FIP Seminar: Co-hosted with Duke OSA/SPIE Student Optical Chapter "Quantitative Phase Imaging in Biomedicine"

Wednesday, January 23, 2019

12:00 pm - 1:00 pm
Fitzpatrick Center Schiciano Auditorium Side B, room 1466

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Presenter

Dr. Gabriel Popescu, Professor of Electrical and Computer Engineering & Bioengineering, University of Illinois at Urbana-Champaign

Light scattering limits the quality of optical imaging of unlabeled specimens: too little scattering and the sample is transparent, exhibiting low contrast, and too much scattering washes the structure information altogether. As a result, current instruments, target specifically either the thin (low-scattering) specimens or the optically thick (multiply scattering) samples. In 2011 we developed spatial light interference microscopy (SLIM) as a high-sensitivity, high-resolution quantitative phase imaging method, which open new applications for studying structure and dynamics. Color SLIM (cSLIM) is a recent development that allows the phase imaging of stained tissue slices. Using specimens prepared under the standard protocols in pathology, cSLIM yields simultaneously the typical image that the pathologist is accustomed to (e.g., H&E, immunochemical stains, etc.) and a quantitative phase image, which provides new information, currently not available in bright field images (e.g., collagen fiber orientation).

However, SLIM works best for thin specimens, such as single cell layers and tissue slices. To expand this type of imaging to thick, multiply scattering media, we developed gradient light interference microcopy (GLIM). GLIM exploits the principle of low-coherence interferometry to extract phase information, which in turn yields strong, intrinsic contrast of transparent samples, such as single cells. Because it combines multiple intensity images that correspond to controlled phase shifts between two interfering waves, GLIM can suppress the incoherent background due to multiple scattering. We demonstrate the use of GLIM to image various samples, including standard micron size beads, single cells, cell populations, thick bovine embryos, and live brain slices. GLIM operates as an add-on to a conventional microscope and overlays seamlessly with the existing channels (e.g., fluorescence).

Gabriel Popescu is a Professor in Electrical and Computer Engineering, University of Illinois at Urbana-Champaign. He received his Ph.D. in Optics in 2002 from the School of Optics/ CREOL (now the College of Optics and Photonics), University of Central Florida.  He continued his training with Michael Feld at M.I.T., working as a postdoctoral associate. He joined Illinois in August 2007 where he directs the Quantitative Light Imaging Laboratory (QLI Lab) at the Beckman Institute for Advanced Science and Technology. Dr. Popescu served as Associate Editor of Optics Express and Biomedical Optics Express, Editorial Board Member for Journal of Biomedical Optics and Scientific Reports. He authored a book, edited another book, authored 155 journal publications, 200 conference presentations, 32 patents, gave 200 lecture/plenary/invited talks. He founded Phi Optics, Inc., a start-up company that commercializes quantitative phase imaging technology. He is a Fellow of OSA and SPIE.

Contact

Burns, August
660-5598
august.burns@duke.edu