High Resolution 3D Optics Coherence Phase Microscopy
High Resolution 3D Optics Coherence Phase Microscopy
批准号:
8137150
负责人:
JOHANNES F DE BOER
金额:
$13.05万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-10 至 2012-08-31
关键词:
3-DimensionalAction PotentialsAstacoideaAutomobile DrivingAxonB-LymphocytesBehaviorBindingCD3 AntigensCalibrationCell VolumesCell physiologyCellsCellular StructuresCellular biologyDetectionDevelopmentDyesElectrodesEnvironmentFluorescence MicroscopyFoundationsFundingGoalsImageImageryImaging DeviceImaging TechniquesIndividualLateralLeadLifeLightLobsterMeasuresMedicineMethodsMicroscopeMicroscopyMonitorNerveNeurobiologyNeuronsOptical Coherence TomographyOpticsPerformancePhasePhase-Contrast MicroscopyPhotonsProcessResearchResolutionSpecimenStaining methodStainsStimulusStructureSwellingSystemT-Cell ReceptorT-LymphocyteTechniquesTechnologyThree-Dimensional ImageThree-Dimensional ImagingTissuesbasecell behaviorcellular imagingdesignfluorescence imagingimaging modalityinsightlight microscopynanometernoveloptical imagingphase changeprogramspublic health relevancerelating to nervous systemresponsesubmicronthree dimensional structuretransmission processtwo-photonvoltage
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Three-dimensional imaging of cells and sub cellular structures has enormous potential in studies on cell physiology and medicine, since it enables the observation of cell behavior in a variety of environments. Many three-dimensional imaging techniques to date require cells to be stained or dyed to produce images of structures that are normally not observable. We propose to develop a three-dimensional optical coherence phase-contrast microscope (OCPM) based on Spectral Domain Optical Coherence Tomography (SD-OCT) technology that can reveal three-dimensional structures and dynamics of cells in their natural state by measuring depth resolved phase differences with high sensitivity. The OCPM will be integrated with Two Photon Microscopy (TPM) into a standard inverted microscope. Phase sensitivity, lateral resolution, and structural imaging capability will be evaluated on calibration objects and cells, where nanometer axial and sub-micron lateral resolution are targeted. Interpretation of OCPM images will be investigated by simultaneous two-photon fluorescence imaging of the same specimen. The potential of OCPM will be studied by imaging cell responses to external stimuli. The ability for deep tissue imaging (250 ¿m) and the exploitation of phase sensitivity will be investigated by monitoring action potentials in axons embedded in larger nerve bundles. Neural activity has been demonstrated to induce rapid changes in nerves (swelling) on the order of 1-3 nanometers. The spatio-temporal resolution of OCPM is capable of detecting these rapid changes during action potential propagation. OCPM will serve as a powerful imaging tool for processes in cell biology and will enhance the understanding of the structure, function, and the behavior of living cells. The overall goal of this research is A) to develop an OCPM system for 3 dimensional high resolution phase contrast imaging of cells, B) to determine the phase resolution and sectioning capability of OCPM, C) to investigate the potential of OCPM for the study of cell dynamics in response to external stimuli, D) to non- invasively measure action potentials of axons within nerve bundles.
PUBLIC HEALTH RELEVANCE: Three-dimensional imaging of cells and sub cellular structures has enormous potential in studies on cell physiology and medicine, since it enables the observation of cell behavior in a variety of environments. Many three-dimensional imaging techniques to date require cells to be stained or dyed to produce images of structures that are normally not observable. We will develop a new form of microscopy (OCPM) that is able to detect minute changes in cells on the order of nanometers. OCPM will serve as a powerful imaging tool for processes in cell biology and will enhance the understanding of the structure, function, and the behavior of living cells.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1364/oe.20.015253
发表时间:
2012-07-02
期刊:
Optics express
影响因子:
3.8
作者:
[de Groot M, Evans CL, de Boer JF]
通讯作者:
de Boer JF
DOI:
10.1364/ol.38.000431
发表时间:
2013
期刊:
Optics letters
影响因子:
3.6
作者:
[Helderman,Frank, Haslam,Bryan, deBoer,JohannesF, deGroot,Mattijs]
通讯作者:
deGroot,Mattijs
Field-based dynamic light scattering microscopy: theory and numerical analysis.
基于场的动态光散射显微镜:理论和数值分析。
DOI:
10.1364/ao.52.007618
发表时间:
2013
期刊:
Applied optics
影响因子:
1.9
作者:
[Joo,Chulmin, deBoer,JohannesF]
通讯作者:
deBoer,JohannesF
High Resolution 3D Optics Coherence Phase Microscopy
-
批准号:7929461
-
项目类别:
-
资助金额:$13.18万
-
财政年份:2009
-
负责人:JOHANNES F DE BOER
-
依托单位:
Video Rate OCT for Evaluating Glaucoma
-
批准号:6878966
-
项目类别:
-
资助金额:$47.75万
-
财政年份:2004
-
负责人:JOHANNES F DE BOER
-
依托单位:
Video Rate OCT for Evaluating Glaucoma
-
批准号:6780055
-
项目类别:
-
资助金额:$54.46万
-
财政年份:2004
-
负责人:JOHANNES F DE BOER
-
依托单位:
Video Rate OCT for Evaluating Glaucoma
-
批准号:7057271
-
项目类别:
-
资助金额:$42.32万
-
财政年份:2004
-
负责人:JOHANNES F DE BOER
-
依托单位:
Video Rate OCT for Evaluating Glaucoma
-
批准号:6950954
-
项目类别:
-
资助金额:$4.22万
-
财政年份:2004
-
负责人:JOHANNES F DE BOER
-
依托单位:
Fast OCT technology for comprehensive diagnostic imaging
-
批准号:6799690
-
项目类别:
-
资助金额:$40.56万
-
财政年份:2003
-
负责人:JOHANNES F DE BOER
-
依托单位:
Fast OCT technology for comprehensive diagnostic imaging
-
批准号:6909774
-
项目类别:
-
资助金额:$46.83万
-
财政年份:2003
-
负责人:JOHANNES F DE BOER
-
依托单位:
Fast OCT technology for comprehensive diagnostic imaging
-
批准号:6730243
-
项目类别:
-
资助金额:$53.16万
-
财政年份:2003
-
负责人:JOHANNES F DE BOER
-
依托单位:
Fast OCT technology for comprehensive diagnostic imaging
-
批准号:7107962
-
项目类别:
-
资助金额:$57.08万
-
财政年份:2003
-
负责人:JOHANNES F DE BOER
-
依托单位:
海外基金