The long-term goal of this technology development project is improve the rehabilitation of veterans suffering from lung diseases through the development of the first truly portable, biocompatible, artificial lung capable of short and long term respiratory support. Artificial lungs are currently used to rehabilitate lung disease patients; however, significant advances in gas exchange, biocompatibility, and portability are required to fully realize their potential. Microfluidic artificial lungs promise to enable a new class of truly portable artificial lungs through feature sizes and blood channel designs that more closely mimic those found in their natural counterpart. Our small-scale microfluidic artificial lungs achieved the highest gas exchange efficiency of any artificial lung to date. Their lifetimes were significantly improved through the application of biocompatible surface coatings. Initial in vivo demonstrations were performed in an animal (rat) model. However, current microfabrication techniques limit the microfluidic networks in these devices to two dimensions, thereby severely limiting potential device topologies and resulting in inefficient blood distribution networks. Further, current construction techniques may not be suitable for the large area production required for human applications. In this study, we will for the first time harness high resolution 3D polymer printing technology to create large area microfluidic lungs with truly three dimensional blood flow networks and topologies. Constructed 3D printed microfluidic artificial lungs will exhibit gas exchange suitable for some human applications, while using a fraction of the blood contacting surface area, blood volume, and total volume of current commercial devices. The objectives of the current technology-development SPiRE proposal are thus to: 1) Determine optimal 3D printing parameters for microfluidic artificial lungs; and, 2) Construct and test the first 3D printed microfluidic artificial lung in the laboratory using whole animal blood. At the conclusion of this study, we will be ready to test our 3D printed microfluidic artificial lungs in a large animal model. The listed objectives are thus critical to advancing this promising technology towards initial acute systems for veteran pulmonary rehabilitation.

Public Health Relevance

Chronic obstructive pulmonary disease (COPD) affects approximately 16% of the veteran population. COPD is the fourth most prevalent disease in the VA population and one of the most costly to the VA health care system. Over 500,000 service-connected respiratory disabilities have been diagnosed in veterans and 6.5% of all Gulf War service-connected disabilities are respiratory system related. Operation Enduring Freedom and Operation Iraqi Freedom Veterans have been exposed to chemicals known to cause acute and chronic respiratory conditions including CARC paint and chromium dust. Other veterans have experienced acute lung injury and failure from blast injury or smoke inhalation. Over 2.3 million veterans reported having some form of ?lung trouble? in the 2001 National Survey of Veterans. This project has the potential to revolutionize the rehabilitation of veterans suffering from lung disease through the development of a truly portable, biocompatible, artificial lung.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Veterans Administration (I21)
Project #
1I21RX002403-01A1
Application #
9349646
Study Section
Rehabilitation Research and Development SPiRE Program (RRDS)
Project Start
2017-07-01
Project End
2019-06-30
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Veterans Health Administration
Department
Type
DUNS #
096318480
City
Ann Arbor
State
MI
Country
United States
Zip Code
48105