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Artificial spleen to treat bloodstream infections: Sepsis therapeutic device under development

Date:
March 30, 2013
Source:
Wyss Institute
Summary:
Scientists are developing blood-cleansing technology. The device will be used to treat bloodstream infections that are the leading cause of death in critically ill patients and soldiers injured in combat. To rapidly cleanse the blood of pathogens, the patient's blood is mixed with magnetic nanobeads coated with a genetically engineered version of a human blood 'opsonin' protein that binds to a wide variety of bacteria, fungi, viruses, parasites, and toxins.

The Spleen-on-a-chip, developed at the Wyss Institute, will be used to treat bloodstream infections that are the leading cause of death in critically ill patients and soldiers injured in combat.
Credit: Wyss Institute

The Wyss Institute for Biologically Inspired Engineering at Harvard University announced today that it was awarded a $9.25 million contract from the Defense Advanced Research Projects Agency (DARPA) to further advance a blood-cleansing technology developed at the Institute with prior DARPA support, and help accelerate its translation to humans as a new type of sepsis therapy.

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The device will be used to treat bloodstream infections that are the leading cause of death in critically ill patients and soldiers injured in combat.

To rapidly cleanse the blood of pathogens, the patient's blood is mixed with magnetic nanobeads coated with a genetically engineered version of a human blood 'opsonin' protein that binds to a wide variety of bacteria, fungi, viruses, parasites, and toxins. It is then flowed through microchannels in the device where magnetic forces pull out the bead-bound pathogens without removing human blood cells, proteins, fluids, or electrolytes -- much like a human spleen does. The cleansed blood then flows back to the patient.

"In just a few years we have been able to develop a suite of new technologies, and to integrate them to create a powerful new device that could potentially transform the way we treat sepsis," said Wyss founding director and project leader, Don Ingber, M.D., Ph.D. "The continued support from DARPA enables us to advance our device manufacturing capabilities and to obtain validation in large animal models, which is precisely what is required to enable this technology to be moved towards testing in humans."

The team will work to develop manufacturing and integration strategies for its core pathogen-binding opsonin and Spleen-on-a-Chip fluidic separation technologies, as well as a novel coating technology called "SLIPS," which is a super-hydrophobic coating inspired from the slippery surface of a pitcher plant that repels nearly any material it contacts. By coating the inner surface of the channels of the device with SLIPS, blood cleansing can be carried out without the need for anticoagulants to prevent blood clotting.

In addition to Ingber, the multidisciplinary team behind this effort includes Wyss core faculty and Harvard School of Engineering and Applied Science faculty member Joanna Aizenberg, Ph.D., who developed the SLIPS technology; Wyss senior staff member Michael Super, Ph.D., who engineered the human opsonin protein; and Mark Puder, M.D., Ph.D., Associate Professor of Pediatric Surgery at Boston Children's Hospital and Harvard Medical School who will be assisting with animal studies.


Story Source:

The above story is based on materials provided by Wyss Institute. Note: Materials may be edited for content and length.


Cite This Page:

Wyss Institute. "Artificial spleen to treat bloodstream infections: Sepsis therapeutic device under development." ScienceDaily. ScienceDaily, 30 March 2013. <www.sciencedaily.com/releases/2013/03/130330130531.htm>.
Wyss Institute. (2013, March 30). Artificial spleen to treat bloodstream infections: Sepsis therapeutic device under development. ScienceDaily. Retrieved March 28, 2015 from www.sciencedaily.com/releases/2013/03/130330130531.htm
Wyss Institute. "Artificial spleen to treat bloodstream infections: Sepsis therapeutic device under development." ScienceDaily. www.sciencedaily.com/releases/2013/03/130330130531.htm (accessed March 28, 2015).

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