Sterilization validation system and method
A sterilization validation system and method are disclosed that ensure sterilization of packaging materials that contain certain sterilized items that have been sterilized in a cleanroom environment. In accordance with the disclosed subject matter, garments (or other items or materials) that are sterilized inside autoclave or breather bags may be secured within tote liners that ensure sterility of the exterior of the breather bags containing the garments. Not only is it possible to ensure a recipient that the garment is sterile, but it is also possible to verify that the outside of the breather bag itself is also sterile, since the breather bag will remain sterilized inside the tote liner during shipping.
1. A sterilization validation method comprising:
loading a sealed breather bag containing a cleaned item into a CO 2 compatible tote liner, the tote liner comprising a CO 2 permeable sleeve and containing a biological indicator to indicate a level of sterility;
sealing the tote liner and exposing the sealed tote liner to a cleaning cycle utilizing CO 2 and a sterilant;
lowering a pressure following the cleaning cycle slowly to prevent damage to the biological indicator; and
confirming sterilization using the biological indictor; and packaging the sterilized tote liner into a container for shipping.
2. The method of claim 1 wherein the cleaned item is one of equipment, an instrument, a garment, and material.
3. The method of claim 1 wherein the exposing comprises utilizing a solution comprising between 15% and 30% weight to volume of hydrogen peroxide as the sterilant.
4. The method of claim 1 wherein the exposing comprises utilizing a high pressure, low temperature cleaning cycle.
5. The method of claim 4 wherein the high pressure, low temperature cleaning cycle achieves a pressure of about 250 psi to about 1000 psi inside a wash cylinder of a machine configured to execute the cleaning cycle.
6. The method of claim 5 wherein the high pressure, low temperature cleaning cycle achieves a temperature of about 0° Celsius to about 40° Celsius inside the wash cylinder.
7. The method of claim 5 wherein the lowering comprises lowering the pressure inside the wash cylinder at a rate of approximately 2 psi/sec to approximately 7 psi/sec.
8. The method of claim 1 wherein the confirming comprises certifying that an exterior surface of the breather bag is sterile inside the tote liner.
9. The method of claim 8 wherein the confirming comprises certifying the level of sterility to at least a Sterility Assurance Level of 10 −6 .
10. The method of claim 9 wherein the biological indicator comprises Bacillus Atrophaeus.
11. A tote liner for use in a sterilization validation method, the tote liner comprising:
a CO 2 permeable sleeve, the sleeve allowing liquid CO 2 and a sterilant to permeate a material of the sleeve during a pressurized cleaning cycle, wherein the sleeve is sized and dimensioned to accommodate a breather bag containing a sterilized item; and
a biological indicator to indicate a level of sterility to at least a Sterility Assurance Level of 10 −6 , wherein the biological indicator comprises Bacillus Atrophaeus ; and
a sealing mechanism to prevent contamination of the breather bag, the sealing mechanism comprising a cleanroom compatible coil zipper designed to maintain sterility of the breather bag inside the sleeve.
12. The tote liner of claim 11 wherein the biological indicator is contained in an interior space within the sleeve.
13. The tote liner of claim 11 wherein the biological indicator is integrated into a structure of the sleeve.
14. The tote liner of claim 11 wherein the sterilant comprises a solution comprising between 15% and 30% weight to volume of hydrogen peroxide and wherein the sleeve is constructed of a material to allow the solution to permeate.
15. A tote liner for use in a sterilization validation method, the tote liner comprising:
a CO2 permeable sleeve, the sleeve allowing liquid CO2 and a sterilant to permeate a material of the sleeve during a pressurized cleaning cycle, wherein the sleeve is sized and dimensioned to accommodate a breather bag containing a sterilized item;
a biological indicator to indicate a level of sterility to at least a Sterility Assurance Level of 10-6; and
a sealing mechanism to prevent contamination of the breather bag, the sealing mechanism comprising a cleanroom compatible coil zipper designed to maintain sterility of the breather bag inside the sleeve.
16. The tote liner of claim 15 wherein the biological indicator is contained in an interior space within the sleeve.
17. The tote liner of claim 15 wherein the biological indicator is integrated into a structure of the sleeve.
18. The tote liner of claim 15 wherein the sterilant comprises a solution comprising between 15% and 30% weight to volume of hydrogen peroxide and wherein the sleeve is constructed of a material to allow the solution to permeate.