Light Seminars
May 5, 2017
L4H Seminar AYDOGAN OZCAN 'Mobile Microscopy, Sensing and Diagnostics through Computational Photonics'
L4H Seminar AYDOGAN OZCAN 'Mobile Microscopy, Sensing and Diagnostics through Computational Photonics'
AYDOGAN OZCAN
Seminar, May 5, 2017, 12:00. Seminar Room
AYDOGAN OZCAN
UCLA & California NanSystems Institute
AYDOGAN OZCAN
UCLA & California NanSystems Institute
My research focuses on the use of computation/algorithms to create new optical microscopy, sensing, and diagnostic techniques, significantly improving existing tools for probing micro- and nano-objects while also simplifying the designs of these analysis tools. In this presentation, I will introduce a new set of computational microscopes which use lens-free on-chip imaging to replace traditional lenses with holographic reconstruction algorithms. Basically, 3D images of specimens are reconstructed from their “shadows” providing considerably improved field-of-view (FOV) and depth-of-field, thus enabling large sample volumes to be rapidly imaged, even at nanoscale. These new computational microscopes routinely generate >1–2 billion pixels (giga-pixels), where even single viruses can be detected with a FOV that is >100 fold wider than other techniques. At the heart of this leapfrog performance lie self-assembled liquid nano-lenses that are computationally imaged on a chip. These self-assembled nano-lenses are stable for >1 hour at room temperature, and are composed of a biocompatible buffer that prevents nano-particle aggregation while also acting as a spatial “phase mask.” The field-of-view of these computational microscopes is equal to the active-area of the sensor-array, easily reaching, for example, >20 mm2 or >10 cm2 by employing state-of-the-art CMOS or CCD imaging chips, respectively.
In addition to this remarkable increase in throughput, another major benefit of this technology is that it lends itself to field-portable and cost-effective designs which easily integrate with smartphones to conduct giga-pixel tele-pathology and microscopy even in resource-poor and remote settings where traditional techniques are difficult to implement and sustain, thus opening the door to various telemedicine applications in global health. Some other examples of these smartphone-based biomedical tools that I will describe include imaging flow cytometers, immunochromatographic diagnostic test readers, bacteria/pathogen sensors, blood analyzers for complete blood count, and allergen detectors. Through the development of similar computational imagers, I will also report the discovery of new 3D swimming patterns observed in human and animal sperm. One of this newly discovered and extremely rare motion is in the form of “chiral ribbons” where the planar swings of the sperm head occur on an osculating plane creating in some cases a helical ribbon and in some others a twisted ribbon. Shedding light onto the statistics and biophysics of various micro-swimmers’ 3D motion, these results provide an important example of how biomedical imaging significantly benefits from emerging computational algorithms/theories, revolutionizing existing tools for observing various micro- and nano-scale phenomena in innovative, high-throughput, and yet cost-effective ways.
Seminar, May 5, 2017, 12:00. Seminar Room
Hosted by Prof. Romain Quidant
In addition to this remarkable increase in throughput, another major benefit of this technology is that it lends itself to field-portable and cost-effective designs which easily integrate with smartphones to conduct giga-pixel tele-pathology and microscopy even in resource-poor and remote settings where traditional techniques are difficult to implement and sustain, thus opening the door to various telemedicine applications in global health. Some other examples of these smartphone-based biomedical tools that I will describe include imaging flow cytometers, immunochromatographic diagnostic test readers, bacteria/pathogen sensors, blood analyzers for complete blood count, and allergen detectors. Through the development of similar computational imagers, I will also report the discovery of new 3D swimming patterns observed in human and animal sperm. One of this newly discovered and extremely rare motion is in the form of “chiral ribbons” where the planar swings of the sperm head occur on an osculating plane creating in some cases a helical ribbon and in some others a twisted ribbon. Shedding light onto the statistics and biophysics of various micro-swimmers’ 3D motion, these results provide an important example of how biomedical imaging significantly benefits from emerging computational algorithms/theories, revolutionizing existing tools for observing various micro- and nano-scale phenomena in innovative, high-throughput, and yet cost-effective ways.
Seminar, May 5, 2017, 12:00. Seminar Room
Hosted by Prof. Romain Quidant
Light Seminars
May 5, 2017
L4H Seminar AYDOGAN OZCAN 'Mobile Microscopy, Sensing and Diagnostics through Computational Photonics'
L4H Seminar AYDOGAN OZCAN 'Mobile Microscopy, Sensing and Diagnostics through Computational Photonics'
AYDOGAN OZCAN
Seminar, May 5, 2017, 12:00. Seminar Room
AYDOGAN OZCAN
UCLA & California NanSystems Institute
AYDOGAN OZCAN
UCLA & California NanSystems Institute
My research focuses on the use of computation/algorithms to create new optical microscopy, sensing, and diagnostic techniques, significantly improving existing tools for probing micro- and nano-objects while also simplifying the designs of these analysis tools. In this presentation, I will introduce a new set of computational microscopes which use lens-free on-chip imaging to replace traditional lenses with holographic reconstruction algorithms. Basically, 3D images of specimens are reconstructed from their “shadows” providing considerably improved field-of-view (FOV) and depth-of-field, thus enabling large sample volumes to be rapidly imaged, even at nanoscale. These new computational microscopes routinely generate >1–2 billion pixels (giga-pixels), where even single viruses can be detected with a FOV that is >100 fold wider than other techniques. At the heart of this leapfrog performance lie self-assembled liquid nano-lenses that are computationally imaged on a chip. These self-assembled nano-lenses are stable for >1 hour at room temperature, and are composed of a biocompatible buffer that prevents nano-particle aggregation while also acting as a spatial “phase mask.” The field-of-view of these computational microscopes is equal to the active-area of the sensor-array, easily reaching, for example, >20 mm2 or >10 cm2 by employing state-of-the-art CMOS or CCD imaging chips, respectively.
In addition to this remarkable increase in throughput, another major benefit of this technology is that it lends itself to field-portable and cost-effective designs which easily integrate with smartphones to conduct giga-pixel tele-pathology and microscopy even in resource-poor and remote settings where traditional techniques are difficult to implement and sustain, thus opening the door to various telemedicine applications in global health. Some other examples of these smartphone-based biomedical tools that I will describe include imaging flow cytometers, immunochromatographic diagnostic test readers, bacteria/pathogen sensors, blood analyzers for complete blood count, and allergen detectors. Through the development of similar computational imagers, I will also report the discovery of new 3D swimming patterns observed in human and animal sperm. One of this newly discovered and extremely rare motion is in the form of “chiral ribbons” where the planar swings of the sperm head occur on an osculating plane creating in some cases a helical ribbon and in some others a twisted ribbon. Shedding light onto the statistics and biophysics of various micro-swimmers’ 3D motion, these results provide an important example of how biomedical imaging significantly benefits from emerging computational algorithms/theories, revolutionizing existing tools for observing various micro- and nano-scale phenomena in innovative, high-throughput, and yet cost-effective ways.
Seminar, May 5, 2017, 12:00. Seminar Room
Hosted by Prof. Romain Quidant
In addition to this remarkable increase in throughput, another major benefit of this technology is that it lends itself to field-portable and cost-effective designs which easily integrate with smartphones to conduct giga-pixel tele-pathology and microscopy even in resource-poor and remote settings where traditional techniques are difficult to implement and sustain, thus opening the door to various telemedicine applications in global health. Some other examples of these smartphone-based biomedical tools that I will describe include imaging flow cytometers, immunochromatographic diagnostic test readers, bacteria/pathogen sensors, blood analyzers for complete blood count, and allergen detectors. Through the development of similar computational imagers, I will also report the discovery of new 3D swimming patterns observed in human and animal sperm. One of this newly discovered and extremely rare motion is in the form of “chiral ribbons” where the planar swings of the sperm head occur on an osculating plane creating in some cases a helical ribbon and in some others a twisted ribbon. Shedding light onto the statistics and biophysics of various micro-swimmers’ 3D motion, these results provide an important example of how biomedical imaging significantly benefits from emerging computational algorithms/theories, revolutionizing existing tools for observing various micro- and nano-scale phenomena in innovative, high-throughput, and yet cost-effective ways.
Seminar, May 5, 2017, 12:00. Seminar Room
Hosted by Prof. Romain Quidant
All Insight Seminars
Light Seminars
November 22, 2017
L4H Seminar BRIAN POGUE 'Optical Imaging of Radiation Dose & Molecular Features of Cancer Treatment'
Light Seminars
November 8, 2017
L4H Seminar JULIETTE GRIFFIE 'On the Need of New Analysis Tools for the Quantification of Molecular Clustering in Super Resolution Pointillist Data Sets'
Light Seminars
October 2, 2017
L4H Seminar ALF HONIGMANN '3D-STED Microscopy to Dissect the Supra-Molecular Structure of Cell Junctions'
Light Seminars
September 22, 2017
L4H Seminar JULIE S. BITEEN 'Single-Molecule Imaging and Plasmon-Enhanced Fluorescence: Understanding Bacterial Function on the Nanoscale'
Light Seminars
September 19, 2017
L4H Seminar ÁLVARO INGLÉS-PRIETO 'Optogenetic Activation of membrane receptors. Implications in Cancer Drug Screening and Parkinson’s Disease'
Light Seminars
July 19, 2017
L4H Seminar RICARDO HENRIQUES 'Democratising Live-Cell High-Speed Low-Illumination Super-Resolution Microscopy'
Light Seminars
June 14, 2017
L4H Seminar JONAS RIES 'Towards Structural Cell Biology with Superresolution Microscopy'
Light Seminars
June 2, 2017
L4H Seminar DAVID R. BUSCH 'Cerebral Hemodynamics Monitoring in the Critically Ill Child: Beyond Trend Monitoring with Quantitative Optical Tools'
Light Seminars
May 24, 2017
L4H SEMINAR JANA KAINERSTORFER 'Blood Flow Autoregulation and Intracranial Pressure Influences on Cerebral Hemodynamic Signals Measured with Near Infrared Spectroscopy'