IP Library Granted Patent US 12,390,621
Granted Patent B1
US 12,390,621 · App. 17/671,296 · Granted Aug 19, 2025

System and method for selective pressure-controlled therapeutic delivery

Inventors: Aravind Arepally (Atlanta, GA); James E. Chomas (Denver, CO); Bryan Pinchuk (Miami, FL); David Benjamin Jaroch (Arvada, CO)
Assignee: TriSalus Life Sciences, Inc.
A61M25/10A61F2/013A61L29/16B05D1/18B05D3/0272A61F2240/001A61L2430/36A61M25/0108A61M2025/1052A61M39/22A61M2039/229A61M2205/3334A61M2230/06A61M2230/30
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Quick Facts
Patent No.
US 12,390,621
App. No.
17/671,296
Granted
Aug 19, 2025
Kind
B1
Abstract

A treatment system includes a guide sheath, and a catheter provided with a pressure-controlled element. The pressure-control element preferably includes an expanded configuration adapted to extend across a small feeder vessel branching from the splenic vein. The pressure-control element is positioned with the feeder vessel, and a therapeutic agent is delivered under pressure directly into the feeder vessel, where it is forced to penetrate deep into tissue. Pressure responsive elements for monitoring intravascular pressure are also provided to time delivery of the therapeutic agent for maximum uptake by the target organ. Methods for treating tissues and organs via vascular pathways are provided.

Claims (66)

1. A method for delivering a therapeutic agent for treatment of a solid tumor in a target organ, the target organ in fluid communication with a vein in a patient, the method comprising:

a) introducing a treatment system into the vein of the patient, the treatment system comprising a microvalve comprising a filamentary braid coated with a polymeric filter comprising pores, the microvalve movable between a collapsed configuration for delivery through the vein, and an expanded configuration adapted to extend across the vein;

b) advancing the microvalve into the vein in the collapsed configuration, the vein subject to a systemic venous pressure on a distal side of the microvalve; then

c) expanding the microvalve into the expanded configuration to block flow within the vein in a distal to proximal direction past the microvalve; and

d) injecting the therapeutic agent at a first pressure, distal of the microvalve and into the vein to cause the therapeutic agent to flow through the vein and into the target organ at a pressure higher than the systemic venous pressure, wherein a pressure of the injected therapeutic agent generates a net increase in fluid pressure in the vein of 10 mmHg to 200 mmHg above the systemic venous pressure.

2. The method according to claim 1 , wherein:

the first pressure is below 300 psi.

3. The method according to claim 1 , wherein:

the microvalve is dynamic such that the microvalve automatically expands to the expanded configuration and contracts to a smaller configuration in response to fluid pressure within the vein on proximal and distal sides of the microvalve, wherein in the smaller configuration the microvalve is not adapted to block flow within the vein.

4. The method according to claim 3 , wherein:

the microvalve is located on a catheter, the catheter comprising a proximal end, a distal end, a first lumen extending between the proximal and distal ends and having a distal orifice, and the microvalve located at the distal end, proximal of the distal orifice.

5. The method according to claim 1 , wherein:

the treatment system further comprises is a static occlusion element.

6. The method according to claim 5 , wherein:

the static occlusion element is a balloon.

7. The method according to claim 4 , wherein:

the proximal end of the catheter comprises an implantable injection port, and

further comprising implanting the implantable injection port in the patient and injecting a bolus of a second agent, such that the injecting the therapeutic agent and the injecting the bolus of the second agent both occur through the implanted injection port.

8. The method according to claim 1 , wherein:

the therapeutic agent comprises one of a radio-embolization agent and a biologic agent.

9. The method according to claim 1 , wherein:

the therapeutic agent is a biologic agent selected from the group consisting of one of CAR-T cells, CAR-NK cells, TCR-R cells, TCR-NK cells, B-cells, and a combination of two or more of the cells.

10. The method according to claim 1 , wherein:

the therapeutic agent comprises one or more of a biologic cell, a checkpoint inhibitor, and an oncolytic virus.

11. The method according to claim 1 , wherein:

the target organ is one of the pancreas, the kidneys, and the liver.

12. The method according to claim 1 , wherein:

the vein is a portal vein or a feeder vessel extending therefrom.

13. The method according to claim 1 , wherein:

the vein is a splenic vein or a feeder vessel extending therefrom.

14. A method for delivering a therapeutic agent under pressure to a target organ for treatment of a solid tumor in the target organ, the target organ in fluid communication with a vein in a patient, the method comprising:

a) introducing a treatment system into the vein of the patient, the treatment system comprising a microvalve comprising a filamentary braid coated with a polymeric filter comprising pores, the microvalve movable between a collapsed configuration for delivery through the vein, and an expanded configuration adapted to extend across the vein;

b) advancing the microvalve in the collapsed configuration into the vein, wherein the vein is subject to a systemic venous pressure on a distal side of the microvalve; then

c) expanding the microvalve into the expanded configuration across the vein to block flow within the vein in a distal to proximal direction past the microvalve; and

d) injecting the therapeutic agent at a first pressure below 300 psi to exit distal of the microvalve and into the vein to cause the therapeutic agent to flow through the vein at a pressure higher than the systemic venous pressure and into the target organ, the therapeutic agent comprising a biologic agent selected from the group consisting of one of CAR-T cells, CAR-NK cells, TCR-R cells, TCR-NK cells, B-cells, and a combination of two or more of the cells.

15. The method according to claim 14 , wherein:

the target organ is one of the pancreas, the kidneys, and the liver.

16. The method according to claim 14 , wherein:

the vein is a portal vein or a feeder vessel extending therefrom.

17. The method according to claim 14 , wherein:

the vein is a splenic vein or a feeder vessel extending therefrom.

18. A method for delivering a therapeutic agent under pressure to a target organ for treatment of a solid tumor in the target organ, the target organ in fluid communication with a vein in a patient, the method comprising:

a) introducing a treatment system into the vein of the patient, the treatment system comprising a microvalve comprising a filamentary braid coated with a polymeric filter comprising pores, the microvalve movable between a collapsed configuration for delivery through the vein, and an expanded configuration adapted to extend across the vein;

b) advancing the microvalve in the collapsed configuration into the vein, wherein the vein is subject to a systemic venous pressure on a distal side of the microvalve; then

c) expanding the microvalve into the expanded configuration across the vein to block flow within the vein in a distal to proximal direction past the microvalve; and

d) injecting the therapeutic agent at a first pressure below 300 psi to exit distal of the microvalve and into the vein to cause the therapeutic agent to flow through the vein at a pressure higher than the systemic venous pressure and into the target organ, the therapeutic agent comprising one or more of a biologic cell, a checkpoint inhibitor, and an oncolytic virus.

19. The method according to claim 18 , wherein:

the target organ is one of the pancreas, the kidneys, and the liver.

20. The method according to claim 18 , wherein:

the vein is a portal vein or a feeder vessel extending from the portal vein.

21. The method according to claim 18 , wherein:

the vein is a splenic vein or a feeder vessel extending from the splenic vein.

22. A method for delivering a therapeutic agent under pressure to a target organ for treatment of a solid tumor in the target organ, the target organ in fluid communication with one or more vessels in a patient, the method comprising:

a) introducing a treatment system into a vessel of the patient in fluid communication with the target organ, the treatment system comprising a microvalve comprising a filamentary braid coated with a polymeric filter comprising pores, the microvalve having shape memory to an expanded configuration adapted to extend across the vessel;

b) advancing the microvalve into the vessel, wherein the vessel is subject to a systemic venous pressure on a distal side of the microvalve; then

c) expanding the microvalve across the vessel to block flow within the vessel in a distal to proximal direction past the microvalve;

d) injecting the therapeutic agent at a first pressure below 300 psi to exit distal of the microvalve and into the vessel to cause the therapeutic agent to flow through the vessel at a pressure higher than the systemic venous pressure and into the target organ, the therapeutic agent comprising a biologic agent selected from the group consisting of one of CAR-T cells, CAR-NK cells, TCR-R cells, TCR-NK cells, β-cells, and a combination of two or more of the cells; and

e) injecting a bolus of a second fluid different than the therapeutic agent at a second pressure at or above 300 psi, the second fluid entering the vessel and forcing the therapeutic agent to flow deeper through the vessel to therapeutically treat the solid tumor in the target organ with the therapeutic agent.

23. The method of claim 22 , wherein the target organ is not located within an extremity.

24. A method for delivering a therapeutic agent under pressure to a target organ for treatment of a solid tumor in the target organ, the target organ in fluid communication with one or more vessels in a patient, the method comprising:

a) introducing a treatment system into a vessel of the patient in fluid communication with the target organ, the treatment system comprising a microvalve comprising a filamentary braid coated with a polymeric filter comprising pores, the microvalve having shape memory to an expanded configuration adapted to extend across the vessel;

b) advancing the microvalve into the vessel, wherein the vessel is subject to a systemic venous pressure on a distal side of the microvalve; then

c) expanding the microvalve across the vessel to block flow within the vessel in a distal to proximal direction past the microvalve;

d) injecting the therapeutic agent at a first pressure below 300 psi to exit distal of the microvalve and into the vessel to cause the therapeutic agent to flow through the vessel at a pressure higher than the systemic venous pressure and into the target organ, the therapeutic agent comprising one or more of a biologic cell, a checkpoint inhibitor, and an oncolytic virus; and

e) injecting a bolus of a second fluid different than the therapeutic agent at a second pressure at or above 300 psi, the second fluid entering the vessel and forcing the therapeutic agent to flow deeper through the vessel to therapeutically treat the solid tumor in the target organ with the therapeutic agent.

25. The method of claim 24 , wherein the target organ is not located within an extremity.

Assignments (3)
SECURITY INTEREST Recorded Apr 30, 2024
From: TRISALUS LIFE SCIENCES, INC.
To: ORBIMED ROYALTY & CREDIT OPPORTUNITIES IV, LP
Reel/Frame 067274/0733 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 17, 2022
From: CHOMAS, JAMES E.; JAROCH, DAVID BENJAMIN; PINCHUK, BRYAN; AREPALLY, ARAVIND
To: SUREFIRE MEDICAL, INC.
Reel/Frame 059036/0471 →
CHANGE OF NAME Recorded Feb 17, 2022
From: SUREFIRE MEDICAL, INC.
To: TRISALUS LIFE SCIENCES, INC.
Reel/Frame 059174/0245 →
Continuity (3)
Continuation 15871326 · Jan 15, 2018
Continuation In Part 15703951 · Sep 13, 2017
Provisional Application 62396622 · Sep 19, 2016
References Cited (68)
US 4738740A · Pinchuk et al. · 1988 [cited by applicant]
US 5171299A · Heitzmann · 1992 [cited by applicant]
US 5397308A · Ellis · 1995 [cited by applicant]
US 5534287A · Lukic · 1996 [cited by applicant]
US 6641553B1 · Chee · 2003 [cited by examiner]
US 6699231B1 · Sterman et al. · 2004 [cited by applicant]
US 6743196B2 · Barbut · 2004 [cited by applicant]
US 8696698B2 · Chomas et al. · 2014 [cited by applicant]
US 9737693B2 · Helkowski · 2017 [cited by applicant]
US 11090468B2 · Chappa · 2021 [cited by applicant]
US 11324619B1 · Yacoby · 2022 [cited by applicant]
US 11400263B1 · Arepally · 2022 [cited by examiner]
US 20010041862A1 · Glickman · 2001 [cited by examiner]
US 20030135255A1 · Sundar · 2003 [cited by applicant]
US 20040006305A1 · Hebert · 2004 [cited by applicant]
US 20040063805A1 · Pacetti et al. · 2004 [cited by applicant]
US 20040098099A1 · McCullagh et al. · 2004 [cited by applicant]
US 20040167385A1 · Rioux et al. · 2004 [cited by applicant]
US 20050113798A1 · Slater · 2005 [cited by applicant]
US 20060149141A1 · Sheets · 2006 [cited by applicant]
US 20060178695A1 · DeCant et al. · 2006 [cited by applicant]
US 20060263301A1 · Vernon · 2006 [cited by applicant]
US 20060264898A1 · Beasley · 2006 [cited by examiner]
US 20070042018A1 · Shalaby · 2007 [cited by applicant]
US 20070191931A1 · Weber et al. · 2007 [cited by applicant]
US 20080051758A1 · Rioux · 2008 [cited by applicant]
US 20080234796A1 · Dorn · 2008 [cited by applicant]
US 20090060973A1 · Hunter et al. · 2009 [cited by applicant]
US 20100069841A1 · Miesel · 2010 [cited by applicant]
US 20100113939A1 · Mashimo et al. · 2010 [cited by applicant]
US 20140276411A1 · Cowan · 2014 [cited by examiner]
US 20140364835A1 · Allen et al. · 2014 [cited by applicant]
US 20150272716A1 · Pinchuk et al. · 2015 [cited by applicant]
US 20150306311A1 · Pinchuk et al. · 2015 [cited by applicant]
US 20160082178A1 · Agah et al. · 2016 [cited by applicant]
US 20160242893A1 · Joshi et al. · 2016 [cited by applicant]
US 20160249969A1 · Santoinanni · 2016 [cited by applicant]
US 20160310148A1 · Allen · 2016 [cited by examiner]
US 20170368306A1 · Tal · 2017 [cited by examiner]
US 20200205840A1 · Adawi · 2020 [cited by applicant]
US 20200383688A1 · Olson · 2020 [cited by applicant]
US 20210244473A1 · Cook · 2021 [cited by applicant]
US 20230025500A1 · Jaroch et al. · 2023 [cited by applicant]
EP 1743524A1 · 2007 [cited by examiner]
JP 2002537909 · 2002 [cited by applicant]
JP 2006051144A · 2006 [cited by applicant]
JP 2006523515 · 2006 [cited by applicant]
WO 9902093A1 · 1999 [cited by applicant]
WO WO2000051675 · 2000 [cited by applicant]
WO 02055146A1 · 2002 [cited by applicant]
WO 2004075776 · 2004 [cited by applicant]
WO WO2011068946 · 2011 [cited by applicant]
WO 2016149653 · 2016 [cited by applicant]
WO WO2018175148 · 2018 [cited by applicant]
WO WO2019140381 · 2019 [cited by applicant]
Canadian Office Action 2 dated Jun. 3, 2022 of Application No. 3,139,118. [cited by applicant]
International Search Report and Written Opinion of Application No. PCT/US2020/034626 dated Aug. 26, 2020. [cited by applicant]
Japanese Office Action dated Apr. 28, 2021 of Application No. 2020-082002. [cited by applicant]
Japanese Office Action dated May 10, 2022 of Application No. 2021-572025. [cited by applicant]
U.S. Appl. No. 17/375,779, Arepally et al. [cited by applicant]
U.S. Appl. No. 19/054,055, Arepally et al. [cited by applicant]
Jedwab et al., A Study of the Geometrical and Mechanical Properties of a Self-Expanding Metallic Stent Theory and Experiment, Journal of Applied Biomaterials, Spring 1993, pp. 77-85, 4.1. [cited by applicant]
Rose et al., Temporary Splenic Artery Balloon Occlusion for Protection of Nonsplenic Vascular Beds During Splenic Embolization, American Journal of Roentgenology, May 1998, pp. 1186-1188, 170.5. [cited by applicant]
Rose et al., Downstream Hepatic Arterial Blood Pressure Changes Caused by Deployment of the Surefire AntiReflux Expandable Tip, Cardiovascular and Interventional Radiology, Oct. 2013, pp. 1262-1269, 36. [cited by applicant]
Rose et al., Feasibility of Intraprocedural Transluminal Hepatic and Femoral Artery Blood Pressure Measurements as an Alternative Embolization Safety Endpoint When Antireflux Devices Are Used During Lobar Chemoembolizat… [cited by applicant]
Rose et al., Quantification of Blood Pressure Changes in the Vascular Compartment When Using an Anti-Reflux Catheter during Chemoembolization versus Radioembolization: A Retrospective Case Series, Journal of Vascular an… [cited by applicant]
Rose et al., The Beauty and Bane of Pressure-Directed Embolotherapy: Hemodynamic Principles and Preliminary Clinical Evidence, American Journal of Roentgenology, Mar. 2019, pp. 686-695, 212.3. [cited by applicant]
Iranpour et al. Altered Doppler Flow Patterns in Cirrhosis Patients: An Overview, Ultrasonography, Jan. 2016, pp. 2-12, 35.1. [cited by applicant]