0.001% to about 2.0 % based on the total volume of a chemical sterilization additive, wherein the additive is selected from the group consisting of acetic acid, peracetic acid, trifluoroacetic acid, acetic acid derivatives or mixtures thereof, and (b) maintaining said contact with the sterilant fluid under said temperature and pressure conditions while mechanically agitating for a time sufficient to achieve a 6-log reduction or greater in colony forming units (CFUs) of bacterial spores. 2. The sterilization method of claim 1, which comprises agitating the sterilant fluid by stirring. 3. Apparatus for sterilizing an article in need of sterilization through the application of a sterilant fluid comprising: a pressure vessel for containing the article in need of sterilization a source of supercritical carbon dioxide connected to the pressure vessel; a source of a liquid chemical sterilization additive selected from the group consisting of acetic acid, peracetic acid, trifluoroacetic acid, acetic acid derivatives or mixtures thereof connected operatively to the pressure vessel; means for introducing the supercritical carbon dioxide and sterilization additive to the pressure vessel in an amount of between about 0.001% to about 2.0% of the additive based on a total volume of the sterilant fluid introduced; means for introducing an article in need of sterilization into the pressure vessel so as to bring the article into contact with the sterilant fluid at supercritical pressure and temperature conditions and maintaining the article in contact with the sterilant fluid under said temperature and pressure conditions while mechanically agitating for a time sufficient to achieve a 6-log reduction or greater in colony forming units (CFUs) of bacterial spores; and a depressurization line fluid-connected to the pressure vessel for evacuating at least some portion of the carbon dioxide and sterilization additive from the pressure vessel so as to depressurize the same. 4. Apparatus as in claim 3, further comprising a liquid-gas separator in said depressurization line for separating carbon dioxide gas from the liquid sterilization additive. 5. Apparatus as in claim 3, further comprising a valve in said depressurization line to allow said at least some portion of the carbon dioxide and sterilization additive to be evacuated from the pressure vessel through the depressurization line. 6. The sterilization method of claim 1, wherein materials treated are selected from the group consisting of thermally or hydrolytically sensitive, medically-important materials. 7. The sterilization method of claim 6, wherein the materials treated are selected from the group consisting of tissue for implantation or transplantation. 8. The sterilization method of claim 6, wherein the materials treated are selected from the group consisting of biodegradable and other medical polymers. 9. The sterilization method of claim 6, wherein the materials treated are selected from the group consisting of drugs, drug delivery systems and/or medical equipment.