William
M. Deen, Ph.D.
Carbon P. Dubbs Professor of Chemical and Biological Engineering
Research
group web site
Email: wmdeen@mit.edu
Office: 66-572
Phone: (617) 253-4535
Fax: (617) 258-8224
Administrative Assistant: Glorianne
Collver-Jacobson, Peter
Romanow
Courses: 10.50, BE.430J
|
| Honors
and Awards |
| 1992 |
Founding Fellow, American Institute for Medical
and Biological Engineering |
| 1982 |
Western Electric Fund Award American Society for Engineering
Education |
Research Focus
Bioengineering, Transport Phenomena, Membrane
Separations
The common theme of our research group is the application of
engineering principles to biological materials or systems. Most
of the problems we work on are motivated by a desire to understand
normal or pathophysiological processes occurring in the body,
and their implications for the prevention, diagnosis, or treatment
of human disease. Much of the work entails collaboration with
physicians, physiologists, and other biological scientists.
One area of focus involves the fundamentals of water and macromolecule
transport in liquid-filled spaces of molecular dimensions. This
is important for understanding mass transfer in body tissues,
as well as for designing membranes or other separation devices.
A key objective of our work is to develop models to predict transport
hindrances in porous or fibrous materials, based on the size,
shape, and electrical charge of the permeating molecule and the
nanostructural properties of the material. The theoretical models
are tested using membranes or gels of well-defined structure.
They are used also to interpret experiments that probe the permeability
properties of mammalian kidney capillaries in health and disease.
We are endeavoring to relate the ultrastructure of those capillaries
to their transport characteristics, through detailed analyses
of convection and diffusion at the cellular and subcellular levels.
Another area of interest is transport and reaction of nitric
oxide (NO) in biological systems. It has been shown in recent
years that NO is synthesized throughout the body and that it is
a key intercellular messenger molecule (e.g., in the regulation
of blood pressure). Transient increases in NO synthesis are important
also in the response of the immune system to infection, in that
the toxicity of NO helps to kill invading microorganisms. However,
sustained high levels of NO synthesis (as may occur with chronic
infection or inflammation) carries with it the risk of collateral
damage to host tissues, including mutational changes that may
lead to cancer. To provide insight into the biological effects
of NO and of the various reactive NOx species derived from NO,
we are studying reaction kinetics and diffusion in aqueous solutions
and cell cultures. Using such data, we are developing computational
models to predict the consequences of NO synthesis by cells in
vivo or in vitro.
Representative Publications & Lectures
"Analysis of the effects of cell spacing and
liquid depth on nitric oxide and its oxidation products in cell
cultures," Chem. Res. Toxicol., 14, 135-147 (2001), (with
B. Chen).
"Concentration polarization in stirred ultrafiltration cells,"
AIChE J., 47, 1115-1125 (2001), (with S.T. Johnston and K.A. Smith).
"Equilibrium partitioning of flexible macromolecules in
fibrous membranes and gels," Macromolecules, 33, 8504-8511
(2000), (with J.A. White).
"Effects of multisolute steric interactions on membrane
partition coefficients," J. Colloid Interface Sci., 226,
112-122 (2000), (with M.J. Lazzara and D. Blankschtein).
"Ultrastructural model for size selectivity in glomerular
filtration," Am. J. Physiol., 276, F892-F902 (1999), (with
A. Edwards and B.S. Daniels).
"Diffusion and reaction of nitric oxide in suspension cell
cultures," Biophys. J., 75, 745-754 (1998), (with B. Chen
and M. Keshive).