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A complete understanding of how the surface properties of inorganic materials influence blood clot initiation and propagation is essential for the further development of implantable biomaterials and hemostatic agents. Our goal is to create a surface science model that predicts how material surface properties can be manipulated to create a completely biocompatible surface, where thrombus formation does not occur, or a highly effective hemostatic agent where thrombus formation occurs very rapidly.
Our approach is to relate changes in the surface chemistry and physical properties of inorganic materials to observed changes in the in vitro clotting response to those materials. To date, we have found that properties such as surface potential, surface area, heat of hydration, and ion exchange capacity play a critical role in thrombus formation at the surface of inorganic materials. In addition, our work with mesocellular foams has shown the “protein-accessible” surface area of porous materials can be optimized by tuning their pore-opening diameter to match the hydrodynamic radius of certain blood clotting zymogens. The results of this work have lead to the development of several, highly effective hemostatic agents that are currently used by the United States Military to control hemorrhage due to traumatic injury.
asawvel [at] chem.ucsb.edu