Microscopic probing of two-photon fluorescence for cancer diagnosis.
作者信息
Kumar DE Arijit, Mutyal Nikhil N, Goswami Debabrata
机构信息
Department of Chemistry, Indian Institute of Technology, Kanpur 208 016, India.
出版信息
Curr Sci. 2011 Feb 10;100(3):294-295.
Abstract
摘要
相似文献
1
Microscopic probing of two-photon fluorescence for cancer diagnosis.用于癌症诊断的双光子荧光显微镜探测
Curr Sci. 2011 Feb 10;100(3):294-295.
2
Probing nucleocytoplasmic transport by two-photon activation of PA-GFP.通过PA-GFP的双光子激活探究核质运输
Microsc Res Tech. 2006 Mar;69(3):220-6. doi: 10.1002/jemt.20252.
3
A two-photon fluorescence silica nanoparticle-based FRET nanoprobe platform for effective ratiometric bioimaging of intracellular endogenous adenosine triphosphate.一种基于双光子荧光硅纳米粒子的 FRET 纳米探针平台，可有效用于细胞内内源性三磷酸腺苷的比率型生物成像。
Analyst. 2021 Jul 26;146(15):4945-4953. doi: 10.1039/d1an00419k.
4
Aggregation-Induced Emission Luminogen with Near-Infrared-II Excitation and Near-Infrared-I Emission for Ultradeep Intravital Two-Photon Microscopy.具有近红外-II 激发和近红外-I 发射的聚集诱导发光团用于超深活体双光子显微镜。
ACS Nano. 2018 Aug 28;12(8):7936-7945. doi: 10.1021/acsnano.8b02452. Epub 2018 Aug 1.
5
Aggregation-Induced Emission Luminogen with Deep-Red Emission for Through-Skull Three-Photon Fluorescence Imaging of Mouse.用于小鼠颅透过三光子荧光成像的深红光发射聚集诱导发光团。
ACS Nano. 2017 Oct 24;11(10):10452-10461. doi: 10.1021/acsnano.7b05645. Epub 2017 Oct 12.
6
Simultaneous two-photon excitation of distinct labels for dual-color fluorescence crosscorrelation analysis.用于双色荧光互相关分析的不同标记物的同时双光子激发。
Proc Natl Acad Sci U S A. 2000 Sep 12;97(19):10377-82. doi: 10.1073/pnas.180317197.
7
Photophysical properties of Na -indicator dyes suitable for quantitative two-photon fluorescence-lifetime measurements.适用于定量双光子荧光寿命测量的 Na 指示剂染料的光物理性质。
J Microsc. 2018 Nov;272(2):136-144. doi: 10.1111/jmi.12754. Epub 2018 Sep 7.
8
[Intensity loss of two-photon excitation fluorescence microscopy images of mouse oocyte chromosomes].[小鼠卵母细胞染色体的双光子激发荧光显微镜图像的强度损失]
Guang Pu Xue Yu Guang Pu Fen Xi. 2014 Jul;34(7):1754-7.
9
Resolution in three-photon fluorescence scanning microscopy.
Opt Lett. 1996 Jul 1;21(13):988-90. doi: 10.1364/ol.21.000988.
10
Acetylene-substituted two-photon absorbing molecules with rigid elongated pi-conjugation: synthesis, spectroscopic properties and two-photon fluorescence cell imaging applications.
J Fluoresc. 2007 Sep;17(5):573-9. doi: 10.1007/s10895-007-0219-8. Epub 2007 Jun 26.
引用本文的文献
1
Towards controlling molecular motions in fluorescence microscopy and optical trapping: a spatiotemporal approach.迈向荧光显微镜和光镊中分子运动的控制：一种时空方法。
Int Rev Phys Chem. 2011 Sep 26;30(3):275-299. doi: 10.1080/0144235X.2011.603237.
本文引用的文献
1
Q&A: Cancer: clues from cell metabolism.问答：癌症：细胞代谢的线索
Nature. 2010 Jun 3;465(7298):562-4. doi: 10.1038/465562a.
2
Two-photon autofluorescence dynamics imaging reveals sensitivity of intracellular NADH concentration and conformation to cell physiology at the single-cell level.双光子自发荧光动力学成像揭示了单细胞水平下细胞内烟酰胺腺嘌呤二核苷酸（NADH）浓度和构象对细胞生理状态的敏感性。
J Photochem Photobiol B. 2009 Apr 2;95(1):46-57. doi: 10.1016/j.jphotobiol.2008.12.010. Epub 2008 Dec 25.
3
Tumor cell metabolism: cancer's Achilles' heel.肿瘤细胞代谢：癌症的致命弱点。
Cancer Cell. 2008 Jun;13(6):472-82. doi: 10.1016/j.ccr.2008.05.005.
4
Metabolic mapping of MCF10A human breast cells via multiphoton fluorescence lifetime imaging of the coenzyme NADH.通过辅酶NADH的多光子荧光寿命成像对MCF10A人乳腺细胞进行代谢图谱分析。
Cancer Res. 2005 Oct 1;65(19):8766-73. doi: 10.1158/0008-5472.CAN-04-3922.
5
Autofluorescence spectroscopy of normal and malignant human breast cell lines.正常和恶性人乳腺癌细胞系的自体荧光光谱分析
Photochem Photobiol. 2003 Nov;78(5):462-9. doi: 10.1562/0031-8655(2003)078<0462:asonam>2.0.co;2.
6
High-resolution multiphoton tomography of human skin with subcellular spatial resolution and picosecond time resolution.具有亚细胞空间分辨率和皮秒时间分辨率的人体皮肤高分辨率多光子断层扫描术。
J Biomed Opt. 2003 Jul;8(3):432-9. doi: 10.1117/1.1577349.
7
Two-photon fluorescence spectroscopy and microscopy of NAD(P)H and flavoprotein.NAD(P)H和黄素蛋白的双光子荧光光谱学与显微镜检查
Biophys J. 2002 May;82(5):2811-25. doi: 10.1016/S0006-3495(02)75621-X.
8
Multiphoton excitation provides optical sections from deeper within scattering specimens than confocal imaging.与共聚焦成像相比，多光子激发能够从散射样本更深的内部提供光学切片。
Biophys J. 1998 Oct;75(4):2015-24. doi: 10.1016/S0006-3495(98)77643-X.
9
Measuring serotonin distribution in live cells with three-photon excitation.利用三光子激发测量活细胞中血清素的分布。
Science. 1997 Jan 24;275(5299):530-2. doi: 10.1126/science.275.5299.530.
10
Multiphoton fluorescence excitation: new spectral windows for biological nonlinear microscopy.多光子荧光激发：用于生物非线性显微镜的新光谱窗口
Proc Natl Acad Sci U S A. 1996 Oct 1;93(20):10763-8. doi: 10.1073/pnas.93.20.10763.
Zotero 插件