Nanotube-reinforced balloons for delivering therapeutic agents within or beyond the wall of blood vessels, and methods of making and using same

Abstract

A dilatation catheter for delivering a therapeutic agent within a body lumen having a wall with a thickness is provided having a balloon having a flexible wall including a polymer with dispersed nanotubes and pores configured to close below a predefined pressure and to open at or above a predefined pressure. In some embodiments, an actuator is provided to controllably inflate the balloon with a fluid at a pressure sufficient to bring the flexible wall of the balloon into contact with at least a portion of the wall of the body lumen but below the predefined pressure, and to controllably increase the pressure of the fluid within the inflated balloon to at least the predefined pressure at a rate and with a force sufficient to deliver the therapeutic agent from the pores and through at least a portion of the thickness of the wall of the body lumen.

1 . A catheter for delivering a therapeutic agent into a wall of a body lumen, the wall having a thickness, the catheter comprising:
 an elongated shaft having proximal and distal ends and a lumen therebetween; and   a balloon affixed to the elongated shaft near the distal end, the balloon comprising a polymer with a plurality of fibers dispersed therein forming a flexible wall defining a plurality of pores positioned so as to be disposed in apposition to the wall of the body lumen when the balloon is inflated, the pores being configured to transition between a closed state below a predefined pressure and an open state at or above the predefined pressure to inject the therapeutic agent into the wall of the body lumen,   wherein the fibers are other than carbon nanotubes.   
     
     
         2 . The catheter of  claim 1 , further comprising:
 a pressurized reservoir of fluid in fluidic communication with the balloon via the lumen in the shaft; and   an actuator for controllably inflating the balloon with the fluid at a pressure sufficient to bring the flexible wall of the balloon into contact with at least a portion of the wall of the body lumen but below the predefined pressure, and for controllably increasing the pressure of the fluid within the inflated balloon to at least the predefined pressure at a rate and with a force sufficient to deliver the therapeutic agent from the pores and through at least a portion of the thickness of the wall of the body lumen.   
     
     
         3 . The catheter of  claim 2 , wherein the actuator controllably increases the pressure of the fluid within the inflated balloon to a selected pressure at a rate and with a force sufficient to deliver the therapeutic agent from the pores and through a entirety of at least one of a tunica intima, a tunica media, and a tunica adventitia of the body lumen. 
     
     
         4 . The catheter of  claim 2 , wherein the fluid comprises the therapeutic agent and a pharmaceutically acceptable carrier, and wherein the actuator controllably increases the pressure of the fluid within the inflated balloon to at least the predefined pressure at a rate and with a force sufficient to jet the fluid through the pores and through at least a portion of the thickness of the wall of the body lumen. 
     
     
         5 . The catheter of  claim 2 , wherein the therapeutic agent is particulate and is disposed within the pores, and wherein the actuator controllably increases the pressure of the liquid within the inflated balloon to at least the predefined pressure at a rate and with a force sufficient to eject the therapeutic agent from the pores and through at least a portion of the thickness of the wall of the body lumen. 
     
     
         6 . The catheter of  claim 1 , wherein the fibers form a reinforcing web within the flexible wall. 
     
     
         7 . The catheter of  claim 1 , wherein the fibers are substantially evenly dispersed in the polymer. 
     
     
         8 . The catheter of  claim 1 , wherein the fibers are present in a concentration of less than 5% w/w in the polymer. 
     
     
         9 . The catheter of  claim 1 , wherein the predefined pressure is based at least in part on a size of the pores, a thickness of the flexible wall, a composition of the polymer, and a concentration of fibers in the polymer. 
     
     
         10 . The catheter of  claim 1 , wherein the therapeutic agent comprises an agent for creating an in-situ stent within the wall of the body lumen. 
     
     
         11 . The catheter of  claim 10 , wherein the agent comprises at least one of an enzyme, a cross-linking agent, a small molecule, a protein, and an antibody selected to modify an elasticity of an intracellular matrix. 
     
     
         12 . The catheter of  claim 1 , wherein the therapeutic agent is selected from the group consisting of: antithrombotics, thrombolytic agents, antiproliferative agents, anti-inflammatory agents, growth factors, smooth muscle cell migration and matrix degradation inhibitors, and re-endothelialization agents. 
     
     
         13 . A method of delivering a therapeutic agent within a wall of a body lumen, the wall having a thickness, the method comprising:
 inserting into the body lumen at least a portion of a catheter comprising:
 an elongated shaft having proximal and distal ends and a lumen therebetween; and 
 a balloon affixed to the elongated shaft near the distal end, the balloon consisting of a polymer with a plurality of fibers dispersed therein forming a flexible wall defining a plurality of pores positioned so as to be disposed in apposition to the wall of the body lumen when the balloon is inflated, the pores being configured to transition between a closed state below a predefined pressure and an open state at or above the predefined pressure to inject the therapeutic agent into the wall of the body lumen; 
   controllably inflating the balloon with a fluid at a pressure sufficient to bring the flexible wall of the balloon into contact with at least a portion of the wall of the body lumen but below the predefined pressure; and   controllably increasing the pressure of the fluid within the inflated balloon to at least the predefined pressure at a rate and with a force sufficient to deliver the therapeutic agent from the pores and through at least a portion of the thickness of the wall of the body lumen,   wherein the fibers are other than carbon nanotubes.   
     
     
         14 . The method of  claim 13 , wherein the fibers form a reinforcing web within the flexible wall. 
     
     
         15 . The method of  claim 13 , wherein the fibers are substantially evenly dispersed in the polymer. 
     
     
         16 . The method of  claim 13 , wherein the fibers are in a concentration of less than 5% w/w in the polymer. 
     
     
         17 . The method of  claim 13 , comprising selecting a size of the pores, a thickness of the flexible wall, a composition of the polymer, and a concentration of fibers in the polymer to define the predefined pressure. 
     
     
         18 . The method of  claim 13 , comprising increasing the pressure of the fluid within the inflated balloon to a selected pressure at a rate and with a force sufficient to deliver the therapeutic agent from the pores and through a entirety of at least one of a tunica intima, a tunica media, and a tunica adventitia of the body lumen. 
     
     
         19 . The method of  claim 13 , wherein the fluid comprises the therapeutic agent and a pharmaceutically acceptable carrier, and comprising increasing the pressure of the fluid within the inflated balloon to at least the predefined pressure at a rate and with a force sufficient to jet the fluid through the pores and through at least a portion of the thickness of the wall of the body lumen. 
     
     
         20 . The method of  claim 13 , wherein the therapeutic agent is particulate and is disposed within the pores, and comprising controllably increasing the pressure of the liquid within the inflated balloon to at least the predefined pressure at a rate and with a force sufficient to eject the therapeutic agent from the pores and through at least a portion of the thickness of the wall of the body lumen. 
     
     
         21 . The method of  claim 13 , wherein the therapeutic agent comprises an agent for creating an in-situ stent within the wall of the body lumen. 
     
     
         22 . The method of  claim 21 , wherein the agent comprises at least one of an enzyme, a cross-linking agent, a small molecule, a protein, and an antibody selected to modify an elasticity of an intracellular matrix. 
     
     
         23 . The method of  claim 13 , wherein the therapeutic agent is selected from the group consisting of: antithrombotics, thrombolytic agents, antiproliferative agents, anti-inflammatory agents, growth factors, smooth muscle cell migration and matrix degradation inhibitors, and re-endothelialization agents. 
     
     
         24 . The method of  claim 13 , wherein the fibers are selected from the group consisting of inorganic nanotubes, graphene fibers, and polymeric fibers. 
     
     
         25 . The catheter of  claim 1 , wherein the fibers are selected from the group consisting of inorganic nanotubes, graphene fibers, and polymeric fibers.