Humidity-management packaging systems and methods

Patent metadata

Field	Value
Publication number	US-10631968-B2
Application number	US-201815909111-A
Country	US
Kind code	B2
Filing date	Mar 1, 2018
Priority date	Mar 6, 2017
Publication date	Apr 28, 2020
Grant date	Apr 28, 2020

Abstract

Packaging systems and methods are disclosed for storing a bioprosthetic device comprising a bioprosthetic tissue and maintaining a target relative humidity across a temperature range. The packaging system includes a sealed package defining an internal space having an internal volume, and a humidity control device and bioprosthetic device within the internal space. The humidity control device includes a barrier defining an enclosed space and a humidity control solution comprising glycerol in the enclosed space. At least a portion of the barrier comprises a gas-permeable membrane. The target relative humidity is provided within the internal volume of the sealed package and the control device maintains the target relative humidity across the temperature range by selectively liberating and absorbing water vapor.

First claim

What is claimed is:

1. A packaging system for storing a bioprosthetic device, wherein the packaging system maintains a target relative humidity across a temperature range, the packaging system comprising:
a sealed package defining an internal space having an internal volume;
at least one bioprosthetic device disposed within the internal space; and
at least one humidity control device disposed within the internal space, the humidity control device having a barrier defining an enclosed space and a humidity control solution comprising glycerol in the enclosed space;
wherein at least a portion of the barrier comprises a gas-permeable membrane;
wherein the target relative humidity is provided within the internal volume of the sealed package; and
wherein the humidity control device maintains the target relative humidity across the temperature range by selectively liberating and absorbing water vapor.

2. The packaging system of claim 1 , wherein the gas-permeable membrane has a water vapor transfer rate of from about 3 to about 10 mg/cm 2 per 24 hours.

3. The packaging system of claim 1 , wherein the gas-permeable membrane has a surface area, and a ratio of the surface area of the gas-permeable membrane to the internal volume of the sealed package is from about 6 to about 30 mg/mL.

4. The packaging system of claim 1 , wherein the gas-permeable membrane has an average porosity of about 8 to about 36 Gurley units.

5. The packaging system of claim 1 , wherein the sealed package has a water vapor transfer rate of less than about 0.002 grams per day.

6. The packaging system of claim 1 , wherein the packaging system maintains the target relative humidity within a tolerance of about ±10%.

7. The packaging system of claim 1 , wherein the bioprosthetic device comprises a bioprosthetic tissue that has a reduced water content of about 25% by weight or less.

8. The packaging system of claim 7 , wherein the bioprosthetic device is a heart valve; and
wherein the bioprosthetic tissue forms leaflets of the heart valve.

9. A packaging system for storing a bioprosthetic device, wherein the packaging system maintains a target relative humidity across a temperature range, the packaging system comprising:
a sealed package having an internal space;
a bioprosthetic device disposed within the internal space; and
a humidity control device disposed within the internal space, the humidity control device having a barrier defining an enclosed space in vapor communication with the internal space of the sealed package and a humidity control solution comprising glycerol in the enclosed space.

10. The packaging system of claim 9 , wherein the humidity control solution has a total weight, and a ratio of the total weight of the humidity control solution to an internal volume of the sealed package is at least about 6 mg/mL.

11. The packaging system of claim 9 , wherein the humidity control solution releases and absorbs water vapor in response to changes in temperature, thereby maintaining the target relative humidity.

12. The packaging system of claim 9 , wherein the packaging system maintains the target relative humidity across the temperature range from about −18° C. to about 45° C.

13. The packaging system of claim 9 , wherein the target relative humidity is from about 15% to about 95%.

14. The packaging system of claim 9 , wherein the humidity control solution further comprises an aqueous solution, wherein the glycerol is provided in a concentration of from about 34% to about 96% (by weight) of the humidity control solution and the aqueous solution is provided in a concentration of from about 4% to about 66% (by weight) of the humidity control solution.

15. The packaging system of claim 9 , wherein a concentration of the glycerol (G w ) in the humidity control solution is substantially related to the target relative humidity (RH) according to Eq. 1:
G w =383(−0.189( RH )+19.9) 0.0806 −383  Eq. 1.

16. The packaging system of claim 9 , wherein the target relative humidity (RH) is substantially related to a concentration of the glycerol (G w ) in the humidity control solution according to Eq. 2:

RH
=

-

(

G
w

+
383

383

)

12.4

-
19.9

0.189

.

Eq
.

⁢
2

17. The packaging system of claim 9 , wherein the humidity control solution further comprises a microbicidal agent.

18. The packaging system of claim 17 , wherein the microbicidal agent comprises an aqueous solution comprising about 97% (by volume) water and about 3% (by volume) of a solution of about 0.625% (by weight) glutaraldehyde.

19. A method of storing one or more bioprosthetic devices within a packaging system that maintains a target relative humidity across a temperature range, the method comprising the steps of:
determining an internal volume of an outer packaging;
selecting the target relative humidity;
providing one or more humidity control devices comprising a humidity control solution disposed within an at least partially gas-permeable enclosure, the humidity control solution comprising glycerol; and
sealing the one or more humidity control devices and the one or more bioprosthetic devices within the internal volume of the outer packaging.

20. The method of claim 19 , wherein selecting the target relative humidity comprises selecting a target relative humidity from about 15% to about 95%.

21. The method of claim 19 , wherein a concentration of the glycerol (G w ) (by weight) in the humidity control solution is substantially related to the target relative humidity (RH) according to Eq. 1:
G w =383(−0.189( RH )+19.9) 0.0806 −383  Eq. 1.

22. The method of claim 19 , wherein the target relative humidity (RH) is substantially related to a concentration of the glycerol (G w ) in the humidity control solution according to Eq. 2:

RH
=

-

Assignees

• Edwards Lifesciences Corp

Inventors

• Mourhatch Ryan
• Liburd Gregory G

Classifications

• A61F2/0095 Primary

  Packages or dispensers for prostheses or other implants (for intraocular lenses A61F2/1691; for dental surgery A61C19/02) · CPC title

• B65D81/22

  in moist conditions or immersed in liquids · CPC title

• B65D81/264

  for absorbing liquids · CPC title

• B65B5/045

  in bags · CPC title

• B65B7/2842

  Securing closures on containers (in general B65B51/00) · CPC title