Sealing members

Inventors: Martin David Spayne (Berkshire, GB); Derek Anthony Mclaughlin (Berkshire, GB); Simon Robert Payne (Berkshire, GB); Matthew James William Leary (Berkshire, GB); Mark Jennings (Berkshire, GB)

Assignee: INTERSURGICAL AG

A61M16/0622 B29C44/0461 B29C45/1676 B29C45/1704 A61M2207/00 B29L2031/4835

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Quick Facts

Patent No.: US 12697454
App. No.: 18/021,968
Granted: Aug 4, 2026
Kind: B2

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Abstract

There is provided a method of manufacturing a sealing member ( 42 ). The method comprises the steps of: (a) providing a mould having a cavity, a polymer injection port and a gas inlet port ( 38 ); (b) injecting a polymer and a blowing agent through the polymer injection port ( 28 ) into the cavity of the mould; and (c) introducing gas through the gas inlet port ( 38 ) into the cavity of the mould, to form a sealing member ( 42 ). The sealing member ( 42 ) comprises an internal chamber ( 44 ) at least partially bounded by a resiliently deformable enclosing wall formed of the polymer, the enclosing wall including an external surface, the external surface having a form that is determined by the cavity of the mould.

Claims (26)

1 . A method of manufacturing a sealing member, the method comprising the steps of:

(a) providing a mould having a cavity, a polymer injection port and a gas inlet port;

(b) injecting a polymer and a blowing agent through the polymer injection port into the cavity of the mould; and

wherein the sealing member comprises an internal chamber at least partially bounded by a resiliently deformable enclosing wall formed of the polymer, the enclosing wall including a patient-contacting surface, the patient-contacting surface having a form that is determined by the cavity of the mould.

2 . A method of manufacturing a sealing member according to claim 1 , wherein the dimensions of the patient-contacting surface are determined by the cavity of the mould, and/or wherein the volume of the sealing member is determined by the cavity of the mould.

3 . A method of manufacturing a sealing member according to claim 1 , wherein the final form of the material formed from the polymer and the blowing agent is determined by the cavity of the mould, and/or wherein the sealing member fully sets or fully solidifies in the cavity of the mould.

4 . A method of manufacturing a sealing member according to claim 1 , wherein the shape and/or dimensions of the patient-contacting surface matches, or corresponds to, the shape and/or dimensions of the cavity of the mould, and/or wherein the volume of the sealing member matches, or corresponds to, the volume of the cavity of the mould.

5 . A method of manufacturing a sealing member according to claim 1 , wherein the sealing member adopts its final form in the cavity of the mould.

6 . A method of manufacturing a sealing member according to claim 1 , wherein the sealing member cools in the cavity of the mould before opening of the mould to a temperature low enough for the sealing member to undergo no substantial change in inherent shape or dimensions upon opening of the cavity or removal of the sealing member from the cavity of the mould.

7 . A method of manufacturing a sealing member according to claim 1 , wherein the blowing agent is a physical blowing agent that provides gas expansion by a physical process.

8 . A method of manufacturing a sealing member according to claim 7 , wherein the blowing agent is caused to expand by one of, or a combination of, the application of heat and a reduction in pressure on injection of the polymer and blowing agent mix into the cavity of the mould.

9 . A method of manufacturing a sealing member according to claim 1 , wherein the blowing agent expands in the cavity of the mould before opening of the mould.

10 . A method of manufacturing a sealing member according to claim 1 , wherein the patient contacting-surface provides an anatomical fit with a patient.

11 . A method of manufacturing a sealing member according to claim 10 , wherein the patient-contacting surface has a leading portion, which is a portion that contacts a surface of the patient before any deformation of the sealing member, that is anatomically shaped at least in a direction of engagement of the sealing member with the surface of the patient, such that a position of the leading portion of the patient-contacting surface varies in this direction, at different positions along the patient-contacting surface.

12 . A sealing member manufactured by the method according to claim 1 .

13 . A respiratory interface device comprising a sealing member manufactured by the method according to claim 1 .

14 . A method of manufacturing a sealing member according to claim 1 , wherein the gas is first introduced through the gas inlet port into the cavity of the mould after the cavity of the mould is at least partially charged by a mixture of the polymer and blowing agent, and/or wherein the polymer and the blowing agent are injected through the polymer injection port into the cavity of the mould such that the cavity of the mould is only partially charged.

15 . A sealing member comprising an enclosed internal chamber at least partially bounded by a resiliently deformable enclosing wall, the enclosing wall including an external surface, the enclosing wall having a plurality of gas pockets formed therein, the sealing member having the form of a loop, and the internal chamber of the sealing member being continuous and extending around at least a majority of the loop.

16 . A sealing member according to claim 15 , wherein the enclosed internal chamber has a central longitudinal axis that follows a curved path, and the curved path extends around at least the majority of the loop.

17 . A sealing member according to claim 15 , wherein the gas pockets have an appearance akin to bubbles, a cellular structure, or a matrix of holes.

18 . A sealing member according to claim 15 , wherein a majority of gas pockets have a diameter in the range of 50-500 μm.

19 . A respiratory interface device comprising a sealing member as claimed in claim 15 .

20 . A sealing member according to claim 15 , wherein an aperture is formed in the enclosing wall of the sealing member, and the aperture is in fluid communication with the internal chamber of the sealing member, such that ambient air may enter and exit the internal chamber during use.

21 . A respiratory interface device comprising a body portion and a sealing member, the body portion comprising a first polymer, and the sealing member comprising a second polymer, the sealing member being fixed to the body portion, wherein the sealing member comprises an enclosed internal chamber at least partially bounded by a resiliently deformable enclosing wall formed of the second polymer, the enclosing wall including a patient-contacting surface and having a plurality of gas pockets formed therein, the sealing member having the form of a loop, and the internal chamber of the sealing member being continuous and extending around at least a majority of the loop.

22 . A respiratory interface device according to claim 21 , wherein an aperture is formed in the enclosing wall of the sealing member, and the aperture is in fluid communication with the internal chamber of the sealing member, such that ambient air may enter and exit the internal chamber during use.