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Kathryn Uhrich
Professor
Email

B.S. 1986, University of North Dakota (Grand Forks, ND)
Ph.D. 1992, Cornell University (Ithaca, NY)
Postdoctoral Research Fellow 1992, Bell Laboratories
Postdoctoral Research Fellow 1993-95, MIT
 

Contact

 

Links

Phone: (732) 445-0361
Fax: (732) 445-7036
Lab: (732) 445-5630 (WL-371)
Dept: Kristina Wetter, Sr. Admin. Assistant: (732) 445-8388, Email

Office: WL-311
Mail: Chemistry & Chemical Biology, 610 Taylor Road, Piscataway, NJ 08854

Research

Summary

The focus in my laboratory is on the synthesis and characterization of biocompatible polymers for medical and dental applications such as drug delivery and tissue engineering. Our polymers are designed to be degradable as well as biocompatible.

Polymeric Micelles

Polymeric micelles are nanocarriers that water-solubilize hydrophobic drug molecules yet can also be bioactive by themselves. These polymers were designed with a branched, hydrophobic interior (core) and hydrophilic exterior (shell) to maintain physical properties characteristic of conventional micelles, but with enhanced thermodynamic stability.

Two general classes of nanoscale polymeric micelles are under investigation: amphiphilic starlike macromolecules (ASMs) and amphiphilic scorpion-like macromolecules (AScMs). These two systems are chemically similar, but structurally different. ASMs behave as unimolecular micelles, whereas AScMs must first aggregate to form micellar structures.





Micropatterns

Micropatterns of protein on biocompatible polymeric substrates can mimic cues to promote neuron growth. While both physical and chemical cues direct regrowth in vivo, these cues are not always enough to bridge the gap caused by injury and restore function to the nerve (target). Currently, we are developing alternate patterning methods to generate nanoscale features and protein gradients, as well as creating synthetic nerve guidance conduits.





PolymerDrugs

PolymerDrugs such as PolyAspirin are novel polyanhydrides that hydrolytically degrade into salicylic acid (or related drug molecules), which can locally reduce post-operative inflammation and pain. In addition to non-steroidal anti-inflammatory drugs (NSAIDs), several other drug classes are investigated, including antiseptics, antiproliferatives, and antibiotics. We are evaluating food-based bioactives to control bacteria in packaging.










Awards & Honors