IP Library Granted Patent US 9,687,597
Granted Patent B2
US 9,687,597 · App. 15/132,846 · Granted Jun 27, 2017

Antithrombogenic hollow fiber membranes and filters

Inventors: Sanjoy Mullick (Brampton, CA); Weilun Chang (Toronto, CA); Hanje Chen (Toronto, CA); Mark A. Steedman (Toronto, CA); Roseita Esfand (Mississauga, CA)
Assignee: Interface Biologies, Inc.
A61M1/3673A61L33/062A61M1/3672B01D63/022B01D63/023B01D67/0093B01D69/02B01D69/08B01D69/087B01D71/44B01D71/68A61M2202/0413B01D2323/30B01D2323/36B29C47/00B29C47/0014B29C47/0026B29L2023/00B29L2031/731
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Quick Facts
Patent No.
US 9,687,597
App. No.
15/132,846
Granted
Jun 27, 2017
Kind
B2
Abstract

The invention relates to extracorporeal blood circuits, and components thereof (e.g., hollow fiber membranes, potted bundles, and blood tubing), including 0.005% to 10% (w/w) surface modifying macromolecule. The extracorporeal blood circuits have an antithrombogenic surface and can be used in hemofiltration, hemodialysis, hemodiafiltration, hemoconcentration, blood oxygenation, and related uses.

Claims (20)

1. A blood tubing comprising a base polymer admixed with from 0.005% to 10% (w/w) surface modifying macromolecule, wherein said blood tubing is antithrombogenic when contacted with blood, as measured by y-count, and wherein said surface modifying macromolecule is described by formula:

F T —[B-(Oligo)] n -B—F T ,  (VII)

wherein

(i) Oligo is polypropylene oxide having a theoretical molecular weight of from 500 to 2,000 Daltons;

(ii) B is a hard segment formed from hexamethylene diisocyanate;

(iii) F T is a polyfluoroorgano group; and

(iv) n is an integer from 1 to 10.

2. The blood tubing of claim 1 , wherein said base polymer comprises polyvinyl chloride.

3. The blood tubing of claim 1 , wherein n is an integer from 1 to 3.

4. The blood tubing of claim 1 , wherein F T is a polyfluoroalkyl having a theoretical molecular weight of between 100-1,500 Da.

5. The blood tubing of claim 1 , wherein F T is CF 3 (CF 2 ) r CH 2 CH 2 —, wherein r is 2-20.

6. The blood tubing of claim 1 , wherein F T is CF 3 (CF 2 ) s (CH 2 CH 2 O) x —, wherein X is 1-10 and s is 1-20.

7. The blood tubing of claim 1 , wherein F T is CH m F (3−m) (CF 2 ) r CH 2 CH 2 — or CH m F (3−m) (CF 2 ) s (CH 2 CH 2 O) x —, wherein m is 0, 1, 2, or 3; X is an integer between 1-10; r is an integer between 2-20; and s is an integer between 1-20.

8. The blood tubing of claim 1 , wherein F T is formed from 1H,1H,2H,2H-perfluoro-1-decanol;

1H,1H,2H,2H-perfluoro-1-octanol; 1H,1H,5H-perfluoro-1-pentanol; or 1H,1H, perfluoro-1-butanol, or a mixture thereof.

9. The blood tubing of claim 8 , wherein F T is formed from 1H,1H,2H,2H-perfluoro-1-octanol.

10. The blood tubing of claim 1 , wherein F T is (CF 3 )(CF 2 ) 5 CH 2 CH 2 O—, (CF 3 )(CF 2 ) 7 CH 2 CH 2 O—, (CF 3 )(CF 2 ) 5 CH 2 CH 2 O—, CHF 2 (CF 2 ) 3 CH 2 O—, or (CF 3 )(CF 2 ) 2 CH 2 O—.

11. The blood tubing of claim 1 , wherein said surface modifying macromolecule is described by formula:

wherein the [CH(CH 3 )CH 2 O] n unit has a theoretical molecular weight of from 500 to 2,000 Daltons.

12. The blood tubing of claim 11 , wherein the [CH(CH 3 )CH 2 O] n unit has Mw of 1000 g/mol.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2017
From: MULLICK, SANJOY; CHANG, WEILUN; CHEN, HANJE; ESFAND, ROSEITA; STEEDMAN, MARK
To: INTERFACE BIOLOGICS, INC.
Reel/Frame 041004/0322 →
Continuity (5)
Division 14491324 · Sep 19, 2014
Division 12834730 · Jul 12, 2010
Continuation In Part 12780200 · May 14, 2010
Provisional Application 61178861 · May 15, 2009
Related Publication 20160228632A1 · Aug 11, 2016