# US 11,077,287 B2 · Non-occluding balloon for cardiovascular drug delivery

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- Number: US 11,077,287 B2
- Document ID: US11077287B2
- Status: Granted
- Kind: B2
- Application number: 16/148,221
- Filed: 2018-10-01
- Published: 2019-04-04
- Granted: 2021-08-03
- Earliest claimed: 2017-10-02
- Assignees: Anlvr, LLC
- Applicants: Anlvr, LLC
- Inventors: Vijay Sitharam Ramanath; Brett Allyn Williams
- Web page: https://patentgrep.com/patent/US11077287B2

## CPC

- A61M 25/10: Balloon catheters ({A61M25/0125 takes precedence; embolectomy A61B17/22032; retractors A61B17/02;} inflatable balloons for placing stents or stent-grafts A61F2/958 {; stomach balloons for treatment of obesity A61F5/0003; oesophagal tubes A61J15/00})
- A61M 25/1029: {Production methods of the balloon members, e.g. blow-moulding, extruding, deposition or by wrapping a plurality of layers of balloon material around a mandril}
- A61M 25/104: {used for angioplasty}
- A61M 2025/0183: {Rapid exchange or monorail catheters}
- A61M 2025/105: {having a balloon suitable for drug delivery, e.g. by using holes for delivery, drug coating or membranes}
- A61M 2025/1072: {having balloons with two or more compartments}
- A61M 2025/1075: {having a balloon composed of several layers, e.g. by coating or embedding}
- A61M 2025/1079: {having radio-opaque markers in the region of the balloon}
- A61M 2025/1086: {having a special balloon surface topography, e.g. pores, protuberances, spikes or grooves}
- A61M 2025/1097: {with perfusion means for enabling blood circulation only while the balloon is in an inflated state, e.g. temporary by-pass within balloon}
- A61M: DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY (introducing media into or onto the bodies of animals A61D7/00; means for inserting tampons A61F13/26; devices for administering food or medicines orally A61J; containers for collecting, storing or administering blood or medical fluids A61J1/05); DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY (surgery A61B; chemical aspects of surgical articles A61L); DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR {(Electrotherapy, e.g. producing anaesthesia by the use of alternating or intermittent currents A61N1/36021)}

## Abstract

A non-occluding drug-coated balloon catheter device for use in a blood vessel transporting blood comprises a catheter shaft including a guidewire lumen, a fluid lumen and a connector port. A balloon is mounted on the catheter shaft and includes an outer envelope surrounding the guidewire lumen in fluid communication with the fluid lumen; a drug coating applied on the exterior surface of the outer envelope; and at least one bypass lumen forming a passage extending from the proximal end of the outer envelope to the distal end of the outer envelope. When the balloon is positioned in a blood vessel and inflated, the exterior surface of the outer envelope presses the drug coating against the blood vessel and the bypass lumen is open between the distal end of the outer envelope and the proximal end of the outer envelope such that blood transport continues through the bypass lumen.

## Claims

### Claim 1

A non-occluding medical balloon apparatus comprising:
a proximal preform portion having a constant cross section along a central axis, the constant cross section defining a continuous annular preform sidewall having an outer surface, an inner surface defining a central passage, a plurality of preform inflation passages disposed between the outer and inner surfaces and fluidly isolated from the central passage, and a plurality of preform septums, each of the respective preform septums extending between the inner and outer surfaces of the continuous annular preform sidewall between a respective pair of the preform inflation passages to fluidly isolate the respective pair of preform inflation passages from one another;
a nosecone defining an extension of the central passage;
an expanded balloon portion disposed between, and connected to, the proximal preform portion and the nosecone, the expanded balloon portion including:
a substantially cylindrical central portion having a nominal diameter that is greater than a distal diameter of the proximal preform portion and greater than a proximal diameter of the nosecone;
wherein the central portion includes a continuous annular central sidewall having an outer surface, an inner surface defining a central portion of an expanded central passage, a plurality of central inflation passages disposed between the outer and inner surfaces, and a plurality of central septums, each of the respective central septums extending between the inner and outer surfaces of the continuous annular central sidewall between a respective pair of the central inflation passages to fluidly isolate the respective pair of central inflation passages from one another;
wherein there is a one-to-one correspondence between each one of the preform inflation passages and a respective one of the central inflation passages, and a one-to-one correspondence between each one of the preform septums and a respective one of the central septums; and
a proximal end portion connected between the central portion and the proximal preform portion and tapering from the nominal diameter of the central portion to the distal diameter of the proximal preform portion;
wherein the proximal end portion includes a continuous annular proximal end sidewall having an outer surface, an inner surface defining a proximal end portion of the expanded central passage, a plurality of proximal end inflation passages disposed between the outer and inner surfaces, and a plurality of proximal end septums, each of the respective proximal end septums extending between the inner and outer surfaces of the continuous annular proximal end sidewall between a respective pair of the proximal end inflation passages to fluidly isolate the respective pair of proximal end inflation passages from one another;
wherein there is a one-to-one correspondence between each one of the preform inflation passages and a respective one of the proximal end inflation passages, and a one-to-one correspondence between each one of the preform septums and a respective one of the proximal end septums; and
a distal end portion connected between the central portion and the nosecone and tapering from the nominal diameter of the central portion to the proximal diameter of the nosecone;
wherein the distal end portion includes a continuous annular distal end sidewall having an outer surface, an inner surface defining a distal portion of the expanded central passage, a plurality of distal end inflation passages disposed between the outer and inner surfaces, and a plurality of distal end septums, each of the respective distal end septums extending between the inner and outer surfaces of the continuous annular distal end sidewall between a respective pair of the distal end inflation passages to fluidly isolate the respective pair of distal end inflation passages from one another;
wherein there is a one-to-one correspondence between each one of the preform inflation passages and a respective one of the distal end inflation passages, and a one-to-one correspondence between each one of the preform septums and a respective one of the distal end septums; and
wherein each respective preform inflation passage of the proximal preform portion is in fluid communication with the respective proximal end inflation passage, the respective central inflation passage and the respective distal end inflation passage having the respective one-to-one correspondence therewith of the expanded balloon portion;
wherein each respective preform septum of the proximal preform portion is operatively connected to respective proximal end septum, the respective central septum and the respective distal end septum having the respective one-to-one correspondence therewith of the expanded balloon portion, to collectively fluidly isolate the respective pair of preform inflation passages, the respective pair of proximal end inflation passages, the respective pair of central inflation passages and the respective pair of distal end inflation passages on each respective side thereof from one another;
wherein, on the proximal end portion of the expanded balloon portion, some overlying areas of the outer and inner surfaces of the continuous proximal end sidewall between a selected pair of proximal septums are joined to form a proximal sealed area;
wherein, a first hole is defined extending through the proximal sealed area of the continuous proximal end sidewall from an exterior of the balloon into the expanded central passage to form a proximal perfusion port, the first hole being fluidly isolated from the proximal end inflation passages;
wherein, on the distal end portion of the expanded balloon portion, some overlying areas of the outer and inner surfaces of the continuous distal end sidewall between a selected pair of distal septums are joined to form a distal sealed area;
wherein, a second hole is defined extending through the distal sealed area of the continuous distal end sidewall from the expanded central passage to the exterior of the balloon to form a distal perfusion port, the second hole being fluidly isolated from the distal end inflation passages; and
a guide wire lumen is disposed through the central passage of the proximal preform portion, the respective expanded central passages of the balloon portion and the central passage of the nose cone.

### Claim 2 (depends on 1)

The non-occluding medical balloon apparatus in accordance with claim 1, further comprising a drug-eluting coating disposed on the outer surface of the central portion of the balloon.

### Claim 3 (depends on 2)

The non-occluding medical balloon apparatus in accordance with claim 2, wherein the drug-eluting coating comprises the drug Paclitaxel.

### Claim 4 (depends on 1)

The non-occluding medical balloon apparatus in accordance with claim 1, further comprising a plurality of micro-pores formed through the outer surface of the sidewall into the inflation passage.

### Claim 5 (depends on 4)

The non-occluding medical balloon apparatus in accordance with claim 4, wherein the dimensions of the micro-pores include a length LMP and a diameter DMP, which are selected relative to a surface tension and/or to a viscosity of a fluid medium within the inflation passage such that the fluid medium is not released from the micro-pores until a predetermined pressure differential DMP is present between the inflation passage and the exterior of the balloon.

### Claim 6 (depends on 1)

The non-occluding medical balloon apparatus in accordance with claim 1, further comprising:
a catheter shaft attached to the proximal preform of the balloon, the catheter shaft including:
a guide wire lumen; and
an inflation lumen; and
wherein the guide wire lumen of the catheter shaft is connected to the guidewire lumen of the balloon; and
wherein the inflation lumen of the catheter shaft is fluidly connected to the inflation passages of the balloon.

### Claim 7 (depends on 1)

The non-occluding medical balloon apparatus in accordance with claim 1, wherein the expanded central passage of the expanded balloon portion is empty except for the guide wire lumen.