2015
DOI: 10.1364/boe.6.001219
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Spectral and lifetime domain measurements of rat brain tumors

Abstract: During glioblastoma surgery, delineation of the brain tumor margins is difficult because the infiltrated and normal tissues have the same visual appearance. We use a fiber-optical fluorescence probe for spectroscopic and time domain measurements to assist surgeon in differentiating the healthy and the infiltrated tissues. First study was performed on rats that were previously injected with tumorous cells. Measurements of endogenous tissue fluorescence were performed on fresh and fixed rat tumor brain slices. S… Show more

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Cited by 40 publications
(60 citation statements)
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“…In addition, by calculating the integral under the curve of the emission spectra of NADH, FAD and the porphyrins, using a Matlab program developed by our team 17 , we obtained two different ratios under 405 nm and 375 nm excitation wavelengths 11 , 18 . …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In addition, by calculating the integral under the curve of the emission spectra of NADH, FAD and the porphyrins, using a Matlab program developed by our team 17 , we obtained two different ratios under 405 nm and 375 nm excitation wavelengths 11 , 18 . …”
Section: Resultsmentioning
confidence: 99%
“…At 375 nm, the calculated ratio has negative values because NADH is more present in brain tissues than FAD at the excitation wavelength 17 , 19 . As shown in Fig.…”
Section: Resultsmentioning
confidence: 99%
“…It was a bi-fiber setup, one fiber to excite the fluorophore at 345nm and 405nm and the other one to collect the intensity of fluorescence and send it to the spectrometer or to the Photo Multiplier Tube for lifetime measurement analysis. This set-up has been previously published [3]. 2) Multimodal wide-field excitation imaging: one and twophotons: At the IMNC laboratory, samples were imaged using a Leica TCS SP8-FLIM microscope on PIMPA platform.…”
Section: B Set-upsmentioning
confidence: 99%
“…We could also measure SHG at 445 nm using 890 nm excitation wavelength. We developed a Matlab script to fit these different fluorophores [3], we will use it here to fit the spectra and observe the change in the mean intensity of fluorescence between fresh and fixed samples. Fig.…”
Section: A Two Photon Spectral Analysismentioning
confidence: 99%
“…Optical tomography in the near IR region is now a reality, 67 and it has proven possible to use fluorescence lifetime measurements to distinguish between healthy and unhealthy cells. 68 An interesting challenge for chemists and biochemists is to be able to tag fluorophores or other radiative molecules to enable them to access specific cells or even specific regions once inside a cell. 69 The higher their specificity, the more useful these molecules will be for diagnostics and therapy.…”
Section: Photobiology: Beyond the Human Bodymentioning
confidence: 99%