Drug dispensing medical electrode lead and method for making same

• US 7,398,126 B2
• Filed: 03/25/2002
• Issued: 07/08/2008
• Est. Priority Date: 03/29/2001
• Status: Expired due to Fees

• Current Assignee: St. Jude Medical AB (Abbott Laboratories)
• Original Assignee: St. Jude Medical AB (Abbott Laboratories)
• Inventors: Wargelius, Maria, Kalling, Sven, Hill, Rolf, Obel, Martin
• Primary Examiner(s): Layno; Carl H.
• Assistant Examiner(s): LEE, YUN H
• Application Number:
  US10/473,552
• Publication Number:
  US 20040172117A1
• Time in Patent Office: 2,297 Days
• Field of Search: 604/890.1, 604/891.1, 607/120
• US Class Current: 607/120
• CPC Class Codes: A61N 1/0568 with drug delivery

Abstract

In an electrically conductive lead adapted for implantation in a human or animal body, and a method for making such a lead, a drug-dispensing member is disposed at a distal end portion of the lead, at which an electrode member is disposed that is adapted to emit and/or sense electrical signals associated with medical therapy. The drug-dispensing member has a configuration so that, after implantation, the amount of drug released into the body per time unit is automatically controlled to smoothly vary with time from al larger amount to a smaller amount in accordance with a predetermined relationship of the amount of drug released as a function of time.

Claims

1. An electrically conductive lead suitable for implantation in a human or animal body, comprising:

a proximal end portion adapted for attachment to an electrical medical therapy device;

a distal end portion having an exterior;

at least one electrode member disposed at said distal end portion for at least one of emitting and sensing electrical signals associated with said medical therapy;

an elongated body extending between, and mechanically and electrically connecting, said proximal end portion and said distal end portion;

a drug-dispensing member disposed at said distal end portion and comprising a drug adapted for release into tissue, said drug-dispensing member having a surface and a configuration so that at least a portion of said surface is exposed at the exterior of said distal end portion and said configuration automatically causing an amount of said drug released into said tissue after implantation to smoothly vary with time from a larger amount to a smaller amount in accordance with a predetermined relationship of the amount of drug released as a function of time; and

said distal end portion having at least one cavity therein with an opening disposed at said exterior of said distal end portion, and said drug-dispensing member being disposed in said cavity, said cavity having a shape that configures said dispensing member for said automatic control of said release.

2. An electrically conductive lead as claimed in claim 1 wherein said drug comprises an anti-inflammatory agent.

3. An electrically conductive lead as claimed in claim 1 wherein said drug-dispensing member contains respectively different concentrations of said drug in different portions of said drug-dispensing member, causing said automatically controlled release.

4. An electrically conductive lead as claimed in claim 1 wherein said drug-dispensing member is comprised of materials of respectively different compositions of materials that interact with said tissue at respectively different rates, selected from the group consisting of materials that are soluble in body fluids and materials that are resorbable in body fluids, and wherein said different parts are disposed to cause said automatically controlled release.

5. An electrically conductive lead suitable for implantation in a human or animal body, comprising:

a proximal end portion adapted for attachment to an electrical medical therapy device;

a distal end portion having an exterior;

at least one electrode member disposed at said distal end portion for at least one of emitting and sensing electrical signals associated with said medical therapy;

an elongated body extending between, and mechanically and electrically connecting, said proximal end portion and said distal end portion;

a drug-dispensing member disposed at said distal end portion and comprising a drug adapted for release into tissue, said drug-dispensing member having a surface and a configuration so that at least a portion of said surface is exposed at the exterior of said distal end portion and said configuration automatically causing an amount of said drug released into said tissue after implantation to smoothly vary with time from a larger amount to a smaller amount in accordance with a predetermined relationship of the amount of drug released as a function of time; and

said drug dispensing member having a configuration causing a decrease in said amount of said drug released into tissue from a maximum amount released in first hours after implantation to an amount approximately one-third of said maximum amount, occurs over at least 24 hours.

6. An electrically conductive lead as claimed in claim 5 wherein said cavity has a cross-sectional area varying smoothly from a maximum area at said opening to a smaller area at a position in said cavity spaced from said opening.

7. An electrically conductive lead as claimed in claim 6 wherein said cavity has a maximum cross-sectional area at said opening that is at least twice a smallest cross-sectional area of said cavity.

8. An electrically conductive lead as claimed in claim 5 wherein said at least one electrode member has a first surface portion at said exterior of said distal end portion and a second surface portion disposed in an interior of said distal end portion, and wherein said cavity is disposed with said opening in said first surface portion.

9. An electrically conductive lead as claimed in claim 8 wherein said cavity does not extend to said second surface portion and terminates inside of said electrode member.

10. An electrically conductive lead as claimed in claim 8 wherein said cavity extends from said first surface portion and has a minimum cross-sectional area at an intermediate position within said cavity that is smaller than a cross-sectional area of said cavity at a position proximal of said intermediate position.

11. An electrically conductive lead as claimed in claim 5 wherein said distal end portion has a distal end tip and a longitudinal axis, and wherein said cavity is disposed with said opening at said distal end tip and extending in a direction of said longitudinal axis.

12. An electrically conductive lead as claimed in claim 5 wherein said distal end portion has a plurality of cavities therein with respective portions of said drug-dispensing member being disposed in said plurality of cavities, said plurality of cavities, in combination, configuring said drug-dispensing member for said automatically controlled release.

13. An electrically conductive lead as claimed in claim 5 wherein said drug-dispensing member is comprised of a material selected from the group consisting of materials soluble in body fluids and materials resorbable in body fluids.

14. An electrically conductive lead as claimed in claim 5 wherein an entirety of said drug-dispensing member is disposed in said cavity.

15. An electrically conductive lead as claimed in claim 5 wherein said drug comprises an anti-inflammatory agent.

16. An electrically conductive lead as claimed in claim 5 wherein said drug-dispensing member contains respectively different concentrations of said drug in different portions of said drug-dispensing member, causing said automatically controlled release.

17. An electrically conductive lead as claimed in claim 5 wherein said drug-dispensing member is comprised of materials of respectively different compositions of materials that interact with said tissue at respectively different rates, selected from the group consisting of materials that are soluble in body fluids and materials that are resorbable in body fluids, and wherein said different parts are disposed to cause said automatically controlled release.

18. A method for producing an electrically conductive lead adapted for implantation in a human or animal body, comprising the steps of:

mechanically and electrically connecting a proximal end portion, adapted for attachment to an electrical medical therapy device, to a distal end portion having an exterior, with an elongated body portion;

disposing at least one electrode member at said distal end portion adapted for at least one of emitting and sensing electrical signals associated with said medical therapy;

disposing a drug-dispensing member at said distal end portion containing a drug for release into tissue and configuring said dug-dispensing member to expose a portion of a surface of said drug-dispensing member at said exterior of said distal end portion and, by said configuration, automatically controlling release of an amount of said drug into tissue after implantation per time unit to smoothly vary over time from a larger amount to a smaller amount according to a predetermined relationship of the amount of drug released as a function of time; and

providing said distal end portion with at least one cavity therein with an opening disposed at said exterior of said distal end portion, and disposing said drug-dispensing member in said cavity and providing said cavity with a shape that configures said dispensing member for said automatic control of said release.

19. A method as claimed in claim 18 comprising using an anti-inflammatory agent as said drug.

20. A method as claimed in claim 18 comprising providing said drug-dispensing member with respectively different concentrations of said drug in different portions of said drug-dispensing member, causing said automatically controlled release.

21. A method as claimed in claim 18 comprising forming said drug-dispensing member as a plurality of member portions respectively comprising materials of different compositions that interact with said tissue at respectively different rates, and selecting said materials from the group consisting of materials that are soluble in body fluids and materials that are resorbable in body fluids, and disposing said different member portions to cause said automatically controlled release.

22. A method for producing an electrically conductive lead adapted for implantation in a human or animal body, comprising the steps of:

mechanically and electrically connecting a proximal end portion, adapted for attachment to an electrical medical therapy device, to a distal end portion having an exterior, with an elongated body portion;

disposing at least one electrode member at said distal end portion adapted for at least one of emitting and sensing electrical signals associated with said medical therapy;

disposing a drug-dispensing member at said distal end portion containing a drug for release into tissue and configuring said dug-dispensing member to expose a portion of a surface of said drug-dispensing member at said exterior of said distal end portion and, by said configuration, automatically controlling release of an amount of said drug into tissue after implantation per time unit to smoothly vary over time from a larger amount to a smaller amount according to a predetermined relationship of the amount of drug released as a function of time; and

configuring said drug dispensing member to cause a decrease in said amount of said drug released into tissue from a maximum amount released in first hours after implantation to an amount approximately one-third of said maximum amount, occurs over at least 24 hours.

23. A method as claimed in claim 22 comprising providing said cavity with a cross-sectional area varying smoothly from a maximum area at said opening to a smaller area at a position in said cavity spaced from said opening.

24. A method as claimed in claim 23 comprising providing said cavity with a maximum cross-sectional area at said opening that is at least twice a smallest cross-sectional area of said cavity.

25. A method as claimed in claim 22 wherein said at least one electrode member has a first surface portion at said exterior of said distal end portion and a second surface portion disposed in an interior of said distal end portion, and comprising disposing said cavity with said opening in said first surface portion.

26. A method as claimed in claim 25 comprising configuring said cavity so that said cavity does not extend to said second surface portion and terminates inside of said electrode member.

27. A method as claimed in claim 25 comprising extending said cavity from said first surface portion and providing said cavity with a minimum cross-sectional area at an intermediate position within said cavity that is smaller than a cross-sectional area of said cavity at a position proximal of said intermediate position.

28. A method as claimed in claim 22 wherein said distal end portion has a distal end tip and a longitudinal axis, and comprising disposing said cavity with said opening at said distal end tip and extending in a direction of said longitudinal axis.

29. A method as claimed in claim 22 comprising disposing a plurality of cavities in said distal end portion and disposing respective portions of said drug-dispensing member in said plurality of cavities, and configuring said plurality of cavities, in combination, to configure said drug-dispensing member for said automatically controlled release.

30. A method as claimed in claim 22 comprising selecting a material, as said drug-dispensing member, from the group consisting of materials soluble in body fluids and materials resorbable in body fluids.

31. A method as claimed in claim 22 comprising disposing an entirety of said drug-dispensing member in said cavity.

32. A method as claimed in claim 22 comprising using an anti-inflammatory agent as said drug.

33. A method as claimed in claim 22 comprising providing said drug-dispensing member with respectively different concentrations of said drug in different portions of said drug-dispensing member, causing said automatically controlled release.

34. A method as claimed in claim 22 comprising forming said drug-dispensing member as a plurality of member portions respectively comprising materials of different compositions that interact with said tissue at respectively different rates, and selecting said materials from the group consisting of materials that are soluble in body fluids and materials that are resorbable in body fluids, and disposing said different member portions to cause said automatically controlled release.