Relevant bibliographies by topics / Near infrared imaging probes

Academic literature on the topic 'Near infrared imaging probes'

Author: Grafiati
Published: 10 December 2022
Last updated: 28 January 2023

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Journal articles on the topic "Near infrared imaging probes"

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Li, Benhao, Jing Lin, Peng Huang, and Xiaoyuan Chen. "Near-infrared probes for luminescence lifetime imaging." Nanotheranostics 6, no. 1 (2022): 91–102. http://dx.doi.org/10.7150/ntno.63124.

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Klohs, Jan, Andreas Wunder, and Kai Licha. "Near-infrared fluorescent probes for imaging vascular pathophysiology." Basic Research in Cardiology 103, no. 2 (March 2008): 144–51. http://dx.doi.org/10.1007/s00395-008-0702-7.

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Ntziachristos, Vasilis, Christoph Bremer, Edward E. Graves, Jorge Ripoll, and Ralph Weissleder. "In Vivo Tomographic Imaging of Near-Infrared Fluorescent Probes." Molecular Imaging 1, no. 2 (April 1, 2002): 153535002002011. http://dx.doi.org/10.1162/15353500200201121.

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Fluorescence imaging is increasingly used to probe protein function and gene expression in live animals. This technology could enhance the study of pathogenesis, drug development, and therapeutic intervention. In this article, we focus on three-dimensional fluorescence observations using fluorescence-mediated molecular tomography (FMT), a novel imaging technique that can resolve molecular function in deep tissues by reconstructing fluorescent probe distributions in vivo. We have compared FMT findings with conventional fluorescence reflectance imaging (FRI) to study protease function in nude mice with subsurface implanted tumors. This validation of FMT with FRI demonstrated the spatial congruence of fluorochrome activation as determined by the two techniques.
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Shieh, P., M. S. Siegrist, A. J. Cullen, and C. R. Bertozzi. "Imaging bacterial peptidoglycan with near-infrared fluorogenic azide probes." Proceedings of the National Academy of Sciences 111, no. 15 (March 31, 2014): 5456–61. http://dx.doi.org/10.1073/pnas.1322727111.

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Ntziachristos, Vasilis, Christoph Bremer, Edward E. Graves, Jorge Ripoll, and Ralph Weissleder. "In Vivo Tomographic Imaging of Near-Infrared Fluorescent Probes." Molecular Imaging 1, no. 2 (April 1, 2002): 82–88. http://dx.doi.org/10.1162/153535002320162732.

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Ma, Zhuoran, Feifei Wang, Weizhi Wang, Yeteng Zhong, and Hongjie Dai. "Deep learning for in vivo near-infrared imaging." Proceedings of the National Academy of Sciences 118, no. 1 (December 28, 2020): e2021446118. http://dx.doi.org/10.1073/pnas.2021446118.

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Detecting fluorescence in the second near-infrared window (NIR-II) up to ∼1,700 nm has emerged as a novel in vivo imaging modality with high spatial and temporal resolution through millimeter tissue depths. Imaging in the NIR-IIb window (1,500–1,700 nm) is the most effective one-photon approach to suppressing light scattering and maximizing imaging penetration depth, but relies on nanoparticle probes such as PbS/CdS containing toxic elements. On the other hand, imaging the NIR-I (700–1,000 nm) or NIR-IIa window (1,000–1,300 nm) can be done using biocompatible small-molecule fluorescent probes including US Food and Drug Administration-approved dyes such as indocyanine green (ICG), but has a caveat of suboptimal imaging quality due to light scattering. It is highly desired to achieve the performance of NIR-IIb imaging using molecular probes approved for human use. Here, we trained artificial neural networks to transform a fluorescence image in the shorter-wavelength NIR window of 900–1,300 nm (NIR-I/IIa) to an image resembling an NIR-IIb image. With deep-learning translation, in vivo lymph node imaging with ICG achieved an unprecedented signal-to-background ratio of >100. Using preclinical fluorophores such as IRDye-800, translation of ∼900-nm NIR molecular imaging of PD-L1 or EGFR greatly enhanced tumor-to-normal tissue ratio up to ∼20 from ∼5 and improved tumor margin localization. Further, deep learning greatly improved in vivo noninvasive NIR-II light-sheet microscopy (LSM) in resolution and signal/background. NIR imaging equipped with deep learning could facilitate basic biomedical research and empower clinical diagnostics and imaging-guided surgery in the clinic.
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Hielscher, A. H., A. Y. Bluestone, G. S. Abdoulaev, A. D. Klose, J. Lasker, M. Stewart, U. Netz, and J. Beuthan. "Near-Infrared Diffuse Optical Tomography." Disease Markers 18, no. 5-6 (2002): 313–37. http://dx.doi.org/10.1155/2002/164252.

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Diffuse optical tomography (DOT) is emerging as a viable new biomedical imaging modality. Using near-infrared (NIR) light, this technique probes absorption as well as scattering properties of biological tissues. First commercial instruments are now available that allow users to obtain cross-sectional and volumetric views of various body parts. Currently, the main applications are brain, breast, limb, joint, and fluorescence/bioluminescence imaging. Although the spatial resolution is limited when compared with other imaging modalities, such as magnetic resonance imaging (MRI) or X-ray computerized tomography (CT), DOT provides access to a variety of physiological parameters that otherwise are not accessible, including sub-second imaging of hemodynamics and other fast-changing processes. Furthermore, DOT can be realized in compact, portable instrumentation that allows for bedside monitoring at relatively low cost. In this paper, we present an overview of current state-of-the -art technology, including hardware and image-reconstruction algorithms, and focus on applications in brain and joint imaging. In addition, we present recent results of work on optical tomographic imaging in small animals.
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Gao, Jinhao, Xiaoyuan Chen, and Zhen Cheng. "Near-Infrared Quantum Dots as Optical Probes for Tumor Imaging." Current Topics in Medicinal Chemistry 10, no. 12 (August 1, 2010): 1147–57. http://dx.doi.org/10.2174/156802610791384162.

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Murtagh, Julie, Daniel O. Frimannsson, and Donal F. O’Shea. "Azide Conjugatable and pH Responsive Near-Infrared Fluorescent Imaging Probes." Organic Letters 11, no. 23 (December 3, 2009): 5386–89. http://dx.doi.org/10.1021/ol902140v.

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Josephson, Lee, Moritz F. Kircher, Umar Mahmood, Yi Tang, and Ralph Weissleder. "Near-Infrared Fluorescent Nanoparticles as Combined MR/Optical Imaging Probes." Bioconjugate Chemistry 13, no. 3 (May 2002): 554–60. http://dx.doi.org/10.1021/bc015555d.

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Dissertations / Theses on the topic "Near infrared imaging probes"

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Quartel, John Conrad. "A study of near-field optical imaging using an infrared microscope." Thesis, Imperial College London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.313413.

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Bordy, Mathieu. "Synthèse et évaluation biologique de sondes fluorogènes pour la détection d’activités enzymatiques." Thesis, Lyon, 2019. http://www.theses.fr/2019LYSEN072.

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Cette thèse de doctorat traite de la conception et de l’évaluation de sondes fluorogènes pour la détection d’activités enzymatiques dans des contextes biologiques d’intérêt. L’élaboration de sondes fluorogéniques stables incorporant l’ELF-97 est une des thématiques de recherche activement poursuivie par notre équipe. Le développement avec succès de sondes peptidases et glycosidases a ouvert de nombreuses perspectives. Un premier chapitre sera dédié à la diversification de ces sondes, tout d’abord par la variation de substrats pour la détection de nouvelles glycosidases, puis par le développement d’un espaceur innovant dans un contexte particulier de sénescence cellulaire. Une sonde pour la détection de la β-galactosidase en milieu acide a notamment pu être synthétisée et testée. En parallèle, des travaux ont porté sur une nouvelle génération de sondes ciblant une famille d’enzymes à fort intérêt scientifique et sociétal : les β-lactamases. La synthèse et l’évaluation biologique préliminaire d’une première sonde modèle a démontré l’efficacité de cette nouvelle architecture moléculaire. Cette sonde a, par la suite, permis l’élaboration de premiers résultats d’imagerie dans le cadre d’une collaboration active avec une équipe de recherche japonaise. Enfin, un dernier volet sera consacré à un projet dont l’objectif n’est pas récent dans l’équipe : le développement d’alternatives à l’ELF-97 présentant une émission décalée vers le rouge ou le proche infrarouge. Ainsi, la synthèse de nouveaux fluorophores, leurs caractérisations physico-chimiques et des tests d’incorporation dans des dispositifs répondeurs ont notamment été réalisés. Plusieurs candidats se sont révélés à fort potentiel pour leur émission fortement décalée vers le rouge ou leur haute insolubilité. Ils pourraient permettre à terme l’adaptation de la technologie à une utilisation in vivo, but ultime de la technologie dans le cadre de l’imagerie moléculaire
This doctoral thesis deals with the design and evaluation of fluorogenic probes for the detection of enzymatic activities in biological contexts of interest.The development of stable fluorogenic probes incorporating ELF-97 is one of the research themes actively pursued by our team. The successful development of peptidases and glycosidases probes have opened many perspectives. A first chapter will be dedicated to the diversification of these probes, firstly by the variation of substrates for the detection of new glycosidases, then by the development of an innovative spacer in the context of cell senescence. In particular, a probe for the detection of β-galactosidase in acidic medium has been synthesized and tested.In parallel, work has focused on a new generation of probes targeting an enzyme family with strong scientific and societal interest : β-lactamases. The synthesis and the preliminary biological evaluation of a first model probe demonstrated the effectiveness of this new molecular architecture. This probe subsequently led to the development of first imaging results as part of an active collaboration with a Japanese research team.Finally, a last part will be devoted to a project whose objective is not recent in the team : the development of alternatives to the ELF-97 presenting a shifted emission towards the red or the near infrared. For this purpose, the synthesis of new fluorophores, their physicochemical characterizations and incorporation tests in responding devices have been carried out. Several candidates have proved to have high potential for two main reasons : strongly red-shifted emission or high insolubility. They could eventually allow the adaptation of the technology to an in vivo use, the ultimate goal of the technology in the context of molecular imaging
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Meyer, Yves. "Conception et développement de bras réactifs auto-immolables pour la synthèse de sondes pro-fluorescentes : applications à la détection de peptidases dans un contexte in-vivo." Thesis, Rouen, INSA, 2010. http://www.theses.fr/2010ISAM0018.

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L'objectif de cette thèse est la conception et le développement de bras espaceurs auto-immolables originaux situés entre le substrat peptidique et un fluorophore à phénol. Une première partie de ces travaux porte sur le développement de bras réactifs auto-immolables adaptés à la détection d'exopeptidases et à leur application pour la synthèse de sondes destinées à l'imagerie in-vivo de la caspase 3, une enzime impliquée dans le processus apoptotique. La seconde partie de ce travail relate les efforts effectués afin d'étendre l'utilisation des bras réactifs auto-immolables à la détection des endopeptidases, notamment les MMPs, une famille d'enzimes fortement impliquée dans la progression cancéreuse
The aim of this PhD work is the design and development of novel self-immolative species linking a peptide susbstrate to a phenolic fluorophore. A first part was dedicated to the development of self-immolative linkers for exopeptidases detection and their incorporation in caspase 3 probes to stain the apoptotic process. A second part was devoted to the extension of the strategy to endopeptidases, especially MMPs, an enzyme family mainly involved in cancer progression
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Damin, Craig Anthony. "Instrument Development and Application for Qualitative and Quantitative Sample Analyses Using Infrared and Raman Spectroscopies." Miami University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=miami1385774823.

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Lescure, Robin. "Développement d’azaBODIPYs fonctionnalisables pour la conception de sondes d’imagerie bimodale et d’agents théranostiques." Thesis, Bourgogne Franche-Comté, 2020. https://nuxeo.u-bourgogne.fr/nuxeo/site/esupversions/21e2771a-9c75-46d7-9377-50e8f2536c32.

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L’utilisation in vivo de l’imagerie optique est encore aujourd’hui principalement limitée par le manque de sondes capables d’émettre dans le proche infrarouge, où les tissus biologiques sont plus transparents à la lumière. Les travaux présentés dans ce manuscrit abordent l’optimisation et la valorisation d’une plateforme fluorescente hydrosoluble dont les propriétés optiques peuvent permettre une utilisation in vivo. Deux applications distinctes ont été envisagées pour cette plateforme WazaBY (Water-soluble azaBODIPY) : une utilisation comme sonde bimodale TEP (ou TEMP) et optique, et une utilisation en tant qu’agent théranostique. Lors du premier projet issu de ces travaux de thèse, nous avons pu développer une sonde bimodale TEMP/optique radiométallée par l’indium-111 et vectorisée par un anticorps (trastuzumab). Sur modèles murins porteurs de tumeurs xénogreffées, il a été possible de réaliser une imagerie bimodale optique/TEMP, témoignant d’une très nette accumulation au sein de la tumeur dès 24 heures après injection. La sonde a également été validée pour la réalisation de chirurgie assistée par fluorescence. Dans le cadre du second projet de cette thèse, une première génération d’agents théranostiques, porteurs de complexes d’or pour la thérapie, ont été synthétisées. L’objectif de ce projet a été de développer une nouvelle entité thérapeutique traçable in vitro et in vivo par imagerie optique. Les résultats préliminaires in vitro ont indiqué une activité antiproliférative des théranostiques sur lignées cellulaires cancéreuses (4T1, MDA MB 231, CT26 et SW480) voisine de celle de l’auranofine. Dans une seconde partie, nous nous sommes focalisés sur le développement de sondes théranostiques dites « intelligentes », pour lesquelles une modification des propriétés photophysiques est attendu lors du relargage éventuel du centre métallique. Deux molécules ont ainsi pu être synthétisées, chacune présentant un comportement de type on/off
The in vivo use of optical imaging is still limited by the lack of near infrared emitting probes. This thesis work focuses on the optimization and valorization of a water-soluble fluorescent platform whose optical properties enable an in vivo use. Two distinct applications were investigated for this WazaBY (Water-soluble azaBODIPY) platform: use as a PET (or SPECT) / optical bimodal probe, and as a theranostic agent. Concerning the first project, we were able to develop a targetted SPECT/optical bimodal probe, which was radiometallated with indium 111. Using xenografted murine models, we were able to show a clear accumulation of the probe in the tumor 24 hours after injection. Moreover, the probe was validated as a contrast agent for fluorescence guided surgery experiment. The second project of this thesis began by the synthesis of a first generation of gold based theranostic agents. The goal was to develop a new therapeutic complex, which can be tracked in vitro and in vivo thanks to optical imaging. In vitro preliminary results showed that the theranostics displayed a cytotoxicity comparable to auranofin on the tested cell lines (4T1, MDA MB 231, CT26 and SW480). A second part of this project focused on the develoment of « smart » probes for a theranostic use. Those probes are designed to undergo photophysical properties changes, when their metallic centre, responsible for the therapeutic role, is released. Two molecules were synthesized, both displaying an on/off behavior
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Minchin, Nigel Robert. "Near-infrared imaging polarimetry of bipolar nebulae." Thesis, University of Hertfordshire, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293286.

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Cheng, Hok Yan. "Near infrared fluorescence probes : towards applications in fluorescence guided surgery." Thesis, University of Hull, 2017. http://hydra.hull.ac.uk/resources/hull:16529.

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Surgery has been a popular method for the treatment of cancers, in particular solid tumours; but the surgical margins for cancerous tissues are often indistinct and in most cases, the poor identification of residual cancer tissues can result in re-excision. Therefore, near infrared (NIR) fluorescence-guided surgery (FGS) is being developed as a real time intra-operative imaging technique to assist surgeons by improving the accuracy and precision of the removal of tumours. However, current FDA approved fluorophores suffer from poor chemical stability, limited water-solubility, and lack selectivity toward neoplastic tissue, limiting their clinical application. These current challenges have led to the development of new and improved fluorophores capable of absorbing and emitting light at NIR wavelengths, negating autofluorescence and improving deeper light transmission. Throughout this project, a series of BODIPYs, aza-BODIPYs and bacteriochlorins were synthesised and developed for bioimaging applications. Despite many of them showing interesting fluorescence properties, the investigation suggested aza-BODIPYs were the most promising red / NIR fluorophores (λem 600-700 nm) due to their excellent photostability. Methods have been developed to incorporate functionalities suitable for bioconjugation. Different bioconjugation strategies have been explored to covalently conjugate the NIR fluorophores to a clinically relevant protein, peptide and antibody under mild conditions. The viability of aza-BODIPY conjugates against biological targets were investigated and a range of other novel targeted NIR fluorophores were successfully developed. In vitro fluorescence imaging was subsequently carried out to demonstrate the enhanced selectivity of the targeting NIR fluorophores toward overexpressed receptors on various cancer cells lines. This project has demonstrated the potential of aza-BODIPY in biological imaging and developed targeted NIR fluorophores. Further biological evaluation is progressing with the eventual aim of developing a pre-clinical model for NIR FGS in oncology.
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Packham, Christopher Charles. "Near infrared imaging and polarimetry of active galactic nuclei." Thesis, University of Hertfordshire, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338568.

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Servati, A. "Nanoparticles for simultaneous near-infrared and magnetic biomolecular imaging." Thesis, University College London (University of London), 2012. http://discovery.ucl.ac.uk/1367959/.

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Nanoparticle probes can unlock the potential for multimodal biomedical imaging (in vivo and in vitro) with enhanced spatial resolution and penetration depth and targeted visualization of complex organisms. This thesis demonstrates synthesis and characterization of magnetic upconversion Gd2O3 nanoparticles that can serve as bimodal probes for optical imaging in near infrared (NIR) biomedical window, where minimal tissue auto uorescence is expected, as well as magnetic resonance imaging. More speci cally, Gd2O3:Yb3+,Tm3+ and Gd2O3:Yb3+,Er3+ nanoparticles are synthesized using urea-based homogeneous precipitation method (UHP) as well as Y2O3:Yb3+/Er3+ micro and nanoparticles using conventional combustion and thermal synthesis methods. The morphological and compositional properties of nanoparticles as well as their photonic and magnetic responses are systematically analyzed to understand the role of synthesis methods and initial synthesis materials including the concentrations of Tm and Er dopants and urea solution on the properties of the synthesized particles. The upconversion nanoparticles synthesized using UHP method are spherical and monodisperse with a size distribution in the range of 60 to 150 nm and controllable dopant concentration through manipulation of initial synthesis chemistry. When excited with 975 nm NIR radiation, Gd2O3:Yb3+,Tm3+ nanoparticles show a pure near infrared emission centered at around 810 nm (i.e., NIR-to-NIR upconversion) in NIR biological window with potential for high depth optical imaging while Er3+ doped particles emit light mainly in visible red centred at around 661 nm. The photoluminescence and transient optical decay measurements demonstrate distinctly di erent energy transfer mechanisms for Er and Tm doped samples. While these measurements signify a dominant role for Yb3+ dopants in strong upconversion emission of Tm3+ samples with a double exponential decay behaviour, they show less important role of Yb3+ in Er3+ samples with a single exponential decay. Systematic magnetic characterization demonstrate strong paramagnetic behaviour for the optically active upconversion nanoparticles, demonstrating their potential for bimodal optical and magnetic resonant imaging.
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Houston, Jessica Perea. "Near infrared optical lymphography for cancer diagnostics." Diss., Texas A&M University, 2005. http://hdl.handle.net/1969.1/4807.

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A new molecular imaging modality has been developed to detect and locate positive axillary and sentinel lymph nodes non-invasively in breast cancer patients undergoing lymphoscintigraphy. The modality is based on fluorescent photon detection to locate the presence of indocyanine green (ICG) in the lymph subsequent to peritumoral injection of ICG into the breast. The imaging system consists of a gain-modulated intensified charge-coupled device (ICCD) camera, which captures low-intensity, near-infrared, and frequency-modulated photons. A four-fold ‘optical lymphography’ study was conducted to (1) examine fluorescence depth penetration and ICCD system accuracy at clinically relevant depths, (2) compare image quality of the ICCD system vs. conventional gamma imaging, (3) measure ICG pharmacokinetics in vivo, and (4) develop a clinical protocol while examining pre-clinical factors such as the outcome of combining ICG with sulfur colloids used in lymphoscintigraphy. The frequency-domain ICCD system was found to precisely detect modulation amplitude, IAC, and phase, θ, at depths up to 9 cm and with IAC accuracy less than 20% and θ less than 2º using an 80-mW laser incident on phantoms having ranging tissue optical properties. Significant differences in the mean depth of penetration owing to 0.62-ns lifetime and 100-MHz frequency increases were detected. An in vivo optical vs. nuclear image quality comparison demonstrated statistically similar (α=0.05) target-to-background ratios for optical (1.4+/-0.3) and nuclear (1.5+/-0.2). Alternatively, resulting image signal-to-noise ratios (SNR) from the ICCD system were greater than that achieved with a conventional gamma camera (pvalue<<0.01). Analysis of SNR versus contrast showed greater sensitivity of optical over nuclear imaging for subcutaneous tumors. In vivo and rapid detection of ICG in the blood-stream of nude mice was accomplished with a home-built avalanche photodiode dynamic fluorescence measurement system. Intensity data upon i.v. injection were regressed with a pharmacokinetic model describing the partitioning of ICG from the blood to the surrounding tissues. ICG blood-clearance was detected approximately 15 min after injection. Lastly, a human subject protocol was written, practiced, and federally approved for the application of optical lymphography. Furthermore, ICG was unaffected when mixed with sulfur colloids thus supporting the feasibility for combining fluorescence imaging with lymphoscintigraphy in breast cancer patients.
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Books on the topic "Near infrared imaging probes"

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Raman, infrared, and near-infrared chemical imaging. Hoboken, N.J: Wiley, 2010.

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Šašić, Slobodan, and Yukihiro Ozaki, eds. Raman, Infrared, and Near-Infrared Chemical Imaging. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470768150.

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Siegfried, Dähne, Resch-Genger Ute, Wolfbeis Otto S, North Atlantic Treaty Organization. Scientific Affairs Division., and NATO Advanced Research Workshop on Syntheses, Optical Properties and Applications of Near-Infrared (NIR) Dyes in High Technology Fields (1997 : Třešt̕, Czechoslovakia), eds. Near-infrared dyes for high technology applications. Dordrecht: Kluwer, 1998.

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Aleassa, Essa M., and Kevin M. El-Hayek, eds. Video Atlas of Intraoperative Applications of Near Infrared Fluorescence Imaging. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-38092-2.

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(Society), SPIE, Optical Society of America, and European Optical Society, eds. Diffuse optical imaging II: 14-17 June 2009, Munich, Germany. Bellingham, Wash: SPIE, 2009.

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Hielscher, Andreas H. Diffuse optical imaging III: 22-24 May 2011, Munich, Germany. Edited by SPIE (Society), Optical Society of America, Deutsche Gesellschaft für Lasermedizin, German Biophotonics Research Program, Photonics4Life (Group), and United States. Air Force. Office of Scientific Research. Bellingham, Wash: SPIE, 2011.

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Ozaki, Yukihiro, and Slobodan Sasic. Raman, Infrared, and near-Infrared Chemical Imaging. Wiley & Sons, Incorporated, John, 2010.

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Ozaki, Yukihiro, and Slobodan Sasic. Raman, Infrared, and near-Infrared Chemical Imaging. Wiley & Sons, Incorporated, John, 2011.

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Ozaki, Yukihiro, and Slobodan Sasic. Raman, Infrared, and near-Infrared Chemical Imaging. Wiley & Sons, Incorporated, John, 2011.

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Ozaki, Yukihiro, and Slobodan Sasic. Raman, Infrared, and near-Infrared Chemical Imaging. Wiley & Sons, Incorporated, John, 2011.

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Book chapters on the topic "Near infrared imaging probes"

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Huang, Rui, Peter S. Conti, and Kai Chen. "In Vivo Tumor Angiogenesis Imaging Using Peptide-Based Near-Infrared Fluorescent Probes." In In Vivo Fluorescence Imaging, 73–84. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3721-9_8.

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Klohs, Jan, and Markus Rudin. "In Vivo Imaging of Vascular Targets Using Near-Infrared Fluorescent Probes." In Advanced Fluorescence Reporters in Chemistry and Biology III, 313–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-18035-4_10.

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Kalchenko, Vyacheslav, Michal Neeman, and Alon Harmelin. "Whole-Body Imaging of Hematopoietic and Cancer Cells Using Near-Infrared Probes." In Advanced Fluorescence Reporters in Chemistry and Biology III, 329–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-18035-4_11.

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Lewis, E. Neil, Joseph W. Schoppelrei, Lisa Makein, Linda H. Kidder, and Eunah Lee. "Near-Infrared Chemical Imaging for Product and Process Understanding." In Process Analytical Technology, 245–79. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470689592.ch8.

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Yoshida, Sanichiro, Tomohiro Sasaki, Masaru Usui, Shuuichi Sakamoto, Ik-keun Park, Hyunchul Jung, and Kyeongsuk Kim. "Near Weld Stress Analysis with Optical and Acoustic Methods." In Residual Stress, Thermomechanics & Infrared Imaging, Hybrid Techniques and Inverse Problems, Volume 9, 119–27. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-21765-9_16.

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Werts, Martinus H. V. "Near-Infrared Luminescent Labels and Probes Based on Lanthanide Ions and Their Potential for Applications in Bioanalytical Detection and Imaging." In Lanthanide Luminescence, 133–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/4243_2010_9.

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Shindo, Yutaka, Yuma Ikeda, Yuki Hiruta, Daniel Citterio, and Kotaro Oka. "Development of Near-Infrared Fluorescent Mg2+ Probe and Application to Multicolor Imaging of Intracellular Signals." In Methods in Molecular Biology, 217–35. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1258-3_19.

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Zhang, C., J. Marty, A. Maynadier, P. Chaudet, J. Réthoré, and M. C. Baietto. "Experimental Investigation of Emissivity Influence to Obtain Thermal Field by Near Infrared Thermography." In Residual Stress, Thermomechanics & Infrared Imaging, Hybrid Techniques and Inverse Problems, Volume 7, 35–37. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-95074-7_6.

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Chighizola, Christopher R., Christopher R. D’Elia, and Michael R. Hill. "Intermethod Comparison and Evaluation of Near Surface Residual Stress in Aluminum Parts Subject to Various Milling Parameters." In Residual Stress, Thermomechanics & Infrared Imaging and Inverse Problems, Volume 6, 67–74. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-30098-2_10.

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Ishikawa, Daitaro, Mika Ishigaki, and Aoife Ann Gowen. "NIR Imaging." In Near-Infrared Spectroscopy, 517–51. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-8648-4_22.

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Conference papers on the topic "Near infrared imaging probes"

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Yu, Shuai, Yuan Liu, Jayanth Kandukuri, Tingfeng Yao, and Baohong Yuan. "Near-infrared time-domain ultrasound-switchable fluorescence imaging." In Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/omp.2017.omm2d.2.

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Patonay, Gabor, Garfield Beckford, Lucjan Strekowski, Maged Henary, Jun Seok Kim, and Sidney Crow. "Near-infrared dyes for molecular probes and imaging." In SPIE BiOS: Biomedical Optics, edited by Samuel Achilefu and Ramesh Raghavachari. SPIE, 2009. http://dx.doi.org/10.1117/12.813562.

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Shao, Pin, Shaojuan Zhang, and Mingfeng Bai. "Near Infrared Fluorescent Quaterrylenediimide-cored Dendrimers for Bio-imaging." In Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/omp.2015.om4d.6.

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Garcia-Allende, P. Beatriz, Maximilian Koch, Jürgen Glatz, Panagiotis Symvoulidis, and Vasilis Ntziachristos. "Near-infrared fluorescence molecular guidance in oncologic surgery and surveillance endoscopy." In Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/omp.2015.ow1d.1.

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Smith, Bradley D. "Storable near-infrared chemiluminescent probes for in vivo optical imaging." In SPIE BiOS, edited by Samuel Achilefu and Ramesh Raghavachari. SPIE, 2011. http://dx.doi.org/10.1117/12.876709.

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Ptaszek, Marcin, Hooi Ling Kee, Chinnasamy Muthiah, Ralph Nothdurft, Walter Akers, Samuel Achilefu, Joseph P. Culver, and Dewey Holten. "Near-infrared molecular imaging probes based on chlorin-bacteriochlorin dyads." In BiOS, edited by Samuel Achilefu and Ramesh Raghavachari. SPIE, 2010. http://dx.doi.org/10.1117/12.842007.

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Taue, Shuji, Hirotsugu Yamamoto, Yoshio Hayasaki, Nobuo Nishida, and Hajime Miura. "Functional near-infrared imaging system using adaptable multi-channel probes." In 19th Congress of the International Commission for Optics: Optics for the Quality of Life, edited by Giancarlo C. Righini and Anna Consortini. SPIE, 2003. http://dx.doi.org/10.1117/12.523834.

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Zhou, Haiying, Walter Akers, Steven Brody, Matthew Wood, and Mikhail Y. Berezin. "Detecting inflammatory responses in live animal models with near-infrared ROS probes." In Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/omp.2019.om2d.3.

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Kobayashi, Hisataka. "Near infrared photo-immunotherapy: A newly developed, target cell-specific cancer theranostic technology." In Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/omp.2015.om2d.2.

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Ahn, Hyo-Yang, Sheng Yao, Xuhua Wang, and Kevin D. Belfield. "Near-infrared emitting squaraine dyes for multiphoton fluorescence imaging with high 2PA cross sections." In Optical Molecular Probes, Imaging and Drug Delivery. Washington, D.C.: OSA, 2011. http://dx.doi.org/10.1364/omp.2011.omd5.

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Reports on the topic "Near infrared imaging probes"

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Kleinmann, S. G. Near-Infrared Imaging of Selected Areas. Fort Belvoir, VA: Defense Technical Information Center, May 1994. http://dx.doi.org/10.21236/ada283519.

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Piao, Daqing. Transrectal Near-Infrared Optical Tomography for Prostate Imaging. Fort Belvoir, VA: Defense Technical Information Center, March 2009. http://dx.doi.org/10.21236/ada509892.

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Yalavarthy, Phaneendra K. Three-Dimensional near Infrared Imaging of Pathophysiological Changes within the Breast. Fort Belvoir, VA: Defense Technical Information Center, March 2007. http://dx.doi.org/10.21236/ada468530.

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Yalavarthy, Phaneendra K. Three-Dimensional Near Infrared Imaging of Pathophysiological Changes Within the Breast. Fort Belvoir, VA: Defense Technical Information Center, March 2008. http://dx.doi.org/10.21236/ada480855.

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Rudy, R. J., R. H. Fujino, S. M. Mazuk, W. J. Skinner, and C. C. Venturini. Adaptation of the Aerospace Near-Infrared Imaging Spectrograph for Observation of Rocket Launches. Fort Belvoir, VA: Defense Technical Information Center, May 2004. http://dx.doi.org/10.21236/ada423789.

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Rudy, R. J., and D. J. Gutierrez. Focus and Tip-Tilt Alignment Procedure for the Enhanced Aerospace Near-Infrared Imaging Spectograph. Fort Belvoir, VA: Defense Technical Information Center, August 2004. http://dx.doi.org/10.21236/ada428138.

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Dehghani, Hamid. Three Dimensional Reconstruction Algorithm for Imaging Pathophysiological Signal within Breast Tissue Using Near Infrared Light. Fort Belvoir, VA: Defense Technical Information Center, July 2004. http://dx.doi.org/10.21236/ada428927.

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Dehghani, Hamid. Three Dimensional Reconstruction Algorithm for Imaging Pathophysiological Signals Within Breast Tissue Using Near Infrared Light. Fort Belvoir, VA: Defense Technical Information Center, July 2006. http://dx.doi.org/10.21236/ada459783.

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Zheng, Gang, Juan Chen, and Klara Stefflova. Near-Infrared Fluorescence Imaging Guided Therapy: Molecular Beacon-Based Photosensitizers Triggered by Breast Cancer-Specific mRNA. Fort Belvoir, VA: Defense Technical Information Center, May 2007. http://dx.doi.org/10.21236/ada472022.

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Deng, Chun, Zhenyu Zhang, Zhi Guo, Hengduo Qi, Yang Liu, Haimin Xiao, and Xiaojun Li. Assessment of intraoperative use of indocyanine green fluorescence imaging on the number of lymph node dissection during minimally invasive gastrectomy: a systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, November 2021. http://dx.doi.org/10.37766/inplasy2021.11.0062.

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Abstract:
Review question / Objective: Whether is indocyanine green fluorescence imaging-guided lymphadenectomy feasible to improve the number of lymph node dissections during radical gastrectomy in patients with gastric cancer undergoing curative resection? Condition being studied: Gastric cancer was the sixth most common malignant tumor and the fourth leading cause of cancer-related death in the world. Radical lymphadenectomy was a standard procedure in radical gastrectomy for gastric cancer. The retrieval of more lymph nodes was beneficial for improving the accuracy of tumor staging and the long-term survival of patients with gastric cancer. Indocyanine green(ICG) near-infrared fluorescent imaging has been found to provide surgeons with effective visualization of the lymphatic anatomy. As a new surgical navigation technique, ICG near-infrared fluorescent imaging was a hot spot and had already demonstrated promising results in the localization of lymph nodes during surgery in patients with breast cancer, non–small cell lung cancer, and gastric cancer. In addition, ICG had increasingly been reported in the localization of tumor, lymph node dissection, and the evaluation of anastomotic blood supply during radical gastrectomy for gastric cancer. However, it remained unclear whether ICG fluorescence imaging would assist surgeons in performing safe and sufficient lymphadenectomy.
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