Contact CaRE LabTBRC, C2798 Department of Biomedical Engineering Medical College of Wisconsin 8701 W Watertown Plank Rd Milwaukee, WI 53226 PH: 414-955-4785
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For this project, the Cardiovascular Regenerative Engineering Laboratory is synthesizing magnetic nanoparticles for use in labeling autologous cells, a process based on the concept of using magnetic cell targeting to improve endothelial cell performance. When this is complete, CaRE will work to fabricate the next generation of magnetic vascular grafts for implantation in the animal model. These grafts are expected to bridge the existing knowledge gap in the field of regenerative medicine by providing an alternative therapeutic strategy for patients with coronary artery disease while yielding better clinical outcomes.
In addition to the above, the synthesized magnetic nanoparticles will be used to fabricate biosynthetic magnetic heart valves—a necessary step in addressing the challenges associated with current prosthetic valves, including design limitations, thrombosis, dual antiplatelet therapy, and calcification— and testing the hydrodynamic performance of the engineered cardiac valves using the Heart Valve Assessment Platform and in vivo model. Along with other major technological advancements, these functional heart valves are expected to improve the efficacy of valve replacement procedures in the future.
Hailey is an undergraduate student in the Marquette-MCW Joint Department of Biomedical Engineering. Her interests include prosthetics and implantable devices.
Tefft BJ, Uthamaraj S, Harbuzariu A, Harburn JJ, Witt TA, Newman B, Psaltis PJ, Hlinomaz O, Holmes DR Jr, Gulati R, Simari RD, Dragomir-Daescu D, Sandhu GS. Nanoparticle-Mediated Cell Capture Enables Rapid Endothelialization of a Novel Bare Metal Stent. Tissue Eng Part A. 2018 07;24(13-14):1157-1166 PMID: 29431053 PMCID: PMC6033300 SCOPUS ID: 2-s2.0-85049639118 02/13/2018
Tefft BJ, Uthamaraj S, Harburn JJ, Hlinomaz O, Lerman A, Dragomir-Daescu D, Sandhu GS. Magnetizable stent-grafts enable endothelial cell capture. J Magn Magn Mater. 2017 Apr 01;427:100-104 PMID: 28286359 PMCID: PMC5341609 03/14/2017