Creating Biomedical Technologies to Improve Health


NIBIB-Supported Biomedical Technology Resource Centers

  • Bruce Tromberg
    University of California-Irvine
  • Ravinder Reddy
    University of Pennsylvania
  • K Shung
    University of Southern California

    The focus of this resource is to develop very high frequency (above 20 MHz) ultrasonic transducers/arrays for applications in medicine and biology that include ophthalmology, dermatology, vascular surgery, and small animal imaging. The research is pursued simultaneously in three directions: novel piezoelectric materials, very high frequency single element transducers and linear arrays, and finite element modeling and material property measurements.

  • Mehmet Toner
    Massachusetts General Hospital
  • David D'Argenio
    University of Southern California

    The Biomedical Simulations Resource (BMSR) in the Department of Biomedical Engineering at the University of Southern California is dedicated to the advancement of the state-of-the-art in biomedical modeling and simulation through Core and Collaborative Research projects, as well as the dissemination of this knowledge and related software through Service, Training and Dissemination activities aimed at the biomedical community at large. The BMSR includes four core research projects:Pharmacokinetic/Pharmacodynamic Systems Analysis – David Z. D'Argenio, Ph.D., Co-DirectorNonlinear Modeling of Complex Biomedical Systems – Vasilis Z. Marmarelis, Ph.D., Co-DirectorModeling of Autonomic, Metabolic and Vascular Control Interactions – Michael C.K. Khoo, Ph.D., Co-InvestigatorNonlinear Modeling of the Hippocampus – Theodore W. Berger, Ph.D., Co-InvestigatorFifteen Collaborative Research Projects serve as challenging test grounds for the Resource's methodologies and expertise. The BMSR's service activities include the development and distribution of four software packages (ADAPT, LYSIS, PNEUMA +amp; EONS).The Resource's Training and Dissemination activities include short courses, advanced workshops and the publication of associated research volumes.

  • Steven Soper
    University of Kansas Lawrence
  • Jonathan Wolpaw
    Wadsworth Center
  • Daniel Sodickson
    New York University School of Medicine
  • Gary Glover
    Stanford University
  • Brett Bouma
    Massachusetts General Hospital
  • Howard Halpern
    University of Chicago
  • Bruce Rosen
    Massachusetts General Hospital
  • Lars Furenlid
    University of Arizona
  • Georges El Fakhri
    Massachusetts General Hospital
  • Richard Superfine
    Univ of North Carolina Chapel Hill
  • Arnold Caplan
    Case Western Reserve University
  • Daniel Vigneron
    University of California, San Francisco

    This Center will develop, investigate, and disseminate new hyperpolarized MR techniques, new 13C agents and specialized analysis open-source software for data reconstruction and interpretation. The Technology Research +amp; Development projects will leverage the extensive DNP facilities and experience of the project leaders to develop improved, robust hyperpolarized MRI methods. These technology developments will be driven by Collaborative Projects led by outstanding clinical and basic scientists who aim to use hyperpolarized 13C MRI to accomplish the scientific goals of their funded research. These technical developments will also be disseminated to the Service Project investigators for extramural feedback and then widely to the scientific community via a dedicated website and onsite training. This center will provide state-of-the-art training in this new metabolic imaging field and sponsor a yearly symposium focused on hyperpolarized MR technology development.

  • Clare Tempany
    Brigham And Women'S Hospital
  • George Johnson
    Duke University
  • Joachim Kohn
    Rutgers, The State Univ of N.J.
  • Arthur Toga
    University of Southern California
  • Peter So
    Massachusetts Institute of Technology

    The MIT Laser Biomedical Research Center (LBRC) develops the basic scientific understanding and new techniques required for advancing the clinical applications of lasers and spectroscopy. To fulfill the significant and ever growing need for a more comprehensive and potentially non-invasive understanding of the human body, the LBRC merges optical spectroscopy, imaging, scattering, and interferometry techniques. Specifically, researchers at the LBRC study the biophysics and biochemistry of healthy and diseased biological structures from the subcellular to the entire-organ scale. For example, spectral diagnosis instruments based on near-infrared Raman scattering, intrinsic fluorescence, diffuse reflectance, and single light scattering provide complementary data on human disease. Combining these techniques into a single, multimodal instrument is applied for diagnostics in various organs, including cervix, oral cavity, Barrett's esophagus, artery, breast, skin, as well as for transcutaneous measurements of blood constituents. The LBRC has been and continues to be a pioneer in the field of developing novel optical probes for use under direct visualization or with endoscopes and biopsy devices.Similarly, new microscopy tools based on interferometry are designed and exploited for measuring cellular structures and their dynamics. In particular, these techniques provide the crucial and unique ability to non-invasively study cells in their native states at remarkably high spatial and temporal resolutions. Using these novel microscopy tools, the LBRC has conducted critical studies to elucidate the fundamental biology of diseases as diverse as malaria and multiple myeloma, and physiological processes such as cell growth and cell division. The interferometry concepts have also been vital in Center’s research efforts to develop optical tools for deep-tissue imaging while minimizing the adverse effects of light scattering or diffusion. Furthermore, the unique and powerful combination of the interferometric microscopy and vibrational spectroscopy tools adds a hitherto unexplored dimension to optical sensing by simultaneous probing of morphological and chemical information.A unique feature of the LBRC is its ability to form strong clinical collaborations with outside investigators in areas of common interest that further the Center's mandated research objectives. A major focus of these collaborations is to rapidly translate the novel photonic technologies introduced at the LBRC into the clinic and potentially into the field. Another focal point of the collaborations is to enable external researchers to exploit laser-based techniques for medical applications such as the spectral diagnosis of disease, investigation of biophysical and biochemical properties of cells and tissues, and development of novel imaging techniques.

  • Robert Griffin
    Massachusetts Institute of Technology

    The Harvard/MIT Center for Magnetic Resonance (CMR) is a joint effort between Harvard Medical School and the Massachussetts Institute of Technology. The CMR core research program is focused on the development and applicaton of new magnetic resonance technologies directed at structural biology using a cluster of high field solution and solid state NMR spectrometers. Investigations includes studies of membrane proteins, translation initiation, and amyloid fibrils associated with several diseases. Membrane proteins are examined in nanodiscs using solution NMR and in lipsomes and 2D crystals using magic angle spinning (MAS) dipolar recoupling techniques. Translation initiation is investigated with solution NMR. MAS is the method of choice for experiments on amyloid fibrils since they are both insoluble and do not diffract to high resolution. The CMR is also heavily involved in the development of new software and instrumentation for magnetic resonance. These include methods for non uniform sampling (NUS) to enable efficient acquisiton of higher dimensional NMR spectra and high frequency microwave technology (~150-600 GHz) is being developed for both DNP-NMR and EPR experiments at high magnetic fields. Recent DNP experiments have yielded significant signal enhancments from membrane and amyloid protein samples and enabled experiments that are otherwise not possible. The CMR has pioneered the development of low temperature MAS technology. In addition, there is an extensive effort focused on the creation of new pulse sequences for performing assignments and determining structures in both solution and MAS experiments. Finally, the staff at the CMR interact extensively with outside investigators.

  • Candice Klug
    Medical College of Wisconsin
  • Craig Malloy
    Ut Southwestern Medical Center

    The Southwestern NMR Center for In Vivo Metabolism exists to develop and apply new methods for analysis of metabolic networks in intact tissues, animals and human patients. The importance of understanding abnormal metabolism in common diseases such as cancer, diabetes and heart disease has long been appreciated. Because of constraints in technology, however, much of this research has been conducted in isolated systems where clinical relevance may be uncertain. Progress in magnetic resonance technology provides a foundation for major advances towards new ways of imaging metabolism in patients. These new techniques offer the advantage of imaging biochemical pathways without radiation. The focus of this Resource is to bring these technologies to a level where clinical research is feasible through the development of new MR contrast agents, NMR spectroscopy at high fields, and imaging of hyperpolarized 13C.

  • Ron Kikinis
    Brigham And Women'S Hospital
  • Kamil Ugurbil
    University of Minnesota
  • David Brenner
    Columbia University Health Sciences

    The Columbia University Radiological Research Accelerator Facility (RARAF) is a dedicated facility for radiobiological research with available ionizing radiations such as protons, alpha particles, and neutrons. RARAF is well-established and highly user-friendly. The focus of RARAF is the development of high-throughput single-cell/single-particle microbeams, which can deliver defined amounts of ionizing radiation into individual cells with a spatial resolution of a few microns or better. The ability of a microbeam to put double strand break damage at any specific known location in a given cell has allowed new approaches to the study of damage signaling.

  • Martin Pomper
    Johns Hopkins University
  • Stanley Opella
    University of California San Diego
  • Peter Van Zijl
    Hugo W. Moser Res Inst Kennedy Krieger
  • David Castner
    University of Washington
  • David Kaplan
    Tufts University Medford