
Technology
The present technology consists of tissue engineered vascular grafts (TEVG's), blood vessel mimics (BVMs), and methods for using these in in vitro model systems for evaluation of intravascular drugs and devices. The present invention includes devices and methods for preparing TEVGs, BVMs and model systems that mimic blood vessel or tubular structure aneurysms. These structures make use of tubular polymeric scaffolds having luminal surfaces that include at least one layer of cells. These tubular scaffolds are comprised of either expanded polymers or electrospun materials while Stromal Vascular Fraction (SVF) cells are utilized for the generation of luminal surfaces having at least one layer of cells. The present technology also includes of methods of development of aneurysm models using serum-free conditions and scaffold variations.

Markets Addressed
Coronary artery disease, the most common form of heart disease, resulted in over 600,000 deaths in 2012, making it the single leading cause of death in the United States. A frequently utilized technique aimed at treating the disease and restoring adequate blood flow to the heart is percutaneous coronary angioplasty accompanied by placement of a stent. Present methods of pre-clinical stent assessment rely on in vivo animal models, including rabbit and pig models. These methods, however, create considerable challenges, namely the long periods of time associated with animal preparation and testing execution, the high costs of animal modeling, and animal to human variability. The technology developed by researchers at the University of Louisville alleviates these problems by providing for blood vessel mimics and methods for preparing the same. Further, this technology allows for development of aneurysm models to allow for improved pre-clinical stent design and testing for the treatment of aneurysms.
Technology Status
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accompanied
technology
bvms
aneurysm
stent
vessel
methods
serum-free
mimics
blood
