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BIOENGINEERING &BIOMEDICAL ENGINEERING
1:00PMWONG 1030SEPTEMBER 28, 2018
Department of Bioengineering
Dr. Qiyin FangProfessor of Engineering Physics and Biomedical EngineeringMcMaster University
Dr. Christine Tardif ([email protected]) Dr. Sebastian Wachsmann Hogiu ([email protected])
ABSTRACT
InIn confocal microscopy, a single foci is raster scanned to form a 2-dimension or 3-dimension image. To speed up such a slow scanning process, multiple foci can be used, e.g. through the use of a spinning disc. We developed a new multiplexing confocal technique that scans a 2D foci array only on the target, but not on the imager. Such methods allowallow the use of next generation discrete CMOS detector arrays and can achieves high throughput without sacricing resolution, ideal for drug screening applications.
BIO
QiyinQiyin Fang is currently a Professor at McMaster University and a Canada Research Chair in Biophotonics. Prior to joining McMaster, Dr. Fang was with the Minimally Invasive Surgical Technology Institute of Cedars-Sinai Medical Center in Los Angeles. Dr. Fang obtained his BSc (Physics) from Nankai University, his MSc (applied physics)physics) and PhD (Biomedical Physics) from East Carolina University. His current research interests include optical spectroscopy and image guided minimally invasive diagnostic and therapeutic devices, miniaturized MOEMS sensors and imaging systems, and advanced optical microscopy and their emerging applications. Dr. Fang is a senior member and visiting lecturer of SPIE. member and visiting lecturer of SPIE.
FAST AND FLUORESCENT MULTIPLEXING FLUORESCENCE LIFETIME IMAGING FOR HIGH CONTENT
