Kathryn Uhrich

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Kathryn Uhrich
Uhrich2.jpg
Kathryn Uhrich, April 2008
Born1965 (age 5657)
NationalityAmerican
Education Grand Forks Central High School
Alma mater University of North Dakota,
Cornell University
Known forPrevention of biofilm formation
Scientific career
Fields Cardiology
InstitutionsRutgers University,
Polymerix Corporation

Kathryn Uhrich (born 1965) is Dean of the College of Natural and Agricultural Sciences, at The University of California, Riverside, [1] and founder of Polymerix Corporation. [2] She has received many awards for her research and work including the ACS Buck-Whitney Award and the Sioux Award. She was a fellow at both the National Academy of Inventors and the American Chemical Society in 2014.

Contents

Research

Her research mainly focuses on biodegradable polymers for use in dental and medical applications. These polymers consist of esters, amides and anhydrides, all of which are susceptible to hydrolysis, thus ensuring the breakdown of the polymer in the body's watery milieu. [3]

The oldest version of aspirin came from Hippocrates in the fifth century BC, [4] while the latest version, PolyAspirin, comes from Uhrich's lab at Rutgers University. [5] Polyaspirine consists of anhydrides and esters that hydrolytically degrade into the active ingredient in aspirin (salicylic acid). Her research was highlighted in "Aspirin: The Remarkable Story of a Wonder Drug" by Diarmuid Jeffreys. [6] Although the polymer was originally designed for biodegradable sutures, PolyAspirin is now undergoing clinical trials as a material for a new type of cardiac stent. This biodegradable stent controls the inflammation effects occurring after angioplasty, called restenosis and disappears when no longer needed. [7] [8]

Kathryn Uhrich at Rutgers UhrichKE wiki.jpg
Kathryn Uhrich at Rutgers

Uhrich has collaborated with Professor Michael Tchikindas in the Rutgers Food Science department to investigate PolyAspirin and other plant-based polymers as a method for prevention of biofilm formation by microbes such as E. coli and Salmonella in food. [9] [10]

In 1997, Uhrich first patented PolyAspirin. [11] All of Uhrich's inventions were originally licensed to Polymerix Corporation in 2000, to develop biodegradable polymerized drugs, and now being licensed through Rutgers. The technology includes more efficient delivery to targeted areas such as orthopedic implants, coronary stents and arthritic joints. Uhrich has at least 16 patents in the US and 160 patent applications pending worldwide, all of which are coordinated by Rutgers OCLTT. [12]

Uhrich's second research line is on polymeric micelles. Like soap, these polymers have a hydrophilic 'head' and a hydrophobic 'tail'. These molecules form a spherical particle in which you can pack a hydrophobic drug molecule. Uhrich's research group investigates two general classes of nanoscale polymeric micelles: amphiphilic star-like macromolecules (ASMs) and amphiphilic scorpion-like macromolecules (AScMs); both systems facilitate drug transport. ASMs behave as unimolecular micelles, where four polymer particles are covalently bound. AScMs consist of part of the star like macromolecules, and must first aggregate to form micellar structures. Because AScMs are easier to synthesize and have similar properties, the polymers are undergoing further proof of principle research in gene delivery of siRNA and plasmid DNA with Professor Charlie Roth. [13]

Also, the anionic (negatively charged) scorpion-like molecules inhibit cellular uptake of oxidized LDL, the 'bad' cholesterol in the body. This type of LDL is usually incorporated in macrophages, resulting in foam cell formation and formation of an atherosclerotic plaque which narrows or blocks the arteries. [14] Contrary to most anti-atherosclerotic drugs, the anionic polymer only targets LDL particles and not HDL particles. The delivery of these polymeric particles is now undergoing investigation with Professor Prabhas Moghe. [15] [16]

Thirdly, her group is interested in micro-sized striped patterns of protein (such as serum albumin, immunoglobulin G, laminin and other growth factors) on biocompatible polymeric substrates (such as poly(methylmethacrylate) or PMMA). These proteins promote neuron cell growth, but are not always large enough to bridge the gap caused by injury and restore function to the nerve. Thus, Uhrich investigates the optimal dimensions for promoting neuronal growth in conjugation with Professors Helen Buettner, [17] Martin Grumet [18] and David Shreiber, [19] and the most effective patterning method to generate protein gradients. More recently, Uhrich's group is collaborating with Professor Sally Meiners of UMDNJ to create nerve guidance conduits from biodegradable polymers. [20]

Awards

Education

Professional career

Related Research Articles

In polymer chemistry, ring-opening polymerization (ROP) is a form of chain-growth polymerization, in which the terminus of a polymer chain attacks cyclic monomers to form a longer polymer. The reactive center can be radical, anionic or cationic. Some cyclic monomers such as norbornene or cyclooctadiene can be polymerized to high molecular weight polymers by using metal catalysts. ROP is a versatile method for the synthesis of biopolymers.

<span class="mw-page-title-main">Malonic acid</span> Carboxylic acid with chemical formula CH2(COOH)2

Malonic acid (IUPAC systematic name: propanedioic acid) is a dicarboxylic acid with structure CH2(COOH)2. The ionized form of malonic acid, as well as its esters and salts, are known as malonates. For example, diethyl malonate is malonic acid's diethyl ester. The name originates from the Greek word μᾶλον (malon) meaning 'apple'.

<span class="mw-page-title-main">Copolymer</span> Polymer derived from more than one species of monomer

In polymer chemistry, a copolymer is a polymer derived from more than one species of monomer. The polymerization of monomers into copolymers is called copolymerization. Copolymers obtained from the copolymerization of two monomer species are sometimes called bipolymers. Those obtained from three and four monomers are called terpolymers and quaterpolymers, respectively. Copolymers can be characterized by a variety of techniques such as NMR spectroscopy and size-exclusion chromatography to determine the molecular size, weight, properties, and composition of the material.

<span class="mw-page-title-main">Dendrimer</span>

Dendrimers are highly ordered, branched polymeric molecules. Synonymous terms for dendrimer include arborols and cascade molecules. Typically, dendrimers are symmetric about the core, and often adopt a spherical three-dimensional morphology. The word dendron is also encountered frequently. A dendron usually contains a single chemically addressable group called the focal point or core. The difference between dendrons and dendrimers is illustrated in the top figure, but the terms are typically encountered interchangeably.

<span class="mw-page-title-main">Robert S. Langer</span> American scientist

Robert Samuel Langer Jr. FREng is an American chemical engineer, scientist, entrepreneur, inventor and one of the twelve Institute Professors at the Massachusetts Institute of Technology.

<span class="mw-page-title-main">Sebacoyl chloride</span> Chemical compound

Sebacoyl chloride (or sebacoyl dichloride) is a di-acyl chloride, with formula (CH2)8(COCl)2. A colorless oily liquid with a pungent odor, it is soluble in hydrocarbons and ethers. Sebacoyl chloride is corrosive; like all acyl chlorides, it hydrolyzes, evolving hydrogen chloride. It is less susceptible to hydrolysis though than shorter chain aliphatic acyl chlorides.

<span class="mw-page-title-main">Polyphosphazene</span>

Polyphosphazenes include a wide range of hybrid inorganic-organic polymers with a number of different skeletal architectures with the backbone P-N-P-N-P-N-. In nearly all of these materials two organic side groups are attached to each phosphorus center. Linear polymers have the formula (N=PR1R2)n, where R1 and R2 are organic (see graphic). Other architectures are cyclolinear and cyclomatrix polymers in which small phosphazene rings are connected together by organic chain units. Other architectures are available, such as block copolymer, star, dendritic, or comb-type structures. More than 700 different polyphosphazenes are known, with different side groups (R) and different molecular architectures. Many of these polymers were first synthesized and studied in the research group of Harry R. Allcock.

<span class="mw-page-title-main">Biodegradable polymer</span>

Biodegradable polymers are a special class of polymer that breaks down after its intended purpose by bacterial decomposition process to result in natural byproducts such as gases (CO2, N2), water, biomass, and inorganic salts. These polymers are found both naturally and synthetically made, and largely consist of ester, amide, and ether functional groups. Their properties and breakdown mechanism are determined by their exact structure. These polymers are often synthesized by condensation reactions, ring opening polymerization, and metal catalysts. There are vast examples and applications of biodegradable polymers.

Polyelectrolytes are charged polymers capable of stabilizing colloidal emulsions through electrostatic interactions. Their effectiveness can be dependent on molecular weight, pH, solvent polarity, ionic strength, and the hydrophilic-lipophilic balance (HLB). Stabilized emulsions are useful in many industrial processes, including deflocculation, drug delivery, petroleum waste treatment, and food technology.

<span class="mw-page-title-main">Polyaspartic acid</span> Chemical compound

Polyaspartic acid (PASA) is a biodegradable, water-soluble condensation polymer based on the amino acid aspartic acid. It is a biodegradable replacement for water softeners and related applications. PASA can be chemically crosslinked with a wide variety of methods to yield PASA hydrogels. The resulting hydrogels are pH-sensitive such that under acidic conditions, they shrink, while the swelling capacity increases under alkaline conditions.

Poly(ethylene adipate) Chemical compound

Poly(ethylene adipate) or PEA is an aliphatic polyester. It is most commonly synthesized from a polycondensation reaction between ethylene glycol and adipic acid. PEA has been studied as it is biodegradable through a variety of mechanisms and also fairly inexpensive compared to other polymers. Its lower molecular weight compared to many polymers aids in its biodegradability.

<span class="mw-page-title-main">Matthew Tirrell</span> American chemical engineer (born 1950)

Matthew V. Tirrell is an American chemical engineer. In 2011 he became the Founding Pritzker Director and Dean of the Institute for Molecular Engineering (IME) at the University of Chicago, in addition to serving as senior scientist at Argonne National Laboratory. Tirrell's research specializes in the manipulation and measurement of polymer surface properties, polyelectrolyte complexation, and biomedical nanoparticles.

Polyorthoesters are polymers with the general structure –[–R–O–C(R1, OR2)–O–R3–]n– whereas the residue R2 can also be part of a heterocyclic ring with the residue R. Polyorthoesters are formed by transesterification of orthoesters with diols or by polyaddition between a diol and a diketene acetal, such as 3,9-diethylidene-2,4,8,10-tetraoxaspiro[5.5]undecane.

Anne Hiltner was an American polymer scientist who founded the Center for Applied Polymer Research (CAPRI) and was later instrumental in the founding of the Center for Layer Polymeric Systems (CLiPS), a National Science Foundation Science and Technology Center at Case Western Reserve University. She served as Director of the Center for Layered Polymeric Systems from its founding in 2006 until her death in 2010.

Nanoparticle drug delivery systems are engineered technologies that use nanoparticles for the targeted delivery and controlled release of therapeutic agents. The modern form of a drug delivery system should minimize side-effects and reduce both dosage and dosage frequency. Recently, nanoparticles have aroused attention due to their potential application for effective drug delivery.

Theresa M. Reineke is an American chemist and Distinguished McKnight University Professor at the University of Minnesota. She designs sustainable, environmentally friendly polymer-based delivery systems for targeted therapeutics. She is the Associate Editor of ACS Macro Letters.

β-Butyrolactone Chemical compound

β-Butyrolactone is the intramolecular carboxylic acid ester (lactone) of the optically active 3-hydroxybutanoic acid. It is produced during chemical synthesis as a racemate. β-Butyrolactone is suitable as a monomer for the production of the biodegradable polyhydroxyalkanoate poly(3-hydroxybutyrate) (PHB). Polymerisation of racemic (RS)-β-butyrolactone provides (RS)-polyhydroxybutyric acid, which, however, is inferior in essential properties to the (R)-poly-3-hydroxybutyrate originating from natural sources.

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<span class="mw-page-title-main">Dextran drug delivery systems</span> Polymeric drug carrier

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Pullulan bioconjugates are systems that use pullulan as a scaffold to attach biological materials to, such as drugs. These systems can be used to enhance the delivery of drugs to specific environments or the mechanism of delivery. These systems can be used in order to deliver drugs in response to stimuli, create a more controlled and sustained release, and provide a more targeted delivery of certain drugs.

References

  1. Grant, James (October 6, 2015). "Kathryn Uhrich Named Dean of College of Natural and Agricultural Sciences". Inside UCR.
  2. Trevor, Greg (November 3, 2003). "Polymer chemistry expert wins two major New Jersey awards". Rutgers Focus. Archived from the original on November 30, 2016. Retrieved November 29, 2016.
  3. Acton, Ashton, ed. (2013). Anhydrides—Advances in Research and Application. ISBN   978-1-4816-9716-3.
  4. Goldberg, Daniel R. (Summer 2009). "Aspirin: Turn of the Century Miracle Drug". Chemical Heritage Magazine. Chemical Heritage Foundation. 27 (2): 26–30. Retrieved March 24, 2018.
  5. "From Willow Bark to PolyAspirin: Discovery and Invention". Program Listing The 37th Middle Atlantic Regional Meeting (May 22–25, 2005) New Brunswick, NJ. Retrieved November 29, 2016.
  6. Jeffreys, Diarmuid (2004). Aspirin. The Remarkable Story of a Wonder Drug. Bloomsbury Publishing. ISBN   978-1-59691-816-0.
  7. "Three Rutgers Profs Honored for Inventions". Rutgers Office of Research and Economic Development. 2012. Retrieved November 29, 2016.
  8. Ono, Miyu (January 25, 2016). "A Way to the Heart with Polymers". Curious Science Writers.
  9. Rosenberg, L.E.; Carbone, A.L.; Römling, U.; Uhrich, K.E.; Chikindas, M.L. (May 2008). "Salicylic acid-based poly(anhydride esters) for control of biofilm formation in Salmonella enterica serovar Typhimurium". Letters in Applied Microbiology. 46 (5): 593–599. doi:10.1111/j.1472-765X.2008.02356.x. PMID   18373656. S2CID   205628108.
  10. "Michael L. Chikindas, Ph. D." Rutgers. Department of Food Science. Archived from the original on November 30, 2016. Retrieved November 29, 2016.
  11. "Polymers vs. Pain". Chemical Heritage Foundation. Archived from the original on June 15, 2010.
  12. 1 2 3 4 "KATHRYN ELIZABETH UHRICH" (PDF). Rutgers University. Retrieved November 29, 2016.
  13. "Roth, Uhrich and Team Issued Patent". Rutgers School of Engineering. 2016. Retrieved November 29, 2016.
  14. Chnari, Evangelia; Nikitczuk, Jessica S.; Uhrich, Kathryn E.; Moghe, Prabhas V. (February 2006). "Nanoscale Anionic Macromolecules Can Inhibit Cellular Uptake of Differentially Oxidized LDL". Biomacromolecules. 7 (2): 597–603. doi:10.1021/bm0506905. PMID   16471936.
  15. "Novel nanotherapeutics target plaque formations in the artery, preventing rupture and debilitating heart disease". Translational Nanomedicine for Heart Disease.
  16. "Prof. Prabhas Moghe". Rutgers. Retrieved November 29, 2016.
  17. Professor Helen Buettner's website Archived May 10, 2008, at the Wayback Machine
  18. Professor Martin Grumet's website
  19. David Shreiber's website
  20. Griffin, Jeremy; Delgado-Rivera, Roberto; Meiners, Sally; Uhrich, Kathryn E. (June 1, 2011). "Salicylic acid-derived poly(anhydride-ester) electrospun fibers designed for regenerating the peripheral nervous system". Journal of Biomedical Materials Research Part A. 97A (3): 230–242. doi:10.1002/jbm.a.33049. PMC   3096072 . PMID   21442724.
  21. "Professor Kathryn Uhrich Named ACS Fellow". Rutgers. Archived from the original on November 30, 2016. Retrieved July 18, 2014.
  22. Feiner, Fred (February 24, 2014). "Rutgers Chemistry Professors Kohn and Uhrich Named Fellows of the National Academy of Inventors". CentralNewJersey.com. Retrieved November 29, 2016.
  23. "The Sioux Award goes to Kathryn Uhrich" (PDF). Chemistry Newsletter. University of North Dakota. Fall 2013. p. 9. Retrieved November 29, 2016.
  24. "Common Pathways Award". New Jersey Association for Biomedical Research. Archived from the original on October 29, 2016. Retrieved November 29, 2016.
  25. "Kathryn Uhrich". Blavatnik Awards Young Scientists. Retrieved November 29, 2016.
  26. "The Buck-Whitney Award". Eastern New York Section A Local Section of the American Chemical Society. Retrieved November 29, 2016.
  27. "UND Chemistry Department Alumn a and Grand Forks Native Kathryn Uhrich Named Fellow of American Chemical Society" (PDF). University of North Dakota. July 18, 2014.
  28. "UND Graduate Kathryn Uhrich becomes Dean of Mathematical and Physical Sciences at Rutgers University". University of North Dakota News and Events Blog. April 21, 2009. Retrieved November 29, 2016.
  29. "Successful Women in Chemistry An Interview with Kathryn E. Uhrich, Rutg ers, the State University of New Jersey" (PDF). Women Chemists. Fall–Winter: 8–9. 2009. Retrieved November 29, 2016.