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- (3dy) Advanced Polymeric and Bionanocomposite Solutions for Tissue Engineering and Drug Delivery Applications
The rapidly evolving toolset available to polymer scientists is enabling the birth of a new generation of smart composite devices which can be tailored to suit the specific and demanding requirements of advanced biomaterials applications from efficient and site-specific drug delivery to the regeneration of complex tissue. With a strong background in polymer synthesis, characterization, and transport phenomena and development of polymeric therapies for tissue engineering applications, I am well-positioned to push the boundaries of scientific discovery at the interface of polymer science and biomedical research. Within this broad scope, early efforts will focus on three primary research thrusts:
I) Injectable In Situ Forming Hydrogels for Tissue Engineering and Drug Delivery
II) Bionanocomposite Polymers for Drug Delivery and Imaging
III) 3-Dimensional Bioprinted Composite Scaffolds for Tissue Engineering
Background:
My doctoral research focused on observing and comprehending the transport of small penetrant molecules in glassy polymers and elucidating the effects of structure and network parameters on the transport mechanism, with a particular emphasis on the occurrence of non-Fickian transport dynamics. Novel structure property relationships were developed for penetrant transport dynamics in the Case II transport regime, material-based mechanisms for controlling the nature of penetrant transport in glassy polymers were elucidated, and high-resolution X-ray computed tomography was adapted as a novel technique for quantitative, in situ imaging of penetrant transport processes.
In my post-doctoral studies, I have moved to the interface of polymer science and biomedical research, focusing on the design and application of injectable hydrogel-cell composite scaffolds for tissue regeneration in craniofacial defects. Specifically, we have developed and filed a provisional patent on a novel class of two-component, in situ dual-hardening hydrogels combining near-instantaneous temperature-induced gelation with epoxy-based crosslinking utilizing degradable polyamidoamine macromers. Such in situ dual-hardening, dimensionally stable, defect-filling, and degradable hydrogels with high gel water content are attractive substrates for tissue engineering and cellular delivery applications. In particular, the use of water-soluble and degradable polyamidoamine polyaddition-formed macromers offers tremendous synthetic flexibility and control over subsequent gel properties.
Post-doctoral Advisor: Professor Antonios G. Mikos, Departments of Bioengineering and Chemical and Biomolecular Engineering, Rice University
Ph.D. Advisor: Professor Nicholas A. Peppas, Departments of Chemical and Biomedical Engineering, The University of Texas at Austin
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