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DESCRIPTION (provided by applicant): The purpose of this project is to develop a multifocal optical coherence microscope (OCM). The proposed OCM will allow noninvasive imaging of unstained biological specimens, with millisecond temporal resolution and sub-cellular spatial resolution in three dimensions. During this project, we expect to achieve three specific aims as follows: 1) Construction of a full-field OCM: We plan to develop a digital camera based full-filed OCM. An electro- optic phase modulator will be used for rapid, vibration-free phase modulation of the reference beam. A near infrared light will be employed to ensure high penetrating depth of OCM imaging. A four-step phase shifting algorithm will be used for concurrent reconstruction of intensity-sensitive and phase-sensitive OCM images. Polarization-sensitive imaging capability will be added to achieve high contrast imaging of biological specimens with birefringence characteristics. 2) Development of a multifocal OCM: In order to ensure the stability of sampling volume, we will employ a multifocal illumination and virtual pinhole confocal imaging strategy for further improvement of the full-field OCM. The combination of the virtual pinhole confocal imaging and low coherence gating mechanism will provide a two-stage `filtering' system for effective rejection of undesired noise light: 1) Computer- synthesized virtual pinholes will be used to reject out-of-focus light; 2) Low coherence gating mechanism will be used to reject cross-talk noise light between adjacent sampling volumes. Using a near infrared light (center wavelength: ~800 nm) with 100 nm bandwidth, we anticipate a depth resolution better than 3 ¿m. The lateral (perpendicular to the light axis) resolution will be optical diffraction limited. 3) Functional test of the multifocal OCM: A series of biological tissues/cells will be used to assess the intensity-sensitive, phase-sensitive, and polarization-sensitive imaging capabilities of the proposed OCM. Multi-modal OCM imaging of human skin will be also implemented for preliminary test of imaging stability of the proposed instrument for in vivo application. Although the proposed OCM promises a versatile imaging platform for a variety of biomedical applications, this project will focus on proof-of-concept of the imaging system. PUBLIC HEALTH RELEVANCE: The proposed multifocal optical coherence microscope can provide fast, noninvasive imaging with sub-cellular spatial resolution in three dimensions. We anticipate that the multifocal OCM will find a wide range of applications in cell biology, neurobiology, tissue engineering, dermatology, and ophthalmology.
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Functional imaging of retinal photoreceptors and inner neurons using stimulus-evoked intrinsic optical signals.
使用刺激诱发的内在光信号对视网膜感光器和内部神经元进行功能成像。
DOI: 10.1007/978-1-61779-848-1_20
发表时间: 2012
期刊: Methods in molecular biology (Clifton, N.J.)
影响因子: --
作者: [Yao,Xin-Cheng, Li,Yi-Chao]
通讯作者: Li,Yi-Chao
Circular polarization intrinsic optical signal recording of stimulus-evoked neural activity.
刺激诱发神经活动的圆偏振内在光信号记录。
DOI: 10.1364/ol.36.001866
发表时间: 2011
期刊: Optics letters
影响因子: 3.6
作者: [Lu,Rong-Wen, Zhang,Qiu-Xiang, Yao,Xin-Cheng]
通讯作者: Yao,Xin-Cheng
DOI: 10.1364/boe.4.001673
发表时间: 2013-09
期刊: Biomedical optics express
影响因子: 3.4
作者: [Rongwen Lu;Benquan Wang;Qiuxiang Zhang;Xincheng Yao]
通讯作者: Rongwen Lu;Benquan Wang;Qiuxiang Zhang;Xincheng Yao
DOI: 10.1080/09500340.2012.687464
发表时间: 2012-06-20
期刊: Journal of modern optics
影响因子: 1.3
作者: [Li YC, Luo JM, Lu RW, Liu KM, Levy AM, Yao XC]
通讯作者: Yao XC
7
    Functional tomography of neurovascular coupling interactions in healthy and diseased retinas
    Functional tomography of neurovascular coupling interactions in healthy and diseased retinas
    Super-resolution ophthalmoscopy for in vivo retinal imaging
    Functional imaging of retinal photoreceptors
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