Theoretical and experimental study on the difference of the time-resolved fluorescence spectrum between the tumor and the adjacent normal tissue

2006 ◽  
Author(s):  
Mingzhao Li ◽  
Tao Xu
2004 ◽  
Vol 44 (supplement) ◽  
pp. S101
Author(s):  
K. Koike ◽  
K. Kawaguchi ◽  
A. Kimura ◽  
T. Yamato

2021 ◽  
Vol 23 (37) ◽  
pp. 21029-21041
Author(s):  
Amita Mahapatra ◽  
Manjari Chakraborty ◽  
Sahadev Barik ◽  
Moloy Sarkar

This work investigates the difference in the microscopic behaviour of imidazolium and pyrrolidinium based ILs employing combined steady state and time-resolved fluorescence, EPR and NMR spectroscopy.


2021 ◽  
Vol 2058 (1) ◽  
pp. 012028
Author(s):  
Yu S Maklygina ◽  
I D Romanishkin ◽  
A S Skobeltsin ◽  
T A Savelyeva ◽  
A A Potapov ◽  
...  

Abstract The paper presents a new approach to assessing the state of tissues that differ in phenotype and in the degree of immunocompetent cells activity using photosensitizers (PS) and time-resolved fluorescence analysis methods. The main attention is paid to the detection of differences between tumor cells and tumor-associated macrophages (TAM) using spectroscopic and microscopic methods by the fluorescent kinetics signal and the difference in the accumulation of PS (the accumulation is several times greater in macrophages). The results of the PS photoluminescence study were obtained using two different techniques: time-resolved spectroscopy and time-resolved fluorescence microscopy (FLIM). Time-resolved spectroscopic analysis of the PS fluorescence lifetime was performed on adult female rats with induced C6 glioma in vivo. 5-ALA-induced Pp IX, which is widely used in clinical practice for carrying out effective conduction photodiagnostics and PDT, was used as the PS.


eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
John Repass ◽  
Elizabeth Iorns ◽  
Alexandria Denis ◽  
Stephen R Williams ◽  
Nicole Perfito ◽  
...  

As part of the Reproducibility Project: Cancer Biology, we published a Registered Report (Repass et al., 2016), that described how we intended to replicate an experiment from the paper ‘Fusobacterium nucleatum infection is prevalent in human colorectal carcinoma’ (Castellarin et al., 2012). Here we report the results. When measuring Fusobacterium nucleatum DNA by qPCR in colorectal carcinoma (CRC), adjacent normal tissue, and separate matched control tissue, we did not detect a signal for F. nucleatum in most samples: 25% of CRCs, 15% of adjacent normal, and 0% of matched control tissue were positive based on quantitative PCR (qPCR) and confirmed by sequencing of the qPCR products. When only samples with detectable F. nucleatum in CRC and adjacent normal tissue were compared, the difference was not statistically significant, while the original study reported a statistically significant increase in F. nucleatum expression in CRC compared to adjacent normal tissue (Figure 2; Castellarin et al., 2012). Finally, we report a meta-analysis of the result, which suggests F. nucleatum expression is increased in CRC, but is confounded by the inability to detect F. nucleatum in most samples. The difference in F. nucleatum expression between CRC and adjacent normal tissues was thus smaller than the original study, and not detected in most samples.


Sign in / Sign up

Export Citation Format

Share Document