WO2012162668A1

WO2012162668A1 - Method and apparatus for delivering oxygen and/or other gases and/or pharmacological agents to tissue, and medical wire for use within the body

Info

Publication number: WO2012162668A1
Application number: PCT/US2012/039716
Authority: WO
Inventors: Todd F. Davenport; Orlando Soto; John S. Geis; Michael Braun
Original assignee: Oxira Medical, Inc.
Priority date: 2011-05-25
Filing date: 2012-05-25
Publication date: 2012-11-29

Abstract

Apparatus for oxygenating blood, said apparatus comprising: a container comprising an interior chamber, a first port communicating with said interior chamber and a second port communicating with said interior chamber; and a porous membrane disposed within said interior chamber of said container, said porous membrane having a porosity such that an oxygen-rich perfluorocarbon solution may be incorporated into said porous membrane and, when a blood fluid is brought into contact with said porous membrane incorporating the oxygen-rich perfluorocarbon solution, the oxygen-rich perfluorocarbon solution elutes out of said porous membrane and into the blood fluid, whereby to oxygenate the blood fluid.

Description

METHOD AND APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES AND/OR PHARMACOLOGICAL AGENTS TO TISSUE,

AND MEDICAL WIRE FOR USE WITHIN THE BODY Inventors

Todd F. Davenport

Orlando Soto

John S. Geis

Michael Braun

Reference To Pending Prior Patent Applications

This patent application:

(i) is a continuation-in-part of pending prior U.S. Patent Application Serial No. 13/431,598, filed 03/27/12 by Christoph Hehrlein et al. for METHOD AND

APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES TO

TISSUE (Attorney's Docket No. OXIRA-5 CON), which patent application is a continuation of prior U.S. Patent Application Serial No. 12/008,130, filed 01/09/08 by Christoph Hehrlein et al. for METHOD AND APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES TO TISSUE (Attorney's Docket No. OXIRA- 5), which patent application (a) is itself a continuation-in-part of prior U.S. Patent

Application Serial No. 10/038,468, filed 01/03/02 by Christoph Hehrlein et al. for DELIVERY SOURCE OF OXYGEN (Attorney's Docket No. 2869/OXIRA-l), and (b) claims benefit of prior U.S. Provisional Patent Application Serial No. 61/002,174, filed 11/07/07 by Christoph Hehrlein et al. for METHOD AND APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES TO TISSUE (Attorney' s

Docket No. OXIRA-5 PROV);

(ii) is a continuation-in-part of pending prior U.S. Patent Application Serial No. 12/472,759, filed 05/27/09 by Michael Braun et al. for METHOD AND APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES AND/OR PHARMACOLOGICAL AGENTS TO TISSUE (Attorney's Docket No. OXIRA-6), which patent application (a) is itself a continuation-in-part of the aforementioned prior U.S. Patent Application Serial No. 12/008,130, filed 01/09/08 by Christoph Hehrlein et al. for METHOD AND APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES TO TISSUE (Attorney's Docket No. OXIRA-5), and (b) claims benefit of prior U.S. Provisional Patent Application Serial No. 61/128,965, filed 05/27/08 by Michael Braun et al. for METHOD AND APPARATUS FOR

DELIVERING OXYGEN AND/OR OTHER GASES AND/OR

PHARMACOLOGICAL AGENTS TO TISSUE (Attorney's Docket No. OXIRA-6 PROV);

(iii) is a continuation-in-part of pending prior U.S. Patent Application Serial No. 12/578,342, filed 10/13/09 by Michael Braun et al. for METHOD AND

APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES AND/OR PHARMACOLOGICAL AGENTS TO TISSUE AND MEDICAL WIRE FOR USE

WrmiN THE BODY (Attorney's Docket No. OXIRA-7), which patent application (a) is itself a continuation-in-part of the aforementioned prior U.S. Patent Application Serial No. 12/008,130, filed 01/09/08 by Christoph Hehrlein et al. for METHOD AND APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES TO TISSUE (Attorney's Docket No. OXIRA-5), and (b) claims benefit of prior U.S. Provisional Patent Application Serial No. 61/104,557, filed 10/10/08 by Michael Braun et al. for METHOD AND APPARATUS FOR DELIVERING OXYGEN AND/OR OTHER GASES AND/OR PHARMACOLOGICAL AGENTS TO TISSUE AND MEDICAL WIRE FOR USE WITHIN THE BODY (Attorney's Docket No. OXIRA-7 PROV); and

(iv) claims benefit of pending prior U.S. Provisional Patent Application Serial No. 61/489,927, filed 05/25/11 by Todd F. Davenport for NEUROX™ CHAMBER (Attorney's Docket No. OXIRA-11 PROV). The nine (9) above-identified patent applications are hereby incorporated herein by reference.

Field Of The Invention

This invention relates to percutaneously delivering oxygen and/or other gases to tissue for the treatment of cardiovascular disease and/or for other treatment purposes, and a medical wire for use within the body. Among other things, the method and apparatus disclosed herein may be used to reduce the risks of ischemic events during an angioplasty procedure and/or a plaque removal procedure, to improve healing of hypoxic tissues, and/or to slow down restenosis after vascular interventions.

Background Of The Invention

A percutaneous transluminal angioplasty (PTA) of blood vessels, including the coronary arteries (PTCA), is a very common procedure to reduce vessel narrowing (i.e., stenosis) that obstructs blood flow to tissue, especially human organs. The angioplasty procedure typically involves inflating a balloon within the constricted region of the blood vessel so as to re-open the blood vessel. The success rates of coronary angioplasty procedures are typically inversely related to (i) the extent of the vascular disease, and (ii) the patient's intolerance to myocardial ischemia (i.e., blood flow obstruction) during the temporary blood vessel occlusion which is associated with a PTA procedure.

More particularly, one of the principle limitations of a coronary angioplasty procedure is the complete obstruction of blood flow during the inflation of the angioplasty balloon. After a short period of balloon occlusion, patients experience myocardial ischemia due to the interruption of oxygenated blood to the myocardium. Myocardial ischemia is usually indicated by angina pectoris and/or cardiac arrhythmias. In the past, several perfusion balloon catheters have been developed to overcome the problem of total blood flow obstruction during percutaneous coronary interventions. By way of example but not limitation, U.S. Patent No. 4,944,745 (Sograd) discloses a perfusion balloon catheter that allows passive perfusion of blood through a catheter whose balloon is obstructing blood flow. U.S. Patent No.

4,909,252 (Goldberger) discloses a perfusion balloon catheter with a central opening which allows blood flow through the catheter when the balloon is fully inflated. U.S. Patent No. 5,087,247 (Horn et al.) discloses a balloon perfusion catheter with an elongated flexible perfusion shaft, with multiple openings proximal and distal to the balloon, in order to permit blood flow through an artery during balloon inflation. International Patent Publication No.

WO 9732626 (Cox et al.) discloses an inflatable balloon envelope allowing blood passage during inflation of the device.

While such perfusion balloon catheters permit some continued blood flow while their balloons are inflated, they are nonetheless limited to a flow rate which is something less than the normal flow rate of the blood passing through the vessel. In other words, perfusion balloon catheters can provide, at best, only some fraction of the normal flow rate which existed in the blood vessel prior to insertion of the catheter and inflation of the balloon. Thus, when perfusion balloon catheters are placed into relatively small arteries (e.g., the coronary arteries) which already have modest flow rates, the further reduction of an already-low flow rate is frequently clinically unacceptable. The inadequacies of the perfusion balloon catheter were characterized in a publication by Ferrari et al. (Coronary Artery Disease, 1997) who conclude their studies with the statement that in "high-risk patients dependent on adequate coronary perfusion, autoperfusion balloons are not able to provide sufficient distal coronary blood flow during balloon inflation". Insufficient blood flow distal to an inflated balloon causes ischemia and hence hypoxia (i.e., oxygen deprivation) in tissue (e.g., the end organs) because the oxygenation of tissue previously supplied with blood is reduced.

For this reason, angioplasty in the coronary arteries is a relatively high risk procedure in patients who require dilatation of the unprotected trunk of the left main coronary artery. Tan et al. (Circulation, 2001) concluded that although percutaneous balloon interventions are a generally accepted treatment modality for coronary artery disease, left main PTCA procedures remain a high risk procedure for the patient.

Another limitation of a coronary angioplasty is restenosis. Restenosis after a PTCA procedure has been successfully inhibited by ionizing radiation therapy (i.e., brachytherapy) applied prior to, or shortly after, angioplasty. Thus, vascular brachytherapy using radioactive sources has become a new treatment option to prevent restenosis. More particularly, radioactive stents disclosed in U.S. Patent No.

5,059,166 (Fischell et al.) and/or radioactive catheters disclosed in U.S. Patent No. 5,199,939 (Dake et al.) have been used to minimize or eliminate neointimal hyperplasia after angioplasty. However, the logistical complexities of using radiation sources in coronary arteries, and radiation safety issues, have prompted researchers to improve the irradiation technology. To this end, U.S. Patent No. 5,951,458 (Hastings et al.) discloses a radiation catheter that releases oxidizing agents such as H₂0₂ to prevent restenosis after a cardiovascular intervention. The method described by Hastings et al. helps to reduce the radiation doses, or treatment times, necessary to prevent restenosis.

Oxygenated perfluorocarbon (PFC) emulsions have been used to treat ischemic and hypoxic disorders. Oxygen-transferable PFC emulsions became known as artificial blood substitutes more than twenty years ago. By way of example but not limitation, in U.S. Patent No. 3,958,014 (Watanabe et al.) and U.S. Patent No.

4,252,827 (Yokoyama et al.), perfluorocarbon (PFC) emulsions are disclosed that have a small PFC "particle" size of 0.02 microns to 0.25 microns, and which were injected into the bloodstream. Additionally, U.S. Patent No. 4,445,500 (Osterholm) teaches that oxygenated perfluorocarbon (PFC) emulsions can be injected into the cerebrospinal pathway to improve aerobic respiration of tissue. Furthermore, U.S. Patent No. 4,795,423 (Osterholm) discloses an intraocular perfusion with

perfluorinated substances to treat ischemic retinopathy.

Unfortunately, clinical experience has shown that the current approaches for using PFCs to oxygenate tissue are highly problematic. More particularly, and as will hereinafter be discussed in further detail, the current approaches for using

perfluorocarbons (PFCs) prevent the use of "pure" PFC solutions and, instead, require the use of PFC emulsions. These emulsions themselves introduce a whole new set of problems which effectively limit the clinical use of PFCs in the bloodstream.

More particularly, it has been found that a pure perfluorocarbon (PFC) solution, with or without a "passenger" gas (e.g., oxygen), cannot be safely injected directly into the arterial or venous bloodstream, e.g., using a standard intravenous (IV) line or syringe. This is because introducing pure PFC solutions in this manner creates dangerous (and potentially fatal) embolisms in the bloodstream. These embolisms are created due to the fact that the PFCs are hydrophobic and are not soluble in blood. Thus, when a pure PFC solution is injected directly into the bloodstream (e.g., for hyperoxic medical therapy), the PFC tends to aggregate into relatively large bodies (or "particles") within the bloodstream. These relatively large aggregations of PFC tend to create embolisms in the bloodstream. For this reason, introducing pure PFCs (with or without a "passenger" gas) directly into the bloodstream, without the provision of some sort of PFC-dispersing mechanism, is not feasible due to the creation of dangerous embolisms.

Furthermore, it is not possible to eliminate the problematic PFC aggregations by simply diluting the PFC with another liquid prior to its introduction into the bloodstream, because the PFCs are not easily soluble in biocompatible fluids (e.g., the PFCs are insoluble in saline). Thus, the PFC tends to re-aggregate even when it is diluted with another liquid, so that the problematic PFC aggregations remain.

As a result, and as noted above, emulsifying agents (such as egg yolk, phospholipids, Pluronic-F68 and other emulsifiers) have been added to the PFC prior to the injection of the PFC into the bloodstream, whereby to "break up" the PFC particles and minimize aggregations of the PFC within the bloodstream. See, for example, U.S. Patent Nos. 3,958,014 (Watanabe et al.), 4,252,827 (Yokoyama et al.), 4,445,500 (Osterholm) and 4,795,423 (Osterholm). Thus, with the prior art approach, emulsifying agents are used as a PFC-dispersing mechanism to break up the PFC and prevent the problematic PFC aggregations which can lead to embolisms.

However, clinical studies in humans evaluating such PFC emulsions (e.g., Fluosol and others) have shown that the use of these emulsions, infused into blood with the PFC for hyperoxic therapy, can cause respiratory insufficiency and pulmonary edema (W all TC et al., Circulation 1994), most likely due to fluid overload and subsequent congestive heart failure. Thus, PFC emulsions can be considered as PFC "particles" (i.e., aggregations) that are accompanied by large quantities of another therapeutic agent (i.e., the emulsifier) which serves to emulsify (i.e., disperse) the pure PFC within the bloodstream. However, these large quantities of additional therapeutic agent (i.e., the emulsifier) in turn significantly increase intravascular volumes and thereby induce unwanted side effects such as respiratory insufficiency and pulmonary edema.

In addition, PFC emulsions are capable of uploading and releasing, per unit of volume, far less oxygen than a pure PFC solution. Thus, where emulsions are added to the PFC in order to avoid the creation of embolisms, it is generally necessary to provide additional systemic oxygenation to the patient via the lung (e.g., by breathing 100% oxygen) so as to create a sufficiently therapeutic oxygen tension of the PFC emulsions (Kim HW et al., Artificial Organs, Vol. 28, No. 9 2004). However, such intensive systemic oxygenation is normally to be avoided clinically, due to the adverse affects of elevated oxygen concentration on the lungs (e.g., oxygen toxicity) (Kim HW et al., Artificial Organs, Vol. 28, No. 9 2004).

Moreover, the use of emulsions to disperse the PFC in blood can also cause allergic reactions in the patient. Mattrey et al. showed that PFC emulsions can cause allergic reactions (Mattrey RF et al., Radiology 1987). More particularly, in an investigation of Fluosol-DA 20% as a contrast agent using Pluoronic-F68 and others as emulsifiers for PFC in humans, it was reported that Fluosol-DA 20% caused allergic reactions which are most likely triggered by complement activation of the substance Pluoronic-F68 (Mattrey RF et al., Radiology 1987). Since pure PFCs are chemically inert and contain no emulsifiers, no allergic reactions are to be expected when using pure PFCs in the blood; thus it has been concluded that it is the presence the emulsifiers which trigger the allergic reaction in the patient.

For these reasons, using oxygenated PFCs in conjunction with emulsifiers to prevent hypoxia has not heretofore been clinically successful.

Thus it will be seen that pure PFCs (with or without a "passenger" gas) cannot be introduced directly into the bloodstream without also providing some PFC- dispersing mechanism to prevent embolisms. However, it will also be seen that the prior art approach of using emulsions as the PFC-dispersing mechanism for the PFC introduces a whole new set of problems which effectively limit the clinical use of PFCs in the bloodstream.

For these reasons, prior art PFC systems for delivering oxygen to tissue have not heretofore been clinically successful.

In addition to the foregoing, medical wires are well known in the art. By way of example, such medical wires may be a coronary wire, a guide wire, a perfusion wire, etc. Many of these medical wires need to be thin and have substantial flexibility at their distal end, a lesser degree of flexibility in their midsection, and a least degree of flexibility at their proximal end. It can be difficult and/or expensive to produce medical wires of this type which have the necessary structural integrity and the desired degrees of flexibility along their length.

Summary Of The Invention

The present invention provides a radically new (i.e., non-emulsifier) PFC- dispersing mechanism to permit the introduction of a pure PFC solution in the bloodstream while preventing the formation of large, embolism-inducing PFC aggregations in the bloodstream.

More particularly, among other things, the present invention employs a carefully constructed porous membrane (which may also be referred to as a porous substrate) to safely dispense pure, chemically inert PFCs directly into the bloodstream at sufficiently low rates, and in sufficiently small bodies, as to prevent the creation of the aforementioned large PFC aggregations which lead to embolisms.

This carefully constructed porous membrane may be mounted on, and/or disposed within and/or otherwise carried by, a catheter or wire or other intravascular device or structure (e.g., an atherectomy device, a stent, etc.); a pure PFC solution loaded into the porous membrane; and the catheter or wire or other intravascular device or structure advanced into the vascular system of the patient so that the porous membrane is located at a selected site within the bloodstream; whereupon the porous membrane will act as a PFC-dispersing mechanism to dispense the pure PFC solution directly into the bloodstream - in a carefully controlled, highly dispersed manner - so that micro-, nano-, and subnano- sized quantities of PFC molecules safely enter the bloodstream, without the occurrence of large, embolism-inducing PFC aggregations. The pure PFC solution preferably carries a sizable quantity of therapeutic gas (e.g., oxygen) therein, so that the gas-rich (e.g., oxygen-rich) PFC solution can deliver the therapeutic gas to downstream tissue (e.g., for oxygenation purposes.

An important aspect of the present invention is that the porous membrane must be carefully constructed so as to permit the gas-rich (e.g., oxygen-rich) PFC to enter the bloodstream at the appropriate rate. In fact, it has been discovered that it is important to form the porous membrane with a porosity which permits the gas-rich PFC to disperse into the bloodstream in very small volumes, and at a highly controlled rate which is both (i) sufficiently high to provide therapeutic benefit to the patient by the delivery of adequate quantities of therapeutic gas (e.g., oxygen) molecules to tissue, and (ii) sufficiently low so as to avoid the creation of embolisms in the bloodstream, even when using pure PFC solutions.

In practice, it has been discovered that, for a catheter or wire or other intravascular device or structure (e.g., atherectomy device, stent, etc.) placed into an artery having a typical rate of blood flow, forming the porous membrane with a porosity in the range of 0.001-200 microns, and preferably in the range of 20-200 microns, permits appropriate dispersion of the gas-rich PFC into the bloodstream without inducing embolisms.

It has been discovered that a pore size of greater than 200 microns can increase the likelihood of creating embolisms in the bloodstream.

It has also been discovered that a pore size which is too small (e.g., less than 20 microns) can make it difficult to deliver enough gas molecules to a site to provide certain therapeutic benefits. Thus, for example, where it is desired to provide oxygenation therapy in larger diameter blood vessels, it may not be desirable to use a pore size of less than 20 microns, since this may not provide enough oxygen molecules to the downstream tissue. However, where the oxygenation therapy is to be provided in smaller diameter vessels, or where some other, non-oxygenation therapy is to be provided to the patient, smaller quantities of therapeutic gas molecules may be adequate, in which case smaller pore sizes (e.g., 0.001 microns) may be satisfactory.

It has been discovered that, for oxygenation therapy, a pore size of 20-200 microns provides excellent therapeutic benefits while still preventing the creation of embolisms.

In one preferred form of the invention, there is provided a system comprising: a hollow tube having a distal end, a proximal end, and a lumen extending between the distal end and the proximal end;

at least a portion of the tube comprising a porous membrane; and

a gas-rich perfluorocarbon solution incorporated in the porous membrane; wherein the porous membrane has a porosity in the range of 0.001-200 microns, in order that:

(i) the gas-rich perfluorocarbon solution is effectively incorporated into the porous membrane; and

(ii) when the porous membrane is positioned in blood, the gas-rich perfluorocarbon solution elutes out of the porous membrane, in aggregations small enough to prevent the creation of embolisms in the blood, with the elution of the gas- rich perfluorocarbon solution into the blood varying between minutes and several hours, depending on the temperature and the hemodynamics of the blood.

In another form of the invention, there is provided a system comprising: a medical wire;

at least a portion of the medical wire comprising a porous membrane; and a gas-rich perfluorocarbon solution incorporated in the porous membrane; wherein the porous membrane has a porosity in the range of 0.001-200 microns, in order that:

(ii) when the porous membrane is positioned in blood, the gas-rich perfluorocarbon solution elutes out of the porous membrane, in aggregations small enough to prevent the creation of embolisms in the blood, with the elution of the gas- rich fluorocarbon solution into the blood varying between minutes and several hours, depending on the temperature and the hemodynamics of the blood.

In another form of the invention, there is provided a method for treating a patient, comprising: providing:

(i) a hollow tube having a distal end, a proximal end, and a lumen extending between the distal end and the proximal end, at least a portion of the tube comprising a porous membrane; and

(ii) a gas-rich perfluorocarbon solution;

loading the gas-rich perfluorocarbon solution into the porous membrane; and positioning the tube in the vascular system of the patient so that porous membrane is exposed to blood;

wherein the porous membrane has a porosity in the range of 0.001-200 microns, in order that:

In another form of the invention, there is provided a method for treating a patient, comprising:

providing:

(i) a medical wire, at least a portion of the medical wire comprising a porous membrane; and

(ii) a gas-rich perfluorocarbon solution;

loading the gas-rich perfluorocarbon solution into the porous membrane; and positioning the medical wire in the vascular system of the patient so that porous membrane is exposed to blood;

wherein the porous membrane has a porosity in the range of 0.001-200 microns, in order that: (i) the gas-rich perfluorocarbon solution is effectively incorporated into the porous membrane; and

In another form of the invention, there is provided an intravascular treatment device comprising:

an intravascular device having a distal end and a proximal end;

at least a portion of the intravascular device comprising a porous membrane; and

a perfluorocarbon solution incorporated in the porous membrane;

(i) the perfluorocarbon solution is effectively incorporated into the porous membrane; and

(ii) when the porous membrane is positioned in blood, the perfluorocarbon solution elutes out of the porous membrane, in aggregations small enough to prevent the creation of embolisms in the blood.

providing:

an intravascular device having a distal end and a proximal end; at least a portion of the intravascular device comprising a porous membrane; and

a perfluorocarbon solution;

loading the perfluorocarbon solution into the porous membrane; and positioning the intravascular device in the vascular system of the patient so that porous membrane is exposed to blood;

(ii) when the porous membrane is positioned in blood, the

perfluorocarbon solution elutes out of the porous membrane, in aggregations small enough to prevent the creation of embolisms in the blood.

In another form of the invention, there is provided

an intravascular treatment device comprising:

an intravascular device having a distal end and a proximal end; and at least a portion of the intravascular device comprising a porous membrane; wherein the porous membrane has a porosity in the range of 0.001-200 microns, in order that when a perfluorocarbon solution is introduced to the porous membrane:

(ii) when the porous membrane is positioned in blood, the

The present invention may also utilize the aforementioned porous membrane (which may also be referred to as a porous substrate) to deliver pharmacological agents to tissue, with the porous membrane regulating the rate of delivery so as to avoid overdosing or underdosing of the pharmacological agent.

The present invention also provides a novel medical wire for use in the body. In another form of the invention, there is provided a medical wire comprising: an elongated body having a distal section terminating in a distal end, a proximal section terminating in a proximal end, and an intermediate section disposed between the distal section and the proximal section;

the distal section being configured so as to have a substantial degree of flexibility, the intermediate section being configured so as to have a lesser degree of flexibility, and the proximal end being configured so as to have a least degree of flexibility;

wherein at least the intermediate section and the proximal section are formed out of a single piece of hypotube.

providing a medical wire comprising:

an elongated body having a distal section terminating in a distal end, a proximal section terminating in a proximal end, and an intermediate section disposed between the distal section and the proximal section;

wherein at least the intermediate section and the proximal section are formed out of a single piece of hypotube; and

positioning the medical wire in the patient.

providing a medical wire comprising:

an elongated body having a distal section terminating in a distal end, a proximal section terminating in a proximal end, and an intermediate section disposed between the distal section and the proximal section; the distal section being configured so as to have a substantial degree of flexibility, the intermediate section being configured so as to have a lesser degree of flexibility, and the proximal end being configured so as to have a least degree of flexibility;

wherein at least the intermediate section and the proximal section are formed out of a single piece of hypotube;

and further wherein at least a portion of the tube comprises a porous membrane having a porosity in the range of 0.001-200 microns, in order that when the porous membrane is exposed to a gas-rich perfluorocarbon solution: (i) the gas-rich perfluorocarbon solution is effectively incorporated into the porous membrane; and (ii) when the porous membrane is thereafter positioned in blood, the gas-rich perfluorocarbon solution elutes out of the porous membrane, in aggregations small enough to prevent the creation of embolisms in the blood;

loading a gas-rich perfluorocarbon solution into the porous membrane; and positioning the medical wire in the vascular system of the patient so that the porous membrane is exposed to blood.

In another form of the invention, there is provided apparatus for oxygenating blood, the apparatus comprising:

a container comprising an interior chamber, a first port communicating with the interior chamber and a second port communicating with the interior chamber; and a porous membrane disposed within the interior chamber of the container, the porous membrane having a porosity such that an oxygen-rich perfluorocarbon solution may be incorporated into the porous membrane and, when a blood fluid is brought into contact with the porous membrane incorporating the oxygen-rich perfluorocarbon solution, the oxygen-rich perfluorocarbon solution elutes out of the porous membrane and into the blood fluid, whereby to oxygenate the blood fluid.

In another form of the invention, there is provided

a method for oxygenating blood, the method comprising: providing apparatus for oxygenating blood, the apparatus comprising:

a container comprising an interior chamber; and

a porous membrane disposed within the interior chamber of the container, the porous membrane having a porosity such that an oxygen-rich perfluorocarbon solution may be incorporated into the porous membrane and, when a blood fluid is brought into contact with the porous membrane incorporating the oxygen-rich perfluorocarbon solution, the oxygen-rich perfluorocarbon solution elutes out of the porous membrane and into the blood fluid, whereby to oxygenate the blood fluid;

introducing an oxygen-rich perfluorocarbon solution to the porous membrane, and transferring a blood fluid from the body of a patient into the interior chamber of the container, whereby to oxygenate the blood fluid; and

returning the oxygenated blood fluid to the body of the patient.

Brief Description Of The Drawings

These and other objects, features and advantages of the present invention will be more fully disclosed in, or rendered obvious by, the following detailed description of the preferred embodiments of the invention, which is to be considered together with the accompanying drawings wherein like numbers refer to like parts, and further wherein:

Fig. 1 is a schematic view of a novel catheter formed in accordance with the present invention;

Figs. 2 and 3 are schematic views illustrating the porous membrane of the novel catheter of Fig. 1, and how the gas-rich (e.g., oxygen-rich) PFC elutes out of the porous membrane;

Figs. 4-7 are schematic views showing how the catheter's porous membrane may be loaded with gas-rich (e.g., oxygen-rich) PFC; Figs. 8-10 are schematic views illustrating how a balloon catheter, incorporating the porous membrane and the gas-rich PFC of the present invention, may be deployed in a blood vessel, so that the gas-rich PFC elutes out of the porous membrane and into the bloodstream;

Fig. 11 is a schematic view showing another catheter formed in accordance with the present invention, wherein the catheter comprises multiple layers of porous membrane;

Figs. 12-16 are schematic views showing a balloon catheter formed in accordance with the present invention, and how it may be used to apply gas-rich (e.g., oxygen-rich) PFC directly to the walls of a blood vessel;

Fig. 17 is a schematic perspective view of a microporous, or nanoporous, thin film membrane, with the pores releasably storing the gas-rich (oxygen-rich) PFC in accordance with the present invention, wherein the microporous or nanoporous membrane may be (i) part of a medical device inserted into a blood vessel, and/or (ii) used as a tissue patch for the improved closure of wounds and/or the topical treatment of surface tissue;

Fig. 18 is a schematic longitudinal view of a novel balloon catheter formed in accordance with the present invention, with the balloon carrying the porous membrane and with the porous membrane carrying the gas-rich (e.g., oxygen-rich) PFC in accordance with the present invention;

Fig. 19 is a schematic longitudinal view of a stent delivery system comprising a porous membrane for appropriately dispersing a supply of gas-rich (e.g., oxygen- rich) PFC - in this embodiment, the porous membrane is located on the shaft of the catheter, proximally and/or distally to the balloon;

Fig. 20 is a schematic cross-sectional view of the distal part of a medical device (e.g., a catheter) containing a porous membrane holding a supply of gas-rich (e.g., oxygen-rich) PFC, with the porous membrane being encompassed by a housing which seals off the porous membrane (and its supply of gas-rich PFC) in accordance with the present invention;

Fig. 21 is a schematic view showing a medical wire formed in accordance with the present invention, wherein the porous membrane is disposed on the exterior of the wire;

Fig. 22 is a schematic view showing a medical wire formed in accordance with the present invention, wherein the wire is cannulated, and further wherein the porous membrane is in the form of a tube disposed within the cannulated wire;

Fig. 23 is a schematic view showing a medical wire formed in accordance with the present invention, wherein the wire is cannulated, and further wherein the porous membrane is in the form of a wick disposed within the interior of the cannulated wire;

Fig. 24 is a schematic view showing a novel medical wire formed in accordance with the present invention;

Fig. 25 is a schematic view of the distal section of the novel medical wire shown in Fig. 24;

Fig. 26 is a schematic view of the intermediate section of the novel medical wire shown in Fig. 24;

Fig. 27 is a schematic view of the proximal section of the novel medical wire shown in Fig. 24;

Fig. 28 is a schematic view of the novel medical wire shown in Fig. 24, modified to carry a porous membrane on its outer surface;

Fig. 29 is a schematic view of the novel medical wire shown in Fig. 24, modified to carry a porous membrane in or on its inner lumen;

Fig. 30 is a schematic view of another novel medical wire formed in accordance with the present invention;

Fig. 31 is a schematic view of still another novel medical wire formed in accordance with the present invention; Fig. 32 is a schematic view of yet another novel medical wire formed in accordance with the present invention;

Fig. 33 is a schematic view of another novel medical wire formed in accordance with the present invention;

Fig. 34 is a schematic view of still another novel medical wire formed in accordance with the present invention;

Fig. 35 is a schematic view of yet another novel medical wire formed in accordance with the present invention;

Figs. 36 and 37 are schematic views of another novel medical wire formed in accordance with the present invention;

Figs. 38 and 39 are schematic views of still another novel medical wire formed in accordance with the present invention;

Figs. 40-45 are schematic views showing apparatus for extracorporeally oxygenating a blood fluid;

Figs. 46-51 are schematic views showing other apparatus for extracorporeally oxygenating a blood fluid;

Figs. 52-54 are schematic views showing still other apparatus for extracorporeally oxygenating a blood fluid;

Figs. 55 and 56 are schematic views showing further apparatus for extracorporeally oxygenating a blood fluid;

Figs. 57 and 58 are schematic views showing additional apparatus for extracorporeally oxygenating a blood fluid;

Figs. 60-63 are schematic views showing still other apparatus for

extracorporeally oxygenating a blood fluid;

Figs. 64 and 65 are schematic views showing further apparatus for extracorporeally oxygenating a blood fluid; and

Figs. 66 and 67 are schematic views showing other apparatus for

extracorporeally oxygenating a blood fluid. Detailed Description Of The Preferred Embodiments

In General

As noted above, it has been found that a pure PFC solution, with or without a "passenger" gas saturation, cannot be safely injected directly into the arterial or venous bloodstream, e.g., using a standard intravenous (IV) line or syringe. This is because introducing pure PFC solutions in this manner creates dangerous embolisms in the blood. These embolisms are created due to the fact that the PFCs are hydrophobic and are not soluble in blood. Thus, when the PFC is injected directly into the bloodstream of a patient, the PFC tends to aggregate into relatively large bodies (or "particles") within the bloodstream. These relatively large aggregations of PFC tend to create embolisms in the bloodstream. For this reason, introducing pure PFCs (with or without a "passenger" gas) directly into the bloodstream of the patient, without using some sort of PFC-dispersing mechanism to "break up" the large PFC aggregations (or "particles"), is not feasible due to the creation of embolisms.

However, as also noted above, the use of emulsifiers as the PFC-dispersing mechanism introduces a whole new set of problems. Among other things, the use of emulsifiers as the PFC-dispersing mechanism can cause respiratory insufficiency and pulmonary edema, require the use of additional systemic oxygenation via the lung (with the associated risk of oxygen toxicity), and may cause allergic reactions.

Thus, a new PFC-dispersing mechanism is needed in order to permit a pure PFC solution (with or without "passenger" gas) to be safely and efficaciously introduced into the bloodstream.

The present invention provides a radically new (i.e., non-emulsifier) PFC- dispersing mechanism to permit the introduction of a pure PFC solution in the bloodstream while preventing the formation of large, embolism-inducing PFC aggregations in the bloodstream. More particularly, the present invention employs a carefully constructed porous membrane (which may also be referred to as a porous substrate) to safely dispense pure, chemically inert PFCs directly into the bloodstream at sufficiently low rates, and in sufficiently small bodies, to prevent the creation of the aforementioned large PFC aggregations which lead to embolisms.

This carefully constructed porous membrane may be mounted on a catheter or wire or other device or intravascular structure (e.g., an atherectomy device, a stent, etc.); a pure PFC solution loaded into the porous membrane; and the catheter or wire or other intravascular device structure advanced into the vascular system of the patient so that the porous membrane is located at a selected site within the bloodstream;

whereupon the porous membrane will act as a PFC-dispersing mechanism to dispense the pure PFC solution directly into the bloodstream - in a carefully controlled, highly dispersed manner - so that micro-, nano-, and subnano- sized quantities of PFC molecules safely enter the bloodstream, without the occurrence of large, embolism- inducing PFC aggregations. The pure PFC solution carries a sizable quantity of therapeutic gas (e.g., oxygen) therein, so that the gas-rich (e.g., oxygen-rich) PFC solution can deliver the therapeutic gas to downstream tissue (e.g., for oxygenation purposes).

An important aspect of the present invention is that the porous membrane must be carefully constructed so as to permit the gas-rich (e.g., oxygen-rich) PFC to enter the bloodstream at the appropriate rate. In fact, it has been discovered that it is important to form the porous membrane with a porosity which permits the gas-rich PFC to disperse into the bloodstream in very small volumes, and at a highly controlled rate which is both (i) sufficiently high to provide therapeutic benefit to the patient by the delivery of adequate quantities of therapeutic gas (e.g., oxygen) molecules to tissue, and (ii) sufficiently low so as to avoid the creation of embolisms in the bloodstream, even when using pure PFC solutions. In practice, it has been discovered that, for a catheter or wire or other intravascular device or structure (e.g., atherectomy device, stent, etc.) placed into an artery having a typical rate of blood flow, forming the porous membrane with a porosity in the range of 0.001-200 microns, and preferably in the range of 20-200 microns, permits appropriate dispersion of the gas-rich PFC into the bloodstream without inducing embolisms.

It has also been discovered that a pore size of greater than 200 microns can increase the likelihood of creating embolisms in the bloodstream.

It has also been discovered that a pore size which is too small (e.g., less than 20 microns) can make it difficult to deliver enough gas molecules to a site to provide certain therapeutic benefits. Thus, for example, where it is desired to provide oxygenation therapy in larger diameter blood vessels, it may not be desirable to use a pore size of less than 20 microns, since this may not provide enough oxygen molecules to the downstream tissue. However, where the oxygenation therapy is to be provided in smaller blood vessels, or where some other, non-oxygenation therapy is to be provided to the patient, smaller quantities of therapeutic gas molecules may be adequate, in which case smaller pore sizes (e.g., 0.001 microns) may be satisfactory.

Construction Details

The present invention uses pure perfluorocarbon (PFC) as a media for delivering therapeutic gas molecules (e.g., 0₂, NO, CO, etc., or any combination thereof) to cells at a target site. Although any PFC media may be used, PFO

(perfluoro-n-octane) is preferred. As used herein, the term "pure PFC" is intended to mean a PFC solution with or without a gas therein, but which does not include emulsifiers therewith. Thus, the term "pure PFC" as used herein is intended to mean non-emulsified PFC. Furthermore, wherever the term "PFC" is used herein, it is intended to refer to pure (i.e., non-emulsified) PFC, unless it is otherwise stated.

The PFC is loaded with the desired therapeutic gas molecules (i.e., the "passenger" gas) until a certain percentage of saturation is achieved (preferably 100%). Preferably, the gas-rich (e.g., oxygen-rich) PFC is produced under normobaric or hyperbaric conditions at a production facility and then stored in a vial until use (e.g., until the gas-rich PFC is loaded into the porous membrane in the operating room).

As noted above, with prior art approaches, introducing a pure PFC solution (with or without gas molecules) directly into the bloodstream (e.g., via a needle) is not clinically acceptable due to the creation of dangerous embolisms. As also noted above, it is not practical to dilute the PFC with another liquid prior to injection, so as to reduce PFC aggregations in the bloodstream, due to the insoluble nature of the PFCs. Furthermore, as also noted above, it is not practical to use emulsifiers to disperse the PFCs within the bloodstream, since the use of emulsifiers can lead to problems of high fluid volume, less efficient oxygen delivery and possible allergic reactions.

The invention described herein overcomes these problems by dispensing a pure, chemically-inert PFC solution (with "passenger" therapeutic gas molecules carried therein) directly into the bloodstream, using a porous membrane (also sometimes referred to as a porous substrate) as a PFC-dispersing mechanism. The porous membrane dispenses the pure PFC solution directly into the bloodstream in a carefully controlled, highly dispersed manner so that micro-, nano-, and subnano- sized quantities of the PFC molecules enter the bloodstream. These tiny quantities of PFC molecules are small enough to avoid the creation of dangerous embolisms in the bloodstream.

Therefore, the present invention provides a unique approach for solving the aforementioned problems associated with prior art PFC delivery and makes it possible - for the first time - to clinically use a pure (i.e., non-emulsified) PFC solution to deliver a therapeutic gas (e.g., oxygen) to treat a medical condition (e.g., to prevent ischemia).

More particularly, the present invention provides a safe and effective way to deliver a gas-rich (e.g., oxygen-rich) PFC solution directly into the bloodstream, without the creation of embolisms, by loading the gas-rich PFC into a porous membrane which is part of a catheter or wire or other intravascular device or structure (e.g., atherectomy device, stent, etc.). The porous membrane is specifically constructed so that the PFCs elute out of the porous membrane, and are dispersed into the bloodstream, in a highly controlled manner, at a reproducible rate, and in small enough volumes, to avoid the creation of dangerous embolisms. This makes it practical, for the first time, to introduce a pure (i.e., non-emulsified) PFC solution directly into the bloodstream, without the risk of embolisms.

To this end, the porous membrane is formed out of a suitable porous material, e.g., Teflon, polyethylene, polyethylene terephthalate, nylon, silicon, cellulose acetate, etc. The porous material has a porosity which permits the gas-rich (e.g., oxygen-rich) PFC to be loaded into the porous membrane outside of the body and then, once the porous membrane is positioned in the bloodstream, to automatically disperse out of the porous material and into the bloodstream in very small volumes, and at a highly controlled rate which is both (i) sufficiently high to provide therapeutic benefit to the patient by the delivery of adequate quantities of therapeutic gas molecules to tissue, and (ii) sufficiently low so as to avoid the creation of fluid overload and/or embolisms in the bloodstream, even when using pure PFCs.

In practice, for oxygenation applications, forming the porous membrane with a porosity in the range of 20-200 microns has been found to permit appropriate dispersion of the oxygen-rich PFC into the bloodstream to adequately oxygenate tissue without causing embolisms. It has been found, however, that a pore size of >200 microns will tend to increase the likelihood of embolisms. Reducing the pore size of the porous membrane to the range of 0.001-20 microns further decreases the size of the PFC particles and hence further reduces the possibility of embolisms. However, it is believed that less PFC can be uploaded (per unit of membrane surface area, per unit of time) when the substrate is nanoporous and, in oxygenation applications, it may be necessary to use larger (e.g., 20-200 micron) pore sizes when the PFC is to be used to oxygenate tissue in larger diameter blood vessels. However, smaller pore sizes (e.g., 0.001-20 microns) may still be satisfactory when the PFC is being used to oxygenate tissue from within smaller diameter blood vessels, or when the therapeutic gas is something other than oxygen.

Further, it is believed that less PFC can be held in a porous membrane with smaller pore sizes than with a porous membrane with larger pore sizes. Thus, where substantial quantities of gas must be delivered to the tissue, and where it is desired to use smaller pore sizes, the overall surface area of the porous membrane may need to be increased, and/or the thickness of the porous membrane may need to be increased, in order to provide an adequate quantity of the therapeutic gas to the tissue.

Thus, a porous membrane formed with an appropriate pore size can be used to dispense the gas-rich (oxygen-rich) PFC into the bloodstream while limiting the size of the PFC aggregations within the bloodstream. For oxygenation applications, a pore size of 20-200 microns has been found to provide excellent therapeutic benefit while still preventing the creation of embolisms.

As noted above, the porous membrane (i.e., the porous substrate) preferably comprises an appropriate polymer. Teflon, polyethylene, polyethylene terephthalate, nylon, silicone, and cellulose acetate, etc. may all be used to form the porous membrane. The porous membrane preferably comprises a

hydrophobic material which binds the hydrophobic perfluorocarbon (PFC) solution non-covalently via London forces (named after Fritz London, the German- American physicist). London forces are exhibited by non-polar molecules because electron density moves about a molecule probabilistically. The London forces become stronger with larger amounts of surface contact. Greater surface area contact means closer interaction between different molecules. A porous membrane with a porosity of between 0.001 and 200 microns, and preferably between 20 and 200 microns, offers a sufficient surface area, and is therefore ideal, for PFC applications where the PFC is to be released into the bloodstream in relatively small (i.e., non-embolism-causing) aggregations.

If the hydrophobic (non-polar) porous membrane is brought into contact with the hydrophobic (non-polar) perfluorocarbon (PFC) solution, the contact angle (e.g., wettability) of the pores of the porous membrane is 0°, which means that the PFC solution will be taken up by the porous membrane. In contrast, when the hydrophobic porous membrane is brought into contact with water or saline, the contact angle (e.g., wettability) is about 120°. The water or saline solution will therefore not be taken up by the hydrophobic porous membrane, and the perfluorocarbon (PFC) solution will not be diluted by other fluids, e.g., the water or saline solution.

The carefully-selected porosity of the hydrophobic polymer substrate (i.e., the porous membrane) allows the pure perfluorocarbon (PFC) solution to disperse into the bloodstream in PFC "particles" of micro, nano and sub-nano sizes. Forming the porous membrane out of polymers with a pore size of 0.001-200 microns, and preferably 20-200 microns, provides an effective incorporation of the gas-rich

(oxygen-rich) perfluorocarbon (PFC) solution into the porous membrane, and provides a safe and effective rate of dispersion of the PFC solution into blood. A pore size above 200 microns increases the aggregation of the perfluorocarbon (PFC) molecules into the large aggregates that increase the likelihood of creating dangerous embolisms in blood. Therefore, a pore size above 200 microns is generally not preferred in the present invention.

Due to the construction of the porous membrane, predominantly nano- and micro- sized PFC aggregates (or "particles") are dispersed from the surface of the porous membrane into the bloodstream. In order to achieve a sufficient amount of oxygen delivery into blood so as to create a substantial hyperoxia in the blood for hyperoxic therapy, a sufficient amount of the nano- and micro- PFC particles have to be released from the surface of a catheter or wire or other intravascular device or structure (e.g., atherectomy device, stent, etc.) introduced into the bloodstream. Of course, many different catheter configurations, or wire configurations, or intravascular device or structure configurations, are possible, and many different porous membrane lengths (and/or surface areas) and porosities are possible, so it should be appreciated that variations and combinations of length (and/or surface area)/porosity/thickness may be employed in order to achieve the desired degree of gas deployment without the creation of embolisms. Furthermore, it should be appreciated that many different degrees of gas deployment may be desirable, depending on the therapeutic gas therapy which is to be effected (e.g., oxygenation or otherwise), the size of the blood vessel involved (e.g., larger or smaller), the quantity of tissue to be treated (e.g., oxygenated), etc.

In animal studies using a porous membrane to dispense a pure PFC solution carrying oxygen molecules, the actual pore size of the porous membrane was set to a mean size of 100 microns (range 20-200 microns). Animal studies in rabbits and pigs, studying the safety and efficacy of a catheter comprising a polymer membrane having a mean pore size of 100 microns (range 20-200 microns), clearly indicated that pores in the range of 20-200 microns are capable of delivering sufficient oxygen-rich perfluorocarbon (PFC) particles to blood so as to provide effective hyperoxic therapy. Moreover, in two different animal models of rabbits and pigs, no embolization of the PFC particles was detected in any of the studied animals. Pathology of pig hearts revealed that no perfluorocarbon (PFC) particles could be detected in the small arterioles and capillaries of the heart muscle (i.e., vessels of the end organ), and thus it was concluded that no embolization of the PFC particles had occurred during use of the inventive catheter in blood.

The amount (i.e., the quantity of molecules) of uptake of the gas-rich PFC solution into the porous membrane, and the amount (i.e., the quantity of molecules) of release of the gas-rich PFC solution from the porous membrane into the bloodstream generally depends on the length, the thickness and the porosity of the substrate membrane. The rate of release of the gas-rich PFC solution from the porous membrane into the bloodstream generally depends on the pore size of the porous membrane. Therefore, in order to induce adequate hyperoxic therapy with the present invention, e.g., elevating the oxygen tension of the blood for hyperoxic therapy without inducing embolisms, the pore size of the substrate (i.e., porous membrane) should preferably be in the range of 20-200 microns for blood vessels of a typical size.

The pore size required to achieve the desired rate of dispersion is effectively determined by the size of the PFC molecules, and is not dependent upon the type or concentration of the therapeutic gas molecules which are bound to the PFC. Thus, a catheter having a porous membrane with a porosity of 0.001-200 microns can be used to safely deliver PFC carrying substantially any therapeutic gas molecule (e.g., 0₂, NO, CO, etc., or any combination thereof), at substantially any percentage of saturation (up to 100% saturation).

As noted above, in practice, it has been found that the pore size of the porous membrane governs the rate of release of the PFC from the catheter. Furthermore, it has been found that the surface area (i.e., length and circumference) and thickness of the porous membrane, together with the pore size, governs the total volume of PFC which may be carried by the device (and hence the total volume of the therapeutic "passenger" gas which may be carried by the medical device).

In one preferred form of the present invention, the porous membrane comprises multiple layers, with the multiple layers being deployed one on top of another.

And in one preferred form of the present invention, the porous membrane comprises multiple layers, with the porosity of the layers varying from one another. More particularly, in one preferred form of the present invention, the innermost layers of the porous membrane (i.e., those lying closest to the center axis of the catheter or wire or other intravascular device or structure) comprise relatively large pore sizes so as to accommodate relatively large amounts of PFC and so as to release that PFC to the outermost layers of the porous membrane as rapidly as the PFC may be accepted by the outermost layers of the porous membrane. At the same time, however, it is preferred that the outermost layers of the porous membrane (i.e., those contacting the bloodstream) be provided with smaller pore sizes (e.g., in the range of 0.001-200 microns, and preferably in the range of 20-200 microns) so as to control the rate of release of the PFC from the catheter in order to avoid the creation of dangerous embolisms.

At the time of use, the catheter (or wire or other intravascular device or structure) is immersed in a vial of gas-rich PFC so that its porous membrane is loaded with the gas-rich PFC, similar to how a sponge is loaded with water. The catheter (or wire or other intravascular device or structure) is then inserted into the vascular system of the patient. Due to the carefully selected porosity of the porous membrane, the gas- rich PFC then elutes out of the porous membrane and disperses into the patient's bloodstream at a rate which limits aggregations of the gas-rich (e.g., oxygen-rich) PFC within the bloodstream to a relatively small size, e.g., 0.001-200 microns. This controlled dispersion of the gas-rich PFC from the porous membrane into the bloodstream prevents embolisms from occurring while still providing sufficient quantities of the therapeutic gas (e.g., oxygen) molecules to provide the desired treatment to the patient. In other words, the porous membrane is carefully engineered so as to elute the gas-rich (e.g., oxygen-rich) PFC at a rate which effectively disperses the PFC in the bloodstream so as to avoid the creation of embolisms. Thus, the present invention permits the direct introduction of pure PFC solutions into the bloodstream, without requiring the use of emulsifiers to avoid the creation of embolisms (and hence without the aforementioned disadvantages associated with the use of emulsifiers). As the gas-rich PFC travels downstream, most of the gas molecules remain attached to the PFC. Some of the gas molecules may also be released from the PFC into the blood. The gas molecules which are released from the PFC into the blood may or may not be picked up by various blood components (e.g., hemoglobin).

At the target tissue site, the gas (e.g., oxygen) molecules bound to the PFC are released to the cells of the patient's tissue. It will be appreciated that the manner in which the gas molecules are released from the PFC is dependent upon both the hemodynamics of the blood environment and time, in much the same way that oxygen molecules are normally released from the blood components of the patient.

More particularly, the gas-rich PFC enters the target tissue region. Due to the fact that the gas (e.g., oxygen) concentration ("tension") in the cells is lower than the gas (e.g., oxygen) concentration ("tension") in the capillary blood, the gas-rich PFC releases the therapeutic gas (e.g., oxygen) molecules. The therapeutic (e.g., oxygen) molecules can then enter the cells of the patient's tissue.

At the target tissue site, the PFC molecules are also available to pick up waste materials (e.g., gases such as carbon dioxide) and carry those waste materials away from the target site, in essentially the same manner that hemoglobin carries away waste materials from the cells. More particularly, the carbon dioxide (C0₂) level increases after cellular activity, and therefore the C0₂ concentration ("tension") in the cells is higher than the C0₂ concentration ("tension") in the capillary blood. As a result, the C0₂ molecules move from the cells into the capillary blood and become attached to the "gas-poor" PFC, which has previously given up its "passenger" gas (e.g., oxygen) to the cells. The PFC, now loaded with C0₂, enters the venous bloodstream and is transported to the lungs, where the C0₂is expelled from the body.

It should also be appreciated that the PFC solution incorporated in the porous membrane need not necessarily carry a therapeutic gas. More particularly, where the primary concern is to remove waste materials (e.g., carbon dioxide) from tissue, the PFC solution loaded into the porous membrane may not be loaded with, or at least may not be completely saturated with, a therapeutic gas. In this case, the gas-poor PFC solution (which is still released safely from the porous membrane without the creation of embolisms) can pick up waste materials (e.g., carbon dioxide) at the tissue and carry it downstream for purging (e.g., by the lungs).

The present invention may be incorporated in various medical devices, in the form of various embodiments, according to the therapy which is to be provided to the patient.

More particularly, in one form of the present invention, there is provided a therapeutic gas delivery apparatus (e.g., a catheter or wire or other intravascular device or structure) for the treatment of disorders (e.g., cardiovascular diseases) that allows the local diffusion of a gas-rich (e.g., oxygen-rich) PFC solution into blood (and/or tissue), whereby to deliver that gas to the blood (and/or tissue). The invention is characterized by a porous membrane which is part of an appropriate medical device, with the porous membrane being impregnated with a gas-loaded (e.g., 0₂, NO, CO, etc.) perfluorocarbon (PFC) solution, e.g., by the application of a heating or cooling solution, or by utilizing heating or cooling apparatus such as resistance heaters, thermoelectric heaters and/or coolers, etc.).

The release kinetics of the PFC solution from the porous membrane may be modulated by controlled temperature changes of the environment. In other words, the rate of release of the PFC solution from the porous membrane may be modulated by heating or cooling the porous membrane with a warm or cold PFC solution. The preferred cooling temperature is 30°C-35°C and the preferred heating temperature is 40°C- 2°C.

The PFC-impregnated porous membrane is preferably sealed in a protective housing made of plastic or metal, allowing the medical device to be pre-loaded with the gas-rich (e.g., oxygen-rich) PFC solution and then stored without the loss of the therapeutic gas and/or the gas-carrying PFC solution. One of the goals of the present invention is to improve oxygen supply to ischemic organs during an angioplasty procedure. For instance, the present invention may be used to prolong balloon inflation times during high-risk PTCA procedures such as balloon or stent treatment of the trunk of the left main coronary artery.

Moreover, the present invention may be used to reduce the extent of acute or subacute myocardial infarction and ischemic stroke. The gas-rich PFC prevents cell death by providing oxygen and other gases, such as nitric oxide (NO) and/or carbon monoxide (CO), thereby preventing excessive inflammation of an organ's tissue. This can be particularly true in infarctions with massive inflammation occurring as a response to tissue damage, where adding small amounts of nitric oxide (NO) and/or carbon monoxide (CO) to oxygen may reduce the negative effects of inflammatory cells such as neutrophils and macrophages. In other words, where infarctions have massive inflammation, providing a PFC solution rich in oxygen and smaller amounts of nitric oxide (NO) and/or carbon monoxide (CO) can have substantial therapeutic benefit. In addition, cooling the treated tissues by injecting a cold fluid (e.g., a fluid having a temperature between 30°C-35°C) through the catheter helps to reduce tissue damage in the brain and in the heart in the presence of an ischemic event, thus improving myocardial or cerebral tissue salvage and reducing the risks of infarction.

Alternatively, in the event of a standard percutaneous coronary intervention procedure in patients without serious ischemia or an infarction, fluid temperatures in the range of 40°C-42°C may be utilized to increase the release kinetics of the therapeutic gases and to prevent restenosis after angioplasty.

Furthermore, in another embodiment characterized by a setting of cardiac arrest, the present invention may be used to oxygenate the body via the endovascular approach while chest compressions are performed. Thus, the body will be oxygenated without a ventilation of the lung during the resuscitation.

Furthermore, the invention disclosed herein may be utilized to reduce restenosis following an angioplasty procedure. The invention disclosed herein presents a novel approach for an angioplasty procedure (including a stent implantation) by improving not only the acute safety of the procedure but also the long-term outcome of the procedure.

In a similar manner, the present invention also may be used to prolong procedure times for plaque removal procedure times with atherectomy devices, for example, atherectomy devices that use mechanical blades or laser energy as a means to extract or ablate atherosclerotic plaque within an artery.

A major aspect of the present invention is the local delivery of oxygen (or other therapeutic gases) into blood (and/or tissue) via a perfluorocarbon (PFC) solution delivered via a percutaneously deliverable device. In addition, with the present invention, the local delivery of oxygen (or other therapeutic gases) can be achieved without requiring the use of software, electronic equipment, or mechanical pumping equipment or hardware (e.g., pumps, chambers, computers, bubble detectors, etc.). The gas-rich (e.g., oxygen-rich) PFC is released to the target area from a porous membrane carried by a catheter (e.g., a tube catheter, a balloon catheter, a perfusion balloon catheter, etc.) or a wire (e.g., a coronary wire, a guidewire, etc.) or other intravascular device or structure (e.g., an atherectomy device, a stent, etc.).

The apparatus presented herein allows for the local diffusion of an oxygen-rich PFC solution into hypoxic target tissues, where oxygen is safely released from the PFC into the bloodstream and increases the oxygen tension of the target tissue.

A porous membrane is used to releasably hold the gas-rich PFC on the device. Preferably the porous membrane comprises a polymer. During the manufacture of the porous membrane polymer, the porosity of the basic polymer material is induced in the range of 0.001-200 microns, and preferably in the range of 20-200 microns.

The porous membrane may be formed as an integral part of an appropriate medical device, or it may be securely attached to the medical device, or it may be securely attached to another component which is itself attached to the medical device. In addition, a surface or portion of the catheter or wire or other intravascular device or structure which itself comes in contact with the bloodstream may be manufactured (e.g., etched or chemically treated) so as to induce the desired porosity on such surface or portion of the catheter or wire or other intravascular device or structure, so as to create the desired porosity in the range of 0.001-200 microns in order to releasably hold and safely disperse the gas-rich (e.g., oxygen-rich) PFC. It should be noted that a catheter and/or wire and/or other intravascular device or structure with a surface so treated so as to create the desired porosity may also be configured so as to further incorporate a porous membrane(s) within one or more lumens of the catheter or wire or other intravascular device or structure.

It is disclosed herein that the microporous material is carried by a medical device, and the microporous material is impregnated with a gas-rich (e.g., oxygen- rich) PFC solution. Perfusion channels carrying liquids around the medical device may also be provided to allow the perfusion of warm and/or cold liquids so as to modulate the release of the gas-rich (e.g., oxygen-rich) PFC from the porous membrane. These induced local temperature changes modulate (i.e., increase or decrease) the rate of release of the PFC solution from the porous membrane, whereby to modulate the rate of delivery of the therapeutic gas (e.g., oxygen) molecules to the tissue.

Polymer tubes formed out of a porous structure and/or incorporating a porous material, and impregnated with oxygenated perfluorocarbon (PFC) solutions, may be used to supplement oxygen delivery to the blood during a cardiopulmonary bypass procedure.

Modified stent delivery catheters, (e.g., balloon catheters with a pre-mounted stent), and/or perfusion balloon catheters, and/or wires (e.g., cardiac wires, guidewires, etc.) and/or arterial plaque-removing atherectomy devices, and/or other intravascular devices or structures are all among the preferred embodiments of the invention. The porous membrane may be dispersed substantially anywhere on the medical device, including on an outer surface of the device, an interior surface of the device, and on the outer surface of any balloon carried by those devices. Endo vascular stents themselves may also be coated with a thin film porous membrane which incorporates the gas-rich (e.g., oxygen-rich) perfluorocarbon (PFC) solution.

For restenosis prevention, the local delivery of a oxygenated perfluorocarbon (PFC) solution may be combined with the application of ionizing radiation or low energy ultraviolet light so as to increase the production of oxygen free radicals in the target cell of an arterial wall. The effect of increased oxygen free radical production on the proliferating target cell in the arterial wall is DNA damage, which will cause a reduction of restenosis formation.

A therapeutic device that provides local tissue oxygenation may also be applied to other fields of vascular medicine. By way of example but not limitation, wound healing of skin in patients with peripheral occlusive arterial disease and impaired blood flow in the lower limb organs may be significantly improved with the local delivery of an oxygenated perfluorocarbon (PFC) solution via a skin patch placed onto the ischemic skin, where the skin patch includes the porous membrane therein. These oxygenated tissue patches promote the growth of new blood vessels into the area of ischemia, for instance in surgically-opened wounds. Gangrenes of the lower limb due to arteriosclerosis may be reduced in size through the use of the present invention.

By way of example but not limitation, the tissue patch carrying the gas-rich PFC solution may be incorporated in a bandage or other wound dressing.

In addition, these skin patches can deliver therapeutic gases in addition to oxygen.

Furthermore, these oxygenated tissue patches can be used to oxygenate tissue other than skin. By way of example but not limitation, these oxygenated tissue patches can be used to topically apply a gas-rich (e.g., oxygen-rich) PFC to internal tissues (e.g., the intestines), whereby to supply a therapeutic gas (e.g., oxygen) to such tissues.

Thus, in one form of the present invention, there is provided a tissue patch for delivering a therapeutic gas to tissue, wherein the tissue patch comprises a porous membrane which is impregnated with a gas-rich PFC solution.

In another preferred embodiment of the present invention, the porous membrane is located on the surface of a balloon of an angioplasty catheter. The porous membrane comprises a porous polymer, preferably at a thickness of between 0.5-4 mm (and most preferably at a thickness of between 0.6-1.4 mm). Among other things, the thickness of the porous membrane may be constrained by the inner diameter of the guiding catheter used, i.e., in the case of coronary and cerebal artery guiding catheters, the limit of membrane thickness might typically be in the range of 1-2 mm. The porous membrane can be integrated into the balloon, and/or into the catheter shaft structure, or can be wrapped around the balloon and/or the catheter shaft structure. The thin film porous polymer membrane is impregnated with an oxygenated perfluorocarbon (PFC) solution. The porous membrane is preferably sealed within a housing so as to prevent premature release of the gas-rich PFC (and/or the therapeutic gas itself). Prior to the intended angioplasty procedure, the housing is removed from the medical device, and the medical device is then advanced into the bloodstream. At the target site, the porous membrane may be brought into contact with the vessel wall. The release kinetics of the gas-rich PFC may also be modified by changes of local temperature between about 0 degrees Celsius and 50 degrees Celsius, e.g., by the injection of cold and/or warm fluids via the guiding catheter prior to inflation of the balloon. The oxygen enters the blood vessel wall by diffusion. Direct contact of the medical device with the target tissue typically improves oxygen delivery. The local increase in oxygen molecules creates an excess of oxygen free radicals when either (i) ionizing radiation with beta-particle emitters (such as Sr-90/Y- 90 or P-32) is applied to the target area, or (ii) ultraviolet light is applied to the target area. A simultaneous application of the oxygenated PFC solution with vessel irradiation (using ionizing radiation or ultraviolet light) is the preferred treatment modality for restenosis prevention.

The oxygen saturation of an end organ increases with improved oxygenated blood flow. Therefore, in another embodiment of the present invention, the oxygenated PFC is released from a perfusion balloon catheter. The perfusion balloon catheter provides for the flow of blood from the proximal end of the occluding balloon into the vascular bed distal to the occluding balloon (i.e., blockage), and thus increases the distribution of the oxygenated perfluorocarbon (PFC) solution to the end organ. Perfusion of blood through the occluded balloon is permitted, and the blood is oxygenated at the proximal end of the balloon, upstream of the balloon (i.e., upstream of the blood flow blockage), so that the oxygenated blood can flow past the balloon to the tissue.

In yet another embodiment of the present invention, the oxygenated PFC is delivered from a porous membrane which is part of a flexible coronary wire or other medical wire device or structure. In a preferred embodiment, the metallic wire is in the form of a flexible hypo-tube, whereby the wire has a lumen that extends from its proximal end through to the distal tip. The porous membrane, which carries the gas- rich PFC solution, is configured such that the porous membrane is positioned inside the lumen, and can extend within a portion of the lumen or from the proximal end all the way to the distal tip of the metallic wire. For example, the porous membrane could be modified to form a thread-like structure or structures. The gas-rich PFC solution is introduced into the porous membrane from the proximal end of the metallic wire through a delivery mechanism (e.g., including but not limited to a syringe) in the appropriate dose or dosages. In addition, the gas-rich PFC solution could be introduced into the porous membrane by a means providing for continuous delivery, which can be a powered device (e.g., including but not limited to an infusion pump) or a passive device (e.g., including but not limited to a gravity-fed drip, much like how a intravenous solution is infused from an IV bag). Then, as the porous membrane is loaded with the liquid oxygen carrier (i.e., the gas-rich PFC) at the proximal end of the metallic wire, capillary action enables the absorption of the gas-rich PFC from the proximal portion of the modified porous membrane through to the distal end of the modified porous membrane, much like dipping the proximal end of a strip of dry facial tissue into water and watching the water being absorbed up into the tissue to the distal end of the strip of tissue. Then, at the tip of the metallic wire where the distal end of porous membrane terminates, the release kinetics of the gas-rich PFC into the bloodstream (as described herein) draws the gas-rich PFC from the porous membrane at the tip of the flexible hypo-tube wire and into the bloodstream. Thus, the gas-rich PFC can be impregnated throughout the length of the modified porous membrane contained within the internal lumen of the wire and then be dispersed out the tip of the flexible metallic wire and into the blood stream, either in dosages or via a continuous flow, at rates which are both (i) sufficiently high to provide therapeutic benefit of the delivery of adequately high therapeutic gas molecules to tissue, and (ii) sufficiently low so as to avoid the creation of fluid overload and/or large particle embolisms in the bloodstream.

In a similar manner, the membrane carrying the liquid perfluorocarbon (PFC) solution can be modified such that the oxygen carrier membrane forms a tube around a retrievable metallic core that is positioned within the wire lumen. The wire containing the core within it can be advanced beyond the lesion (i.e., coronary obstruction) in the distal coronary artery. Then, as the core holding the porous membrane tube within the wire is held at a fixed position, the wire can be retracted an appropriate distance to expose the tube-shaped carrier membrane so as to allow the tube carrying the oxygen source (i.e., the oxygen-rich PFC solution) to dwell in the bloodstream. Thereafter, in all of the aforementioned flexible wire embodiments, a conventional balloon catheter can be advanced over the wire to a treatment zone preferentially proximal to the oxygen delivery source. These aforementioned embodiments permit prolonged balloon inflation as a result of allowing simultaneous oxygen delivery distal to the lesion during balloon inflation, thus eliminating the risk of myocardial ischemia during balloon inflation. Additionally, supplemental oxygen can continue to be delivered after balloon inflation. It should be noted that it may be desirable to advance a balloon catheter over the wire to a treatment zone distal to the oxygen delivery source, depending on the anatomical structure of the blood vessels, so as to allow

dispersement of gas-rich PFC before and after balloon inflation.

In yet another embodiment, the distal tip of a coronary wire is coated with the porous membrane carrying the liquid perfluorocarbon (PFC) solution. Alternatively, the porous membrane carrying the gas-rich PFC solution is modified such that the porous membrane forms a tube around the wire. The wire is placed in the distal coronary artery, and the porous membrane is allowed to dwell in the bloodstream so as to dispense the gas-rich PFC solution into the bloodstream. Thereafter, a conventional balloon catheter can be advanced over the wire to a treatment zone, which may be proximal or distal to where the gas-rich PFC was released. If desired, the tubular porous membrane can be withdrawn from the wire prior to advancing the balloon catheter over the wire, or the balloon catheter can be advanced over the tubular porous membrane. In either case, this approach permits prolonged balloon inflation without inducing myocardial ischemia.

In some cases it may be preferable to place the porous membrane inside of the lumen of a guidewire. For oxygen delivery, a length of ePTFE "tubing" is placed inside the wire lumen. Because the wire may be designed with an 0.014" outer diameter (which is a typical maximum outer diameter of a coronary wire), it may not always be possible to place the ePTFE tube on the outside of the wire in the case where an angioplasty catheter is to be advanced over the wire. Note that a huge clinical advantage can be obtained where a catheter is to be advanced over an oxygen- delivering wire, thus simultaneously providing balloon dilatation and oxygenation delivery distal to the obstruction. In yet another embodiment of the present invention, the wire is porous. The wire is impregnated with the gas-rich PFC at its distal tip or along its length.

In yet another embodiment of the present invention, the distal tip of the wire forms a plastic thread which is tightly connected to the metallic portion of the wire.

Illustrated Embodiments

Looking now at Figs. 1-3, there is shown a catheter 100 which comprises a shaft 105 comprising a porous membrane 110. Porous membrane 110 is saturated with a gas-rich (e.g., oxygen-rich) PFC solution 115 which is contained in pores 120 formed in porous membrane 110. Porous membrane 110 is preferably formed out of a polymer (e.g., Teflon, polyethylene, polyethylene terephthalate, nylon, silicone, cellulose acetate, etc.). Porous membrane 110 is formed with a porosity which permits gas-rich PFCs to be loaded into the porous membrane and thereafter to be dispersed into the bloodstream at a rate which is both (i) sufficiently high to provide therapeutic benefit by the delivery of a sufficient quantitiy of gas molecules to tissue, and (ii) sufficiently low so as to avoid the creation of fluid overload and/or large PFC- particle embolisms in the bloodstream.

In practice, for a catheter placed into an artery having a typical blood flow, forming the porous membrane with a porosity in the range of 0.001-200 microns has been found to permit appropriate dispersion of the gas-rich PFC into the bloodstream. However, it has also been found that a pore size of >200 microns will increase the likelihood of embolisms. Thus, it is desired to keep the pore size in the range of 0.001-200 microns. This pore size tends to limit gas-rich PFC aggregations within the bloodstream to a very small size, e.g., 0.001-200 microns, which has been found to provide therapeutic benefit while still preventing the creation of embolisms. For oxygenation applications, the porous membrane preferably has a pore size in the range of 20-200 microns. The pore size required to achieve the desired rate and volume of PFC dispersion is effectively determined by the size of the PFC molecules, and is not dependent upon the type or concentration of the therapeutic gas molecules which are bound to the PFC. Thus, a catheter having a porous membrane with a porosity of 0.001-200 microns can be used to deliver PFCs carrying substantially any therapeutic molecule (e.g., 0₂, NO, CO, etc., or any combination thereof), at substantially any percentage of saturation.

Looking now at Figs. 4-7, at the time of use, the catheter 100 is immersed in a vial 125 of pure, gas-rich PFC so that the porous membrane is loaded with the gas-rich PFC, in a manner similar to how a sponge is loaded with water.

Looking next at Fig. 8, catheter 100 (preferentially a monorail balloon catheter or a stent delivery balloon catheter) is then inserted into the vascular system (e.g., blood vessel 130) of the patient, so that porous membrane 110 comes into contact with the patient's blood 135. Due to the carefully selected porosity of porous membrane 110, gas-rich PFC 115 is dispersed out of the porous membrane and into the bloodstream of the patient at a rate which limits aggregations of the gas-rich PFC to a very small size, e.g., one which avoids the creation of embolisms even when using pure (i.e., non-emulsified) PFC. It is this controlled release of the gas-rich PFC from the porous membrane which prevents embolisms.

As the gas-rich PFC travels downstream, most of the gas molecules remain attached to the PFC molecules. Some of the gas molecules, however, may also be released from the PFC molecules into the blood. The gas molecules which are released from the PFC molecules into the blood may or may not be picked up by hemoglobin or other blood components.

At the target tissue site, the gas molecules bound to the PFC are released to the cells. It will be appreciated that the manner in which the gas molecules are released from the PFC is dependent upon both the hemodynamics of the blood environment and time, in much the same way that oxygen is normally released from hemoglobin. More particularly, gas rich PFC enters the target tissue region. Due to the fact that oxygen tension in the cells is lower than the oxygen tension in the capillary blood, the oxygen-rich PFC releases its oxygen molecules. The oxygen molecules can then enter the cells.

At the target site, PFC molecules are also available to pick up waste materials (e.g., gases such as C0₂) and carry them away from the target site, in essentially the same manner that hemoglobin carries away waste materials from cells. More particularly, the C0₂ level increases in a cell after cellular activity, and therefore the C0₂ tension in the cells is higher than the C0₂ tension in the capillary blood. The C0₂ molecules move from the cell into the capillary blood and become attached to the "gas-poor" PFC (which has previously given up its oxygen). The PFC, now loaded with C0₂, enters the venous bloodstream and is transported to the lungs, at which time the C0₂is expelled.

It should also be appreciated that the PFC solution incorporated in the porous membrane need not necessarily carry a therapeutic gas. More particularly, where the primary concern is to remove waste materials (e.g., carbon dioxide) from tissue, the PFC solution loaded into the porous membrane may not be loaded with, or at least may not be completely saturated with, a therapeutic gas. In this case, the gas-poor PFC solution (which is still released safely from the porous membrane without the creation of embolisms) can pick up waste materials (e.g., carbon dioxide) at the tissue and carry it downstream for purging (e.g., at the lungs).

Still looking now at Fig. 8, to the extent that catheter 100 is formed with a balloon 140, the balloon may be inflated as shown in Fig. 9, e.g., so as to dilate the vessel and/or to set a stent. It will be appreciated that as the balloon is inflated, the blood vessel may be occluded. However, inasmuch as the tissue downstream of the balloon has previously been super-oxygenated with oxygen-rich PFC delivered by indwelling catheter 100 prior to balloon inflation, longer periods of occlusion, with less detrimental results, may be achieved. Alternatively, and/or additionally, shaft 105 of catheter 100 may be cannulated so as to provide an oxygen delivery catheter, whereby to permit blood flow through the catheter even when the balloon is inflated.

Thereafter, as shown in Fig. 10, balloon 140 may be deflated, whereby to permit continued delivery of gas-rich PFC, removal of waste materials (e.g. C0₂), and the withdrawal of catheter 100 from blood vessel 130.

Significantly, in one preferred form of the present invention, catheter 100 can be placed into a blood vessel and left to dwell there for several minutes before balloon inflation, whereby to permit the tissue downstream of the lesion to be pre-conditioned with a supply of PFC-delivered oxygen. As a result, when the balloon is subsequently inflated, the patient can tolerate "standard" balloon inflation times with less or no pain. In addition, longer periods of balloon inflation can be achieved with less risk of ischemia, less risk of tissue damage, and less risk of arrhythmias that otherwise could result due to hypoxia.

Furthermore, after balloon deflation, the catheter can be maintained in position within the blood vessel so as to continue to deliver oxygen-rich PFC to the

downstream tissue and remove waste materials (e.g. C0₂), so as to extend the therapeutic event.

If desired, balloon 140 (and preferentially a so-called "Rapid Exchange", or stent delivery, balloon) may be omitted from shaft 105 of catheter 100.

Furthermore, and looking now at Fig. 11, porous membrane 110 may be deployed in single or multiple layers substantially anywhere along shaft 105. In the case of a monorail balloon catheter or stent delivery system, the length of the porous membrane may be limited to the opening of the catheter shaft at the point at which the guidewire channel exits. A catheter of this construction may be used solely as a source of oxygen delivery or, alternatively, the catheter may be configured to deliver working tools, including visualization devices and atherectomy devices, to an internal site even as tissue downstream of the site has been, and continues to be, oxygenated by the gas-rich PFC. In another preferred construction of the present invention, porous membrane 110 may be applied to the walls of balloon 140, in order to deliver oxygen (or another gas) directly to the walls of blood vessel 130. See, for example, Figs. 12-16. In this construction, balloon 140 may donate oxygen and/or other gases to the bloodstream prior to balloon inflation, and thereafter topically apply the oxygen and/or other gases to the walls of the blood vessel during balloon inflation.

The present invention may be incorporated in still other embodiments.

Thus, for example, Fig. 17 shows a perspective view of a porous thin film membrane 1 with pores 2, functioning as a flexible porous substrate for a liquid oxygen carrier 3 in accordance with the present invention. An oxygenated perfluorocarbon (PFC) solution is incorporated in the porous substrate and elutes from the porous substrate. The liquid oxygen carrier (i.e., the oxygenated PFC) diffuses freely out of the porous thin film membrane. Studies on the release kinetics of the oxygenated perfluorocarbons (PFCs) from different polymer membranes show that dispersion of the oxygenated perfluorocarbon (PFC) solution from such a membrane into tissue or blood varies between minutes and several hours, depending on the temperature of the environment. Polymers with small pore sizes, preferably of 0.001- 200 microns, produce an effective delivery mechanism for oxygenated

perfluorocarbon (PFC) solutions. The temperature-dependent release feature of the porous membrane may be used for all of the vascular devices described herein such as tubes, balloons, endovascular stents, wires, atherectomy devices, or tissue patches aimed at modifying the oxygen supply to tissues of various body organs. The release kinetics from the substrate can be controlled by injection of fluids of 0-50°C making direct or indirect contact with the porous substrate carrying the oxygenated perfluorocarbon (PFC) solution.

Fig. 18 shows a schematic longitudinal view of a balloon catheter 4, with the porous substrate 6 being tightly connected with the balloon 5, and with the porous substrate being impregnated with the oxygen carrier (i.e., the oxygen-rich PFC solution). The oxygen carrier solution is incorporated into a membrane 7 which is attached to the surface of the balloon. The liquid oxygen carrier is an oxygenated perfluorocarbon (PFC) solution. A "guidewire" lumen 8 allows positioning of the balloon in the artery with a wire. This guidewire may be a flexible wire 25 emitting ionizing radiation 26 from incorporated beta-particle emitters such as Sr-90/Y-90 (strontium/yttrium) or P-32 (phosphorus) or ultraviolet light (UV) waves 27. In the first case, the flexible wire 25 may be partially coated with the beta-particle-emitters 26 and in the latter case, the flexible wire 25 is an ultraviolet light waveguide connected to an ultraviolet light source and having a surface structure within the balloon 5 to radially emit the UV waves 27. The shaft of the catheter 9 includes an inflation channel 10 for inflation of a balloon with fluids or contrast agents to visualize the balloon under fluoroscopy.

Fig. 19 shows a schematic longitudinal view of a perfusion balloon catheter 11 serving as the substrate source 6 for the liquid oxygen carrier (i.e., the oxygenated PFC solution). In this embodiment, the oxygen delivery source membrane 7 is located on the surface of the balloon 5 and proximally 12 and distally 13 to the balloon end of the catheter 11 on the shaft 9 of the catheter. The shaft 9 of the perfusion balloon catheter includes the guidewire lumen 8, a balloon inflation lumen 14, and a perfusion fluid lumen 15. The perfusion fluid lumen 15 allows perfusion of blood or transport of therapeutic fluids (temperature between 0-50 degrees C) through the inflated balloon. The perfusion fluid lumen 15 is designed to allow injection of therapeutic liquids or drugs with temperatures between 0 degrees C and 50 degrees C to modify the release kinetics of the oxygen carrier from the substrate. Holes beyond the proximal end 16 of the balloon connect a pathway for blood through the shaft 9 of the perfusion balloon catheter to the distal end of the catheter 17. The perfusion fluid lumen 15 connects to the holes at the proximal end 16 and distal end 17 of the balloon. The perfusion holes 16, 17 penetrate through the membrane 12, 13 carrying the liquid oxygen carrier (i.e., the PFC solution). Thus, blood perfusion through the balloon carries blood that is oxygenated by the membrane at the proximal end of the inflated balloon and is oxygenated beyond the distal end of the inflated balloon by the membrane after passage through the balloon. The guidewire 25 contains the oxygen carrier 7 at its distal tip 28. A stent 29 is mounted on the deflated balloon 5. Upon inflation of the balloon via its lumen 14, the stent 29 is expanded and deployed into the vessel.

Fig. 20 shows a schematic cross-sectional view of a medical device containing a liquid oxygen delivery source being encompassed by a removable housing sealing off the impregnated source in accordance with the present invention. The oxygen delivery source such as a perfusion balloon catheter 18 with an attached thin film membrane 19 incorporating the oxygen carrier (i.e., the oxygen-rich PFC solution) is placed in a container 21 filled with a liquid oxygen carrier solution 20. The container eliminates any dissipation of liquid or oxygen, and is used as a storage place for the oxygen delivery source. The inner part 22 of the shaft of the perfusion catheter contains a guidewire lumen 23 and perfusion fluid lumen 24 for the perfusion of blood or therapeutic fluids.

Looking next at Fig. 21, there is shown a

medical wire 200. Medical wire 200 may be coronary wire, a guide wire, etc.

Medical wire 200 comprises a shaft 205. At least a portion of shaft 205 comprises a porous membrane 210 for carrying a gas-rich (e.g., oxygen-rich) PFC solution in accordance with the present invention. Porous membrane 210 may be formed as an integral part of shaft 205, or it may be formed as a separate element and secured to shaft 205 in ways well known in the art (e.g., by bonding).

Looking next at Fig. 22, there is shown a medical wire 300. Medical wire 300 may be coronary wire, a guide wire, etc. Medical wire 300 comprises a shaft 305 and a central lumen 310. A porous membrane 315 is disposed within the interior of lumen 310. Porous membrane 315 is preferably in the form of a hollow tube disposed within lumen 310 of medical wire 300. Porous membrane 310 is constructed to carry a gas- rich (e.g., oxygen-rich) PFC solution in accordance with the present invention. Looking next at Fig. 23, there is shown a medical wire 400. Medical wire 400 may be a coronary wire, a guidewire, etc. Medical wire 400 comprises a shaft 405 and a central lumen 410. A porous membrane 415 is disposed within the interior of lumen 410. Porous membrane 415 is preferably in the form of a single body substantially completely filling lumen 410 so as to form a wick-like structure. Porous membrane 415 is constructed so as to carry a gas-rich (e.g., oxygen-rich) PFC solution, and safely dispense the same into the bloodstream without the creation of dangerous embolisms, in accordance with the present invention. Furthermore, because porous membrane 415 is configured to form a wick-like structure within shaft 405 of medical wire 400, porous membrane 415 can be used to transport gas-rich (e.g., oxygen-rich) PFC to the distal tip of medical wire 400, whereupon the gas-rich PFC may be safely released into the bloodstream.

In one preferred construction, and as shown in Fig. 23, porous membrane 415 extends all of the way from the proximal end of medical wire 400 to the distal tip of medical wire 400. In this construction, porous membrane 415 can be pre-loaded with the gas-rich PFC solution prior to deploying the medical wire in the bloodstream of the patient. Alternatively, with this construction, the proximal end of porous membrane 415 can be placed in contact with a reservoir of gas-rich PFC after medical wire 400 has been deployed in the bloodstream of the patient, whereupon porous membrane 415 will "wick" the gas-rich PFC solution from the proximal end of porous membrane 415 to the distal tip of porous membrane 415, where it is released into the bloodstream of the patient.

In another preferred construction, porous membrane 415 extends along only a portion of lumen 410. More particularly, in this alternative construction, porous membrane 415 extends from the distal tip of medical wire 400 back along a portion of the length of lumen 410. In this construction, the gas-rich PFC solution can be introduced into the proximal end of lumen 410 (either before or after medical wire 400 is deployed in the patient), whereupon porous membrane 415 will "wick" the gas-rich PFC solution down the remainder of lumen 410 to the distal tip of porous membrane 415, where it is released into the bloodstream of the patient.

The invention described herein consists of a gas (e.g., 0₂, NO, CO, etc., or a combination of these gases) delivery source for local rescue of ischemic tissue. The invention consists of porous polymer membranes being part of a medical device from which a liquid gas carrier (i.e., the gas-rich PFC) is locally or systemically released. The porous membrane impregnated with the liquid gas carrier may be a part of a tube, a balloon, a perfusion balloon, a stent, and a wire. The porous membrane is preferably sealed with a removable housing to allow storage of the medical device.

Additional Subject Matter

The foregoing discussion discloses, among other things, a system for delivering oxygen and/or other gases to tissue using a gas-rich perfluorocarbon (PFC) solution releasably incorporated into a porous membrane which is disposed on an intravascular device.

The following discusses further aspects of the present invention, including how the porous membrane can be used to deliver additional therapeutic agents (e.g., pharmacological agents) to tissue.

Method And Apparatus For

Releasing A Lipophilic Pharmacological Agent From The Porous Membrane Into The Blood

Additional Background

Pharmacological agents can be easily over-dosed or under-dosed when injected into the bloodstream to treat arteriosclerosis and/or other forms of coronary artery disease. Over-dosing may result in toxic reactions of a non-target organ, potentially leading to organ failure. Under-dosing may result in a limited drug response or no response, which may lead to the progression of the disease with no beneficial therapeutic effects. Under-dosing easily occurs when the pharmacological agent is injected into the patient's bloodstream and the agent is then diluted as it passes into side branches of the circulatory system. This prevents the pharmacological agent from reaching the target area with a sufficient dosage for the desired therapeutic effect.

Many researchers have previously studied the mechanism of the restenotic process after percutaneous coronary interventions (PCI). The major step by which restenosis (i.e., the repeated narrowing of a vessel lumen) occurs is a repair stimulus of the vascular injury induced during the re-opening of an artery, for instance by means of a balloon inflation. Significantly, after a PCI procedure, the injured vessel wall is more susceptible to the intrusion of pharmacologically active agents than a non- injured vessel wall. Thus, it is not surprising that, after a PCI procedure, the mere injection of a pharmacological agent into the bloodstream can reduce restenosis rates.

Recently, Albrecht et al. published a paper (Invest. Radiol. 2007; 42: 579-585) indicating that the injection of a mixture of the pharmacologically active agent paclitaxel and a contrast agent prevented restenosis after a PCI procedure in pigs. A mixture of contrast agent with paclitaxel was also disclosed in a publication by Speck et al. (ES2289721T). However, under-dosing in the target area, and over-dosing in the non-target area (e.g., the remaining organs of a body), is likely to occur because the injection is systemic and does not limit the therapeutic effect of the drug to only the target area. Therefore, the systemic injection of a pharmacological agent into the circulatory system of the patient is not the preferred method of therapy to prevent restenosis.

Scheller et al. disclosed a paclitaxel-coated balloon (EP Patent No. 1857127). This system is intended to restrict drug delivery to the target area. However, it has been found that particles of the drug coating can be mechanically scraped off the balloon during advancement of the drug-coated balloon through a tight stenosis (i.e., lumen narrowing). In a recent publication discussing use of the Scheller drug-coated balloon in clinical applications, it was shown that only 20% of the paclitaxel mounted on the balloon surface was actually taken up by the target vessel wall. Thus, a disadvantage of the Scheller approach is the significant loss of the therapeutic drug during advancement of the balloon to the target lesion. This can result in under- dosage of the desired drug.

Dornmke et al. published a technique for enhancing the local concentration of a pharmacological agent in blood for the reduction of restenosis (Thromb. Haemost. 2007; 98:674-680). The Dornmke device employed two balloons to occlude the vessel on either side of the treated restenosis zone, with the pharmacological agent being injected out of the catheter and into the treatment zone between the two inflated balloons. Although this device increases the local concentration of the

pharmacological agent in the bloodstream at the target area, it can cause ischemia due to the vessel occlusion from the two balloons. Therefore, the device disclosed by Dornmke, while capable of reducing restenosis rates, is not desirable due to the occurrence of ischemia of the heart.

Intravascular Device Utilizing Porous Membrane For Controlled Delivery Of

Therapeutic Agents To Tissue

The present invention provides a novel method and apparatus for the controlled delivery of therapeutic agents (e.g., pharmacological agents) in an intravascular approach so as to treat coronary artery disease, among other disorders. In the coronary artery disease application, the novel method and apparatus is configured to achieve regression of the size of arteriosclerotic plaques and to prevent restenosis after percutaneous coronary interventions (PCI), including angioplasty. Moreover, the novel device (i.e., catheter) is preferably specifically designed for local drug treatment of multiple atherosclerotic lesions along the vasculature, e.g., along the length of an injured vessel, during one single drug application procedure. The novel catheter may also be configured so that it can be used as a stent delivery system by which the stent is placed to complete any type of catheter revascularization of a stenotic artery. In one preferred construction, the porous membrane is disposed proximal to the stent-setting balloon. After the stent has been placed, the catheter is moved distally into the periphery of the vascular bed, so that the porous membrane is disposed substantially adjacent to the just-placed stent or just upstream of the just-placed stent, and then the catheter remains in this position within the vessel for 2-20 minutes in order to allow complete drug elution from the porous membrane into the bloodstream and the vessel wall.

The method and apparatus of the present invention is preferably also configured to facilitate the introduction of a therapeutic agent (e.g., a pharmacological agent) into the bloodstream so that it will reach the target area of blood vessel with the desired dosage and without creating a temporary vessel occlusion, whereby to reduce ischemia of downstream organs.

In one preferred form of the present invention, the apparatus comprises an intravascular device (e.g., a catheter) which includes a porous membrane which incorporates a lipophilic pharmacological agent such that the application of mechanical stress to the intravascular device does not easily remove the

pharmacological agent from the porous membrane. Thus, with this form of the invention, the catheter can move through tight spaces within the vascular system of the patient without concern that the lipophilic pharmacological agent will be mechanically "stripped off the catheter due to engagement of the porous membrane with the side walls of the blood vessels.

In this form of the invention, the porous membrane is a membrane of the type disclosed above, except that it is adapted to release a lipophilic pharmacological agent instead of the gas-rich perfluorocarbon (PFC) solution (which is also highly lipophilic). To this end, the porous membrane is formed with an appropriate porosity such that, for the particular pharmacological agent which is to be delivered, the rate of elution of the pharmacological agent from the porous membrane matches the desired rate of dosage for the pharmacological agent. The intravascular device is preferably configured to remain in the blood vessel for a period of about 2-20 minutes to release the desired amount of the lipophilic pharmacological agent to the target area, e.g., the site of a previous PCI injury, with the lipophilic pharmacological agent preferably being released exclusively from the porous membrane carried by the catheter.

In one form of the present invention, the porous membrane may be disposed on the catheter shaft but not on the surface of the balloon. In another form of the present invention, the porous membrane may be disposed on both the catheter shaft and on the balloon surface. In other words, the surface of the balloon may or may not comprise a porous membrane, as desired. It is even possible that the porous membrane may be provided on the balloon without being provided on the catheter shaft. However, in this respect it should be appreciated that it is generally preferred to place the porous membrane on at least the catheter shaft in order to incorporate and deliver a sufficient dose of the pharmacological agent.

The porous surface (i.e., porous membrane) may be part of any catheter construction as long as the porous membrane is present to bind the lipophilic pharmacological agents by London Forces.

The length of the porous membrane coating disposed on the catheter shaft may vary in accordance with various factors, e.g., the length of the vessel which is to be treated by local drug delivery, the dose of the pharmacological agent which is desired, etc.

The catheter shaft may consist of a multi-layer of different porous membrane polymers to increase the amount of uploaded and releasable drug. In other words, the porous membrane may be formed as a series of layers, one on top of another, and each of the layers may be formed out of identical or different polymers, and/or each of the layers may have different thicknesses, and/or each of the layers may have different porosities, etc. In the situation where a coronary artery is to be treated, the length of the catheter shaft coating (i.e., porous membrane) may be, by way of example, 3-12 cm, according to the length of the diseased coronary artery. Alternatively, other lengths of porous membrane may be used. In the situation where a peripheral artery is to be treated, the length of the catheter shaft coating (which delivers the lipophilic drug) may vary, by way of example, between 5 and 60 cm. Alternatively, other lengths of porous membrane may be used.

The kinetics by which the lipophilic drug is released from the porous catheter surface depend on the porosity of the porous membrane and the nature of the lipophilic pharmacological agent. The kinetics by which the lipophilic drug is delivered to tissue depend on the blood flow characteristics around the catheter. In other words, a distinction should be recognized between (i) the rate of drug release from the catheter (which is governed by the London Forces reversibly binding the lipophilic drug to the pores of the porous membrane), and (ii) the rate of drug distribution to the tissue (which is governed by blood flow). Thus, by way of example, the greater the blood flow around the porous membrane, the greater the rate of distribution of the eluted drugs to the tissue. Additionally, if the blood flow around the catheter is turbulent, then the lipophilic drug (released from the porous membrane) is distributed more rapidly, e.g., within minutes after the catheter enters the bloodstream. If the porous membrane section of the catheter is withdrawn into a guiding catheter, the release of the lipophilic drug from the porous surface is slowed down because blood flow is reduced while a portion of the porous membrane or all of the porous membrane resides within the tube of the guiding catheter. Therefore, and significantly, the release of the lipophilic pharmaceutical agent can be modified by pushing the porous membrane section of the catheter out of a guiding catheter into the bloodstream and pulling it back into the guiding catheter.

The release of the lipophilic drug from the porous membrane can be further modified by injecting fluids into the guiding catheter while all or a portion of the porous membrane section is located within the tube of the guiding catheter. If these fluids reduce the environmental temperature around the porous membrane section of the catheter, the lipophilic drug will remain longer in the pores of the substrate.

However, when the temperature is increased around the porous membrane section of the catheter, then the release of the lipophilic drug will be increased.

In another embodiment of this invention, the porous membrane may be located on the surface of the balloon of a balloon catheter. This porous membrane may be configured as a multi-layer of polymers so as to increase the amount of drug to be uploaded and delivered. When the porous membrane is placed on the balloon, and when the balloon is thereafter inflated, the porous membrane is stretched and the pores of the substrate change their conformity and configuration. This change in pore size of the substrate provokes changes in the adhesion of the London Forces that reversibly bind the lipophlic drug to the pores of the substrate, and hence the drug is released more quickly from the porous membrane into the blood stream. In this respect it should be appreciated that increased lipophilic drug elution is due to London Forces, not mechanical ejection.

If the lipophilic drug is brought into close contact with the injured vessel wall, then the blood-borne elements (e.g., blood substitutes like leucocytes, macrophages) transport the drug into the vessel wall to support the healing process. Blood borne elements carry important information to start repair mechanisms and blood cascades. By way of example but not limitation, blood borne elements are responsible for and able to drive the growth factor movement from the blood borne elements to the tissue. Thus, the movement of the growth factors of the blood-borne elements which enter the vessel wall and start re-establishing regeneration of the lacerated tissue will also drag the lipophilic drug into the vessel wall. Since liphophilic drugs are known to be easily taken up by human cells, the action of the drug is uniform in the vessel wall and yet localized to the site of vessel injury. Preferred Constructions

In the preferred forms of the present invention, the apparatus comprises an intravascular device (e.g., a catheter) which includes a porous membrane which incorporates a lipophilic pharmacological agent. The porous membrane is of the type disclosed above, except that it is adapted for the controlled release of the lipophilic pharmacological agent instead of the gas-rich perfluorocarbon (PFC) solution. To this end, the porous membrane is formed with an appropriate porosity such that, for the particular pharmacological agent which is to be delivered, the rate of elution of the pharmacological agent from the porous membrane matches the desired rate of dosage for the pharmacological agent.

More particularly, a porous device surface (e.g., a porous membrane carried on a catheter surface) incorporates a lipophilic pharmacological agent and binds the substance reversibly to the porous membrane by the same London forces described above with respect to PFC. The lipophilic pharmacological agent may be a statin (such a simastatin, cerivastatin, lovastatin, pravastatin, etc.), a mitose-inhibiter such as paclitaxel, or an immunosuppressant such as sirolimus, tacrolimus, pimecrolimus, zotarolimus, etc. The rate of release of the lipophilic pharmacological agent from the porous membrane into the bloodstream is controlled by the pore size of the porous membrane. More specifically, the rate of release of the lipophilic pharmacological agent from the porous membrane is regulated by substantially the same release mechanisms discussed above with respect to PFC, except that the pore size is instead coordinated with the characteristics of the specific lipophilic pharmacological agent in order to achieve the desired rate of release, which is preferably in the range between

The rate of release of the pharmacological agent from the porous membrane may also be affected by temperature and/or the local fluid dynamics surrounding the porous membrane. Thus, the intravascular device may also include structure for modifying temperature (e.g., a heated or cooled fluid flush) and/or modifying local fluid dynamics (e.g., a chemically-influencing fluid solution).

The porous construction of the membrane carried by the intravascular device incorporates the pharmacological agent in such a way that the agent cannot be dislodged, or otherwise lost, from the intravascular device due to engagement with vascular structure (e.g., when moved through small diameter vessels and/or a tight stenosis). The profile of the intravascular device with porous membrane preferentially is sized to enable placement of the porous membrane in close proximity to the location of the vessel wall that has been treated during the PCI procedure.

In one preferred construction, the intravascular device comprises a balloon catheter, with the porous membrane being disposed distal to, or proximal to, the balloon. After treatment (balloon inflation) of a stenosis, the uncoated balloon portion of the catheter is moved distal to the area of the vessel which has been treated. The treatment of stenosis (PCI) can be repeated several times and can be combined with a stent implantation. After the PCI procedure has been completed, however, the catheter is not removed from the body. The deflated balloon portion of the catheter is located more proximally, beyond the treated area of the blood vessel, allowing the porous membrane, which is located distal to the balloon, to reside in closer proximity to the treated vessel wall tissue. The catheter remains temporarily within the bloodstream in the vessel for about 2-20 minutes. During this time, the

pharmacological agent elutes from the porous membrane at the appropriate rate of release and makes its way downstream to the treated tissue. Significantly, the balloon of the catheter remains deflated during this local drug delivery. Since the balloon typically is inflated during PCI under high atmospheric pressure (often multiple times), it is stretched and thus increases its natural profile while dilating the vessel wall. Thus used, the higher-profile balloon helps reduce blood flow proximally of the target area (i.e., the site of the previous PCI procedure). In other words, the increased profile of the deflated balloon on the catheter reduces blood flow in the target area or areas of the previous PCI procedure, without completely occluding the vessel and obstructing blood flow. This reduction in blood flow is sufficient for the

pharmacological agent to elute from the porous membrane and dwell in the target area of the previous PCI procedure (i.e., the site or sites of the vessel injury), which enhances absorption of the lipophilic drug by the injured vessel wall while the catheter is indwelling during the above mentioned 2-20 minute time period. Importantly, this preferred construction does not require inflating a balloon at the site of the vessel injury to a diameter greater than the inner diameter of the vessel, thus having to directly contact the vessel wall in order to "press" or "push" the drug into the vessel wall. This is a significant advantage of this preferred construction, since (i) it eliminates the risk of further vessel wall injury from additional balloon dilatation, or dilatations, for the purposes of drug delivery, especially when predilatation with regular PCI balloon catheters (i.e., balloon catheters without drug delivery capabilities) is performed at the lesion site(s), (ii) less precision is required for catheter placement compared to drug eluting balloons, which must be carefully positioned to avoid missing the target site, (iii) there is less risk of ischemia and/or arrhythmias since balloon inflation is avoided and therefore the blood vessel is not occluded during drug delivery, (iv) a single catheter incorporating a standard balloon and the porous membrane can treat multiple lesion sites that are located proximal to the deflated balloon and in close proximity to and/or downstream from the membrane, and (v) the porous membrane can be constructed to deliver a wider range of types of drugs and/or drug delivery rates and dosages.

Example 1

First, the lipophilic pharmacological agent is dissolved in alcohol (e.g., methanol). Then, the alcohol-pharmacological agent mixture is incorporated in the porous membrane by dipping or immersing the intravascular device, or, alternatively, the portion of the intravascular device incorporating the porous membrane, into the mixture of alcohol and pharmacological agent. Thereafter, the intravascular device, or the portion incorporating the porous membrane, is removed from the mixture and air- dried so as to allow the alcohol to dissipate from the porous membrane. At this point, only the lipophilic pharmacological agent remains in the pores of the porous membrane. The rate and quantity of the uptake of the lipophilic pharmacological agent into the porous membrane depends upon (i) the pore size of the porous membrane, (ii) the concentration of the pharmacological agent in the mixture, and (iii) the molecular weight of the pharmacological agent. Once the porous membrane is loaded with lipophilic pharamacological agent, the intravascular device is packaged, sterilized and subsequently stored at room temperature (21°C) until clinical use.

Alternatively, the porous membrane may be loaded with the aforementioned alcohol- lipophilic pharmaceutical agent mixture after the intravascular device incorporating the porous membrane is packaged and sterilized. In this case, the sterilized intravascular device incorporating the porous membrane may be removed from its packaging using a standard sterile technique. The porous membrane may then be immersed or dipped one or more times into the aforementioned alcohol-lipophilic pharmaceutical agent mixture in order to load the porous membrane immediately prior to clinical use.

When the intravascular device enters the bloodstream, the pharmacological agent begins to elute from the porous membrane.

Significantly, since the bloodstream is at body temperature (37° C), the difference in temperatures between the porous membrane and the bloodstream increases the rate of release of the pharmacological agent from the porous membrane.

A further increase in temperature from 37°C to 40°C can further increase the rate of release of the pharmacological agent into the bloodstream.

In a preferred approach, the pharmaceutical agent is carried downstream from the porous membrane to the target treatment area of the vessel prior to performing a percutaneous coronary intervention (PCI). In this case, blood flow is reduced by the narrowed vessel at the site of the untreated lesion. This reduction of blood flow results in greater dwell time of the released pharmaceutical agent at the target treatment area prior to PCI balloon dilatation, thus allowing the pharmaceutical agent to penetrate the tissue and therefore pre-treat the target tissue prior to balloon inflation and/or stent delivery. Then, the interventional device may be advanced within the blood vessel to the point where the balloon on the interventional device is placed across the lesion. The balloon may then be inflated to dilate the lesion to restore more normal blood flow.

Upon deflation of the balloon, the interventional device may thereafter be further advanced within the blood vessel past the treatment area. As described above, the now-enlarged deflated balloon serves to restrict the flow of blood carrying the pharmaceutical agent to allow further penetration of the pharmaceutical agent into the treated target tissue.

It should be appreciated that the present invention allows pre-PCI and/or post- PCI drug delivery using a single interventional device without totally occluding the blood vessel during therapeutic drug delivery, thus significantly reducing the perioperative risks of ischemia, arrhythmias, or myocardial infarction during therapeutic drug delivery.

Example 2

As noted above, the intravascular device may be configured to comprise structure for modifying local fluid dynamics. More particularly, the intravascular device may be surrounded with a tube or guiding catheter filled with a modulating fluid which can be used to modify local fluid dynamics.

At the target area, the fluid may be injected from the intravascular device through the surrounding tube and into the bloodstream. The injection of this modulating fluid at the site of the treated vessel changes the fluid dynamics surrounding the porous membrane and therefore increases the rate of release of the lipophilic pharmacological agent into the bloodstream.

Medical Wire

Looking next at Fig. 24, there is shown a novel medical wire 500 formed in accordance with the present invention. Novel medical wire 500 may be any type of medical wire for use in the body, where the wire should be thin and have substantial flexibility at its distal end, a lesser degree of flexibility in its midsection, and a least degree of flexibility at its proximal end. By way of example but not limitation, medical wire 500 may be a coronary wire, a guide wire, etc.

Novel medical wire 500 may be used for traditional, wire-based purposes (e.g., as a coronary wire for advancement across a coronary lesion, as a guide wire for guiding the delivery of other devices to a remote site within the body, etc.), and/or novel medical wire 500 may also be provided with a porous membrane of the sort disclosed above, in which case the novel medical wire may also be used to deliver a substance (e.g., a gas-rich perfluorocarbon (PFC) solution, a lipophilic

pharmacological agent, a liquid compound, etc.) to the body, with the substance being delivered to the body via the carefully controlled release mechanism discussed above.

More particularly, and looking now at Fig. 24, medical wire 500 generally comprises a distal section 505 terminating in a distal end 510, an intermediate section 515, and a proximal section 520 terminating in proximal end 525. Medical wire 500 preferably also comprises inner lumen 540 beginning at distal end 510, extending through intermediate section 515 and terminating at proximal end 525. Distal section 505 is configured so as to have a substantial degree of flexibility, intermediate section 515 is configured so as to have a lesser degree of flexibility, and proximal section 520 is configured so as to have a least degree of flexibility. In one preferred form of the invention, distal section 505 is approximately 7 cm long, intermediate section 515 is approximately 30-40 cm long, and proximal section 520 is approximately 160 cm long.

In one preferred form of the invention, medical wire 500 is formed out of a single piece of hypotube, with various sections of the hypotube being worked differently so as to provide each of the sections with a different, desired degree of flexibility. In one preferred form of the invention, medical wire 500 is formed out of a hypotube having an outer diameter of approximately 0.35 mm and in inner diameter of approximately 0.1 mm. This is in marked contrast to conventional hypotubes, which traditionally have an outer diameter of 0.352 mm and an inner diameter of 0.22 mm.

As noted above, distal section 505 of medical wire 500 is configured so as to have the greatest degree of flexibility and, to this end, distal section 505 is preferably laser cut so as to introduce the desired high degree of flexibility into this region of the medical wire. In one preferred form of the invention, and looking now at Fig. 25, a helical laser cut 530 is made in the outer surface of the hypotube, with the helical laser cut being in the form of a surface groove. This surface groove reduces the strength of the side wall of the hypotube so as to increase flexibility in distal section 505 to the extent desired. In another preferred form of the present invention, helical laser cut 530 extends completely through the side wall of medical wire 500, which effectively transforms distal section 505 of the medical wire into a spring-like structure with a high degree of flexibility.

Intermediate section 515 is generally desired to have a lesser degree of flexibility than distal section 505. To this end, intermediate section 515 is preferably laser cut so as to introduce the desired degree of flexibility into this region of the medical wire. In one preferred form of the invention, and looking now at Fig. 26, a helical laser cut 535 is made in the outer surface of the hypotube, with helical laser cut 535 being in the form of a surface groove. Again, this surface groove reduces the strength of the side wall of the hypotube so as to increase flexibility in intermediate section 515 to the extent desired. However, in order to introduce less flexibility into intermediate section 515 than is introduced into distal section 505, helical laser cut 535 is preferably different than helical laser cut 530, e.g., helical laser cut 535 is shallower than helical laser cut 530, and/or helical laser cut 535 has a larger period than helical laser cut 530, and/or helical laser cut 535 has a narrower swath than helical laser cut 530, etc.

Proximal section 520 preferably has the least degree of flexibility and so, to this end, the hypotube is preferably left intact, without any surface modification in this area of the medical wire. See Fig. 27.

As a result of this construction, medical wire 500 has a highly flexible distal section 505, a less flexible intermediate section 515 and a least flexible proximal section 520. Accordingly, distal section 505 can act as an atraumatic leading tip when medical wire 500 is advanced through the vascular system of the patient, intermediate section 515 can accommodate the substantial bends which must frequently be traversed within the vascular system of the patient, and proximal section 520 can provide the structure and support needed to advance the medical wire through the vascular system of the patient.

Novel medical wire 500 may be used for traditional, wire-based and/or catheter-based procedures (e.g., as a coronary wire, as a neuroradiology wire, as a guide wire, etc.). Additionally, since novel medical wire 500 is preferably formed out of a hypotube, the inner lumen 540 (Figs. 24-27) of the medical wire may also be used as a passageway to pass fluids to tissue, e.g., medical wire 500 may be used as a perfusion wire to deliver pharmacological agents, such as clot-dissolving drugs, liquid compounds, or other fluids or fluid/gas mixtures through its inner lumen. Where inner lumen 540 of medical wire 500 is to be used to pass fluids down the length of the medical wire, it may be desirable to push the fluid through the lumen under pressure so as to facilitate and/or enable fluid passage. By way of example but not limitation, the fluid may be pushed at a pressure similar to that used to inflate an angioplasty balloon. In one preferred form of the invention, fluid may be pushed through inner lumen 540 of medical wire 500 at a pressure of about 20 atmospheres.

Where it is desired to deliver a substance (e.g., a gas-rich perfluorocarbon (PFC) solution, a lipophilic pharmacological agent, etc.) to the body using the carefully controlled porous membrane release mechanism discussed above, novel medical wire 500 may be provided with a porous membrane for loading with the substance (e.g., the gas-rich perfluorocarbon (PFC) solution, the lipophilic

pharmacological agent, etc.) which is to be delivered to the body.

More particularly, medical wire 500 may be provided with a porous membrane secured to the outer surface of some or all of its distal section 505 and/or its intermediate section 515. See, for example, Fig. 28, where porous membrane 545 is shown secured to the outside surface of some or all of intermediate section 515; and see also, for example, Fig. 29, where porous membrane is shown disposed within the inner lumen 540 of medical wire 500 (the porous membrane may completely fill some or all of the inner lumen as shown, or the porous membrane may simply line some or all of the side wall of the inner lumen). In this form of the invention, all or a desirable portion of medical wire 500 is immersed into the substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) which is to be delivered to the body so that the substance is loaded into porous membrane 545, and then medical wire 500 is deployed in the body so that the porous membrane is exposed to body fluids, whereupon the porous membrane acts as a controlled release mechanism for eluting the substance into the body in the manner previously disclosed. In this respect it should also be appreciated that if portions of porous membrane 545 are deployed within the lumen of an intravascular catheter (e.g. a guiding catheter), physiologic fluids (e.g. saline, plasma, etc.) may be delivered through the lumen of the

intravascular catheter, thus releasing the substance loaded into the porous membrane into such physiologic fluids and subsequently into the bloodstream of the patient. Alternatively, blood may be aspirated into the lumen of the intravascular catheter, e.g., by drawing the patient's blood, or blood combined with saline, up into the catheter. This approach causes the substance to be released from the porous membrane into the intralumenal blood, or blood-saline solution, which is then flushed with saline as may be required so as to deliver the blood or blood-saline solution (carrying the substance released from the porous membrane) into the bloodstream of the patient.

It should be appreciated that, when using a porous membrane to deliver oxygen-rich perfluorocarbon (PFC) solutions to the body, it can be desirable to use physiologic fluids (e.g., saline, plasma, etc.) to elute the oxygen-rich PFC from the porous membrane, since such physiologic fluids are capable of reaching down to the microcirculatory regions of the body, such as the capillaries in the heart (where the oxygen is released from the PFC particles) and then into the oxygen-deprived cells, which are the intended recipients of the oxygen. In this respect it will also be appreciated that the relatively flexible red blood cells can normally twist and turn their way into the microcapillaries of the circulatory system, but diseased microcapillaries may be too constricted for the red blood cells to pass, thereby starving the tissue of oxygen. Therefore, delivering the oxygen-rich PFC solution with a physiologic fluid (e.g., saline or plasma) allows the nanoparticle- sized PFC to enter even the diseased microcapillaries and deliver the much-needed oxygen to the tissues. In this respect it will also be appreciated that oxygen-carrying PFC molecules are substantially smaller than red blood cells but carry proportionally greater amounts of oxygen, thereby enabling extremely efficient and effective oxygenation of downstream tissues.

As noted above, and looking now at Fig. 29, medical wire 500 may be provided with a porous membrane 545 which is disposed within the inner lumen 540 of the hypotube. Porous membrane 545 may extend all the way down to distal end 510 of medical wire 500, or it may terminate short of distal end 510, e.g., porous membrane 545 may terminate at the distal end of intermediate section 515, as shown in Fig. 29. In this respect it should be appreciated that porous membrane 545 may be loaded into inner lumen 540 of the hypotube by first passing a thin wire (not shown) through the inner lumen of the hypotube, and then using that thin wire to pull (or "tow") porous membrane 545 into position within inner lumen 540 of the hypotube. In this form of the invention, the proximal end of porous membrane 545 is preferably placed into contact with a supply of the substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) which is to be delivered to the patient, so that the substance is loaded into porous membrane 545 via a wicking action. Thereafter, medical wire 500 is deployed in the body so that the porous membrane is exposed to body fluids, whereupon the porous membrane provides a controlled release mechanism for eluting the substance into the body in the manner previously disclosed (i.e., through the tip of the wire or through laser-formed openings along the side of the wire— note that the laser-formed openings not shown in Fig. 29). Alternatively, the substance may be eluted from the porous membrane by aspirating the patient's blood, or blood diluted with saline, into the medical wire and then ejecting it back out, e.g., with a saline push. Or the substance may be eluted out of the porous membrane by running an intermittent or continuous saline flush through lumen 540, which may be facilitated by applying a small amount of pressure through the saline flush line.

In another preferred construction, and looking now at Fig. 30, distal section 505 of medical wire 500 may be formed by (i) grinding down (or otherwise removing) sections of the hypotube so as to leave a strut 550 extending distally of intermediate portion 515, and (ii) securing (e.g., by welding) a helical spring 555 to strut 550 (and, optionally, securing one end of helical spring 555 to intermediate portion 515). This construction provides medical wire 500 with a distal section 505 which has the requisite flexibility characteristics. Again, a porous membrane (not shown in Fig. 30) may be added to the outside of the medical wire 500 shown in Fig. 30, and/or disposed within the inner lumen 540 of the medical wire 500 shown in Fig. 30, so as to elute a desired substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) into the body using the aforementioned porous membrane release mechanism. Alternatively, and still looking now at Fig. 30, distal section 505 may be formed by terminating the hypotube at the distal end of intermediate section 515, and welding (or otherwise securing) a strut 550 to the distal end of intermediate section 515. Helical spring 555 may then be secured to strut 550 (and, optionally, to intermediate section 515) in the manner discussed above. Again, this construction provides a distal section 505 which has the requisite flexibility characteristics.

Furthermore, and looking now at Fig. 31, distal section 505 may be formed by terminating the hypotube at the distal end of intermediate section 515, and then securing (by welding, crimping, etc.) a strut 550 within inner lumen 540. Helical spring 555 may then be secured to strut 550 (and, optionally, to intermediate section 515) in the manner discussed above. This construction provides a distal section 505 which has the requisite flexibility characteristics. Again, a porous membrane (not shown in Fig. 31) may be added to the outside of the medical wire 500 shown in Fig. 31, and/or disposed within the inner lumen 540 of the medical wire 500 shown in Fig. 31, so as to elute a desired substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) into the body using the aforementioned porous membrane release mechanism.

And in another preferred form of the present invention, and looking now at Fig. 32, distal section 505 of medical wire 500 may be formed by terminating the hypotube at the distal end of intermediate section 515, and securing (e.g., by welding, etc.) a helical spring 555 to the distal end of intermediate section 515. This construction provides a distal section 505 which has the requisite flexibility characteristics. Again, a porous membrane (not shown in Fig. 32) may be added to the outside of the medical wire 500 shown in Fig. 32, and/or disposed within the inner lumen 540 of the medical wire 500 shown in Fig. 32, so as to elute a desired substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) into the body using the aforementioned porous membrane release mechanism. In yet another preferred form of the invention, and looking now at Fig. 33, medical wire 500 may be formed with a tapered construction so as to provide the various sections of the medical wire with the desired degrees of flexibility. More particularly, the medical wire 500 shown in Fig. 33 is formed with a tapered outer wall, reducing in thickness as it progresses in the distal direction, whereby to provide the desired degrees of flexibility to the distal, intermediate and proximal sections of the medical wire. Such a tapered construction is highly advantageous since it provides "pushability" (i.e., enabling advancement of the wire through the vasculature) plus flexibility - the thicker proximal end provides the column strength desired for pushability, the thinner distal end provides the flexibility needed for atraumatic wire advancement. In one preferred form of the present invention, medical wire 500 comprises a tapered hypotube having an outer diameter of approximately 0.35 mm at its proximal end 510 and an outer diameter of approximately 0.18 mm at its distal end, and a constant inner diameter of approximately 0.1 mm along its length. In this respect it should be noted that conventional hypotubes traditionally have an outer diameter of 0.352 mm and an inner diameter of 0.22 mm. Thus, the present use of an inner diameter of approximately 0.1 mm is important, because this uniquely small inner diameter allows for larger distal wall thickness, which in turn allows tapering from a larger proximal outer diameter towards a smaller distal outer diameter throughout the length of the wire. With a conventional inner diameter of 0.22 mm, it would not be possible to taper the hypotube down to an outer diameter at the distal end that would be flexible enough for safe clinical use. This approach also allows for a controlled production of the hypotube. Again, a porous membrane (not shown in Fig. 33) may be added to the outside of the medical wire 500 shown in Fig. 33, and/or disposed within the inner lumen 540 of the medical wire 500 shown in Fig. 33, so as to elute a desired substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) into the body using the aforementioned porous membrane release mechanism. In another preferred form of the invention, intermediate section 515 has an outer diameter which tapers downward; a distal section 505 which is integral with, and flush, with the distal end of intermediate section 515; proximal section 520 which is integral with, and flush with, the proximal end of intermediate section 515; and the entire medical wire has a constant inner diameter. By way of example but not limitation, proximal section 520 can have a constant outer diameter of 0.35 mm, intermediate section 515 can taper downward from an outer diameter of 0.35 mm at its proximal end to an outer diameter of 0.18 mm at its distal end, distal section 505 can have a constant outer diameter of 0.18 mm, and the entire medical wire 500 can have a constant inner diameter of 0.1 mm. Furthermore, distal section 505 can be formed with or without helical laser cuts to provide a desired degree of flexibility, or distal section 505 can be formed with another distal tip construction, e.g., one such as is disclosed in Figs. 30-32.

Looking next at Fig. 34, there is shown another medical wire 500 also formed in accordance with the present invention. The medical wire 500 shown in Fig. 34 is generally similar to the medical wire 500 shown in Fig. 30, except that helical spring 555 is replaced with a tip 560. Tip 560 comprises a flexible, atraumatic structure formed out of a radio-opaque material, e.g., platinum, stainless steel, etc. Again, a porous membrane (not shown in Fig. 34) may be added to the outside of the medical wire 500 shown in Fig. 34, and/or disposed within the inner lumen 540 of the medical wire 500 shown in Fig. 34, so as to elute a desired substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) into the body using the

aforementioned porous membrane release mechanism.

Looking next at Fig. 35, there is shown still another medical wire 500 also formed in accordance with the present invention. The medical wire shown in Fig. 35 is generally similar to the medical wire 500 shown in Fig. 30, except that helical spring strut 550 is omitted, helical spring 555 is secured directly to intermediate section 515, and a hydrophilic coating 565 is disposed along a portion of the medical wire. Preferably, helical spring 555 tapers downward along its length so as to provide a reduced distal profile. It should be appreciated that in this form of the invention, the helical laser cuts 535 extend completely through the side wall of intermediate section 515 for at least a portion of the length of intermediate section 515, so that fluid passing down the center lumen of medical wire 500 is allowed to flow through the laser- formed section proximal to tip 555, as well as through the side of spiral tip 555.

However, hydrophilic coating 565 prevents fluid from flowing through the helical laser cuts 535 formed in the side wall of the medical wire. And again, a porous membrane (not shown in Fig. 34) may be added to the outside of the medical wire 500 shown in Fig. 34, and/or disposed within the inner lumen 540 of the medical wire 500 shown in Fig. 34, so as to elute a desired substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) into the body using the aforementioned porous membrane release mechanism.

Looking next at Figs. 36 and 37, there is shown still another medical wire 500 formed in accordance with the present invention. The medical wire 500 shown in Figs. 36 and 37 is generally similar to the medical wire 500 shown in Fig. 35, except that helical spring 555 is covered with a porous membrane 570, and hydrophilic coating 565 extends substantially all the way along the medical wire except for the region covered by porous membrane 570. Another porous membrane (not shown in Figs. 36 and 37) may also be disposed within the inner lumen of the medical wire 500 shown in Figs. 36 and 37. Again, these porous membranes can be used to elute a desired substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) into the body using the aforementioned porous membrane release mechanism.

Looking next at Figs. 38 and 39, there is shown yet another medical wire 500 formed in accordance with the present invention. The medical wire 500 shown in Figs. 38 and 39 is generally similar to the medical wire 500 shown in Figs. 36 and 37, except that a plug 575 is disposed within the inner lumen of the medical wire just proximal to the tapered tip. As a result of this construction, fluid passing down the inner lumen 540 of the medical wire cannot flow out the distal end of the medical wire, although it can flow through the helical laser cuts 535 formed in the side wall of the medical wire, and then through the porous membrane secured to the outside of the medical wire, before entering the body. Another porous membrane (not shown in Figs. 36 and 37) may also be disposed within the inner lumen of the medical wire 500 shown in Figs. 36 and 37. Again, these porous membranes can be used to elute a desired substance (e.g., a gas-rich PFC solution, a lipophilic pharmacological agent, etc.) into the body using the aforementioned porous membrane release mechanism.

Additional Subject Matter

The foregoing discussion discloses, among other things, a method and apparatus for delivering oxygen and/or other gases to tissue using a gas-rich perfluorocarbon (PFC) solution releasably carried by a porous membrane which is disposed on an intravascular device, and a method and apparatus for releasing a lipophilic pharmacological agent from a porous membrane into the blood.

The following discusses additional inventive concepts, including how the porous membrane and PFC solution can be used to extracorporeally hyperoxygenate blood (or blood components such as blood plasma) for delivery to tissue, e.g., brain tissue.

Method And Apparatus For Extracorporeally Hyperoxygenating Blood For Delivery

To Tissue

Additional Background

More than 14 million people worldwide suffer from ischemic strokes. An ischemic stroke is typically caused by one or more cerebral artery blockages resulting from blood clots or other emboli that restrict the supply of oxygenated blood to the areas of the brain distal to the blockage. Drugs such as tPA can be delivered to the affected artery by intravenous injection and/or via an intra-arterial (IA) catheter in order to dissolve the clot.

Another technique for clot removal is catheter-mediated clot retrieval. This is an endovascular approach in which the physician aspirates or extracts the blood clot into the lumen of the retrieval catheter or, alternatively, into a microcatheter, thereby removing the blood clot from the artery and restoring the flow of oxygenated blood to downstream portions of the brain.

However, arterial recanalization via endovascular procedures does not always provide the desired clinical results. More particularly, during intra-arterial (IA) procedures, microcatheter access to the blood clot, and to the distal vasculature beyond the occluding clot, is usually achieved within minutes of the start of the procedure. However, the time necessary to achieve arterial recanalization (either with IA-tpa or mechanical clot retrievers) is usually much longer, which can delay reperfusion of the brain tissue which is distal to the blockage (and hence subject to oxygen deprivation).

Until normal blood flow is restored, the tissue distal to the blockage is at serious risk of oxygen deprivation and hence tissue damage. In other words, until normal blood flow is restored, "time is brain". Therefore, any approach that can enhance oxygen delivery to the tissue distal to the blockage while recanalization is achieved (e.g., by IA-tpa or catheter-mediated clot retrieval) will potentially preserve tissue.

In one recent approach, "microcatheter oxygenated blood" (MOB) has been infused through the blockage to supply oxygenated blood to the tissue beyond the blockage. More particularly, with this approach, blood is drawn from the femoral artery via a syringe. This femoral blood is subsequently injected through the blockage using a microcatheter, so that normally-oxygenated blood is delivered distal to the blockage, whereby to help preserve downstream tissue while complete recanalization is achieved. In the past, MOB has been infused intermittently, however, the suggestion has been made to conduct MOB infusion as a continuous mechanical pump-mediated procedure.

Unfortunately, with MOB, the amount of oxygen which can be delivered to the brain is relatively modest, due to the small lumen of the microcatheter and due to the limited amount of oxygen that is contained in normally-oxygenated blood.

The present invention provides a novel method and apparatus for

extracorporeally hyperoxygenating blood for delivery to tissue (e.g., to tissue downstream of a blockage).

Extracorporeal Device Utilizing Porous Membrane For Hyperoxygenating Blood For

Delivery To Tissue

The present invention comprises the provision and use of a novel device to enable microcatheter-mediated delivery of hyperoxygenated blood to the tissue distal to a blockage, e.g., so as to treat patients suffering from ischemic stroke.

In one preferred form of the invention, and looking now at Fig. 40, there is provided a novel device 605 which comprises a hollow cylinder 610 which contains one or more rods or tubes 615 covered with a porous membrane 620 of the sort discussed above (i.e., the "porous membrane" previously described for storing and releasing the gas-rich PFC solution). In one preferred form of the invention, porous membrane 620 comprises ePTFE with appropriately- sized pores for releasably storing an oxygenated PFC solution. Each end of cylinder 610 is closed. Rods or tubes 615 are attached to each end of cylinder 610. A female luer lock connector 625 is formed on one end (i.e., the proximal end) of cylinder 610. A male luer lock connector 630 is formed at the opposite end (i.e., the distal end) of cylinder 610. A port 635 is provided along one side of cylinder 610. Port 635 has a needle 640 embedded at its base.

A vial (not shown) of oxygenated perfluorocarbon (PFC) solution, sealed with an air-tight stopper (e.g., medical grade rubber), is intended to be inserted into port 635, so that needle 640 penetrates the vial of oxygenated PFC solution, whereby to allow the oxygenated PFC solution contained in the vial to drain into cylinder 610. Porous membrane 620 rapidly absorbs the oxygenated PFC solution to the point of saturation. Excess oxygenated PFC solution is then removed from cylinder 610 via female luer lock connector 625 or male luer lock connector 630 or both.

Alternatively, an additional port (not shown) may be provided on cylinder 610 so as to facilitate the removal of excess oxygenated PFC solution from cylinder 610. In any case, after the excess oxygenated PFC solution has been removed from cylinder 610, cylinder 610 will be left empty, except for the porous membrane 620 which is loaded with oxygenated PFC solution.

Looking now at Fig. 41, female luer lock connector 625 on cylinder 610 is attached to a male luer lock connector 645 on a syringe 650, and male luer lock connector 630 at the distal end of cylinder 610 is connected to a blood access line (e.g., to a female luer lock connector 651 formed on the hub 652 of an intra-arterial needle 653 that is inserted into a femoral artery or, alternatively, another arterial blood access source such as, but not limited to, a sheath introducer, a touhy-borst valve, a guiding catheter, etc.). Using syringe plunger 655 of syringe 650, normally- oxygenated blood is then aspirated from the arterial site and passed through cylinder 610 so as to fill syringe 650. As this occurs, the normally-oxygenated blood passes through cylinder 610, coming into contact with the oxygenated PFC solution contained in the porous membrane 620 on rods or tubes 615. Oxygenated PFC nanoparticles in the porous membrane 620 elute out of the porous membrane 620 and into the normally-oxygenated arterial blood as the blood is drawn across the porous membrane carried by rods or tubes 615. As a result, the blood in cylinder 610 and syringe 650 becomes hyperoxygenated due to the oxygenated PFC solution which elutes out of the porous membrane and into the blood. Significantly, the oxygenated PFC solution elutes out of the porous membrane and into the arterial blood at a controlled rate so that the oxygenated PFC solution does not aggregate into large bodies (or "particles") which can cause embolisms. It will be appreciated that at this point, cylinder 610 and syringe 650 are attached to one another so as to create a subassembly 660, with both cylinder 610 and syringe 650 being filled with hyperoxygenated blood.

Once subassembly 660 has been filled with hyperoxygenated blood, subassembly 660 may be detached from the arterial blood access source (e.g., subassembly 660 may be detached from intra-arterial needle 653).

Looking now at Fig. 42, there is shown a microcatheter 665 that is introduced into the target cerebral artery, with the distal tip 670 of the microcatheter advanced across the arterial blockage that is causing ischemia in the brain. Subassembly 660 is attached to female luer lock connector 675 of microcatheter 665 (or, alternatively, the female luer lock connector of an intra-arterial guiding catheter or the female luer lock connectors of other intra-arterial catheters such as those utilized for the

aforementioned blood clot extraction procedures). Plunger 655 of syringe 650 is then slowly depressed, thereby delivering the hyperoxygenated blood contained in subassembly 660 through the lumen of microcatheter 665 and to the vasculature distal to the arterial blockage, whereby to supply oxygen to the downstream tissue and thereby minimize tissue damage due to oxygen deprivation.

Additionally and/or alternatively, hyperoxygenated blood is then delivered (for example, via a guiding catheter with its tip positioned proximal to the site of the blood clot) following the removal of the blood clot, whereby to oxygenate a larger area of tissue.

Significantly, due to the aforementioned retrograde/antegrade blood flow through subassembly 660, residual oxygenated PFC solution remaining in porous membrane 620 after the initial retrograde blood flow can elute into the blood during the subsequent antegrade blood flow across porous membrane 620, thereby increasing the hyperoxygenicity of the blood which is delivered distal to the blockage (e.g., via microcatheter 665). Alternatively, and looking now at Fig. 43, it may be desirable to use a larger volume syringe 680 which can hold the complete volume of the hyperoxygenated blood contained in cylinder 610. In this form of the invention, once subassembly 660 is disconnected from the arterial blood access source, plunger 685 of larger volume syringe 680 is pulled proximally so as to draw all of the hyperoxygenated blood in cylinder 610 into larger volume syringe 680. Then the empty cylinder 610 is disconnected from larger volume syringe 680 (which now contains all of the hyperoxygenated blood). Larger volume syringe 680 is then attached directly to female luer lock connector 675 of microcatheter 665. Plunger 685 of larger volume syringe 680 is then slowly depressed, thus delivering the hyperoxygenated blood in larger volume syringe 680 directly through the lumen of microcatheter 665 and distal to the arterial blockage.

If desired, the porous membrane disposed within cylinder 610 need not be mounted to rods or tubes 615. Other configurations may also be used. By way of example but not limitation, in another preferred embodiment of the invention, and looking now at Fig. 44, device 605 has a hollow cylinder 610 which contains a porous membrane 620.

In another alternative construction of device 605, and looking now at Fig. 45, device 605 may be constructed without the port 635 and needle 640 shown in Figs. 40-44. In this form of the invention, a needle (not shown) attached to a syringe (not shown) is inserted into a vial (not shown) containing oxygenated PFC solution, and a volume of oxygenated PFC solution sufficient to fill cylinder 610 is drawn out of the vial and into the syringe. The user may then withdraw the needle from the vial, remove the needle from the syringe, screw the syringe (which is loaded with oxygenated PFC solution) into female luer lock connector 625 of device 605, and fill cylinder 610 with oxygenated PFC solution by depressing the plunger of the syringe. After porous membrane 620 absorbs the oxygenated PFC solution to the point of saturation, excess oxygenated PFC solution may then be removed from cylinder 610, e.g., in the manner discussed above. Thereafter, device 605 (containing rods or tubes 615 carrying the porous membrane 620 which is saturated with oxygenated PFC solution) may then be used in the manner discussed above to hyperoxygenate arterial blood and deliver that hyperoxygenated blood to tissue downstream of a blockage.

Figs. 46 and 47 show another preferred form of the present invention. In this form of the invention, device 605 comprises the aforementioned hollow cylinder 610 which contains a quantity of porous membrane 620 (preferably ePTFE) for storing and releasing the gas-rich PFC solution). The porous membrane 620 may be in various forms consistent with the present invention, e.g., mounted to internal structure such as rods or tubes, or disposed in a honeycomb structure, etc. Each end of cylinder 610 is closed. Female luer lock connector 625 is formed on one end of cylinder 610. Male luer lock connector 630 is formed at the opposite end of cylinder 610. As seen in Fig. 48, female luer lock connector 625 of cylinder 610 is intended to be connected to a male luer lock adapter of syringe 680, and male luer lock connector 630 of cylinder 610 is intended to be selectively connected to (a) a blood access line (e.g., to a female luer lock connector 651 formed on the hub 652 of an intra-arterial needle 653 that is inserted into a femoral artery or, alternatively, another arterial blood access source such as, but not limited to, a sheath introducer, a touhy-borst valve, a guiding catheter, etc.) for extraction of blood from the body, or (b) a trans-clot blood return line (e.g., a female luer lock connector 675 of microcatheter 665 or, alternatively, the female luer lock connector of an intra-arterial guiding catheter or the female luer lock connectors of other intra-arterial catheters such as those utilized for the aforementioned blood clot extraction procedures) for insertion of hyperoxygenated blood into the body, as will hereinafter be discussed.

In addition to the foregoing, device 605 also comprises a distalmost mesh element 690, an intermediate mesh element 695, and a proximalmost mesh element 700. Distalmost mesh element 690 has a pore size on the order of 5-15 microns in order to (a) filter out red blood cells from arterial blood so that the red blood cells cannot pass further into the device, and (b) allows very low resistance for the return flow of hyperoxygenated blood plasma, which in turn allows the hyperoxygenated blood plasma to re-mix with the red blood cells retained distal to distalmost mesh element 690, as will hereinafter be discussed in further detail. Intermediate mesh element 695 has a pore size on the order of 0.1-1 micron in order to break up any aggregaged micro-droplets of oxygenated PFC solution, in order that emitted droplet size can be controlled and maintained during the deployment cycle. Proximalmost mesh element 700 has a pore size similar to that of intermediate mesh element 695 (i.e., 0.1-1 micron) in order to break up any aggregaged micro-droplets of oxygenated PFC solution when drawing oxygenated blood plasma into the syringe and/or when passing oxygenated blood plasma out of the syringe.

Oxygenated PFC solution is introduced into the porous membrane 620 by passing the oxygenated PFC solution to porous membrane 620 via female luer lock connector 625, male luer lock connector 630, or by using another port (not shown) which allows the oxygenated PFC solution to be introduced to porous membrane 620.

In one preferred manner of use, female luer lock connector 625 is connected to a standard syringe, male luer lock connector 630 is connected to a blood access line (e.g., to luer lock connector 651 formed on the hub 652 of intra- arterial needle 653 inserted into a femoral artery), and then blood is withdrawn from the body and into device 605. As seen in Figs. 49 and 50, as blood passes into the device, red blood cells are filtered out of the blood via distalmost mesh element 690. These red blood cells are retained in the distalmost portion of the device. The plasma from the blood is passed through the intermediate mesh element 695 and then through the chamber containing the porous membrane 620 (which has been previously charged with the oxygenated PFC solution), whereby to oxygenate the blood plasma with oxygenated PFC solution. Then the oxygenated blood plasma is passed through the proximalmost mesh element 700 and into the syringe. As the oxygenated blood plasma is passed through the proximalmost mesh element 700, the small pore size (on the order of 0.1-1 micron) of the proximalmost mesh element breaks up any aggregaged micro-droplets of oxygenated PFC solution before the oxygenated blood plasma enters the syringe. Thereafter, the male luer lock connector 630 is disconnected from the blood access line (e.g., from the femoral artery access) and it is connected to microcatheter 665 which has its distal end extending through the blood clot. Then the oxygenated blood plasma is ejected from the syringe, with the oxygenated blood plasma passing back through the device 605. As this occurs, the oxygenated blood plasma first passes through the proximalmost mesh element 700, where the small pore size of the proximalmost mesh element breaks up any aggregaged micro-droplets of oxygenated PFC solution before the oxygenated blood plasma re-encounters the porous membrane 620. As the oxygenated blood plasma passes by the porous membrane 620, the residual oxygenated PFC solution remaining in porous membrane 620 can elute into the oxygenated plasma during the antegrade flow across porous membrane 620, thereby increasing the hyperoxygenicity of the blood plasma. Next, the oxygenated plasma passes through the intermediate mesh element 695, where the small pore size of the intermediate mesh element breaks up any aggregaged micro-droplets of oxygenated PFC solution before the oxygenated blood plasma re-encounters the distalmost mesh element 690. As the oxygenated blood plasma passes through the distalmost mesh element 690, it is reunited with the red blood cells residing distal to the distalmost mesh element 690, and then the hyperoxygenated blood is delivered (via the microcatheter 665) to the region distal to the blood clot, whereby to oxygenate the tissue distal to the blood clot and minimize tissue damage due to oxygen deprivation.

Additionally and/or alternatively, hyperoxygenated blood is then delivered (for example, via a guiding catheter with its tip positioned proximal to the site of the blood clot) following the removal of the blood clot, whereby to oxygenate a larger area of tissue. As an alternative to the foregoing, and looking now at Fig. 51, if it is desired to return only hyperoxygenated blood plasma to the patient, and not return the red blood cells previously captured in device 605 distal to distalmost mesh 690, the following approach may be used. More particularly, after syringe 680 has been filled with hyperoxygenated blood plasma, device 605 is disconnected from the filled syringe 680, and an alternative device 605A is connected to syringe 680 and then to microcatheter 665. In this form of the invention, the alternative device 605 A is preferably substantially the same as the device 605, except that it omits the aforementioned distalmost mesh element 690 and the porous membrane 620 and, optionally, the proximalmost mesh element 700. As a result of this construction, as the hyperoxygenated blood plasma in syringe 680 is passed through alternative device 605 A and into microcatheter 665, the hyperoxygenated blood plasma passes through intermediate mesh element 695, whereupon the small pore size of the intermediate mesh element breaks up any aggregaged micro-droplets of oxygenated PFC solution before the oxygenated blood plasma is returned to the body via microcatheter 665. If desired, more than one intermediate mesh 695 may be provided in alternative device 605A.

Turning next to Figs. 52-54, there is shown another preferred form of device 605. More particularly, in this form of the invention, device 605 comprises the aforementioned hollow cylinder 610 which contains a quantity of porous membrane 620 (preferably ePTFE) for storing and releasing the gas-rich PFC solution. In this form of the invention, the porous membrane 620 is preferably in the form of a plurality of stacked, spaced discs 705. More particularly, each of the discs 705 comprises the porous membrane 620 and a spacer 710 for separating the porous membrane of one disc 705 from the porous membrane of another disc 705. Thus, a gap 711 is formed between each of the discs 705. Each of the discs 705 preferably includes at least one opening 715 therein for permitting blood to pass by the disc. Each end of cylinder 610 is closed. Female luer lock connector 625 is formed on one end of cylinder 610. Male luer lock connector 630 is formed at the opposite end of cylinder 610. As will be appreciated in view of the foregoing disclosure, female luer lock connector 625 of cylinder 610 is intended to be connected to a male luer lock adapter of syringe 680, and male luer lock connector 630 of cylinder 610 is intended to be selectively connected to (a) a blood access line (e.g., to a female luer lock connector 651 formed on the hub 652 of an intra-arterial needle 653 that is inserted into a femoral artery or, alternatively, another arterial blood access source such as, but not limited to, a sheath introducer, a touhy-borst valve, a guiding catheter, etc.) for extraction of blood from the body, or (b) a trans-clot blood return line (e.g., a female luer lock connector 675 of microcatheter 665 or, alternatively, the female luer lock connector of an intra-arterial guiding catheter or the female luer lock connectors of other intra-arterial catheters such as those utilized for the aforementioned blood clot extraction procedures) for insertion of hyperoxygenated blood into the body, as will hereinafter be discussed.

In one preferred manner of use, female luer lock connector 625 is connected to a syringe 680, male luer lock connector 630 is connected to a blood access line (e.g., to luer lock connector 651 formed on the hub 652 of intra-arterial needle 653 inserted into a femoral artery), and then blood is withdrawn from the body and into device 605. As blood passes into the device, the blood passes by the porous membrane 620 (which has been previously charged with the oxygenated PFC solution), whereby to oxygenate the blood. Then the oxygenated blood is passed into the syringe.

Thereafter, the male luer lock connector 630 is disconnected from the blood access line (e.g., from the femoral artery access) and it is connected to a microcatheter (e.g., the microcatheter 665) which has its distal end extending through the blood clot. Then the oxygenated blood is ejected from the syringe, with the oxygenated blood passing back through the device 605. As this occurs, the oxygenated blood passes by the porous membrane 620, and residual oxygenated PFC solution remaining in porous membrane 620 can elute into the oxygenated blood during the antegrade flow across porous membrane 620, thereby increasing the hyperoxygenicity of the blood before being delivered (via the microcatheter) to the region distal to the blood clot, whereby to oxygenate the tissue distal to the blood clot.

Turning next to Figs. 55 and 56, there is shown another preferred form of device 605. More particularly, in this form of the invention, device 605 comprises the aforementioned hollow cylinder 610 which contains a quantity of porous membrane 620 (preferably ePTFE) for storing and releasing the gas-rich PFC solution. In this form of the invention, the porous membrane 620 is preferably in the form of a loosely wound roll 720 of porous membrane, each wind of the roll 720 being spaced from the adjacent wind of the roll by gaps 725, whereby to expose the porous membrane 620 for greater surface area contact with the blood. Each end of cylinder 610 is closed. Female luer lock connector 625 is formed on one end of cylinder 610. Male luer lock connector 630 is formed at the opposite end of cylinder 610. As will be appreciated in view of the foregoing disclosure, female luer lock connector 625 of cylinder 610 is intended to be connected to a male luer lock adapter of syringe 680, and male luer lock connector 630 of cylinder 610 is intended to be selectively connected to (a) a blood access line (e.g., to a female luer lock connector 651 formed on the hub 652 of an intra-arterial needle 653 that is inserted into a femoral artery or, alternatively, another arterial blood access source such as, but not limited to, a sheath introducer, a touhy- borst valve, a guiding catheter, etc.) for extraction of blood from the body, or (b) a trans-clot blood return line (e.g., a female luer lock connector 675 of microcatheter 665 or, alternatively, the female luer lock connector of an intra-arterial guiding catheter or the female luer lock connectors of other intra-arterial catheters such as those utilized for the aforementioned blood clot extraction procedures) for insertion of hyperoxygenated blood into the body, as will hereinafter be discussed.

In one preferred manner of use, female luer lock connector 625 is connected to a syringe 680, male luer lock connector 630 is connected to a blood access line (e.g., to a luer lock connector 651 formed on the hub 652 of intra-arterial needle 653 inserted into a femoral artery), and then blood is withdrawn from the body and into device 605. As blood passes into the device, the blood passes by the porous membrane 620 (which has been previously charged with the oxygenated PFC solution), whereby to oxygenate the blood. Then the oxygenated blood is passed into the syringe. Thereafter, the male luer lock connector 630 is disconnected from the blood access line (e.g., from the femoral artery access) and it is connected to a microcatheter (e.g., the microcatheter 665) which has its distal end extending through the blood clot. Then the oxygenated blood is ejected from the syringe, with the oxygenated blood passing back through the device 605. As this occurs, the oxygenated blood passes by the porous membrane 620, and residual oxygenated PFC remaining in porous membrane 620 can elute into the oxygenated blood during the antegrade flow across porous membrane 620, thereby increasing the hyperoxygenicity of the blood before being delivered (via the microcatheter) to the region distal to the blood clot, whereby to oxygenate the tissue distal to the blood clot.

Looking next at Figs. 57-59, there is shown another preferred form of device 605. This form of device 605 is identical to the form of device 605 shown in Figs. 55 and 56, except that in the device 605 of Figs. 55 and 56, porous membrane 620 is in the form of a flat, planar web or tape which is loosely coiled so as to create the roll 720 with gaps 725, whereas in the device 605 shown in Figs. 57-59, porous membrane 620 is in the form of a corrugated web or tape which is loosely coiled so as to create the roll 720 with gaps 725. In essence, the corrugated web or tape of the porous membrane 620 of Figs. 57-59 provides increased surface area as compared to the flat, planar web or tape of the porous membrane 620 of Figs. 55 and 56, whereby to facilitate oxygen uploading to the blood. The device 605 of Figs. 57-59 is intended to be used in substantially the same manner as the device 605 of Figs. 55 and 56.

Turning next to Figs. 60-63, there is shown another preferred form of device 605. More particularly, in this form of the invention, device 605 comprises a housing 610 which contains a quantity of porous membrane 620 (preferably ePTFE) for storing and releasing the gas-rich PFC solution. In this form of the invention, the porous membrane 620 is preferably in the form of a pair of planar sheets 731 which are mounted to a support 732, whereby to separate the planar sheets from one another and expose the planar sheets of porous membrane 620 to blood passing through housing 610. Each end of housing 610 is closed. Female luer lock connector 625 is formed on one end of housing 610. Male luer lock connector 630 is formed at the opposite end of housing 610. As will be appreciated in view of the foregoing disclosure, female luer lock connector 625 of housing 610 is intended to be connected to a male luer lock adapter of syringe 680, and male luer lock connector 630 of cylinder 610 is intended to be selectively connected to (a) a blood access line (e.g., to a female luer lock connector 651 formed on the hub 652 of an intra-arterial needle 653 that is inserted into a femoral artery or, alternatively, another arterial blood access source such as, but not limited to, a sheath introducer, a touhy-borst valve, a guiding catheter, etc.) for extraction of blood from the body, or (b) a trans-clot blood return line (e.g., a female luer lock connector 675 of microcatheter 665 or, alternatively, the female luer lock connector of an intra-arterial guiding catheter or the female luer lock connectors of other intra-arterial catheters such as those utilized for the

aforementioned blood clot extraction procedures) for insertion of hyperoxygenated blood into the body, as will hereinafter be discussed.

In one preferred manner of use, female luer lock connector 625 is connected to a syringe 680, male luer lock connector 630 is connected to a blood access line (e.g., to luer lock connector 651 formed on the hub 452 of intra-arterial needle 653 inserted into a femoral artery), and then blood is withdrawn from the body and into device 605. As blood passes into the device, the blood passes by the porous membrane 620 (which has been previously charged with the oxygenated PFC solution), whereby to oxygenate the blood. Then the oxygenated blood is passed into the syringe 680.

Thereafter, the male luer lock connector 630 is disconnected from the blood access line (e.g., from the femoral artery access) and it is connected to a microcatheter (e.g., the microcatheter 665) which has its distal end extending through the blood clot. Then the oxygenated blood is ejected from the syringe, with the oxygenated blood passing back through the device 605. As this occurs, the oxygenated blood passes by the porous membrane 620, and residual oxygenated PFC remaining in porous membrane 620 can elute into the oxygenated blood during the antegrade flow across porous membrane 620, thereby increasing the hyperoxygenicity of the blood before being delivered (via the microcatheter) to the region distal to the blood clot, whereby to oxygenate the tissue distal to the blood clot. Additionally and/or alternatively, hyperoxygenated blood is then delivered (for example, via a guiding catheter with its tip positioned proximal to the site of the blood clot) following the removal of the blood clot, whereby to oxygenate a larger area of tissue.

Turning next to Figs. 64 and 65, there is shown another preferred form of device 605. More particularly, in this form of the invention, device 605 comprises the aforementioned hollow cylinder 610 which contains a quantity of porous membrane 620 (preferably ePTFE) for storing and releasing the gas-rich PFC solution. In this form of the invention, the porous membrane 620 is preferably in the form of a helical wick 735, which is connected to an external source 740 of oxygenated PFC solution, whereby to provide a continuous elution of oxygenated PFC solution to blood within hollow cylinder 610, as will hereinafter be discussed. Each end of cylinder 610 is closed. Female luer lock connector 625 is formed on one end of cylinder 610. Male luer lock connector 630 is formed at the opposite end of cylinder 610. As will be appreciated in view of the foregoing disclosure, female luer lock connector 625 of cylinder 610 is intended to be connected to a male luer lock adapter of syringe 680, and male luer lock connector 630 of cylinder 610 is intended to be selectively connected to (a) luer lock connector 651 formed on the hub 652 of an intra-arterial needle 653, or, alternatively, the female luer lock connector of other arterial blood access devices, including but not limited to a sheath introducer, a touhy-borst valve, or a guiding catheter, for extraction of blood from the body, or (b) female luer lock connector 675 of microcatheter 665, or alternatively, the female luer lock connector of an intra-arterial guiding catheter or the female luer lock connectors of other intraarterial catheters such as those utilized for aforementioned blood clot extraction procedures, for insertion of hyperoxygenated blood into the body, as will hereinafter be discussed.

In one preferred manner of use, female luer lock connector 625 is connected to syringe 680, male luer lock connector 630 is connected to a blood access line (e.g., to luer lock connector 651 formed on the hub 652 of intra-arterial needle 653, or, for example, other arterial blood access lines, including but not limited to devices inserted into a femoral artery), and then blood is withdrawn from the body and into device 605. As blood passes into the device, the blood passes by the helical wick 735 of porous membrane 620 (which is continuously charged with the oxygenated PFC solution from the external source 740 of oxygenated PFC solution), so that oxygenated PFC solution elutes into the blood, whereby to oxygenate the blood. Then the oxygenated blood is passed into the syringe. Thereafter, the male luer lock connector 630 is disconnected from the blood access line (e.g., from the femoral artery access) and it is connected to a microcatheter (e.g., the microcatheter 665 which has its distal end extending through the blood clot or, alternatively, the female luer lock connector of an intra-arterial guiding catheter or the female luer lock connectors of other intra-arterial catheters, such as those utilized for the aforementioned blood clot extraction procedures, which have the distal end positioned proximal to the site of the blood clot following the removal of the blood clot). Then the oxygenated blood is ejected from the syringe, with the oxygenated blood passing back through the device 605. As this occurs, the oxygenated blood passes by the porous membrane 620, so that additional oxygenated PFC solution can elute into the blood, thereby increasing the

hyperoxygenicity of the blood. Hyperoxygenated blood is then delivered (via a microcatheter with its distal tip passed through the clot) to the region distal to the blood clot, whereby to oxygenate the tissue distal to the blood clot.

Turning next to Figs. 66 and 67, there is shown another preferred form of device 605. More particularly, in this form of the invention, device 605 comprises the aforementioned hollow cylinder 610 which contains a quantity of porous membrane 620 (preferably ePTFE) for storing and releasing the gas-rich PFC solution. In this form of the invention, the porous membrane 620 is preferably in the form of a cylinder 745, which extends coaxial within, and spaced from, another cylindrical wall 750 provided in hollow cylinder 610, whereby to provide an annular chamber 755 for holding a supply of oxygenated PFC solution, whereby to provide continuous infusion of oxygenated PFC solution to porous membrane 620, so that the oxygenated PFC solution can elute out of the porous membrane and into the blood contained within a passageway 760 passing through hollow cylinder 610, as will hereinafter be discussed. Each end of cylinder 610 is closed. Female luer lock connector 625 is formed on one end of cylinder 610. Male luer lock connector 630 is formed at the opposite end of cylinder 610. Passageway 760 connects female luer lock connector 625 with male luer lock connector 630. As will be appreciated in view of the foregoing disclosure, female luer lock connector 625 of cylinder 610 is intended to be connected to a male luer lock adapter of syringe 680, and male luer lock connector 630 of cylinder 610 is intended to be selectively connected to (a) a blood access line (e.g., to a female luer lock connector 651 formed on the hub 652 of an intra-arterial needle 653 that is inserted into a femoral artery or, alternatively, another arterial blood access source such as, but not limited to, a sheath introducer, a touhy-borst valve, a guiding catheter, etc.) for extraction of blood from the body, or (b) a trans-clot blood return line (e.g., a female luer lock connector 675 of microcatheter 665 or, alternatively, the female luer lock connector of an intra-arterial guiding catheter or the female luer lock connectors of other intra-arterial catheters such as those utilized for the aforementioned blood clot extraction procedures) for insertion of hyperoxygenated blood into the body, as will hereinafter be discussed.

Oxygenated PFC solution is introduced into annular chamber 755 by passing the oxygenated PFC solution to annular chamber 755 via a port (not shown) which allows the oxygenated PFC solution to be introduced to annular chamber 755. In one preferred manner of use, female luer lock connector 625 is connected to syringe 680, male luer lock connector 630 is connected to a blood access line (e.g., to luer lock connector 651 formed on the hub 652 of intra-arterial needle 653 inserted into a femoral artery), and then blood is withdrawn from the body and into device 605. As blood passes into the device and along passageway 760, the blood passes by the porous membrane 620 (which is continuously charged with the oxygenated PFC solution located within annular chamber 755), so that the oxygenated PFC solution can elute out of the porous membrane and into the blood passing through passageway 760, whereby to oxygenate the blood. Then the oxygenated blood is passed into the syringe. Thereafter, the male luer lock connector 630 is disconnected from the blood access line (e.g., from the femoral artery access) and it is connected to a microcatheter (e.g., the microcatheter 665) which has its distal end extending through the blood clot. Then the oxygenated blood is ejected from the syringe, with the oxygenated blood passing back through the device 605. As this occurs, the oxygenated blood passes by the porous membrane 620, so that additional oxygenated PFC solution can elute into the blood, thereby increasing the hyperoxygenicity of the blood before being delivered (via the microcatheter) to the region distal to the blood clot, whereby to oxygenate the tissue distal to the blood clot.

If desired, the aforementioned distalmost mesh 690, intermediate mesh 695 and/or proximalmost mesh 700 may be incorporated in device 605 of Figs. 40-45, device 605 of Figs. 52-54, device 605 of Figs. 55 and 56, device 605 of Figs. 57-59, device 605 of Figs. 60-63, device 605 of Figs. 64 and 65, and/or device 605 of Figs. 66 and 67. It should be appreciated that the use of the present invention is not limited to providing hyperoxygenated blood to brain tissue downstream of a clot. The invention may also be used to provide hyperoxygenated blood to other body tissue. By way of example but not limitation, the invention may be used to extracorporeally hyperoxygenate blood in the manner previously discussed, and then the

hyperoxygenated blood may be intravascularly delivered (by an appropriate catheter or other device known in the art) to coronary tissue, e.g., coronary tissue downstream from partially or fully obstructed coronary arteries or coronary tissue downstream of an angioplasty site.

Modifications

It is to be understood that the present invention is by no means limited to the particular constructions herein disclosed and/or shown in the drawings, but also comprises any modifications or equivalents within the scope of the invention.

Claims

What Is Claimed Is:

1. Apparatus for oxygenating blood, said apparatus comprising:

a container comprising an interior chamber, a first port communicating with said interior chamber and a second port communicating with said interior chamber; and

a porous membrane disposed within said interior chamber of said container, said porous membrane having a porosity such that an oxygen-rich perfluorocarbon solution may be incorporated into said porous membrane and, when a blood fluid is brought into contact with said porous membrane incorporating the oxygen-rich perfluorocarbon solution, the oxygen-rich perfluorocarbon solution elutes out of said porous membrane and into the blood fluid, whereby to oxygenate the blood fluid.

2. Apparatus according to claim 1 wherein said first port is configured to be connected to a blood line in fluid communication with a blood vessel within a patient.

3. Apparatus according to claim 2 wherein said blood line comprises an intra-arterial needle.

4. Apparatus according to claim 2 wherein said blood line comprises a microcatheter having its distal tip disposed beyond a blockage in the blood vessel.

5. Apparatus according to claim 1 wherein said second port is configured to be connected to a syringe.

6. Apparatus according to claim 1 wherein said porous membrane has a porosity such that the oxygen-rich perfluorocarbon solution elutes out of said porous membrane and into the blood fluid in aggregations small enough to prevent the creation of embolisms in the blood fluid.

7. Apparatus according to claim 6 wherein said porous membrane has a porosity in the range of 0.001-200 microns.

8. Apparatus according to claim 1 wherein said porous membrane comprises ePTFE.

9. Apparatus according to claim 1 wherein said porous membrane is mounted to support structure located within said interior chamber of said container.

10. Apparatus according to claim 9 wherein said support structure comprises at least one cylindrical structure fixed within said interior chamber of said container.

11. Apparatus according to claim 9 wherein said support structure comprises at least one wall.

12. Apparatus according to claim 11 wherein said at least one wall is located within said interior chamber of said container.

13. Apparatus according to claim 11 wherein said at least one wall defines a portion of the perimeter of said interior chamber of said container.

14. Apparatus according to claim 1 wherein said container further comprises a third port communicating with said interior chamber.

15. Apparatus according to claim 14 wherein said third port comprises a hollow needle communicating with said interior chamber.

16. Apparatus according to claim 15 wherein said third port further comprises a cylinder coaxially surrounding said hollow needle, said cylinder having a length greater than said hollow needle so that said hollow needle does not project beyond said cylinder.

17. Apparatus according to claim 14 wherein said porous membrane comprises a wick structure connected to said third port, whereby oxygen-rich perfluorocarbon solution introduced into said third port is infused into said porous membrane.

18. Apparatus according to claim 1 wherein said porous membrane comprises a wall of said interior chamber of said container, said wall separating said interior chamber of said container from a second interior chamber formed within said container, and further wherein said membrane is configured so that when oxygen-rich perfluorocarbon solution is disposed within said second interior chamber of said container, said oxygen-rich perfluorocarbon solution elutes into a blood fluid disposed within said interior chamber of said container.

19. Apparatus according to claim 1 further comprising at least one mesh disposed intermediate said first port and said second port.

20. Apparatus according to claim 19 wherein said at least one mesh comprises a mesh with a porosity of 5-15 microns so as to filter out red blood cells.

21. Apparatus according to claim 19 wherein said at least one mesh comprises a mesh with a porosity of 0.1-1 micron so as to break up any aggregated micro-droplets of oxygen-rich perfluorocarbon solution.

22. Apparatus according to claim 1 wherein said first port comprises a luer lock connector.

23. Apparatus according to claim 1 wherein said second port comprises a luer lock connector.

24. Apparatus according to claim 1 wherein said blood fluid comprises whole blood.

25. Apparatus according to claim 1 wherein said blood fluid comprises blood plasma.

26. A method for oxygenating blood, said method comprising:

providing apparatus for oxygenating blood, said apparatus comprising:

a container comprising an interior chamber; and

a porous membrane disposed within said interior chamber of said container, said porous membrane having a porosity such that an oxygen-rich perfluorocarbon solution may be incorporated into said porous membrane and, when a blood fluid is brought into contact with said porous membrane incorporating the oxygen-rich perfluorocarbon solution, the oxygen-rich perfluorocarbon solution elutes out of said porous membrane and into the blood fluid, whereby to oxygenate the blood fluid; introducing an oxygen-rich perfluorocarbon solution to said porous membrane, and transferring a blood fluid from the body of a patient into said interior chamber of said container, whereby to oxygenate the blood fluid; and

returning the oxygenated blood fluid to the body of the patient.