Technical Presentation Program
Medicine, Biosciences, Biotechnology Symposium
Friday, 9:00am-4:00pm

Medicine, Biosciences, Biotechnology Symposium Chair:

  • Semahat S. Demir, PhD, Assistant Professor, School of Biomedical Engineering, University of Tennessee - Memphis
  • Medicine, Biosciences, Biotechnology Symposium Peer Reviewers:

  • Denis DiAngelo, PhD, School of Biomedical Engineering, University of Tennessee - Memphis
  • Eugene Eckstein, PhD, Hyde Professor Chair of Excellence, School of Biomedical Engineering, University of Tennessee - Memphis
  • Jae Rho, PhD, Assistant Professor, Department of Biomedical Engineering, University of Memphis
  • Robert Malkin, PhD, Assistant Professor, Department of Biomedical Engineering, University of Memphis
  • Presentations
    9:00am-9:25am MBB01 Photopolymerized Hydrogel Barriers Prevent Thrombosis and Restenosis after Balloon Injury: The Roles of Medial and Luminal Growth Factors
    9:30am-9:55am MBB11 Effect of a Novel Keratin Biomaterial on Wound Healing: In Vitro and Preclinical Results
    10:00am-10:25am MBB03 Transmyocardial Laser Revascularization (TMLR)
    10:30am-10:55am MBB04 Cardiopulmonary Bypass Techniques for Neonates and Infants
    1:00pm-1:25pm MBB05 The Future of Diagnostic X-ray and CT Imaging
    1:30pm-1:55pm MBB06 Advances in Computer Technology are Creating New Opportunities for Engineering in Cardiology
    2:00pm-2:25pm Coffee Break - Visit the Open Technical Exchange Poster Session
    2:30pm-2:55pm *MBB07 Joint Kinematics
    3:00pm-3:25pm *MBB08 Bone Remodeling During Space Flight
    3:30pm-3:55pm MBB09 Quantifying Muscle Activation Patterns By Means of Clustering and Classification
    Posters
    MBBP01 Integrating Physiological Data and Mathematical Models to Understand Disease in Cardiac Ventricular Cells
    MBBP02 Electrical Stimulus Application on a Cardiac Pacemaker Cell

    Session Codes
    *xxxnn Both an oral presentation and a poster
    xxxPnn Poster Only


    For technical presentation or Open Technical Exchange information, contact the Houston Convention Team.

    MBB01
    Photopolymerized Hydrogel Barriers Prevent Thrombosis and Restenosis after Balloon Injury: The Roles of Medial and Luminal Growth Factors
    Jennifer West, PhD, T.N. Law Assistant Professor, Rice University, Department of Bioengineering
    Jeffrey A. Hubbell, PhD, ETH (Swiss Federal Institute of Technology), Zurich, Switzerland, Department of Biomedical Engineering
    Friday, 9:00am–9:25am

    An interfacial photopolymerization technique has been developed to allow the synthesis of thin (<50 µm) hydrogel barriers on the luminal surface of arteries. These hydrogels are non-thrombogenic and biodegradable. The polymerization process does not damage the underlying tissue. Application of hydrogel barriers following balloon injury of the rat common carotid artery has been shown to eliminate thrombosis (2 hr post-injury, n = 7, p < 0.005) and to reduce intimal thickening by approximately 80% (14 d post-injury, n = 7, p < 0.001). The efficacy of this short-term, strictly localized treatment for prevention of restenosis is believed to be due to the complete blockade of interaction with thrombus-derived mitogens and chemotactic agents, such as platelet-derived growth factor (PDGF) and thrombin. To probe this possibility, experiments were carried out utilizing non-degradable hydrogel barriers to block thrombosis and contact with blood combined with localized delivery of PDGF and thrombin. Neither of these substances stimulated intimal thickening in the absence of thrombosis, whereas PDGF delivery in the presence of thrombosis increased the intimal thickening response approximately two-fold. Thus, we conclude that while PDGF is a factor in the restenosis cascade, it requires the activity of a blood-derived cofactor.

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    MBB11
    Effect of a Novel Keratin Biomaterial on Wound Healing: In Vitro and Preclinical Results
    C.R. Blanchard, PhD, Manager, Materials Development Section, Southwest Research Institute
    H. Cohly, PhD, Research Associate, University of Mississippi Medical Center
    A.J. Siller, Scientist, Materials Development Section, Southwest Research Institute
    M. Angel, Student, University of Mississippi Medical Center
    B. Rogers, Professor, University of Mississippi Medical Center
    J. Thompson, Student, University of Mississippi Medical Center
    G.E. Abraham III, Student, University of Mississippi Medical Center
    R.A. Smith, MD, Plastic Surgeon, Jackson Plastic Surgery Clinic
    Friday, 9:30am to 9:55 am

    Partial and full thickness wounds often require the application of topical dressings for protection and to promote healing. Keratins, major structural proteins of all epithelial cell types, appear to play an important role in the re-epithelialization process of wound healing. The effect of a new keratin biomaterial (KP) derived from human hair on proliferation of keratinocytes (K), fibroblasts (F), endothelial cells (E), and T cells was studied. In addition, CD/hairless rats (N=28) were randomly divided into two groups. Group A wounds were untreated while Group B wounds were treated with keratin every other day. The KP powder was prepared by cleaning, drying and comminuting human hair harvested from 13-19 year old males. Cells exposed to the KP biomaterial revealed that lymphocytes did not proliferate, activated T cells were not inhibited, keratinocytes proliferated profusely, fibroblasts proliferated modestly, and microvascular endothelial cells proliferated profusely. Non-proliferation of lymphocytes is an indication that the KP biomaterial is non-immunogenic. Failure to inhibit active T cells shows that the KP biomaterial does not interfere with the body's normal immune response. Clinically observed epithelialization in the planimetry studies at day 4 indicated 98.5% coverage in the treated and 76.7% in the non-treated rats (p<0.05). Cellular hyperesponsiveness, coupled with low antigenicity, demonstrates the enhanced wound healing and mitogenic characteristics of keratin. The preclinical study demonstrates that KP enhances healing in partial thickness wounds.

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    MBB03
    Transmyocardial Laser Revascularization (TMLR)
    Kƒmuran A. Kadipasaoglu, PhD, Texas Heart Institute, Cardiovascular Surgical Research
    L.A. Stutts, MA, Texas Heart Institute, Cardiovascular Surgical Research Laboratories
    H.B. Cihan, MD, Texas Heart Institute, Cardiovascular Surgical Research
    D. A. Cooley, MD, Texas Heart Institute, Cardiovascular Surgical Research
    O.H. Frazier, MD, Texas Heart Institute, Cardiovascular Surgical Research
    Friday, 10:00am–10:25am

    TMLR for the treatment of refractory angina is performed using a CO2 laser with a fixed power output of 800 W and a variable pulse energy and pulse duration. Laser energy is transmitted via an articulating arm placed in direct contact with the target tissue. The laser delivers single pulses on the R wave of the EKG waveform. The epicardium is exposed via a left anterolateral thoracotomy. Transmural channels are placed in the beating heart. Reversal of ischemia is believed to occur when blood penetrates the changnels during systole and perfuses the subendocardium via the sinusoidal plexus. The procedure is undergoing safety and efficacy evaluation in randomized clinical trials in the US.

    TMLR using the 800 W CO2 Laser is safe in the patient population described in this study, effectively relieves anginal symptoms, improves exercise tolerance, and increases left ventricular freewall perfusion for at least 12 months.

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    MBB04
    Cardiopulmonary Bypass Techniques for Neonates and Infants
    Akif Undar, PhD, Director, Perfusion Research, Congenital Heart Surgery, Texas Children's Hospital, and Director, Pediatric Perfusion Research, Cullen Cardiovascular Research Laboratory, Texas Heart Institute, and Instructor, Section of Congenital Heart Surgery, Baylor College of Medicine
    Alexis Palacios-Macedo, MD, Clinical Fellow, Congenital Heart Surgery, Texas Children's Hospital and Baylor College of Medicine
    Angela Diamond, MD, Clinical Fellow, Congenital Heart Surgery, Texas Children's Hospital and Baylor College of Medicine
    O. Howard Frazier, MD, Chief, Transplantation Service, Director, CV Surgery Research, Texas Heart Institute
    Charles D. Fraser, MD, Chief, Congenital Heart Surgery, Texas Children's Hospital and Assistant Professor, Department of Surgery, Baylor College of Medicine
    Friday, 10:30am–10:55am

    Every year, approximately 10,000 neonates are born in the United States with congenital heart defects, that require a cardiopulmonary bypass (CPB) procedure during infancy. Although complex surgeries can be done with routine techniques with a lower mortality rate than ever before; the brain injury after CPB is still a significant problem (among 10 to 30% of post-op pediatric heart patients). The common approach has been to repair the congenital heart defect treating neonates and infants as small adults. However, especially neonates, respond to CPB more dramatically and rapidly than adults. For example, cerebral blood flow (CBF), cerebral metabolism (CMRO2), and the CBF/CMRO2 ratio in neonates are significantly higher than adults due to the increased metabolic demand for neuronal growth. Therefore, neonates and infants are not just small adults. Non-pulsatile perfusion, the level of cerebral perfusion pressure (CPP), acid-base management technique during cooling and rewarming, rate of pump flow, degree of hemodilution and hypothermia, and duration of circulatory arrest may influence the brain injury. All of these parameters are controlled during CPB and a little adjustment of any of these parameters may have a significant effect for the outcome of the patient. Currently, the effects of each of these parameters are under investigation by several institutions to develop a safer cardiopulmonary bypass circuit for neonates and infants. We will focus on the effects of pulsatile vs. non-pulsatile perfusion during pediatric open-heart surgery in this paper.

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    MBB05
    The Future of Diagnostic X-ray and CT Imaging
    Frank A. DiBianca, PhD, Director and Crippled Children's Foundation Professor, University of Tennessee at Memphis, School of Biomedical Engineering
    Friday, 1:00pm–1:25pm

    The first window into the human body for medical diagnosis was discovered at the end of the nineteenth century when Professor Konrad Roentgen observed that the mysterious "X-rays" he had recently discovered could penetrate through the body and record images of internal human anatomy on photographic film. Other than by means of highly invasive exploratory surgery, this x-ray imaging technique remained the sole method of studying internal anatomy for over half a century until the advent of alternative diagnostic techniques such as ultrasound, nuclear isotope imaging, CT scanning and, most recently, magnetic resonance imaging. Despite these major advances, diagnosis with x-ray beams still remains the most often used technique due to its generality, high resolution and low cost.

    This talk will survey the relative strengths of the various imaging techniques, summarize current directions in x-ray and CT imaging and attempt to prognosticate their future directions and ability to remain competitive in the 21st century.

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    MBB06
    Advances in Computer Technology are Creating New Opportunities for Engineering in Cardiology
    Sheryl S. Prucka, PE, President and Founding Partner of Prucka Engineering, Inc.
    Friday, 1:30pm–1:55pm

    In the past decade, the application of computerized techniques has dramatically improved health care providers ability to diagnose and treat a variety of cardiac conditions. The trend has led toward safer and less invasive diagnostic methods. As an example, echocardiography is now routinely used as a noninvasive preliminary technique for evaluating ventricular function. Previously, catheterization studies were required to perform such an evaluation, exposing the patient to the risk associated with an invasive procedure. In addition to improving diagnostic tools, computerized approaches to support interventional techniques have improved treatment efficacy and reduced both risk to the patient and the cost of procedures.

    Current research in cardiology is providing many opportunities for the continued application of computerized techniques. Several computerized methods for 3-dimentional localization of catheters have recently been developed, enabling engineers to create accurate 3-D representations of the chamber, and the catheter within it, during an electrophysiologic study. New techniques in imaging, including the use of Intra-Vascular Ultrasound (IVUS) are providing substantial opportunity for the development of new computer-based tools for the analysis and 3-D reconstruction of the chamber or vessel where the image data is collected. Recent advances in computer technology are providing engineers with a powerful foundation which can be effectively used to develop tools to address rapidly changing needs in the field of cardiology, and in medicine in general.

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    *MBB07
    Joint Kinematics
    Rita M. Patterson, PhD, Assistant Professor
    C.K. Hebert, MD, Assistant Professor
    William L. Buford, Jr., PhD, Assistant Professor
    Steven F. Viegas, MD, Professor, The University of Texas Medical Branch, Galveston, Department of Orthopaedic Surgery and Rehabilitation
    Friday, 2:30pm–2:55pm

    Because of the body's structural complexity and morphological variations, a reference database of normal anatomy and kinematics will provide valuable reference information to facilitate diagnosis and treatment of various injuries and diseases.

    The skin on fresh frozen cadaver extremities was dissected and triad pins placed into various bones defining different joints. Transverse images of the joint and pins were obtained with a GE 9800 CT generating contiguous slices 1.5 mm thick. The data was processed and then visualized in 3D computer space in AVS on an Evans and Sutherland Graphic workstation. Optoelectronic-stereo-cinephotogrammetry motion analysis (OSMA) was then performed on the joints during motion.

    Results of the OSMA motion data were combined with CT geometric data to create an animation of the motion. Range of motion (ROM), angles between bones, and instantaneous screw axes (ISA) were calculated.

    This new combination of motion analysis and 3D reconstruction of CT images affords a high speed, dynamic analysis of kinematics. Human Joint motion is complex consisting of both rotation and translation components.

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    *MBB08
    Quantifying Muscle Activation Patterns By Means of Clustering and Classification
    Christina A. Batson, Senior Student, University of Alabama, Department of Mechanical Engineering
    Beth A. Todd, PhD, Assistant Professor, The University of Alabama, Department of Mechanical Engineering
    Tanya G. Cole, Senior Student, The University of Alabama, Department of Mechanical Engineering
    Linda C. Shackelford, MD, Head of the Bone and Mineral Physiology Laboratory, NASA, Johnson Space Center, Life Sciences Research Laboratories
    Friday, 3:00pm–3:25pm

    Research has proven that disuse of bones, such as that seen in a non-gravitational environment, results in bone mineral density (BMD) loss. Under weightless conditions in orbit, astronauts have a tendency to exhibit bone mineral loss in their spine and lower extremities with no net changes in the upper extremities. The main areas of concern include the lumbar spine, femoral neck, and calcaneus regions. It has been found that heavy resistive exercises are the most successful countermeasures for increasing BMD in these areas, while chemical therapies are showing potential. NASA has been exploring these options as a means of preventing BMD loss during space flight. Effective countermeasures for BMD loss found through this research can also be used to prevent and treat osteoporotic bone disorders.

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    MBB09
    Quantifying Muscle Activation Patterns By Means of Clustering and Classification
    Vonda L. Hart, MS, University of Houston, Bioengineering Research Center, Department of Electrical and Computer Engineering
    Ben H. Jansen, PhD, University of Houston, Bioengineering Research Center, Department of Electrical and Computer Engineering
    Demetrios C. Mavrofrides, MS, University of Houston, Bioengineering Research Center, Department of Electrical and Computer Engineering
    Caroline W. Stegink Jansen, PhD, University of Texas Medical Branch, Galveston, School of Allied Health, Department of Physical Therapy
    Friday, 3:30pm–3:55pm

    The electromyogram (EMG) provides a measure of a muscle's involvement in the execution of a motor task. Successful completion of an activity, such as walking, depends on the efficient motor control of a group of muscles. We have developed a technique to quantify the intricate phasing and activation levels of a muscle group during a motor task. At the core of our method is a multidimensional representation of the EMG activity observed during a single stride. This representation, referred to as a "trajectory", is obtained by plotting the activity of one muscle against that of other muscles. A hierarchical clustering procedure is used to identify representative classes of muscle activity patterns, referred to as "templates". Once the templates are identified, single strides from the various sessions recorded are classified by matching them to the templates. Differences in gait patterns between walking conditions can be reflected by changes in the distribution of strides matching individual templates, e.g., one condition results in fewer strides matching a particular template than another condition. Two experimental conditions were used to determine the effectiveness of the algorithm in differentiating between gait patterns. The conditions were horizontal and inclined treadmill gait. Data were collected multiple times over several days. Significant differences between horizontal and inclined gait were found, while the ithin and between day variability was small.

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    MBB10 - Withdrawn

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    MBBP01
    Integrating Physiological Data and Mathematical Models to Understand Disease in Cardiac Ventricular Cells
    Semahat S. Demir, PhD, Assistant Professor, School of Biomedical Engineering, University of Tennessee - Memphis

    The insights gained and results derived from studies on dogs and rats will enhance our understanding of the heart, and provide us with better treatments for diseases in human. Despite nearly five decades of histological, electrophysiological, pharmacological and biochemical investigations, relatively little is known regarding the ionic mechanisms underlying the action potential variation in the canine and rat ventricular myocytes under different pathological conditions. Thus, the action potentials of dog and rat continue to be a topic of considerable interest in cardiac electrophysiology and mathematical modeling for several reasons. First, the canine ventricular action potential is very similar to that of human. On the other hand, the rat ventricular action potential is shorter and lacks a prominent plateau phase compared to those by human, dog, guinea pig and rabbit. Second, mathematical modeling for ventricular cells has been done in guinea pig and relatively less in rat, rabbit and dog. Furthermore, the differences in ventricular membrane ionic currents, especially outward K+ currents in different species have very important practical implications. Different drugs are known to affect different ionic currents and to change action potential waveforms in various mammalian heart preparations under different pathological (normal, tachycardia induced heart failure diabetic, altered thyroid, and hypertrophied) conditions. A better understanding of the role of the ionic currents that control repolarization in the ventricular myocytes obtained from various species including dog and rat will provide explanations for species differences in treatment and drug actions, and also promote pharmacological research that may lead to the development of more specific drugs to be used in humans. In short, the biophysically detailed quantitative dog and rat ventricular cell models can provide good insights into the ionic basis of action potential variation in epicardial and endocardial cells under a variety of disease conditions.

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    MBBP02
    Electrical Stimulus Application on a Cardiac Pacemaker Cell
    Semahat S. Demir, PhD, Assistant Professor, School of Biomedical Engineering, University of Tennessee - Memphis

    A cardiac pacemaker (sinoatrial node, SAN) cell model (Demir et al 1994) was studied to determine the phase-sensitive response of the sinoatrial node cell to a single pulse and periodic pulses of hyperpolarizing electrical current. The simulation data were presented in phase response curves (PRCs) for the single pulse and in entrainment curves (ECs) for the periodically applied pulses. These graphical representations provided a quantitative description of the phase-sensitivity behavior of the SAN cell in rabbit. Our computations showed that the characteristics of the phase-sensitive effects in PRCs and ECs are dependent upon the intensity of the stimulus and that the PRCs and ECs represented the perturbations in the membrane properties of the pacemaker cell caused by the hyperpolarizing stimulus. The mechanisms related to the changes in the ionic currents due to the hyperpolarizing effects are explained in phase planes, in terms of current-voltage plots. Our model depends on quantitative voltage clamp and action potential data, thus it can provide reasonable estimates of the ionic currents and their interactions in setting the pacemaker rate. We found out that the action potential threshold determined by ICa,L was not affected by the perturbations. The currents (INaCa, If, INa and ICa,T) that set the rate of diastolic depolarization were affected by the perturbations. The changes in INaCa, If, INa and ICa,T during diastole determine the rate of diastolic depolarization which results in delaying or advancing the following action potential. This study provides a better understanding of the requirements and mechanisms for controlling pacemaker activity of the heart during diastole.

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    MBBP03 - Withdrawn

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    For technical presentation or Open Technical Exchange information, contact the Houston Convention Team.

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