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MACROMOLECULAR SCIENCE AND ENGINEERING

 
 

GARY E. WNEK


The Joseph F. Toot, Jr., Professor and Chair
Faculty Director, The Institute for Management and Engineering (TiME)
Ph.D. Polymer Science and Engineering, University of Massachusetts, Amherst

Room 314
Phone: (216) 368-4172
Fax: (216) 368-4202
Email: gew5@case.edu

full cv (pdf)

 

Research Interests

Polymers with unusual electrical or optical properties; biomaterials for tissue engineering and regenerative medicine; electric field-mediated processing (electrospinning of nano- and micro fibers and morphology modulation in polymer blends); polymer-based microfluidic platforms; polymer product design

Overview of Research

1. Polymers in Medicine

Over the past several years, we have been involved in the development of electrostatic spinning (electrospinning) as a method of fabrication of scaffolds for tissue engineering, drug delivery, and related applications. The motivation is to create bio-mimicking fibers in a diameter range (ca. 20-100 nm) difficult to access by conventional fiber processing methods. Our group's long-term focus is directed toward exploitation of nanofiber scaffolds for a better understanding of processes in the central nervous system or CNS (the brain and spinal cord), and ultimately to contribute to restoration of function impaired by CNS-related diseases. We believe that much can be learned about fundamental cellular processes if cells are presented with the appropriate 3-D scaffold on which to grow, proliferate, and communicate. We are also interested in the development of platforms for cell encapsulation and, longer term, the fabrication of 'artificial cells.' Toward that end, attention is being directed toward the construction of novel bio-fuel cells.

2. Polymers in Electrochemical Devices: Fuel Cells and Batteries

A growing interest exists in the development of new materials with improved properties for various energy storage and conversion devices, including batteries, fuel cells, and supercapacitors. Over the past 10 years, our group has helped to develop new, low-cost proton-conducting membranes based on simple random and block copolymer structures containing partially sulfonated styrene units. We learned a great deal about the influence of ionic aggregation and morphology in these materials, and are beginning to apply this knowledge to the design of new polymers with, for example, low permeation to methanol for use in direct methanol fuel cells. In addition, we are exploring the use of these and other polymer electrolytes as hosts for luminescent dyes for the development of electroluminescent devices with tunable emission profiles. We have recently embarked on a program to exploit electrostatic processing, specifically electrospraying and electrospinning as a general approach for the fabrication of electrochemical devices, particularly fuel cells and batteries. A typical proton exchange membrane fuel cell, for example, has as its principal components a proton-conducting membrane, anode and cathode electro-catalyst layers with specific compositions and porosities, and a porous and conductive gas diffusion layer to allow good access of hydrogen and oxygen to the electrodes. We propose that this entire device, termed a membrane-electrode assembly, can be fabricated by electroprocessing. We have demonstrated to date that the prototypical proton-conducting membrane, Nafion, can be electrosprayed and has electrical properties identical to that of commercial films. We are now developing electrode compositions for electrospraying, to be shortly followed by electrospinning of gas diffusion layers. Attention is also being directed to fabrication of Li battery components by electroprocessing, including gel electrolytes and metal oxide cathodes.

3. Microfluidics and Sensors

We have helped to develop a new approach to 'lab-on-a-chip' microfluidic devices based on 2-D printing of hydrophilic paths on otherwise hydrophobic surfaces and bringing two such surface in close proximity without actual contact. Water will wet the hydrophilic paths and be drawn along them by capillary action, yet the sidewalls are in contact with air and thus the water channels are confined by the fluid's surface tension. An attractive feature of this approach is that all paths can be easily printed on inexpensive materials rather than inscribed as 3-D channels as is the case with conventional microfluidic devices. Another attribute is that reactive reagents can be 'spotted' along the paths by printing, affording a simple means to fabricate complex assay systems. Our group is also developing impedance-based sensors for live cell cultures, building on the work on electric cell-substrate impedance sensing (ECIS) by Giaever and Keese at RPI. Our focus is sensing in 3-D cell cultures that better mimic the natural environment of cells and tissues, and we have developed a system using thin (ca. 2-10 mm) gold wires in fibrin gels that is the subject of a paper in preparation. The gold wire diameters are similar to those of many mammalian axons, and we plan to focus on the notion of using the wires as artificial axon templates for neural cell growth, with specific attention toward understanding biochemical triggers of myelination and demyelination, the latter being associated with neurodegenerative diseases such as multiple sclerosis.

Current Activity

Coming soon.

Recent Publications

M. J. Swickrath, S. Shenoy, J. A. Mann, Jr., J. Belcher, R. Kovar and G. E. Wnek, “An Alternative Processing Paradigm for Autonomous Surface Tension-Confined Microfluidic Platforms,” Microfluidics and Nanofluidics, in press.

M. J. Swickrath, J. A. Mann and G. E. Wnek, “Surface-Directed Capillary Flow Systems,” Encyclopedia of Micro- and Nano-Fluidics, in press.

I. G. Loscertales, J. E. Diaz Gomez, M. Lallave, J. M. Rosas, J. Rodriguez-Mirasol, T. Cordero, M. Marquez, S. Shenoy, G. E. Wnek, T. Thorsen, A. Fernandez-Nieves and A. Barrero, “Coaxial Electrospinning for Nanostructured Advanced Materials,” Mater. Res. Soc. Symp. Proc., Vol. 948, B06-01 (2007).

M. C. McManus, E. D. Boland, H. P. Koo, C. P. Barnes, K. J. Pawlowski, G. E. Wnek, D. J. Simpson and G. L. Bowlin, “Mechanical Properties of Electrospun Fibrinogen Structures,” Acta Biomaterialia, 2, 19 (2006).

A. Guiseppi-Elie, S. Brahim, G. E. Wnek and R. H. Baughman, “Carbon Nanotube-Modified Electrodes for the Direct Bioelectrochemistry of Pseudoazurin,” Nanobiotechnology, 1, 83 (2005).

T. Telemeco, C. Ayers, G. L. Bowlin, G. E. Wnek, E. D. Boland, N. Cohen, M. Vaida, D. Tang, C. M. Baumgarten, J. Matthews, and D. G. Simpson, “Regulation of Cellular Infiltration into Tissue Engineering Scaffolds Composed of Submicron Diameter Fibrils Produced by Electrospinning,” Acta Biomaterialia, 1, 377 (2005).

S. L. Shenoy, W. D. Bates and G. E. Wnek, “Correlation Between “Electrospinnability” and Physical Gelation,” Polymer, 46, 8990-9004 (2005).

G. E. Wnek and S. G. Cort, “Product and Process Design and Delivery: Invention Through to Innovation,” Proc. ASEE Annual Conference and Exposition, Portland, OR, June 2005.

O. A. Baturina and G. E. Wnek, “Characterization of PEM Fuel Cells with Catalyst Layers Obtained by Electrospraying,” Electrochem. Solid State Lett., 8, A267 (2005).

S.L. Shenoy, H. L. Frisch, W. D. Bates and G. E. Wnek, "Role of Chain Entanglements on Fiber Formation During Electrospinning of Polymer Solutions: Good Solvent, Non-Specific Polymer-Polymer Interaction Limit," Polymer, 46, 3372 (2005).

D. L. Woerdeman, P. Ye, S. Shenoy, R. S. Parnas, G. E. Wnek, and O. Trofimova, “Electrospun Fibers from Wheat Protein: Investigation of the Interplay between Molecular Structure and the Fluid Dynamics of the Electrospinning Process,” Biomacromolecules, 6, 707 (2005).

E. D. Boland, K. J. Pawlowski, D. G. Simpson, G. E. Wnek and G.L. Bowlin. "Electrospinning Collagens and Elastin: Preliminary Vascular Tissue Engineering." Frontiers in Biosciences, 9, 1422 (2004).

E. H. Sanders, K. A. McGrady, G. E. Wnek, C. A. Edmonson, J. M. Mueller, J. J. Fontanella, S. Suarez and S G. Greenbaum, "Characterization of Electrosprayed Nafion Films," J. Power Sources, 129, 55 (2004).

E. H. Sanders, R. Kleofkorn, G. L. Bowlin, D. G. Simpson and G. E. Wnek, “Two-Phase Electrospinning from a Single Electrified Jet: Microencapsulation of Aqueous Reservoirs in Poly(Ethylene-co-Vinyl Acetate) Fibers,” Macromolecules, 36, 3803 (2003).

E.-R. Kenawy, J. M. Layman, J. R. Watkins, G. L. Bowlin, J. A. Matthews, D. G. Simpson and G. E. Wnek, “Electrospinning of Poly(Ethylene-co-Vinyl Alcohol) Fibers,” Biomaterials, 24, 907-913 (2003).

L. Yao, T. W. Haas, A. Guiseppi-Elie, G. L. Bowlin, D. G. Simpson, and G. E. Wnek, “Electrospinning and Stabilization of Fully Hydrolyzed Poly(vinyl alcohol) Fibers,” Chem. Mater, 15, 1860 (2003).

G. E. Wnek, M. E. Carr, D. G. Simpson and G. L. Bowlin, “Electrospinning of Nanofiber Fibrinogen Structures,” Nano Lett., 3, 213-216 (2003).

Awards

John W. Hyatt Award (benefit to society), Society of Plastics Engineers, 2007

Kern Faculty Fellow, NCIIA/Kern Entrepreneurship Education Network, 2006-07

NASA Lecturer, 64th Frontiers in Chemistry Symposium, Case Western Reserve University, 2004

Sidney Negus Memorial Lecturer, Virginia Academy of Sciences, 1999

1996 Eastern New York Intellectual Property Law Association Inventor of the Year Award (for U.S. patent 5,468,574)