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Dissertations / Theses on the topic 'Fluorescent imaging System'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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1

Roy, Debashish. "3D Cryo-Imaging System For Whole Mouse." Case Western Reserve University School of Graduate Studies / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=case1259006676.

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2

Crosby, Kevin C. "Macromolecular Organization and Cell Function: A Multi-System Analysis." Diss., Virginia Tech, 2008. http://hdl.handle.net/10919/30259.

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The interior of the cell is a densely crowded and complex arena, full of a vast and diverse array of molecules and macromolecules. A fundamental understanding of cellular physiology will depend not only upon a reductionist analysis of the chemistry, structure, and function of individual components and subsystems, but also on a sagacious exegesis of the dynamic and emergent properties that characterize the higher-level system of living cells. Here, we present work on two aspects of the supramolecular organization of the cell: the controlled assembly of the mitotic spindle during cell division a

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3

Cho, Hoon-Sung. "Design and Development of a multifunctional nano carrier system for imaging, drug delivery, and cell targeting in cancer research." University of Cincinnati / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1275936260.

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4

Somoza, Eduardo A. Jr. "UTILIZATION OF FLUORESCENCE MOLECULAR IMAGING TO OPTIMIZE RADIONUCLIDE IMAGING." Case Western Reserve University School of Graduate Studies / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=case1338904705.

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5

Wang, Thomas D. (Thomas Duen-Shyr). "Fluorescence endoscopic imaging system for detection of colonic adenomas." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/8972.

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Thesis (Ph.D.)--Massachusetts Institute of Technology, Whitaker College of Health Sciences and Technology, 1996.<br>Includes bibliographical references (p. [137]-144).<br>Background/Aims: Autofluorescence spectra have been collected from colonic mucosa with optical fiber contact probes. This technique was found to be sensitive to the biochemical and microarchitectural differences between normal and pre-malignant tissue. It is desired to extend this method to wide area surveillance using endoscopically-collected fluorescence images. Methods: An analytic model was developed to determine the numb

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6

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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7

Salman, Aljebur Ali, and Yu Zholudov. "System for two photon imaging of biosamples." Thesis, Харків, ХНУРЕ, 2019. http://openarchive.nure.ua/handle/document/8366.

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The work is devoted to development of scanning imaging system for bioobjects based on two-photon fluorescence of nanoparticles. It is based on the use of nanomaterials in imagining systems and some of nonfluorescent imaging applications and labeling with fluorescent nanoparticles. The basics of two photon fluorescence, its imaging application, properties of nanoparticles and biological tissues, used for our system development were analyzed. Based on this analysis we developed the general scheme of the system for scanning imaging of bioobjects using CdTe quantum dot labels and method of two-ph

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8

Sexton, Kristian. "System and Methodology for Receptor-Level Fluorescence Imaging during Surgery." Thesis, Dartmouth College, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3634175.

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<p> Fluorescence molecular imaging will have an important clinical impact in the area of guided oncology surgery, where emerging technologies are poised to provide the surgeon with real-time molecular information to guide resection, using targeted molecular probes. The development of advanced surgical systems has gone hand in hand with probe development, and both aspects are analyzed in this work. A pulsed-light fluorescence guided surgical (FGS) system has been introduced to enable video rate visible light molecular imaging under normal room light conditions. The concepts behind this system d

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9

Souza, Geovane Grossi Araújo de. "X-Ray fluorescence imaging system based on Thick-GEM detectors." Universidade de São Paulo, 2019. http://www.teses.usp.br/teses/disponiveis/43/43134/tde-21032019-233121/.

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GEMs (Gas Electron Multiplier) and Thick-GEMs (Thick-Gas Electron Multiplier) are MPGDs (Micropattern Gas Detector) that make part of the new generation of gaseous detectors, allowing high counting rates, low cost when compared to solid state detectors, high radiation hardness and gain when using multiple structures. Besides that, the handling and maintenance of these detectors is relatively simple, being versatile to detect different types of radiation. Therefore, these detectors are an effective alternative to build imaging systems with large sensitive area. This work consists in the study

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10

Choi, Sungmoon. "Fluorescent noble metal nanodots for biological applications." Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/37195.

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Commercial organic dyes are widely used for cellular staining due to their small size, high brightness, and chemical functionality. However, their blinking and photobleaching are not ideal for studying dynamics inside live cells. An improvement over organics and much larger quantum dots, silver nanodots (Ag NDs) exhibit low cytotoxicity and excellent brightness and photostability, while retaining small size. We have utilized ssDNA hairpin structures to encapsulate Ag NDs with excellent spectral purity, high concentration, and good chemical and photophysical stability in a variety of biological

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11

Kujala, Naresh Gandhi Yu Ping. "Frequency domain fluorescent molecular tomography and molecular probes for small animal imaging." Diss., Columbia, Mo. : University of Missouri--Columbia, 2009. http://hdl.handle.net/10355/7021.

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Title from PDF of title page (University of Missouri--Columbia, viewed on Feb 26, 2010). The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file. Dissertation advisor: Dr. Ping Yu. Vita. Includes bibliographical references.

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12

Steyer, Grant. "Imaging of Cardiovascular Cellular Therapeutics with a Cryo-imaging System." Case Western Reserve University School of Graduate Studies / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1264865581.

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13

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

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14

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.<br>Principal faculty advisors: Fouad Kiamilev and Robert F. Rogers, Dept. of Electrical and Computer Engineering. Includes bibliographical references.

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15

Venius, Jonas. "Fluorescence spectroscopy and imaging studies of functionally different human heart tissues." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2013. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20130124_081732-30187.

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Rhythmical contraction of the heart is controlled by the cardiac conduction system (CCS). However, this highly important system visually could not be distinguished from the surrounding heart tissues – myocardium (MC) and connective tissue (CT); therefore during surgical procedures CCS could be damaged. The reliable method for CCS identification either in vivo or ex vivo does not exist therefore there is a definite need for developing a CCS imaging method. Fluorescence spectroscopy studies of cardiac tissues revealed, that most distinct spectral differences between CCS and the surrounding tissu

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16

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 lar

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17

Chen, Bing. "Dynamic Multispectral Imaging System with Spectral Zooming Capability and Its Applications." Scholarly Repository, 2010. http://scholarlyrepository.miami.edu/oa_dissertations/452.

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The main focus of this dissertation is to develop a multispectral imaging system with spectral zooming capability and also successfully demonstrate its promising medical applications through combining this technique with microscope system. The realization of the multispectral imaging method in this dissertation is based on the 4-f spatial filtering principle. When a collimated light is dispersed by the grating, there exists a clear linear distribution spectral line or spectrum at the Fourier plane of the Fourier transform lens group base on the Abbe imaging theory and optics Fourier Transform

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18

PILLAI, Vinoshene. "Intravital two photon clcium imaging of glioblastoma mouse models." Doctoral thesis, Scuola Normale Superiore, 2021. http://hdl.handle.net/11384/109211.

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19

Rasmussen, John C. "Development of a radiative transport based, fluorescence-enhanced, frequency-domain small animal imaging system." Thesis, [College Station, Tex. : Texas A&M University, 2006. http://hdl.handle.net/1969.1/ETD-TAMU-1067.

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20

Crane, Bryan Lee 1976. "DNA mutation detection via fluorescence imaging in a spatial thermal gradient, capillary electrophoresis system." Thesis, Massachusetts Institute of Technology, 2001. http://hdl.handle.net/1721.1/88874.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2001.<br>"February 2001."<br>Includes bibliographical references (leaves 122-126).<br>by Bryan Lee Crane.<br>S.M.

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21

Dubaj, Vladimir, and 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 diamete

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22

Rose, Cornelia [Verfasser], and 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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23

Uthoff, Ross. "Design of a Smartphone-Camera-based Fluorescence Imaging System for the Detection of Oral Cancer." Thesis, The University of Arizona, 2015. http://hdl.handle.net/10150/593619.

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Shown is the design of the Smartphone Oral Cancer Detection System (SOCeeDS). The SOCeeDS attaches to a smartphone and utilizes its embedded imaging optics and sensors to capture images of the oral cavity to detect oral cancer. Violet illumination sources excite the oral tissues to induce fluorescence. Images are captured with the smartphone’s onboard camera. Areas where the tissues of the oral cavity are darkened signify an absence of fluorescence signal, indicating breakdown in tissue structure brought by precancerous or cancerous conditions. With this data the patient can seek further testi

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24

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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25

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.<br>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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26

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 refl

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27

Godavarty, Anuradha. "Fluorescence enhanced optical tomography on breast phantoms with measurements using a gain modulated intensified CCD imaging system." Texas A&M University, 2003. http://hdl.handle.net/1969.1/2184.

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Fluorescence-enhanced optical imaging using near-infrared (NIR) light developed for in-vivo molecular targeting and reporting of cancer provides promising opportunities for diagnostic imaging. However, prior to the administration of unproven contrast agents, the benefits of fluorescence-enhanced optical imaging must be assessed in feasibility phantom studies. A novel intensified charge-coupled device (ICCD) imaging system has been developed to perform 3-D fluorescence tomographic imaging in the frequency-domain using near-infrared contrast agents. This study is unique since it (i) employs

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28

Chang, Jean H. "Design and fabrication of a precision alignment system and package for a two-photon fluorescence imaging device." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/45776.

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Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2008.<br>Includes bibliographical references (leaf 24).<br>A compact, lightweight precision alignment system and package for an endomicroscope was designed and fabricated. The endomicroscope will consist of a millimeter-scale fiber resonator and a two-axis silicon optical bench. The alignment system provided five degrees of freedom and was designed to align the fiber resonator with the microchip with a resolution of one micron. The alignment system consisted of a system of ultra-fine screws and two compliant

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29

Makhlouf, Houssine. "Integrated Multi-Spectral Fluorescence Confocal Microendoscope and Spectral-Domain Optical Coherence Tomography Imaging System for Tissue Screening." Diss., The University of Arizona, 2011. http://hdl.handle.net/10150/202761.

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A multi-modality imaging system intended for clinical utilization has been developed. It is constructed around an existing fiber-bundle-based fluorescence confocal microendoscope. Additional imaging modalities have been implemented to expand the capabilities of the system and improve the accuracy of disease diagnosis. A multi-spectral mode of operation is one such modality. It acquires fluorescence images of a biological sample across a spectral range of sensitivity and explores the collected image data at any specified wavelength within that spectral range. Cellular structures can be differen

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30

Martin, Phillip A., and Phillip A. Martin. "Investigation of the Feasibility of an Optical Imaging System for the Application of In Vivo Flow Cytometry." Thesis, The University of Arizona, 2016. http://hdl.handle.net/10150/621197.

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This thesis investigates the feasibility of employing an optical imaging system for the application of in vivo flow cytometry for detecting rare circulating tumor cells (CTCs) in vasculature. This investigation presented used three optical imaging configurations: a Nikon Eclipse E600 fluorescence microscope with a PIXIS 2048B CCD camera; a Nikon Eclipse E600 fluorescence microscope with a ThorLabs DCC 3240N CMOS camera; and a custom built confocal microendoscope with a ThorLabs DCC 3240N CMOS camera. These systems were employed to gain insight as to what signal to noise ratios and sensitivitie

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31

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 r

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32

Pincet, Lancelot. "Dynamic excitation systems for quantitative and super-resolved fluorescence microscopy." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASP033.

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La microscopie de localisation de molécule unique (SMLM) est une technique optique super-résolue permettant d'observer des échantillons biologiques marqués par des fluorophores avec une résolution bien inférieure à la limite de diffraction. La qualité de cette imagerie dépend fortement de la capacité à observer les molécules de manière individuelle, ce qui nécessite un contrôle précis de la photophysique des fluorophores pour qu'ils émettent de manière décalée dans l'espace et le temps. Jusqu'à présent, les méthodes d'excitation dynamique visaient à produire une illumination uniforme sur des c

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33

Walde, Marie [Verfasser], Rainer [Gutachter] Heintzmann, and Ute [Gutachter] Neugebauer. "Development of a holoscopic imaging system and applied high-resolution fluorescence microscopy / Marie Walde ; Gutachter: Rainer Heintzmann, Ute Neugebauer." Jena : Friedrich-Schiller-Universität Jena, 2017. http://d-nb.info/1177597233/34.

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34

Chen, Huiyi. "System-Wide Studies of Gene Expression in Escherichia coli by Fluorescence Microscopy and High Throughput Sequencing." Thesis, Harvard University, 2011. http://dissertations.umi.com/gsas.harvard:10044.

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Gene expression is a fundamental process in the cell and is made up of two parts – the information flow from DNA to RNA, and from RNA to protein. Here, we examined specific sub-processes in Escherichia coli gene expression using newly available tools that permit genome-wide analysis. We begin our studies measuring mRNA and protein abundances in single cells by single-molecule fluorescence microscopy, and then focus our attention to studying RNA generation and degradation by high throughput sequencing. The details of the dynamics of gene expression can be observed from fluctuations in mRNA and

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35

Venius, Jonas. "Funkciškai besiskiriančių žmogaus širdies audinių fluorescenciniai tyrimai ir vaizdinimas." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2013. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2013~D_20130124_081724-06694.

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Tvarkingą širdies darbą užtikrina širdies laidžioji sistema (ŠLS). Ją pažeidus sutrinka širdies darbas. Pažeidimo rizika atsiranda operacijos metu, kadangi ŠLS yra raumeninės kilmės audinys ir vizualiai neatskiriamas nuo aplinkinių audinių. ŠLS pažeidimo galima būtų išvengti, jei būtų žinomas tikslus ŠLS išsidėstymas arba egzistuotų ŠLS vaizdinimo metodika. Deja, bet atskirų ŠLS dalių tikslus išsidėstymas vis dar tikslinamas, o patologijų atvejais apskritai nėra žinomas. ŠLS vaizdinimo metodikos, tinkančios in vivo taikymams, taipogi nėra. Atlikus širdies audinių tyrimus nustoviąja fluorescen

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36

Manhat, Beth Ann. "Understanding the Emission from Semiconductor Nanoparticles." PDXScholar, 2012. https://pdxscholar.library.pdx.edu/open_access_etds/465.

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This dissertation describes the synthesis and characterization of fluorescent semiconductor nanoparticles (NPs) in order to optimize their biomedical utility for imaging and sensing applications. While both direct and indirect bandgap semiconductor NPs have been studied, control over their emission properties vary. Quantum confinement (QC), which primarily controls the emission wavelength of nanosized semiconductors, dictates that as the size of semiconductor NPs decrease, the magnitude of the bandgap increases, resulting in changes in the observed emission wavelength: smaller NPs have a large

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37

Nishino, Hiroto. "Real-time Navigation for Liver Surgery Using Projection Mapping With Indocyanine Green Fluorescence: Development of the Novel Medical Imaging Projection System." Kyoto University, 2019. http://hdl.handle.net/2433/242358.

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38

DIMAS, FIRMANDA AL RIZA. "Potato surface defect detection using machine vision systems based on spectral reflection and fluorescence characteristics in the UV-NIR region." Kyoto University, 2019. http://hdl.handle.net/2433/244556.

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Kyoto University (京都大学)<br>0048<br>新制・課程博士<br>博士(農学)<br>甲第22075号<br>農博第2367号<br>新制||農||1072(附属図書館)<br>学位論文||R1||N5229(農学部図書室)<br>京都大学大学院農学研究科地域環境科学専攻<br>(主査)教授近藤直, 准教授小川雄一, 教授清水浩<br>学位規則第4条第1項該当

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Lillro, Ejla. "Image Sensor System for Detection of Bacteria and Antibiotic Resistance." Thesis, KTH, Skolan för teknik och hälsa (STH), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-179399.

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Antibiotic resistance is now a recognized problem in global health. In attempts to find solutions to detect bacteria causing antibiotic resistance we turn to technological solutions that are miniaturized, portable and cheap. The current diagnostic procedures cannot provide correct information outside laboratory settings, at the point-of-care, within necessary time. This has led to ineffective treatment of urinary tract infections causing recurrent infections and multi-drug resistant bacteria to spread. The bacteria genes show which antibiotic that is required to eliminate disease and spread of

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40

Merz, Simon Frederik [Verfasser], and Matthias [Akademischer Betreuer] Gunzer. "Mesoscopic whole organ imaging using light sheet fluorescence microscopy : from experimental systems to clinical application / Simon Frederik Merz ; Betreuer: Matthias Gunzer." Duisburg, 2021. http://d-nb.info/1236502027/34.

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Bozhko, Dmitry [Verfasser], Vasilis [Akademischer Betreuer] Ntziachristos, Alexander W. [Gutachter] Koch, Vasilis [Gutachter] Ntziachristos, and Oliver [Gutachter] Hayden. "Development of a Hybrid System for Intravascular Fluorescence-Ultrasound Imaging / Dmitry Bozhko ; Gutachter: Alexander W. Koch, Vasilis Ntziachristos, Oliver Hayden ; Betreuer: Vasilis Ntziachristos." München : Universitätsbibliothek der TU München, 2019. http://d-nb.info/1201819679/34.

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42

Fantoni, Frédéric. "Méthodes d'illumination et de détection innovantes pour l'amélioration du contraste et de la résolution en imagerie moléculaire de fluorescence en rétrodiffusion." Thesis, Grenoble, 2014. http://www.theses.fr/2014GRENU034/document.

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Depuis quelques années, les techniques d'imagerie de fluorescence font l'objet d'une attention particulière, celles-ci permettant d'étudier de manière non invasive un nombre important de processus cellulaires. En particulier, les techniques de fluorescence en rétrodiffusion (FRI pour Fluorescence Reflectance Imaging) présentent plusieurs avantages en termes de facilité de mise en oeuvre, de rapidité et de coût, mais elles sont aussi sujettes à des limites fortes : la pénétration des tissus reste relativement faible (quelques millimètres seulement), et il est impossible d'avoir une information

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43

Means, John A. "Fluorescence and NMR Characterization of a T Box Antiterminator-tRNA Complex." View abstract, 2007. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&res_dat=xri:pqdiss&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&rft_dat=xri:pqdiss:3289332.

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44

Richards, Christopher I. "Dynamic dark state depletion." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/31831.

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Thesis (Ph.D)--Chemistry and Biochemistry, Georgia Institute of Technology, 2010.<br>Committee Chair: Dickson, Robert; Committee Member: Fahrni, Christoph; Committee Member: Payne, Christine; Committee Member: Petty, Jeff; Committee Member: Srinivasarao, Mohan. Part of the SMARTech Electronic Thesis and Dissertation Collection.

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Madai, Vince István [Verfasser]. "Virtual pre-embedding labeling : a method for correlative fluorescence and electron microscopic imaging and double-labeling in the central nervous system of the rat / Vince István Madai." Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2012. http://d-nb.info/1027307558/34.

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Madai, Vince Istvan [Verfasser]. "Virtual pre-embedding labeling : a method for correlative fluorescence and electron microscopic imaging and double-labeling in the central nervous system of the rat / Vince István Madai." Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2012. http://d-nb.info/1027307558/34.

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47

Poon, Chien Sing. "Early Assessment of Burn Severity in Human Tissue with Multi-Wavelength Spatial Frequency Domain Imaging." Wright State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=wright1484582176416423.

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48

Huisman, Maximiliaan. "Vision Beyond Optics: Standardization, Evaluation and Innovation for Fluorescence Microscopy in Life Sciences." eScholarship@UMMS, 2019. https://escholarship.umassmed.edu/gsbs_diss/1017.

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Fluorescence microscopy is an essential tool in biomedical sciences that allows specific molecules to be visualized in the complex and crowded environment of cells. The continuous introduction of new imaging techniques makes microscopes more powerful and versatile, but there is more than meets the eye. In addition to develop- ing new methods, we can work towards getting the most out of existing data and technologies. By harnessing unused potential, this work aims to increase the richness, reliability, and power of fluorescence microscopy data in three key ways: through standardization, evaluat

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Schädlich, Andreas Verfasser], Karsten [Akademischer Betreuer] [Mäder, Achim [Akademischer Betreuer] Göpferich, and Jörg [Akademischer Betreuer] Kreßler. "Pre‐clinical in vivo studies of parenteral drug delivery systems using non‐invasive multispectral fluorescence imaging : [kumulative Dissertation] / Andreas Schädlich. Betreuer: Karsten Mäder ; Achim Göpferich ; Jörg Kreßler." Halle, Saale : Universitäts- und Landesbibliothek Sachsen-Anhalt, 2013. http://d-nb.info/1045194824/34.

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Agarwal, Abhiruchi. "Nanocarrier mediated therapies for the gliomas of the brain." Diss., Georgia Institute of Technology, 2011. http://hdl.handle.net/1853/39468.

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Abstract:

Existing methods of treating glioma are not effective for eradicating the disease. Therefore, new and innovative methods of treatment alone or in combination with existing therapies are necessary. Delivery of therapeutic agents through delivery carriers such as liposomes diminishes the harmful effects of the agent in healthy tissues and allows increased accumulation in the tumor. In addition, targeted chemotherapy using liposomes provides the opportunity for further increase in drug accumulation in tumor. However, the current targeting strategies suffer accelerated plasma clearance and are not

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