IP Library Granted Patent US 9,700,704
Granted Patent B2
US 9,700,704 · App. 15/154,662 · Granted Jul 11, 2017

Drug releasing coatings for balloon catheters

Inventor: Lixiao Wang (Medina, MN)
Assignee: Lutonix, Inc.
A61M25/10A61K31/337A61K31/436A61L29/08A61L29/085A61L29/16A61L31/08A61L31/16A61L2300/416A61L2300/428A61L2300/606A61L2300/608A61L2300/802A61M2025/105
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Quick Facts
Patent No.
US 9,700,704
App. No.
15/154,662
Granted
Jul 11, 2017
Kind
B2
Abstract

Balloon catheters, methods for preparing balloon catheters, and uses of balloon catheters are disclosed. The balloon catheter includes an elongate member, an expandable balloon, and a coating layer overlying an exterior surface of the expandable balloon. The coating layer includes a total drug load of a hydrophobic therapeutic agent and a combination of additives including a first additive and a second additive. The hydrophobic therapeutic agent is paclitaxel, rapamycin, or paclitaxel and rapamycin. The first additive is a surfactant. The second additive is a chemical compound having one or more hydroxyl, amino, carbonyl, carboxyl, acid, amide, or ester groups.

Claims (48)

1. A balloon catheter for delivering a therapeutic agent to a blood vessel while the balloon catheter is deployed at a target site of the blood vessel, the balloon catheter comprising:

an elongate member having a lumen and a distal end,

an expandable balloon attached to the distal end of the elongate member and in fluidic communication with the lumen; and

a dried coating layer overlying an exterior surface of the expandable balloon, wherein:

the dried coating layer comprises a total drug load of a hydrophobic therapeutic agent and a combination of additives comprising a first additive and a second additive;

the hydrophobic therapeutic agent is one of paclitaxel or analogs thereof, rapamycin or analogs thereof, daunorubicin, doxorubicin, beta-lapachone, biologically active vitamin D, or combinations thereof;

the first additive is one of PEG sorbitan monolaurates, PEG sorbitan monooleates, or combinations thereof; and

the second additive is one of sorbitol, sorbitan, xylitol, gluconolactone, lactobionic acid, or combinations thereof.

2. The balloon catheter of claim 1 , wherein the hydrophobic therapeutic agent is chosen from paclitaxel or analogs thereof.

3. The balloon catheter of claim 1 , wherein the hydrophobic therapeutic agent is chosen from rapamycin or analogs thereof.

4. The balloon catheter of claim 1 , wherein the hydrophobic therapeutic agent is uniformly distributed in the dried coating layer.

5. The balloon catheter of claim 1 , wherein the total drug load of the hydrophobic therapeutic agent is from 1 μg to 20 μg per square millimeter of the expandable balloon.

6. The balloon catheter of claim 1 , wherein the total drug load of the hydrophobic therapeutic agent is from 2.5 μg to 6 μg per square millimeter of the expandable balloon.

7. The balloon catheter of claim 1 , wherein the first additive is a PEG sorbitan monolaurate.

8. The balloon catheter of claim 7 , wherein the PEG sorbitan monolaurate is PEG-20 sorbitan monolaurate.

9. The balloon catheter of claim 1 , wherein the first additive is a PEG sorbitan monooleate.

10. The balloon catheter of claim 9 , wherein the PEG sorbitan monooleate is PEG-20 sorbitan monooleate.

11. The balloon catheter of claim 1 , wherein the first additive is one of PEG-20 sorbitan monolaurate, PEG-20 sorbitan monooleate, or combinations thereof.

12. The balloon catheter of claim 1 , wherein the second additive is one of sorbitol, gluconolactone, or combinations thereof.

13. The balloon catheter of claim 1 , wherein the second additive is sorbitol.

14. The balloon catheter of claim 1 , wherein the second additive is gluconolactone.

15. The balloon catheter of claim 1 , wherein the ratio by weight of the combination of additives in the dried coating layer to the hydrophobic therapeutic agent in the dried coating layer is about 10 to 0.5.

16. The balloon catheter of claim 1 , wherein:

the dried coating layer consists essentially of the hydrophobic therapeutic agent, the first additive, and the second additive;

the hydrophobic therapeutic agent is chosen from paclitaxel or analogs thereof;

the first additive is one of PEG-20 sorbitan monolaurate, PEG-20 sorbitan monooleate, or combinations thereof; and

the second additive is one of sorbitol, gluconolactone, or combinations thereof.

17. The balloon catheter of claim 1 , wherein:

the dried coating layer consists essentially of the hydrophobic therapeutic agent, the first additive, and the second additive;

the hydrophobic therapeutic agent is chosen from paclitaxel or analogs thereof;

the first additive is PEG-20 sorbitan monolaurate; and

the second additive is sorbitol.

18. The balloon catheter of claim 1 , wherein:

the dried coating layer consists essentially of the hydrophobic therapeutic agent, the first additive, and the second additive;

the hydrophobic therapeutic agent is chosen from paclitaxel or analogs thereof;

the second additive is gluconolactone; and

the total drug load of the hydrophobic therapeutic agent is from 2 μg to 6 μg per square millimeter of the expandable balloon.

19. The balloon catheter of claim 1 , wherein the dried coating layer has a thickness of from about 0.1 μm to 15 μm.

20. A balloon catheter for delivering a therapeutic agent to a blood vessel while the balloon catheter is deployed at a target site of the blood vessel, the balloon catheter comprising:

an elongate member having a lumen and a distal end,

an expandable balloon attached to the distal end of the elongate member and in fluid communication with the lumen; and

a dried coating layer overlying an exterior surface of the expandable balloon, wherein:

the dried coating layer comprises a total drug load of a hydrophobic therapeutic agent and a combination of additives comprising a first additive and a second additive;

the total drug load of the hydrophobic therapeutic agent is from 2.5 μg to 6 μg per square millimeter of the expandable balloon;

the hydrophobic therapeutic agent is one of paclitaxel or analogs thereof, rapamycin or analogs thereof, daunorubicin, doxorubicin, beta-lapachone, biologically active vitamin D, or combinations thereof;

the first additive is one of PEG-20 sorbitan monolaurate, PEG-20 sorbitan monooleate, or combinations thereof;

the second additive is one of sorbitol, gluconolactone, or combinations thereof; and

the ratio by weight of the combination of additives in the dried coating layer to the hydrophobic therapeutic agent in the dried coating layer is about 10 to 0.5.

Continuity (20)
Continuation In Part 15067739 · Mar 11, 2016
Continuation 14683612 · Apr 10, 2015
Continuation 13846143 · Mar 18, 2013
Continuation 12731835 · Mar 25, 2010
Continuation In Part 12121986 · May 16, 2008
Continuation In Part 11942452 · Nov 19, 2007
Division 15154662 · May 13, 2016
Continuation In Part 14932033 · Nov 4, 2015
Continuation 13846358 · Mar 18, 2013
Continuation 12549180 · Aug 27, 2009
Provisional Application 60860084 · Nov 20, 2006
Provisional Application 60880742 · Jan 17, 2007
Provisional Application 60897427 · Jan 25, 2007
Provisional Application 60903529 · Feb 26, 2007
Provisional Application 60904473 · Mar 2, 2007
Provisional Application 60926850 · Apr 30, 2007
Provisional Application 60981380 · Oct 19, 2007
Provisional Application 60981384 · Oct 19, 2007
Provisional Application 61092872 · Aug 29, 2008
Related Publication 20160250452A1 · Sep 1, 2016