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Gotowe bibliografie tematyczne / Fluorescence imaging systems

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Gotowa bibliografia na temat „Fluorescence imaging systems”

Autor: Grafiati

Data publikacji: 6 września 2023

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Artykuły w czasopismach na temat "Fluorescence imaging systems"

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Farrell, Joyce, Zheng Lyu, Zhenyi Liu, Henryk Blasinski, Zhihao Xu, Jian Rong, Feng Xiao i Brian Wandell. "Soft-prototyping imaging systems for oral cancer screening". Electronic Imaging 2020, nr 7 (26.01.2020): 212–1. http://dx.doi.org/10.2352/issn.2470-1173.2020.7.iss-212.

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We are using image systems simulation technology to design a digital camera for measuring fluorescent signals; a first application is oral cancer screening. We validate the simulations by creating a camera model that accurately predicts measured RGB values for any spectral radiance. Then we use the excitationemission spectra for different biological fluorophores to predict measurements of fluorescence of oral mucosal tissue under several different illuminations. The simulations and measurements are useful for (a) designing cameras that measure tissue fluorescence and (b) clarifying which fluorophores may be diagnostic in identifying precancerous tissue.

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Yan, Yuling, M. Emma Marriott, Chutima Petchprayoon i Gerard Marriott. "Optical switch probes and optical lock-in detection (OLID) imaging microscopy: high-contrast fluorescence imaging within living systems". Biochemical Journal 433, nr 3 (14.01.2011): 411–22. http://dx.doi.org/10.1042/bj20100992.

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Few to single molecule imaging of fluorescent probe molecules can provide information on the distribution, dynamics, interactions and activity of specific fluorescently tagged proteins during cellular processes. Unfortunately, these imaging studies are made challenging in living cells because of fluorescence signals from endogenous cofactors. Moreover, related background signals within multi-cell systems and intact tissue are even higher and reduce signal contrast even for ensemble populations of probe molecules. High-contrast optical imaging within high-background environments will therefore require new ideas on the design of fluorescence probes, and the way their fluorescence signals are generated and analysed to form an image. To this end, in the present review we describe recent studies on a new family of fluorescent probe called optical switches, with descriptions of the mechanisms that underlie their ability to undergo rapid and reversible transitions between two distinct states. Optical manipulation of the fluorescent and non-fluorescent states of an optical switch probe generates a modulated fluorescence signal that can be isolated from a larger unmodulated background by using OLID (optical lock-in detection) techniques. The present review concludes with a discussion on select applications of synthetic and genetically encoded optical switch probes and OLID microscopy for high-contrast imaging of specific proteins and membrane structures within living systems.

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Etrych, Tomáš, Olga Janoušková i Petr Chytil. "Fluorescence Imaging as a Tool in Preclinical Evaluation of Polymer-Based Nano-DDS Systems Intended for Cancer Treatment". Pharmaceutics 11, nr 9 (12.09.2019): 471. http://dx.doi.org/10.3390/pharmaceutics11090471.

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Targeted drug delivery using nano-sized carrier systems with targeting functions to malignant and inflammatory tissue and tailored controlled drug release inside targeted tissues or cells has been and is still intensively studied. A detailed understanding of the correlation between the pharmacokinetic properties and structure of the nano-sized carrier is crucial for the successful transition of targeted drug delivery nanomedicines into clinical practice. In preclinical research in particular, fluorescence imaging has become one of the most commonly used powerful imaging tools. Increasing numbers of suitable fluorescent dyes that are excitable in the visible to near-infrared (NIR) wavelengths of the spectrum and the non-invasive nature of the method have significantly expanded the applicability of fluorescence imaging. This chapter summarizes non-invasive fluorescence-based imaging methods and discusses their potential advantages and limitations in the field of drug delivery, especially in anticancer therapy. This chapter focuses on fluorescent imaging from the cellular level up to the highly sophisticated three-dimensional imaging modality at a systemic level. Moreover, we describe the possibility for simultaneous treatment and imaging using fluorescence theranostics and the combination of different imaging techniques, e.g., fluorescence imaging with computed tomography.

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Royon, Arnaud, i Noël Converset. "Quality Control of Fluorescence Imaging Systems". Optik & Photonik 12, nr 2 (kwiecień 2017): 22–25. http://dx.doi.org/10.1002/opph.201700005.

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Georgiev, Nikolai I., Ventsislav V. Bakov, Kameliya K. Anichina i Vladimir B. Bojinov. "Fluorescent Probes as a Tool in Diagnostic and Drug Delivery Systems". Pharmaceuticals 16, nr 3 (1.03.2023): 381. http://dx.doi.org/10.3390/ph16030381.

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Over the last few years, the development of fluorescent probes has received considerable attention. Fluorescence signaling allows noninvasive and harmless real-time imaging with great spectral resolution in living objects, which is extremely useful for modern biomedical applications. This review presents the basic photophysical principles and strategies for the rational design of fluorescent probes as visualization agents in medical diagnosis and drug delivery systems. Common photophysical phenomena, such as Intramolecular Charge Transfer (ICT), Twisted Intramolecular Charge Transfer (TICT), Photoinduced Electron Transfer (PET), Excited-State Intramolecular Proton Transfer (ESIPT), Fluorescent Resonance Energy Transfer (FRET), and Aggregation-Induced Emission (AIE), are described as platforms for fluorescence sensing and imaging in vivo and in vitro. The presented examples are focused on the visualization of pH, biologically important cations and anions, reactive oxygen species (ROS), viscosity, biomolecules, and enzymes that find application for diagnostic purposes. The general strategies regarding fluorescence probes as molecular logic devices and fluorescence–drug conjugates for theranostic and drug delivery systems are discussed. This work could be of help for researchers working in the field of fluorescence sensing compounds, molecular logic gates, and drug delivery.

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Fenton, James M., i Antony R. Crofts. "Computer aided fluorescence imaging of photosynthetic systems". Photosynthesis Research 26, nr 1 (październik 1990): 59–66. http://dx.doi.org/10.1007/bf00048977.

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Pawlowski, Michal E., i Yiran Yang. "Achromatization method for multichannel fluorescence imaging systems". Optical Engineering 58, nr 01 (22.01.2019): 1. http://dx.doi.org/10.1117/1.oe.58.1.015106.

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Kudryavtsev, Volodymyr, Suren Felekyan, Anna K. Woźniak, Marcelle König, Carl Sandhagen, Ralf Kühnemuth, Claus A. M. Seidel i Filipp Oesterhelt. "Monitoring dynamic systems with multiparameter fluorescence imaging". Analytical and Bioanalytical Chemistry 387, nr 1 (12.12.2006): 71–82. http://dx.doi.org/10.1007/s00216-006-0917-0.

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Lo, Shih-Jie, Chen-Meng Kuan, Min-Wei Hung, Yun Fu, J. Yeh, Da-Jeng Yao i Chao-Min Cheng. "A Simple Imaging Device for Fluorescence-Relevant Applications". Micromachines 9, nr 8 (20.08.2018): 418. http://dx.doi.org/10.3390/mi9080418.

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This article unveiled the development of an inexpensive, lightweight, easy-to-use, and portable fluorescence imaging device for paper-based analytical applications. We used commercial fluorescent dyes, as proof of concept, to verify the feasibility of our fluorescence imaging device for bioanalysis. This approach may provide an alternative method for nucleotide detection and semen analysis, using a miniaturized fluorescence reader that is more compact and portable than conventional analytical equipment.

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Wang, Li, Mingguang Ren, Zihong Li, Lixuan Dai i Weiying Lin. "A ratiometric two-photon fluorescent probe for the rapid detection of HClO in living systems". Analytical Methods 11, nr 12 (2019): 1580–84. http://dx.doi.org/10.1039/c9ay00205g.

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Rozprawy doktorskie na temat "Fluorescence imaging systems"

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Nadeau, Valerie J. "Fluorescence imaging and spectroscopy systems for cancer diagnostics". Thesis, University of Glasgow, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269513.

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Robinson, Tom. "The application of multi-dimensional fluorescence imaging to microfluidic systems". Thesis, Imperial College London, 2011. http://hdl.handle.net/10044/1/9285.

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This thesis describes the application of multidimensional fluorescence imaging to microfluidic systems. The work focuses on time- and polarisation-resolved fluorescence microscopy to extract information from microchannel environments. The methods are applied to polymerase chain reaction (PCR) and a DNA repair enzyme, uracil DNA glycosylase (UDG). The fluorescence lifetimes Rhodamine B are calibrated over a thermal gradient using time correlated single photon counting. The dye is then introduced in solution into a novel microfluidic PCR device. Fluorescence lifetime imaging microscopy (FLIM) is then performed, and using the calibration curve, the temperature distributions are accurately determined. The device is subsequently optimised for efficient DNA amplification. A line-scanning FLIM microscope is used to characterise a rapid microfluidic mixer via a fluorescence quenching experiment. Fluorescein and sodium iodide are mixed in a continuous flow format and imaged in 3-D. The spatial distributions of the fluorescence lifetimes are converted to the concentrations of sodium iodide to quantify mixing. Computational fluid dynamic (CFD) simulations are validated by comparison to the quantitative concentrations obtained experimentally. The binding reaction between UDG and a hexachlorofluorescein (HEX) labelled DNA strand is characterised spectrally. As well as an increase in fluorescence polarisation anisotropy, a 700 ps increase in the fluorescence lifetime is measured. Confocal microscopy shows the same spectral properties when the reaction is performed in both simple and rapid microfluidic mixers. In the latter experiment, a concentration series allows the determination of kinetics, which agree with conventional stopped-flow data. A two-colour two-photon (2c2p) FLIM microscope is developed and applied to the UDG-DNA system. An oligonucleotide containing 2-aminopurine, a reporter of DNA base flipping, and HEX is mixed with UDG in a microfluidic Y-mixer. The 2c2p excitation allows FLIM of both fluorophores and hence detection of binding and base flipping. Comparison to CFD with known kinetic rate constants confirms the experimental observations.

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Fernando, Nilmi T. "Novel Near-Infrared Cyanine Dyes for Fluorescence Imaging in Biological Systems". Digital Archive @ GSU, 2011. http://digitalarchive.gsu.edu/chemistry_diss/57.

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Heptamethine cyanine dyes are attractive compounds for imaging purposes in biomedical applications because of their chemical and photophysical properties exhibited in the near-infrared region. A series of meso amino-substituted heptamethine cyanine dyes with indolenine, benz[e]indolenine and benz[c,d]indolenine heterocyclic moieties were synthesized and their spectral properties including fluorescence quntum yield were investigated in ethanol and ethanol/water mixture. Upon substitution with amines, the absorption maxima of the dyes shifted to the lower wavelength region (~600 nm), showed larger Stokes shifts and stronger fluorescence which can be attributed to an excited state intramolecular charge transfer (ICT). High quantum yields were observed for primary amine derivatives and lower quantum yields were observed for secondary amine derivatives. Fluorescence quantum yields are greater for dyes with 3H-indolenine terminal moieties than for dyes with benz[e]indolenine end groups. Benz[c,d]indolenine based heptamethine cyanine dyes exhibited the lowest quantum yield due to aggregation in solution. In general, the benz[e]indolenine hepatemethine cyanines showed high Stokes shifts compared to indolenine dyes. For the meso-chloro dyes, the absorption maxima for the dyes shifted bathochromically in the order of indolenine, benz[e]indolenine and benz[c,d]indolenine.

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Vogt, Juergen. "Conception, design and assembly of a high speed, high dynamic range imaging system for fluorescence microscopy". Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 96 p, 2007. http://proquest.umi.com/pqdweb?did=1338919451&sid=18&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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Thesis (M.S.E.C.E.)--University of Delaware, 2007.
Principal faculty advisors: Fouad Kiamilev and Robert F. Rogers, Dept. of Electrical and Computer Engineering. Includes bibliographical references.

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Rose, Cornelia [Verfasser], i Achim [Akademischer Betreuer] Göpferich. "Particulate systems for fluorescence imaging and drug delivery / Cornelia Rose. Betreuer: Achim Göpferich". Regensburg : Universitätsbibliothek Regensburg, 2010. http://d-nb.info/1023312115/34.

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Concia, Massimo. "Fluorescence labeled PEI-based gene delivery systems for near infrared imaging in nude mice". Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-113095.

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Dubaj, Vladimir, i n/a. "Novel optical fluorescence imaging probe for the investigation of biological function at the microscopic level". Swinburne University of Technology, 2005. http://adt.lib.swin.edu.au./public/adt-VSWT20060905.084615.

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Existing optic fibre-bundle based imaging probes have been successfully used to image biological signals from tissue in direct contact with the probe tip (Hirano et al. 1996). These fibre-bundle probe systems employed conventional fluorescence microscopy and thus lacked spatial filtering or a scanned light source, two features used by laser scanning confocal microscopes (LSCMs) to improve signal quality. Improving the methods of imaging tissue in its natural state, deep in-vivo and at cellular resolution is an ever-present goal in biological research. Within this study, a novel (580 μm diameter) optic fibre-bundle direct-contact imaging probe, employing a LSCM, was developed to allow for improved imaging of deep biological tissue in-vivo. The new LSCM/probe system possessed a spatial resolution of 10 μm, and a temporal resolution of 1 msec. The LSCM/probe system was compared to a previously used direct-contact probe system that employed a conventional fluorescence microscope. Quantitative and qualitative data indicated that the LSCM/probe system possessed superior image contrast and quality. Furthermore, the LSCM/probe system was approximately 16 times more effective at filtering unwanted contaminating light from regions below the imaging plane (z-axis). The unique LSCM/probe system was applied to an exploratory investigation of calcium activity of both glial and neuronal cells within the whisker portion of the rat primary somatosensory cortex in-vivo. Fluorescence signals of 106 cells were recorded from 12 female Sprague Dawley rats aged between 7-8 weeks. Fluo-3(AM) fluorophore based calcium fluctuations that coincided with 10 - 14 Hz sinusoidal stimulation of rat whiskers for 0.5-1 second were observed in 8.5% of cells (9 of 106). Both increases and decreases in calcium levels that coincided with whisker stimulation were observed. Of the 8.5 % of cells, 2.8% (3 cells) were categorized as glial and 5.7% (6 cells) as neuronal, based on temporal characteristics of the observed activity. The remaining cells (97 of 106) displayed sufficient calcium-based intensity but no fluctuations that coincided with an applied stimulus. This was partially attributed to electronic noise inherent in the prototype system obscuring potential very weak cell signals. The results indicate that the novel LSCM/probe system is an advancement over previously used systems that employed direct-contact imaging probes. The miniature nature of the probe allows for insertion into soft tissue, like a hypodermic needle, and provides access to a range of depths with minimal invasiveness. Furthermore, when combined with selected dyes, the system allows for imaging of numerous forms of activity at cellular resolution.

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Adair, Kenneth Valloyd. "Diffusive, reactive and orientational dynamics of molecular systems using molecular Fourier imaging correlation spectroscopy /". view abstract or download file of text, 2006. http://proquest.umi.com/pqdweb?did=1251854551&sid=1&Fmt=2&clientId=11238&RQT=309&VName=PQD.

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Thesis (Ph. D.)--University of Oregon, 2006.
Typescript. Includes vita and abstract. Includes bibliographical references (leaves 103-108). Also available for download via the World Wide Web; free to University of Oregon users.

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Ogden, Melinda Anne. "Two-photon total internal reflection microscopy for imaging live cells with high background fluorescence". Thesis, Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/34786.

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Fluorescence microscopy allows for spatial and temporal resolution of systems which are inherently fluorescent or which can be selectively labeled with fluorescent molecules. Temporal resolution is crucial for imaging real time processes in living samples. A common problem in fluorescence microscopy of biological samples is autofluorescence, fluorescence inherent to the system, which interferes with detection of fluorescence of interest by decreasing the signal to noise ratio. Two current methods for improved imaging against autofluorescence are two-photon excitation and total internal reflection microscopy. Two-photon excitation occurs when two longer wavelength photons are absorbed quasi-simultaneously by a single fluorophore. For this to take place there must be a photon density on the order of 1030 photons/(cm2)(s), which is achieved through use of a femtosecond pulsed laser and a high magnification microscope objective. Two-photon excitation then only occurs at the focal spot, significantly reducing the focal volume and therefore background autofluorescence. The second method, total internal reflection, is based on evanescent wave excitation, which decreases exponentially in intensity away from the imaging surface. This allows for excitation of a thin (~200 nm) slice of a sample. Since only a narrow region of interest is excited, an optical slice can be imaged, decreasing excitation of out-of-focus autofluorescence, and increasing the signal to noise ratio. By coupling total internal reflection with two-photon excitation, an entire cell can be imaged while still maintaining the use of lower energy photons to irradiate the sample and achieve two-photon excitation along the length traveled by the evanescent wave. This system allows for more sensitive detection of fluorescence of interest from biological systems as a result of a significant decrease in excitation volume and therefore a decrease in autofluorescence signal. In the two-photon total internal reflection microscopy setup detailed in this work, an excitation area of 20 μm by 30 μm is achieved, and used to image FITC-stained actin filaments in BS-C-1 cells

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Graham, Emmelyn M. "The application of fluorescence lifetime imaging microscopy to quantitatively map mixing and temperature in microfluidic systems". Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/2432.

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The technique of Fluorescence Lifetime Imaging Microscopy (FLIM) has been employed to quantitatively and spatially map the fluid composition and temperature within microfluidic systems. A molecular probe with a solvent-sensitive fluorescence lifetime has been exploited to investigate and map the diffusional mixing of fluid streams under laminar flow conditions within a microfluidic device. Using FLIM, the fluid composition is mapped with high quantification and spatial resolution to assess the extent of mixing. This technique was extended to quantitatively evaluate the mixing efficiency of a range of commercial microfluidic mixers employing various mixing strategies, including the use of obstacles fabricated within the channels. A fluorescently labelled polymer has been investigated as a new probe for mapping temperature within microfluidic devices using FLIM. Time Correlated Single Photon Counting (TCSPC) measurements showed that the average fluorescence lifetime displayed by an aqueous solution of the polymer depended strongly on temperature, increasing from 3 ns to 13.5 ns between 23 and 38 oC. This effect was exploited using FLIM to provide high spatial resolution temperature mapping with sub-degree temperature resolution within microfluidic devices. A temperature-sensitive, water-soluble derivative of the rhodamine B fluorophore, effective over a wide dynamic temperature range (25 to 91 oC) has been used to map the temperature distribution during the mixing of fluid streams of different temperatures within a microchannel. In addition, this probe was employed to quantify the fluid temperature in a prototype microfluidic system for DNA amplification. FLIM has been demonstrated to provide a superior approach to the imaging within microfluidic systems over other commonly used techniques, such as fluorescence intensity and colourimetric imaging.

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Książki na temat "Fluorescence imaging systems"

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Brovko, Lubov. Bioluminescence and fluorescence for in vivo imaging. Bellingham, Wash: SPIE Press, 2010.

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Cartwright, Alexander N. Nanoscale imaging, sensing, and actuation for biomedical applications VI: 27-28 January 2009, San Jose, California, United States. Redaktor SPIE (Society). Bellingham, Wash: SPIE, 2009.

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Cells illuminated: In vivo optical imaging. Bellingham, Wash., USA: SPIE Press, 2010.

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L, Barbour Randall, Carvlin Mark Joseph, Society of Photo-optical Instrumentation Engineers. i Biomedical Optics Society, red. Proceedings of physiological imaging, spectroscopy, and early-detection diagnostic methods: 19-20 January 1993, Los Angeles, California. Bellingham, Wash., USA: SPIE, 1993.

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N, Cartwright Alexander, Nicolau Dan V i Society of Photo-optical Instrumentation Engineers., red. Nanoscale imaging, spectroscopy, sensing, and actuation for biomedical applications IV: 23-24 January 2007, San Jose, California, USA. Bellingham, Wash: SPIE, 2007.

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Nicolau, Dan V., i Alexander N. Cartwright. Nanoscale imaging, sensing, and actuation for biomedical applications VIII: 24 and 26-27, January 2011, San Francisco, California, United States. Bellingham, Wash: SPIE, 2011.

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Enderlein, J. Single molecule spectroscopy and imaging: 19-21 January 2008, San Jose, California, USA. Bellingham, Wash: SPIE, 2008.

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Erdmann, Rainer, J. Enderlein i Zygmunt Gryczynski. Single molecule spectroscopy and imaging IV: 22-23 January 2011, San Francisco, California, United States. Bellingham, Wash: SPIE, 2011.

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Enderlein, J. Single molecule spectroscopy and imaging II: 24-25 January 2009, San Jose, California, United States. Bellingham, Wash: SPIE, 2009.

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N, Cartwright Alexander, Nicolau Dan V i Society of Photo-optical Instrumentation Engineers., red. Nanobiophotonics and biomedical applications III: 23-24 January 2006, San Jose, California, USA. Bellingham, Wash: SPIE, 2006.

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Części książek na temat "Fluorescence imaging systems"

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Ishizawa, Takeaki, i Norihiro Kokudo. "Fluorescence Imaging Systems (PDE, HyperEye Medical System, and Prototypes in Japan)". W Fluorescence Imaging for Surgeons, 81–86. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15678-1_7.

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Iourov, Ivan Y. "Microscopy and Imaging Systems". W Fluorescence In Situ Hybridization (FISH) — Application Guide, 75–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-70581-9_7.

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Malval, J. P., I. Gosse, J. P. Morand i R. Lapouyade. "Integrated Supramolecular Systems: From Sensors to Switches". W Fluorescence Spectroscopy, Imaging and Probes, 87–100. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-56067-5_4.

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Cotlet, M., J. Hofkens, M. Maus i F. C. de Schryver. "Multiparametric Detection of Fluorescence Emitted from Individual Multichromophoric Systems". W Fluorescence Spectroscopy, Imaging and Probes, 131–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-642-56067-5_8.

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Bartolo, Baldassare Di. "Fluorescence Spectroscopy and Energy Transfer Processes in Biological Systems". W Biophotonics: Spectroscopy, Imaging, Sensing, and Manipulation, 107–71. Dordrecht: Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-90-481-9977-8_6.

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Nakanishi, Tomoko M. "Real-Time Element Movement in a Plant". W Novel Plant Imaging and Analysis, 109–68. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-4992-6_4.

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AbstractWe developed an imaging method utilizing the available RIs. We developed two types of real-time RI imaging systems (RRIS), one for macroscopic imaging and the other for microscopic imaging. The principle of visualization was the same, converting the radiation to light by a Cs(Tl)I scintillator deposited on a fiber optic plate (FOS). Many nuclides were employed, including 14C, 18F, 22Na, 28Mg, 32P 33P, 35S, 42K, 45Ca, 48V, 54Mn, 55Fe, 59Fe, 65Zn, 86Rb, 109Cd, and 137Cs.Since radiation can penetrate the soil as well as water, the difference between soil culture and water culture was visualized. 137Cs was hardly absorbed by rice roots growing in soil, whereas water culture showed high absorption, which could provide some reassurance after the Fukushima Nuclear Accident and could indicate an important role of soil in firmly adsorbing the radioactive cesium.28Mg and 42K, whose production methods were presented, were applied for RRIS to visualize the absorption image from the roots. In addition to 28Mg and 42K, many nuclides were applied to image absorption in the roots. Each element showed a specific absorption speed and accumulation pattern. The image analysis of the absorption of Mg is presented as an example. Through successive images of the element absorption, phloem flow in the aboveground part of the plant was analyzed. The element absorption was visualized not only in the roots but also in the leaves, a basic study of foliar fertilization.In the case of the microscopic imaging system, a fluorescence microscope was modified to acquire three images at the same time: a light image, fluorescent image, and radiation image. Although the resolution of the image was estimated to be approximately 50 μm, superposition showed the expression site of the transporter gene and the actual 32P-phosphate absorption site to be the same in Arabidopsis roots.

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Banachowicz, Adrian, Anna Lis-Nawara, Michał Jeleń i Łukasz Jeleń. "Convolutional Neural Networks for Dot Counting in Fluorescence in Situ Hybridization Imaging". W Theory and Applications of Dependable Computer Systems, 21–30. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-48256-5_3.

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George, Graham N., i Ingrid J. Pickering. "X-ray Fluorescence Imaging: Elemental and Chemical Speciation Mapping of Biological Systems". W Encyclopedia of Biophysics, 1–6. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-642-35943-9_681-1.

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George, Graham N., i Ingrid J. Pickering. "X-Ray Fluorescence Imaging: Elemental and Chemical Speciation Mapping of Biological Systems". W Encyclopedia of Biophysics, 2781–85. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-16712-6_681.

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Lewis, Jana L., i Danny A. Sherwinter. "The Pinpoint System". W Fluorescence Imaging for Surgeons, 87–97. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15678-1_8.

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Streszczenia konferencji na temat "Fluorescence imaging systems"

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Mukherjee, Amaradri, i Chrysanthe Preza. "Computational 3D Fluorescence Microscopy Imaging". W Imaging Systems. Washington, D.C.: OSA, 2010. http://dx.doi.org/10.1364/is.2010.iwc2.

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2

Taiti, A., P. Coppo i E. Battistelli. "Fluorescence imaging spectrometer optical design". W SPIE Optical Systems Design, redaktorzy Laurent Mazuray, Rolf Wartmann i Andrew P. Wood. SPIE, 2015. http://dx.doi.org/10.1117/12.2191290.

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3

Preza, Chrysanthe. "Computational imaging for 3D fluorescence microscopy". W Imaging Systems and Applications. Washington, D.C.: OSA, 2014. http://dx.doi.org/10.1364/isa.2014.iw2c.1.

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4

Kim, Ganghun, Naveen Nagarajan, Amihai Meiri, Sean Merrill, Mario Capecchi, Erik M. Jorgensen i Rajesh Menon. "A cannula-based computational fluorescence microscope". W Imaging Systems and Applications. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/isa.2015.it2a.3.

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5

Gorpas, Dimitris, Maximilian Koch, Maria Anastasopoulou, Uwe Klemm i Vasilis Ntziachristos. "Standardization of fluorescence molecular imaging systems". W European Conferences on Biomedical Optics, redaktorzy Arjen Amelink i I. Alex Vitkin. SPIE, 2017. http://dx.doi.org/10.1117/12.2286065.

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6

Dahan, Maxime. "Compressive Fluorescence Microscopy for Biological and Hyperspectral Imaging". W Imaging Systems and Applications. Washington, D.C.: OSA, 2012. http://dx.doi.org/10.1364/isa.2012.im4c.5.

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Ruiz, Alberto J., Edwin A. Robledo, Eammon Littler i Ethan P. M. LaRochelle. "Radiometric characterization methods for fluorescence guidance imaging systems using a calibrated solid-state emitter". W Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: Optica Publishing Group, 2023. http://dx.doi.org/10.1364/omp.2023.oth1e.5.

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Streszczenie:

Methods for radiometric characterization of fluorescence-guided imaging systems using a calibrated solid-state emitter are introduced. Used alongside fluorescence phantoms, we demonstrate quantitative fluorescence imaging that can facilitate cross-system comparisons and multi-center reproducibility.

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8

Koch, Maximilian, Maria Anastasopoulou, Uwe Klemm, Vasilis Ntziachristos i Dimitris Gorpas. "Phantom and methodology for fluorescence molecular imaging systems benchmarking". W Unconventional Optical Imaging, redaktorzy Corinne Fournier, Marc P. Georges i Gabriel Popescu. SPIE, 2018. http://dx.doi.org/10.1117/12.2309766.

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Wang, Wensheng, Yifan Wang, Cuifang Kuang i Xu Liu. "Dual-color super-resolution imaging by fluorescence emission difference microscopy". W Imaging Systems and Applications. Washington, D.C.: OSA, 2016. http://dx.doi.org/10.1364/isa.2016.it1f.4.

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Pang, Shuo. "Compressive high-speed imaging in fluorescence microscopy and 3D photography". W Imaging Systems and Applications. Washington, D.C.: OSA, 2018. http://dx.doi.org/10.1364/isa.2018.itu3b.1.

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Raporty organizacyjne na temat "Fluorescence imaging systems"

1

Nieman, Linda T., Michael B. Sinclair, George S. Davidson, Mark Hilary Van Benthem, David Michael Haaland, Jerilyn Ann Timlin, Darryl Yoshio Sasaki, George David Bachand i Howland D. T. Jones. 3D optical sectioning with a new hyperspectral confocal fluorescence imaging system. Office of Scientific and Technical Information (OSTI), luty 2007. http://dx.doi.org/10.2172/902877.

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2

Chyu, M. K. Use of a laser-induced fluorescence thermal imaging system for film cooling heat transfer measurement. Office of Scientific and Technical Information (OSTI), kwiecień 1996. http://dx.doi.org/10.2172/226040.

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3

Wang, Ziqiang. Fast methods for analysis of neurotransmitters from single cell and monitoring their releases in central nervous system by capillary electrophoresis, fluorescence microscopy and luminescence imaging. Office of Scientific and Technical Information (OSTI), grudzień 1999. http://dx.doi.org/10.2172/754796.

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