Biomedical optical Imaging based on Low Coherence Interferometry and Array Scanning Techniques - 多院系Nanophotonics学术交流

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欧阳世宏

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Apr 29, 2011, 8:37:22 AM4/29/11
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Biomedical optical Imaging based on Low Coherence Interferometry and Array Scanning Techniques - 多院系Nanophotonics学术交流

 

 报告题目:Biomedical optical Imaging based on Low Coherence Interferometry and Array Scanning Techniques

 

 报告人简介:吴继刚,密西根学院

 Jigang Wu is an assistant professor at the University of Michigan-Shanghai Jiao Tong University (UM-SJTU) Joint Institute. He received B.S. and M.S. in Physics from Tsinghua University in 2001 and 2004, respectively, and Ph.D. in Electrical Engineering from the California Institute of Technology in 2008. He then worked as a postdoctoral scholar and research engineer at Caltech before joining the faculty of UM-SJTU Joint Institute in 2011. His current research interests include biomedical optical imaging, biophotonics, and their

 applications in biomedicine

 

 

 时间:201156(星期五)下午4

 地点:电信学院三号楼200号会议室

 

 摘要:

 The recent decades have witnessed rapid development of various biomedical optical imaging methods. Compared with other biomedical imaging techniques, optical methods usually have the advantages of being harmless while providing high resolution and high sensitivity. The first part of my talk will focus on a paired-angle-rotation scanning (PARS) endoscopic probe for optical coherence tomography (OCT). OCT is based on a low-coherence interferometer and is able to obtain in vivo high-resolution images using coherent gate. The development of the forward-imaging PARS probe would be very helpful for many clinic applications. The second part of my talk will focus on array scanning based methods, including optofluidic microscopy (OFM) and wide-field microscopy (WFM). OFM is a low-cost on-chip microscope design based on aperture array scanning and can provide high-resolution microscopic image without the need of bulky and expensive objective lenses. WFM is based on a focus grid scanning scheme. As each focus is equivalent to an objective lens, we can equivalently have multiple objective lenses in the system, and thus expand the field-of-view. In comparison, conventional microscope only provides limited field-of-view, especially for high-magnification images.

 

 

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