R42HL170864
Project Grant
Overview
Grant Description
Manufacturable biomimetic microfluidic oxygenator for safer, simpler treatment of respiratory failure - Project summary/abstract
This fast track STTR project focuses on developing and demonstrating a high-volume manufacturing technology for microfluidic oxygenators for applications requiring extracorporeal membrane oxygenation (ECMO) to treat respiratory failure.
Unlike heart disease and cancer, mortality from lung diseases continue to rise, and a combination of increasing patient populations suffering from chronic obstructive pulmonary disease and acute lung injury associated with respiratory infectious diseases and trauma represent an enormous health care challenge in the US and across the world.
The gold standard treatment for respiratory failure, invasive mechanical ventilation, carries significant risks of mechanical and biochemical injury to the lung along with microbial exposure.
As a result, ECMO has emerged as an alternative therapy that allows injured lungs to rest, directly oxygenating and removing carbon dioxide from the blood in an extracorporeal circuit.
However, ECMO use is limited due to the extreme complexity of the blood circuit, which includes a hollow fiber membrane oxygenator (HFMO) as the functional unit, and bioinspired microfluidic oxygenators capable of more safely oxygenating the blood have emerged.
Our preliminary data demonstrates the first large-scale, extended duration microfluidic oxygenators in large animals, with distinct safety and efficacy advantages over HFMO, but the method of construction is very complex and costly.
We have engaged with high precision injection molding companies to identify a path to produce the devices at high volume and low cost, and the focus here is to develop and demonstrate the injection molded microfluidic oxygenator technology in safety and efficacy studies in a porcine model.
Toward this end, we propose a fast track proposal comprising two phases and four overall aims.
In Phase I, we will 1) define the target product profile for the adult clinical scale microfluidic oxygenator and conduct fluid mechanical and thermal modeling to identify the process window required for high yield injection molding of these devices, 2) iteratively apply computational models to verify the oxygen transfer and blood flow, pressure and shear properties of oxygenators resulting from these designs, and 3) build a casted replica of the injection molding design to confirm gas transfer performance.
Successful identification of a microfluidic oxygenator design that meets the requirements from manufacturability, cost and performance perspectives will lead to advancement to Phase II of the program.
Here we will 1) fabricate the injection molds required for fabrication of larger numbers of microfluidic oxygenators at pediatric and adult scale, and 2) test these pediatric and adult scale oxygenators in extended duration studies in porcine models to confirm safety and efficacy in comparison with HFMO control devices.
This demonstration of safety and efficacy, enabled by the high-volume injection molding process developed on this project, will accelerate the advancement of the technology toward commercialization and clinical translation for treatment of critically ill patients suffering from respiratory failure.
This fast track STTR project focuses on developing and demonstrating a high-volume manufacturing technology for microfluidic oxygenators for applications requiring extracorporeal membrane oxygenation (ECMO) to treat respiratory failure.
Unlike heart disease and cancer, mortality from lung diseases continue to rise, and a combination of increasing patient populations suffering from chronic obstructive pulmonary disease and acute lung injury associated with respiratory infectious diseases and trauma represent an enormous health care challenge in the US and across the world.
The gold standard treatment for respiratory failure, invasive mechanical ventilation, carries significant risks of mechanical and biochemical injury to the lung along with microbial exposure.
As a result, ECMO has emerged as an alternative therapy that allows injured lungs to rest, directly oxygenating and removing carbon dioxide from the blood in an extracorporeal circuit.
However, ECMO use is limited due to the extreme complexity of the blood circuit, which includes a hollow fiber membrane oxygenator (HFMO) as the functional unit, and bioinspired microfluidic oxygenators capable of more safely oxygenating the blood have emerged.
Our preliminary data demonstrates the first large-scale, extended duration microfluidic oxygenators in large animals, with distinct safety and efficacy advantages over HFMO, but the method of construction is very complex and costly.
We have engaged with high precision injection molding companies to identify a path to produce the devices at high volume and low cost, and the focus here is to develop and demonstrate the injection molded microfluidic oxygenator technology in safety and efficacy studies in a porcine model.
Toward this end, we propose a fast track proposal comprising two phases and four overall aims.
In Phase I, we will 1) define the target product profile for the adult clinical scale microfluidic oxygenator and conduct fluid mechanical and thermal modeling to identify the process window required for high yield injection molding of these devices, 2) iteratively apply computational models to verify the oxygen transfer and blood flow, pressure and shear properties of oxygenators resulting from these designs, and 3) build a casted replica of the injection molding design to confirm gas transfer performance.
Successful identification of a microfluidic oxygenator design that meets the requirements from manufacturability, cost and performance perspectives will lead to advancement to Phase II of the program.
Here we will 1) fabricate the injection molds required for fabrication of larger numbers of microfluidic oxygenators at pediatric and adult scale, and 2) test these pediatric and adult scale oxygenators in extended duration studies in porcine models to confirm safety and efficacy in comparison with HFMO control devices.
This demonstration of safety and efficacy, enabled by the high-volume injection molding process developed on this project, will accelerate the advancement of the technology toward commercialization and clinical translation for treatment of critically ill patients suffering from respiratory failure.
Awardee
Funding Goals
THE DIVISION OF LUNG DISEASES SUPPORTS RESEARCH AND RESEARCH TRAINING ON THE CAUSES, DIAGNOSIS, PREVENTION, AND TREATMENT OF LUNG DISEASES AND SLEEP DISORDERS. RESEARCH IS FUNDED THROUGH INVESTIGATOR-INITIATED AND INSTITUTE-INITIATED GRANT PROGRAMS AND THROUGH CONTRACT PROGRAMS IN AREAS INCLUDING ASTHMA, BRONCHOPULMONARY DYSPLASIA, CHRONIC OBSTRUCTIVE PULMONARY DISEASE, CYSTIC FIBROSIS, RESPIRATORY NEUROBIOLOGY, SLEEP AND CIRCADIAN BIOLOGY, SLEEP-DISORDERED BREATHING, CRITICAL CARE AND ACUTE LUNG INJURY, DEVELOPMENTAL BIOLOGY AND PEDIATRIC PULMONARY DISEASES, IMMUNOLOGIC AND FIBROTIC PULMONARY DISEASE, RARE LUNG DISORDERS, PULMONARY VASCULAR DISEASE, AND PULMONARY COMPLICATIONS OF AIDS AND TUBERCULOSIS. THE DIVISION IS RESPONSIBLE FOR MONITORING THE LATEST RESEARCH DEVELOPMENTS IN THE EXTRAMURAL SCIENTIFIC COMMUNITY AS WELL AS IDENTIFYING RESEARCH GAPS AND NEEDS, OBTAINING ADVICE FROM EXPERTS IN THE FIELD, AND IMPLEMENTING PROGRAMS TO ADDRESS NEW OPPORTUNITIES. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, USE SMALL BUSINESS TO MEET FEDERAL RESEARCH AND DEVELOPMENT NEEDS, FOSTER AND ENCOURAGE PARTICIPATION IN INNOVATION AND ENTREPRENEURSHIP BY SOCIALLY AND ECONOMICALLY DISADVANTAGED PERSONS, AND INCREASE PRIVATE-SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT FUNDING. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE TECHNOLOGICAL INNOVATION, FOSTER TECHNOLOGY TRANSFER THROUGH COOPERATIVE R&D BETWEEN SMALL BUSINESSES AND RESEARCH INSTITUTIONS, AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL R&D.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Massachusetts
United States
Geographic Scope
State-Wide
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been extended from 04/16/25 to 08/31/26 and the total obligations have increased 986% from $294,063 to $3,193,069.
Biomembretics was awarded
Biomimetic Microfluidic Oxygenator for Safer Respiratory Treatment
Project Grant R42HL170864
worth $3,193,069
from National Heart Lung and Blood Institute in September 2024 with work to be completed primarily in Massachusetts United States.
The grant
has a duration of 2 years and
was awarded through assistance program 93.837 Cardiovascular Diseases Research.
The Project Grant was awarded through grant opportunity PHS 2023-2 Omnibus Solicitation of the NIH for Small Business Technology Transfer Grant Applications (Parent STTR [R41/R42] Clinical Trial Not Allowed).
SBIR Details
Research Type
STTR Phase I
Title
Manufacturable Biomimetic Microfluidic Oxygenator for Safer, Simpler Treatment of Respiratory Failure
Abstract
PROJECT SUMMARY/ABSTRACT This Fast Track STTR project focuses on developing and demonstrating a high-volume manufacturing technology for microfluidic oxygenators for applications requiring ExtraCorporeal Membrane Oxygenation (ECMO) to treat respiratory failure. Unlike heart disease and cancer, mortality from lung diseases continue to rise, and a combination of increasing patient populations suffering from Chronic Obstructive Pulmonary Disease and acute lung injury associated with respiratory infectious diseases and trauma represent an enormous health care challenge in the US and across the world. The gold standard treatment for respiratory failure, invasive mechanical ventilation, carries significant risks of mechanical and biochemical injury to the lung along with microbial exposure. As a result, ECMO has emerged as an alternative therapy that allows injured lungs to rest, directly oxygenating and removing carbon dioxide from the blood in an extracorporeal circuit. However, ECMO use is limited due to the extreme complexity of the blood circuit, which includes a hollow fiber membrane oxygenator (HFMO) as the functional unit, and bioinspired microfluidic oxygenators capable of more safely oxygenating the blood have emerged. Our preliminary data demonstrates the first large-scale, extended duration microfluidic oxygenators in large animals, with distinct safety and efficacy advantages over HFMO, but the method of construction is very complex and costly. We have engaged with high precision injection molding companies to identify a path to produce the devices at high volume and low cost, and the focus here is to develop and demonstrate the injection molded microfluidic oxygenator technology in safety and efficacy studies in a porcine model. Toward this end, we propose a fast track proposal comprising two phases and four overall aims. In Phase I, we will 1) Define the target product profile for the adult clinical scale microfluidic oxygenator and conduct fluid mechanical and thermal modeling to identify the process window required for high yield injection molding of these devices, 2) Iteratively apply computational models to verify the oxygen transfer and blood flow, pressure and shear properties of oxygenators resulting from these designs, and 3) Build a casted replica of the injection molding design to confirm gas transfer performance. Successful identification of a microfluidic oxygenator design that meets the requirements from manufacturability, cost and performance perspectives will lead to advancement to Phase II of the program. Here we will 1) Fabricate the injection molds required for fabrication or larger numbers of microfluidic oxygenators at pediatric and adult scale, and 2) Test these pediatric and adult scale oxygenators in extended duration studies in porcine models to confirm safety and efficacy in comparison with HFMO control devices. This demonstration of safety and efficacy, enabled by the high-volume injection molding process developed on this project, will accelerate the advancement of the technology toward commercialization and clinical translation for treatment of critically ill patients suffering from respiratory failure.
Topic Code
NHLBI
Solicitation Number
PA23-232
Status
(Ongoing)
Last Modified 9/5/25
Period of Performance
9/17/24
Start Date
8/31/26
End Date
Funding Split
$3.2M
Federal Obligation
$0.0
Non-Federal Obligation
$3.2M
Total Obligated
Activity Timeline
Transaction History
Modifications to R42HL170864
Additional Detail
Award ID FAIN
R42HL170864
SAI Number
R42HL170864-2550498286
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Funding Office
75NH00 NIH National Heart, Lung, and Blood Institute
Awardee UEI
JQGRGECTY9N6
Awardee CAGE
None
Performance District
MA-90
Senators
Edward Markey
Elizabeth Warren
Elizabeth Warren
Modified: 9/5/25