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Transcript
Integrating Nanostructures with Biological Structures
Investigators: M. Stroscio, ECE and BioE; M. Dutta, ECE
Prime Grant Support: ARO, NSF, AFOSR, SRC, DARPA, DHS
Problem Statement and Motivation
• Coupling manmade nanostructures with biological
structures to monitor and control biological
processes.
• For underlying concepts see Biological
Nanostructures and Applications of Nanostructures
in Biology: Electrical, Mechanical, & Optical
Properties, edited by Michael A. Stroscio and Mitra
Dutta (Kluwer, New York, 2004).
Technical Approach
• Synthesis of nanostructures
• Binding nanostructures to manmade structures
• Modeling electrical, optical and mechanical
properties of nanostructures
• Experimental characterization of intergated manmade
nanostructure-biological structures
Key Achievements and Future Goals
• Numerous manmade nanostructures have been
functionalized with biomolecules
• Nanostructure-biomolecule complexes have been used
to study a variety of biological structures including cells
• Interactions between nanostructures with biomolecules
and with biological environments have been modeled for
a wide variety of systems
• Ultimate goal is controlling biological systems at the
nanoscale
Carcinogenic Potential of Wireless Communication Radiation
Investigators: James C. Lin, PhD, Electrical and Computer Engineering; and Bioengineering
Prime Grant Support: Magnetic Health Science Foundation
Problem Statement and Motivation
• Wide Spread Use of Cell Phone Technology
• Concerns about Health and Safety
• Plectin is A High Molecular Weight Protein
• Plectin Immunoreactivity Follows Brain Injury
• Mutation of Plectin Identified With Signs of
Neurodegenerative Disorder
Immunolabeling of Irradiated Rat Brain
Using Monoclonal Antibody, Pletin.
Technical Approach
• Irradiate Young Adult Rats (300 g) in Plexiglass Holder
• Produce Power Deposition Patterns in Rat Brains
Comparable to Those in Humans
• Brains Were Removed and Incubated
• Floating Sections Were Used for Immunocytochemistry
• Use Monoclonal Antibody - plectin - Labeling
• Examination by Light Microscopy
Key Achievements and Future Goals
• Immunolabeling of Irradiated Rat Brain Showed
Increased Glial Fibrillary Acidic Protein
(IFAP)
• GFAP Plays An Important Role in Glial Reactions After
Lesions
• Preliminary Results Indicate There is No Difference in
Expression Pattern of Plectin Among the
Brains Tested at Peak SAR levels of 0, 1.6
and 16 W/kg in the brain.
• Additional Experiments to Establish Statistical Validity
Teaching Sensorimotor Skills with Haptics
Investigators: Miloš Žefran, ECE; Matteo Corno, ECE; Maxim Kolesnikov, ECE
Prime Grant Support: NSF; UIC College of Dentistry
Problem Statement and Motivation
• New surgical procedures are introduced at a high rate.
Each requires costly training.
• Haptic simulators provide a cost-effective alternative
to traditional training: no need to travel, 24/7 availability,
easy to create additional units as needed.
• Existing paradigm for haptics is not suitable for
teaching sensorimotor skills. Lack of good models and
of realistic haptic rendering are main obstacles to
creating useful simulators.
Technical Approach
Key Achievements and Future Goals
• Position and force information are simultaneously
displayed to facilitate motor skill acquisition. The user is
modeled as a three-input, single-output system.
• Developed a new paradigm for teaching of
sensorimotor skills with haptics.
• The model of the human enables stability analysis
through the Lyapunov second method; traditional
passivity techniques can not be used. Time delays are
critical for stability and are explicitly modeled.
• The Euclidean group SE(3) used to develop haptic
rendering algorithms that properly account for
translations and rotations. Kinetic energy provides an
intrinsic way to define the penetration which is in turn
used to compute the reaction force.
• Proposed a new model for a user responding to haptic
and visual stimuli. The model experimentally verified.
• Stability analysis of the system performed. Stability
boundaries explicitly identified.
• Implemented a new method for haptic rendering.
• Future work: applications in medical training, rehabilitation; faster implementation of the haptic rendering;
implementation on cheap haptic displays; extensions of
the new paradigm for collaborative haptics.
Cardiac Sound Separation and Analysis
Investigators: Roland Priemer, ECE; Vivek Nigam , ECE
Prime Grant Support: Prakash Agarwal Foundation
Phonocardiogram Dissection
Mitral Component
Aortic Component
Hole
Apply blind source
separation algorithms to
isolate major delayed
components of the heart
sound.
Murmur
Tricuspid
Component
Background Noise
Pulmonary Component
Utilize dynamics of the
heart to detect and isolate
major heart sounds.
Background Noise
Aortic Component
Pulmonary Component
Mitral Component
Tricuspid Component
Statistically
Independent
Murmur
Primary auscultation sites.
Heart sound with a VSD
murmur.
Motivation, Problems and Goals
Motivation
Problems
Goals
Extract clinically relevant
features from isolated
heart sounds to perform
clinical diagnosis.
S4
Systolic Murmur Classification
Heart disease is the leading cause of death in the world.
One percent of all newborns have some sort of heart
dysfunction. The stethoscope is the most widely used frontline
instrument to detect heart dysfunction.
Ejection
Regurgitant
Ejection
Using the stethoscope requires extensive training .
Interpretation of the phonocardiogram can be subjective .
The phonocardiogram is a mixture of sounds with complexity
that makes it difficult to analyze for diagnosis of heart
dysfunctions .
Extract discrete heart sounds from the phonocardiogram and
develop algorithms for real-time analysis. Non-invasive, easy
to use and inexpensive apparatus. Automated support of
diagnosis of the separated sounds to classify dysfunctions.
S3
Ejection or
Regurgitant
Ejection or
Regurgitant
Simplicity based detection of heart
sounds. Top: Mitral stenosis murmur.
Bottom: Simplicity of mitral stenosis
murmur
Normal
Simplicity based classification of
systolic murmurs.