Process for determining viability of test microorganisms of biological indicator and sterilization detection device for determining same

Patent metadata

Field	Value
Publication number	US-10876144-B2
Application number	US-201715699191-A
Country	US
Kind code	B2
Filing date	Sep 8, 2017
Priority date	Jul 14, 2017
Publication date	Dec 29, 2020
Grant date	Dec 29, 2020

Abstract

A process for determining the viability of a biological indicator includes exposing the biological indicator to a viability detection medium, the biological indicator including test microorganisms, the exposing the biological indicator to the viability detection medium producing a gaseous reaction product when one or more of the test microorganisms are viable. The presence or absence of the gaseous reaction product produced by the biological indicator combined with the viability detection medium is detected with a sensing device, the sensing device comprising an electro-mechanical sensor, wherein the presence of the gaseous reaction product indicates the presence of viable test microorganisms and the absence of the gaseous reaction product indicates the absence of viable test microorganisms. A sterilization detection device includes a container configured to contain the biological indicator, a viability detection medium, and the sensing device.

First claim

The invention claimed is:

1. A process for determining the viability of a biological indicator, the process comprising:
subjecting the biological indicator to a sterilization process in which the biological indicator is exposed to a sterilization medium, the biological indicator comprising test microorganisms on a carrier;
subsequent to the sterilization process, exposing the biological indicator to a viability detection medium comprising hydrogen peroxide, the exposing the biological indicator to the detection medium comprising the hydrogen peroxide producing a gaseous reaction product when one or more of the test microorganisms are viable; and
detecting with a sensing device the presence or absence of the gaseous reaction product produced by the biological indicator combined with the viability detection medium, the sensing device comprising an electro-mechanical sensor, wherein the presence of the gaseous reaction product indicates the presence of viable test microorganisms and the absence of the gaseous reaction product indicates the absence of viable test microorganisms.

2. The process of claim 1 , wherein combination of viable test microorganisms of the biological indicator and the viability detection medium produces the gaseous reaction product.

3. The process of claim 1 , wherein viable test microorganisms of the biological indicator produce a chemical, and combination of the chemical and the viability detection medium produces the gaseous reaction product.

4. The process of claim 3 , wherein the chemical produced by the biological indicator comprises peroxidase.

5. The process of claim 1 , wherein the electro-mechanical sensor comprises a quartz crystal microbalance comprising a coating on a surface of the substrate configured to absorb the gaseous reaction product produced by the biological indicator.

6. The process of claim 5 , wherein the coating comprises a metal oxide.

7. The process of claim 5 , wherein the coating comprises an inorganic material.

8. The process of claim 5 , wherein the coating comprises an organic material.

9. The process of claim 5 , wherein the coating comprises a polymer.

10. The process of claim 5 , wherein the coating further comprises an additive to increase attraction to the gaseous reaction product or catalyze the gas.

11. The process of claim 1 , wherein the sensing device comprises an electronic device capable of measuring a change in a frequency of oscillation of the electro-mechanical sensor when the gaseous reaction product interacts with a coating of the electro-mechanical sensor, the change in the frequency indicating the presence of viable test microorganisms.

12. The process of claim 1 , wherein the biological indicator comprises bacterial spores.

13. The process of claim 1 , wherein the biological indicator comprises bacteria.

14. The process of claim 1 , wherein the biological indicator comprises bacteria of the Bacillus or Clostridia genera.

15. The process of claim 1 , wherein the biological indicator comprises Geobacillus stearothermophilus, Bacillus atrophaeus, Bacillus subtilis, Bacillus pumilus, Bacillus coagulans, Clostridium sporogenes, Bacillus subtilis globigii, Bacillus cereus, Bacillus circulans , or a mixture of two or more thereof.

16. The process of claim 1 , wherein the gaseous reaction product comprises a volatile organic compound.

17. The process of claim 1 , wherein the gaseous reaction product comprises carbon dioxide.

18. The process of claim 1 , wherein the gaseous reaction product comprises oxygen.

19. The process of claim 1 , wherein the gaseous reaction product comprises methane.

20. The process of claim 1 , wherein the step of detecting the presence or absence of the gaseous reaction product is conducted under vacuum.

21. The process of claim 1 , wherein the sterilization medium comprises steam, dry heat, radiation, plasma, ozone, vaporized hydrogen peroxide, vaporized peracetic acid, chlorine dioxide, one or more gaseous sterilants, and/or one or more liquid sterilants.

22. The process of claim 1 , wherein the biological indicator is placed in a sterilization indicator subsequent to being subjected to the sterilization process, the sterilization indicator comprising:
a container configured to contain the biological indicator;
a liquid dispenser containing the viability detection medium and arranged to bring the viability detection medium into contact with the biological indicator in the container; and
the sensing device disposed in the container.

23. The process of claim 22 , wherein the container further comprises a vacuum port, and the method further comprises drawing a vacuum in the container prior to exposing the biological indicator to the viability detection medium.

24. The process of claim 1 , wherein the biological indicator is contained in a sterilization indicator during the sterilization process, the sterilization indicator comprising a container comprising:
a first compartment holding the biological indicator;
a second compartment connected to the first compartment and holding a frangible ampoule containing the viability detection medium;
a third compartment connected to the first compartment and holding the sensing device disposed in the container; and
a lid moveable between an open and a closed position, wherein the sterilization process is conducted with the lid in the open position such that at least the first compartment is exposed to external environment.

25. The process of claim 24 , wherein the exposing the biological indicator to a viability detection medium comprises closing the lid to break the frangible ampoule and isolate the first compartment, the second compartment, and the third compartment from the external environment.

Assignees

• American Sterilizer Co

Inventors

• Centanni Michael A
• Franciskovich Phillip P

Classifications

• C12M37/06

  Means for testing the completeness of the sterilization (testing for sterility conditions C12Q1/22) · CPC title

• C12Q1/22 Primary

  Testing for sterility conditions · CPC title

• A61L2/28

  Devices for testing the effectiveness or completeness of sterilisation or disinfection, e.g. indicators which change colour · CPC title

• G01N27/00

  Investigating or analysing materials by the use of electric, electrochemical, or magnetic means (G01N3/00 – G01N25/00 take precedence; measurement or testing of electric or magnetic variables or of electric or magnetic properties of materials G01R) · CPC title

• G01N2033/4977

  Physics · mapped topic