US5486357A
Expired / Lapsed
US
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Radiofrequency plasma biocompatibility treatment of inside surfaces
Assignee: Cordis Corp
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Filing: 1993-10-27
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Granted: 1996-01-23
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Expires: 2013-10-27
Abstract
Abstract Internal polymeric surfaces of medical devices are provided that have enhanced biocompatibility properties. The internal polymeric surface presents an anti-thrombogenic, fibrinolytic or thrombolytic interface with body fluids such as blood flowing through medical device tubing during implantation for medical procedures. The biocompatibility enhancing agent is secured to the polymeric substrate by a spacer molecule which is covalently bound to the internal polymeric surface which had been subjected to radiofrequency plasma treatment with a low pressure plasma medium of water vapor, oxygen or combination of water vapor and oxygen gas.
Inventors
- 👤 Pallassana V. Narayanan
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 16:12
CPC Classifications
C; C08; C08J; C08J7/00; C08J7/12; C08J7/123; A; A61; A61L; A61L33/00; A61L33/0005; A61L33/0011; A61L33/0029; A61L33/0041; A61L33/0047; A61L33/06; A61L33/08; B; B29; B29C; B29C59/00; B29C59/14; B29C59/142; Y; Y10; Y10S; Y10S522/00; Y10S522/915; Y10S525/00; Y10S525/937; Y10S530/00; Y10S530/81; Y10S530/812; Y10S530/815; Y10S530/816
Claims Analysis
Total Claims: 17
Claim 1
Independent Claim
304 words
A method for enhancing the biocompatibility of interior polymeric surfaces of medical device components, comprising the steps of: positioning a medical device component within a radiofrequency plasma discharge apparatus, the medical device component being catheter tubing with a polymeric surface interior lumen having a diameter of less than about 0.1 inch, said catheter tubing having a length suitable for use as a catheter in humans; providing a reduced pressure environment within the radiofrequency plasma discharge apparatus, said reduced pressure environment being about 0.25 Torr or less; inserting into said reduced pressure environment a plasma medium selected from the group consisting of water vapor, oxygen gas, and mixtures thereof, said plasma medium having a pressure of less than about 0.2 Torr; subjecting said plasma medium to a radiofrequency electric field to induce a gas discharge in order to form reactive species from said plasma medium within the plasma discharge apparatus and within the lumen to form a modified interior polymeric lumen surface comprising reactive sites which had been modified by the subjecting step, said subjecting step being carried out for at least about 10 minutes and while said plasma medium has a pressure of less than about 0.2 Torr; treating said modified interior polymeric lumen surface with a spacer component having amine groups whereby covalent linkages are formed between the spacer component amine groups and the reactive sites of the modified interior polymeric lumen surface to form a spacer component-treated modified polymeric lumen surface; and covalently bonding an anti-thrombogenic, fibrinolytic or thrombolytic agent having acid functionality and biologically active properties to said spacer component-treated modified polymeric lumen surface, whereby said modified polymeric lumen surface is rendered into a biocompatible surface, and the anti-thrombogenic, fibrinolytic or thrombolytic agent of the biocompatible surface is resistant to extraction under in vivo conditions while retaining its biologically active properties.
Claim 2
Independent Claim
304 words
A method for enhancing the biocompatibility of interior polymeric surfaces of medical device components, comprising the steps of: positioning a medical device component within a radiofrequency plasma discharge apparatus, the medical device component being catheter tubing with a polymeric surface interior lumen having a diameter of less than about 0.1 inch, said catheter tubing having a length suitable for use as a catheter in humans; providing a reduced pressure environment within the radiofrequency plasma discharge apparatus, said reduced pressure environment being about 0.25 Torr or less; inserting into said reduced pressure environment a plasma medium selected from the group consisting of water vapor, oxygen gas, and mixtures thereof, said plasma medium having a pressure of less than about 0.2 Torr; subjecting said plasma medium to a radiofrequency electric field to induce a gas discharge in order to form reactive species from said plasma medium within the plasma discharge apparatus and within the lumen to form a modified interior polymeric lumen surface comprising reactive sites which had been modified by the subjecting step, said subjecting step being carried out for at least about 10 minutes and while said plasma medium has a pressure of less than about 0.2 Torr; treating said modified interior polymeric lumen surface with a spacer component having amine groups whereby covalent linkages are formed between the spacer component amine groups and the reactive sites of the modified interior polymeric lumen surface to form a spacer component-treated modified polymeric lumen surface; and covalently bonding an anti-thrombogenic, fibrinolytic or thrombolytic agent having acid functionality and biologically active properties to said spacer component-treated modified polymeric lumen surface, whereby said modified polymeric lumen surface is rendered into a biocompatible surface, and the anti-thrombogenic, fibrinolytic or thrombolytic agent of the biocompatible surface is resistant to extraction under in vivo conditions while retaining its biologically active properties.
Claim 3
Dependent Claim
41 words
The method in accordance with claim 1, wherein said plasma medium includes between about 40 to about 90 volume percent water vapor and between about 10 and about 60 volume percent oxygen, based upon the total volume of the plasma medium.
Claim 4
Dependent Claim
28 words
The method in accordance with claim 1, wherein said treating step utilizes a spacer component selected from the group consisting of primary amines, secondary amines, and mixtures thereof.
Claim 5
Dependent Claim
29 words
The method in accordance with claim 1, wherein said interior polymeric lumen surface modified by said subjecting step includes reactive sites of carboxyl groups, hydroxyl groups or mixtures thereof.
Claim 6
Dependent Claim
21 words
The method in accordance with claim 1, wherein said treating step is carried out in the presence of a coupling agent.
Claim 7
Dependent Claim
22 words
The method in accordance with claim 1, wherein said contacting step contacts said spacer component-treated modified polymeric surface with a heparinous material.
Claim 8
Dependent Claim
27 words
The method in accordance with claim 1, wherein said subjecting step is carried out while said plasma medium has a pressure of less than about 0.1 Torr.
Claim 9
Dependent Claim
25 words
The method in accordance with claim 1, wherein the catheter tubing in said positioning step has a lumen diameter of about 0.072 inch or less.
Claim 10
Dependent Claim
186 words
A medical device component having a biocompatible polymeric surface, wherein said medical device component is catheter tubing, said catheter tubing having a lumen with a diameter of less than about 0.1 inch and having a length suitable for use as a catheter in humans, and said biocompatible polymeric surface comprises an interior polymeric lumen surface which has been modified by subjecting the interior polymeric lumen surface to radiofrequency discharge treatment within a low-pressure plasma medium for at least about 10 minutes to provide a treated interior polymeric lumen surface, the plasma medium selected from the group consisting of water vapor, oxygen gas, and mixtures thereof, said plasma medium having a pressure of less than about 0.2 Torr, followed by treatment of the treated interior polymeric lumen surface with a spacer component having amine groups forming covalent linkages with the treated interior polymeric lumen surface to form a spacer component-treated interior polymeric lumen surface, after which an anti-thrombogenic, fibrinolytic or thrombolytic agent having acid functionality has been covalently bonded to the spacer component-treated interior polymeric lumen surface to provide a biocompatible partially enclosed interior polymeric lumen surface.
Claim 11
Dependent Claim
186 words
A medical device component having a biocompatible polymeric surface, wherein said medical device component is catheter tubing, said catheter tubing having a lumen with a diameter of less than about 0.1 inch and having a length suitable for use as a catheter in humans, and said biocompatible polymeric surface comprises an interior polymeric lumen surface which has been modified by subjecting the interior polymeric lumen surface to radiofrequency discharge treatment within a low-pressure plasma medium for at least about 10 minutes to provide a treated interior polymeric lumen surface, the plasma medium selected from the group consisting of water vapor, oxygen gas, and mixtures thereof, said plasma medium having a pressure of less than about 0.2 Torr, followed by treatment of the treated interior polymeric lumen surface with a spacer component having amine groups forming covalent linkages with the treated interior polymeric lumen surface to form a spacer component-treated interior polymeric lumen surface, after which an anti-thrombogenic, fibrinolytic or thrombolytic agent having acid functionality has been covalently bonded to the spacer component-treated interior polymeric lumen surface to provide a biocompatible partially enclosed interior polymeric lumen surface.
Claim 12
Dependent Claim
27 words
The medical device component in accordance with claim 9, said polymeric surface is a polyurethane, a polyurethane copolymer, a nylon, a polyamide or a silicone rubber polymer.
Claim 13
Dependent Claim
26 words
The medical device component in accordance with claim 9, wherein the medical device component is a component of a catheter, a cannula or a balloon catheter.
Claim 14
Dependent Claim
49 words
The medical device component in accordance with claim 9, wherein said covalent linkages between the modified polymeric lumen surface and the spacer component are between carboxyl or hydroxyl groups formed by the radiofrequency discharge treatment on the polymeric surface and primary or secondary amine groups of the spacer component.
Claim 15
Dependent Claim
37 words
The medical device component in accordance with claim 12, wherein a covalent linkage is present between primary or second amine groups of spacer component molecules and the acid functionality groups of the anti-thrombogenic, fibrinolytic or thrombolytic agent.
Claim 16
Dependent Claim
23 words
The medical device component in accordance with claim 9, wherein said diameter of the catheter tubing lumen is about 0.072 inch or less.
Claim 17
Dependent Claim
21 words
The medical device in accordance with claim 9, wherein said plasma medium has a pressure of less than about 0.1 Torr.
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