scholarly journals Label‐free spectroscopic tissue characterization using fluorescence excitation‐scanning spectral imaging

2019 ◽  
Vol 13 (2) ◽  
Author(s):  
Peter F. Favreau ◽  
Joshua A. Deal ◽  
Bradley Harris ◽  
David S. Weber ◽  
Thomas C. Rich ◽  
...  
2020 ◽  
Vol 13 (2) ◽  
Author(s):  
Peter F. Favreau ◽  
Joshua A. Deal ◽  
Bradley Harris ◽  
David S. Weber ◽  
Thomas C. Rich ◽  
...  

Author(s):  
J. A. Palero ◽  
H. S. de Bruijn ◽  
A. van der Ploeg van den Heuvel ◽  
H. J. C. M Sterenborg ◽  
H. C. Gerritsen

Author(s):  
Yao Alvarez Kossonou ◽  
Jérémie Zoueu

In this paper, we present the progress made in developing multimodal and multispectral light microscopy for label-free malaria diagnosis. Our previously developed light emitting diode (LED) illumination system was replaced by laser diodes as light sources in order to narrow the spectral bands and improve the effectiveness of the contrast function for infected blood cell detection. The acquisition system is now equipped with an algorithm for automatic field scanning and best in-focus determination. We demonstrate the potential of this platform to provide multiple investigation modalities like transmission, reflection, scattering, fluorescence, excitation, emission and polarisation. The application of this platform on malaria-infected samples has shown the effectiveness of such a system in label-free and all-optical malaria detection by allowing the possibility of using a different type of imaging set-up for the samples analysed. Also, fewer illumination sources are used to characterise malaria-infected red blood cells compared to our previous works on malaria detection using LEDs illumination sources.


2021 ◽  
Author(s):  
Yanyu Zhao ◽  
Anahita Pilvar ◽  
Mark C. Pierce ◽  
Darren M. Roblyer

The Analyst ◽  
2017 ◽  
Vol 142 (8) ◽  
pp. 1207-1215 ◽  
Author(s):  
D. Petersen ◽  
L. Mavarani ◽  
D. Niedieker ◽  
E. Freier ◽  
A. Tannapfel ◽  
...  

The great capability of virtual staining for label-free classification of colon cancer tissue has been demonstrated via Raman spectral imaging.


2013 ◽  
Vol 79 (20) ◽  
pp. 6345-6350 ◽  
Author(s):  
Helene Knaus ◽  
Gerhard A. Blab ◽  
Alexandra V. Agronskaia ◽  
Dave J. van den Heuvel ◽  
Hans C. Gerritsen ◽  
...  

ABSTRACTLabel-free nonlinear spectral imaging microscopy (NLSM) records two-photon-excited fluorescence emission spectra of endogenous fluorophores within the specimen. Here, NLSM is introduced as a novel, minimally invasive method to analyze the metabolic state of fungal hyphae by monitoring the autofluorescence of NAD(P)H and flavin adenine dinucleotide (FAD). Moreover, the presence of melanin was analyzed by NLSM. NAD(P)H, FAD, and melanin were used as biomarkers for freshness of mushrooms ofAgaricus bisporus(white button mushroom) that had been stored at 4°C for 0 to 17 days. During this period, the mushrooms did not show changes in morphology or color detectable by eye. In contrast, FAD/NAD(P)H and melanin/NAD(P)H ratios increased over time. For instance, these ratios increased from 0.92 to 2.02 and from 0.76 to 1.53, respectively, at the surface of mushroom caps that had been harvested by cutting the stem. These ratios were lower under the skin than at the surface of fresh mushrooms (0.78 versus 0.92 and 0.41 versus 0.76, respectively), indicative of higher metabolism and lower pigment formation within the fruiting body. Signals were different not only between tissues of the mushroom but also between neighboring hyphae. These data show that NLSM can be used to determine the freshness of mushrooms and to monitor the postharvest browning process at an early stage. Moreover, these data demonstrate the potential of NLSM to address a broad range of fundamental and applied microbiological processes.


ACS Nano ◽  
2009 ◽  
Vol 3 (11) ◽  
pp. 3552-3559 ◽  
Author(s):  
Tatyana Chernenko ◽  
Christian Matthäus ◽  
Lara Milane ◽  
Luis Quintero ◽  
Mansoor Amiji ◽  
...  

2015 ◽  
Vol 7 (12) ◽  
pp. 5157-5161 ◽  
Author(s):  
H. Yoshikawa ◽  
M. Murahashi ◽  
M. Saito ◽  
S. Jiang ◽  
M. Iga ◽  
...  

Parallelized detection of protein interactions using a multi-array chip and a hyper-spectral imaging system.


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