Widefield fluorescence macroscopy with out-of-focus blur rejection
具有离焦模糊抑制功能的宽场荧光肉眼观察
基本信息
- 批准号:7489984
- 负责人:
- 金额:$ 15.93万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2007
- 资助国家:美国
- 起止时间:2007-09-01 至 2010-01-31
- 项目状态:已结题
- 来源:
- 关键词:Animal Cancer ModelAnimalsBlurBrainCharacteristicsClinicDepthDevicesDiagnosisDiscriminationFluorescenceGoalsHybridsImageImageryImaging DeviceKnowledgeLabelLasersLightLightingMethodsMetricMicroscopeMicroscopicMicroscopyModificationMusNeuronsOperative Surgical ProceduresPatternPublic HealthRadiology SpecialtyResearchResolutionSamplingScanningSensitivity and SpecificityStandards of Weights and MeasuresStructureSystemTechniquesTestingThickTissuesWorkanticancer researchbasecharge coupled device cameraclinical applicationdesignfluorescence imagingfluorescence microscopeimprovedin vivoinstrumentinstrumentationliquid crystalmillimetermolecular imagingnovelprototypesubmicrontheoriestissue phantomtooltumor
项目摘要
DESCRIPTION (provided by applicant): Our aim is to develop of a new type of imaging "macroscope" that performs ultra-deep (several millimeters) fluorescence imaging in thick tissue while providing out-of-focus background rejection. Our proposed method for out-of-focus blur rejection is based on a novel technique called Dynamic Speckle Illumination (DSI) microscopy that was recently invented in our lab. Our goal is to build a portable DSI macroscope and establish its potential for in-vivo molecular-imaging applications such as cancer research and diagnosis, as well as small animal imaging and surgery. DSI microscopy consists of a simple modification to a standard widefield fluorescence microscope. Sample illumination is performed with random laser speckle patterns rather than with a lamp. The main advantage of DSI microscopy is that it provides depth discrimination and out-of-focus blur reduction in thick tissues without the use of a complicated scanning mechanism. We have developed the full theory of DSI microscopy and already demonstrated sub-micron-resolution imaging with confocal-like background rejection of GFP-labeled neurons, down to about 100¿m in mice brain. We propose to develop a new instrument that performs much deeper imaging but with lower resolution. Our targeted depth is several millimeters, down to perhaps a centimeter. To attain this goal we propose to significantly re-design of our DSI microscope to incorporate a long working-distance telecentric objective, near-infrared laser illumination, and a more sensitive CCD camera. We also plan to combine DSI with structured illumination contrast and multipsectral imaging (for the latter, we will work with Cambridge Research & Instrumentation). The defining advantage of our DSI macroscope compared to conventional commercially available macroscopes will be that DSI provides out-of-focus background rejection, enabling significantly better localization and visualization of labeled structures within thick tissue. Initial testing of our DSI prototype will be performed on tissue phantoms provided by a radiology lab. Widefield fluorescence macroscopy with out-of-focus blur rejection. Public health: We propose to develop a simple and inexpensive device that performs ultra-deep fluorescence imaging with out-of-focus blur rejection, for small animal cancer-model imaging. Our goal is to build a new tool for cancer research that can eventually be implemented in the clinic.
描述(由申请人提供):我们的目标是开发一种新型的成像“宏观镜”,其在厚组织中执行超深(几毫米)荧光成像,同时提供散焦背景抑制。我们所提出的方法为离焦模糊抑制是基于一种新的技术,称为动态散斑照明(DSI)显微镜,最近在我们的实验室发明的。我们的目标是建立一个便携式的DSI宏观,并建立其潜在的体内分子成像应用,如癌症的研究和诊断,以及小动物成像和手术。DSI显微镜由对标准宽视场荧光显微镜的简单修改组成。用随机激光散斑图案而不是用灯进行样品照明。DSI显微镜的主要优点是,它提供了深度歧视和离焦模糊减少厚组织,而无需使用复杂的扫描机制。我们已经开发了DSI显微镜的完整理论,并且已经证明了亚微米分辨率成像与GFP标记神经元的共焦样背景排斥,在小鼠大脑中低至约100 μ m。我们建议开发一种新的仪器,执行更深的成像,但分辨率较低。我们的目标深度是几毫米,甚至一厘米。为了实现这一目标,我们建议显着重新设计我们的DSI显微镜,将一个长的工作距离远心物镜,近红外激光照明,和一个更敏感的CCD相机。我们还计划将联合收割机DSI与结构照明对比度和多光谱成像相结合(对于后者,我们将与剑桥研究与仪器公司合作)。与传统的市售宏观镜相比,我们的DSI宏观镜的定义优势在于,DSI提供了失焦背景抑制,能够显著更好地定位和可视化厚组织内的标记结构。我们的DSI原型的初始测试将在放射实验室提供的组织体模上进行。具有离焦模糊抑制的宽视场荧光宏观检查。公共卫生:我们建议开发一种简单而廉价的设备,用于小动物癌症模型成像,该设备可以进行具有离焦模糊抑制的超深荧光成像。我们的目标是建立一个新的癌症研究工具,最终可以在临床上实施。
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Jerome Mertz其他文献
Jerome Mertz的其他文献
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- 资助金额:
$ 15.93万 - 项目类别:
Multi-Layer Neuronal Imaging with Reverberation Multiphoton Microscopy
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- 资助金额:
$ 15.93万 - 项目类别:
Multi-layer neuronal imaging with reverberation multiphoton microscopy
使用混响多光子显微镜进行多层神经元成像
- 批准号:
10320482 - 财政年份:2020
- 资助金额:
$ 15.93万 - 项目类别:
Fast, large-scale neuronal imaging with multi-z confocal microscopy
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- 批准号:
10088442 - 财政年份:2020
- 资助金额:
$ 15.93万 - 项目类别:
Fast, large-scale neuronal imaging with multi-z confocal microscopy
使用多 Z 共聚焦显微镜进行快速、大规模神经元成像
- 批准号:
10524735 - 财政年份:2020
- 资助金额:
$ 15.93万 - 项目类别:
Fast, large-scale neuronal imaging with multi-z confocal microscopy
使用多 Z 共聚焦显微镜进行快速、大规模神经元成像
- 批准号:
10304852 - 财政年份:2020
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$ 15.93万 - 项目类别:
Retinal/choroidal imaging with transcranial back-illumination
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- 批准号:
9762120 - 财政年份:2018
- 资助金额:
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Multi-region, extended-depth imaging of neural activity via a novel needle microendoscope
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- 批准号:
8953984 - 财政年份:2015
- 资助金额:
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