IP Library Granted Patent US 10,314,929
Granted Patent B2
US 10,314,929 · App. 15/198,670 · Granted Jun 11, 2019

Apparatus and method for sterilizing endoscope

Inventors: Keyvan Nowruzi (Mission Viejo, CA); Navid Omidbakhsh (Mission Viejo, CA)
Assignee: Ethicon, Inc.
A61L2/24A61L2/14A61L2/186A61L2/20A61L2/202A61L2/208A61L2/28A61L2202/11A61L2202/122A61L2202/14A61L2202/18A61L2202/24
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Quick Facts
Patent No.
US 10,314,929
App. No.
15/198,670
Granted
Jun 11, 2019
Kind
B2
Abstract

A method of sterilizing an article such as a flexible endoscope is performed in a sterilization chamber. A vacuum is applied in the sterilization chamber while the article is contained in the sterilization chamber. A sterilant is then introduced into the sterilization chamber. The pressure within the sterilization chamber is incrementally increased to provide a step-wise transition from a high vacuum state to atmospheric pressure. The article is thereby sterilized.

Claims (50)

1. A method of sterilizing an article, the method comprising:

(a) receiving the article in a sterilization chamber;

(b) verifying the article is properly positioned in the sterilization chamber using at least one of a photo sensor, an imaging device or a weight sensor;

(c) applying a vacuum to the sterilization chamber to reduce the pressure within the sterilization chamber to a first pressure, wherein the first pressure is less than 100 torr;

(d) introducing a sterilant into the sterilization chamber;

(e) maintaining the first pressure in the sterilization chamber for a first period of time;

(f) venting the sterilization chamber to increase the pressure within the sterilization chamber to a second pressure, wherein the second pressure is greater than the first pressure but is still less than 100 torr;

(g) maintaining the second pressure in the sterilization chamber for a second period of time;

(h) venting the sterilization chamber to increase the pressure within the sterilization chamber to a third pressure; and

(i) maintaining the third pressure in the sterilization chamber for a third period of time.

2. The method of claim 1 , wherein the article comprises an endoscope.

3. The method of claim 2 , wherein the endoscope defines a lumen.

4. The method of claim 3 , wherein the lumen has a length of at least 800 mm and an inner diameter less than 6 mm.

5. The method of claim 1 , wherein the second period of time is longer than the first period of time.

6. The method of claim 1 , wherein the first period of time is between approximately 5 seconds and approximately 5 minutes.

7. The method of claim 1 , wherein the first period of time is between approximately 20 seconds and approximately 2 minutes.

8. The method of claim 1 , wherein the second pressure is at least 10 torr greater than the first pressure.

9. The method of claim 1 , wherein the second pressure is between approximately 10 torr greater than the first pressure and approximately 30 torr greater than the first pressure.

10. The method of claim 1 , wherein the third pressure is at least 10 torr greater than the second pressure.

11. The method of claim 1 , wherein the third pressure is approximately 760 torr.

12. The method of claim 1 , further comprising applying a plasma to the sterilization chamber.

13. The method of claim 12 , wherein the step of applying a plasma comprises applying a plasma to the sterilization chamber between the step (c) of applying the vacuum to the sterilization chamber and the step (d) of introducing the sterilant to the sterilization chamber.

14. The method of claim 12 , wherein the step of applying a plasma comprises: (i) vacuuming the sterilization chamber after step (i) of maintaining the third pressure in the sterilization chamber, and then (ii) applying a plasma.

15. The method of claim 1 , further comprising introducing additional sterilant into the sterilization chamber during the step (f) of venting the sterilization chamber to increase the pressure within the sterilization chamber to the second pressure.

16. The method of claim 1 , further comprising applying sterilant to one or more internal spaces within the article before receiving the article in the sterilization chamber.

17. The method of claim 1 , wherein the sterilant is selected from the group consisting of hydrogen peroxide, peroxy acids, ozone, or a mixture thereof.

18. A method of sterilizing an article, the method comprising:

(a) receiving the article and a biological indicator in a sterilization chamber, wherein the biological indicator is configured to measure the effectiveness of a sterilization cycle;

(b) verifying the article is properly positioned in the sterilization chamber using at least one of a photo sensor, an imaging device or a weight sensor;

(c) applying a vacuum to the sterilization chamber to reduce the pressure within the sterilization chamber to a first pressure, wherein the first pressure is less than 100 torr;

(d) introducing a sterilant into the sterilization chamber;

(e) maintaining the first pressure in the sterilization chamber for a first period of time;

(f) venting the sterilization chamber to increase the pressure within the sterilization chamber to a second pressure, wherein the second pressure is greater than the first pressure but is still less than 100 torr;

(g) maintaining the second pressure in the sterilization chamber for a second period of time;

(h) venting the sterilization chamber to increase the pressure within the sterilization chamber to a third pressure, wherein the third pressure is greater than the second pressure but is still less than 100 torr;

(i) maintaining the third pressure in the sterilization chamber for a third period of time; and

(j) venting the sterilization chamber to increase the pressure within the sterilization chamber to atmospheric pressure; and

(k) removing the article from the sterilization chamber,

wherein at least one of steps (f), (h), or (j) further includes introducing additional sterilant into the sterilization chamber.

19. A method of sterilizing an article, the method comprising:

(a) receiving the article in a sterilization chamber;

(b) verifying the article is properly positioned in the sterilization chamber using at least one of a photo sensor, an imaging device or a weight sensor;

(c) applying a vacuum to the sterilization chamber to reduce the pressure within the sterilization chamber below 100 torr;

(d) applying a plasma to the sterilization chamber;

(e) introducing a sterilant into the sterilization chamber;

(f) venting the sterilization chamber to incrementally increase the pressure within the sterilization chamber while introducing additional sterilant into the sterilization chamber, wherein the pressure remains below 100 torr;

(g) maintaining the incrementally increased pressure in the sterilization chamber for a period of time;

(h) repeating steps (f) through (g) at least once; and

(i) venting the sterilization chamber to increase the pressure within the sterilization chamber to atmospheric pressure.

20. The method of claim 19 , wherein step (h) further comprises repeating steps (f) through (g) at least twice.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2019
From: ETHICON, INC.
To: ASP GLOBAL MANUFACTURING GMBH
Reel/Frame 049514/0404 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2016
From: NOWRUZI, KEYVAN; OMIDBAKHSH, NAVID
To: ETHICON, INC.
Reel/Frame 039905/0798 →
Continuity (1)
Related Publication 20180000976A1 · Jan 4, 2018
Cited By (2)
US 12,649,031 US 12,708,681