IP Library › Granted Patent US 12,544,718
Granted Patent B2
US 12,544,718 · App. 18/239,346 · Granted Feb 10, 2026

Method for manufacturing oxygenator

Inventors: Renjo Takama (Kanagawa, JP); Takeshi Sato (Kanagawa, JP)
Assignee: TERUMO KABUSHIKI KAISHA
B01D63/0223B01D71/70B01D71/262
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Quick Facts
Patent No.
US 12,544,718
App. No.
18/239,346
Granted
Feb 10, 2026
Kind
B2
Abstract

A coating layer containing a silicone compound is formed on an inner surface of a hollow fiber membrane for manufacturing an oxygenator having a plurality of porous hollow fiber membranes for gas exchange. The method includes dissolving a silicone compound in an organic solvent having a surface tension of less than 70 dyn/cm to prepare a coating solution; and bringing an inner surface of the hollow fiber membranes into contact with the coating solution while bringing an outer surface of the hollow fiber membranes into contact with water to form a coating layer containing a silicone compound on the inner surface.

Claims (31)

1 . A method for manufacturing an oxygenator having a plurality of porous hollow fiber membranes for gas exchange, comprising the steps of:

dissolving a silicone compound in an organic solvent having a surface tension of less than 70 dyn/cm to prepare a coating solution; and

bringing an inner surface of the hollow fiber membranes into contact with the coating solution while bringing an outer surface of the hollow fiber membranes into contact with water to form a coating layer containing a silicone compound on the inner surface.

2 . The method according to claim 1 , wherein

after bringing the inner surface of the hollow fiber membranes into contact with the coating solution, a fluid is caused to flow through a lumen of the hollow fiber membranes to remove the coating solution.

3 . The method according to claim 2 , wherein

the fluid is selected from the group consisting of air, an inert gas, water, and a lower alcohol.

4 . The method according to claim 1 , wherein a concentration of the silicone compound in the coating solution is more than 400 mg/mL and less than 800 mg/mL.

5 . The method according to claim 1 , wherein the organic solvent is at least one selected from the group consisting of n-hexane, cyclohexane, acetone, butyl alcohol, 1-propanol, isopropanol, chloroform, diethyl ether, an aromatic hydrocarbon, and a fluorine-based solvent.

6 . The method according to claim 1 , wherein at least a part of the hollow fiber membranes are formed of polypropylene or polymethylpentene.

7 . The method according to claim 1 , further comprising the step of:

forming a coat containing an antithrombotic polymer compound on the outer surface of the hollow fiber membranes.

8 . The method according to claim 1 , wherein the silicone compound is represented by the following Formula (1):

and wherein in the above Formula (1), R 1 to R 8 each independently represent an alkyl group having 1 or more and 6 or less carbon atoms, an aromatic hydrocarbon group having 6 or more and 30 or less carbon atoms, or a reactive group selected from the group consisting of an ethylenically unsaturated bond-containing group having 1 or more and 6 or less carbon atoms, an amino group-containing group, a hydroxy group-containing group, a carboxy group-containing group, a maleimide group-containing group, a thiol group-containing group, and a halogen group; and n is 1 or more and 100,000 or less.

9 . A method for manufacturing an oxygenator having a plurality of porous hollow fiber membranes for gas exchange, comprising the steps of:

fixing ends of the hollow fiber membranes to partition walls at opposing ends of a housing such that the ends of the hollow fiber membranes are open, wherein the housing defines a gas chamber inside the hollow fiber membranes and a blood chamber outside the hollow fiber membranes;

dissolving a silicone compound in an organic solvent to prepare a coating solution;

filling the blood chamber with water to bring outer surfaces of the hollow fiber membranes into contact with the water;

filling the gas chamber with the coating solution to bring inner surfaces of the hollow fiber membranes into contact with the coating solution while the water contacts the outer surfaces to form a coating layer containing a silicone compound on the inner surfaces;

removing the coating solution from the gas chamber; and

removing the water from the blood chamber.

10 . The method according to claim 9 , wherein the coating solution is removed by flowing a fluid through the hollow fiber membranes, and wherein the method further comprising the step of:

drying the hollow fiber membranes.

11 . The method according to claim 10 , wherein the fluid is selected from the group consisting of air, an inert gas, water, and a lower alcohol.

12 . The method according to claim 9 , wherein a concentration of the silicone compound in the coating solution is more than 400 mg/mL and less than 800 mg/mL.

13 . The method according to claim 9 , wherein the organic solvent is at least one selected from the group consisting of n-hexane, cyclohexane, acetone, butyl alcohol, 1-propanol, isopropanol, chloroform, diethyl ether, an aromatic hydrocarbon, and a fluorine-based solvent.

14 . The method according to claim 9 , wherein at least a part of the hollow fiber membranes are formed of polypropylene or polymethylpentene.

15 . The method according to claim 9 , further comprising the step of:

forming a coat containing an antithrombotic polymer compound on the outer surface of the hollow fiber membranes.

16 . The method according to claim 9 , wherein the silicone compound is represented by the following Formula (1):

and wherein in the above Formula (1), R 1 to R 8 each independently represent an alkyl group having 1 or more and 6 or less carbon atoms, an aromatic hydrocarbon group having 6 or more and 30 or less carbon atoms, or a reactive group selected from the group consisting of an ethylenically unsaturated bond-containing group having 1 or more and 6 or less carbon atoms, an amino group-containing group, a hydroxy group-containing group, a carboxy group-containing group, a maleimide group-containing group, a thiol group-containing group, and a halogen group; and n is 1 or more and 100,000 or less.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY DATA PREVIOUSLY RECORDED AT REEL: 064750 FRAME: 0457. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Sep 6, 2023
From: TAKAMA, RENJO; SATO, TAKESHI
To: TERUMO KABUSHIKI KAISHA
Reel/Frame 064812/0080 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2023
From: TAKAMA, RENJO; SATO, TAKESHI
To: FORD GLOBAL TECHNOLOGIES, LLC
Reel/Frame 064750/0457 →
Priority Claims (1)
JP 2021-035129 · Mar 5, 2021 · national
Continuity (2)
Continuation PCTJP2022006838 · Feb 21, 2022
Related Publication 20230398495A1 · Dec 14, 2023
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