Fluorescence Imaging for Ultrafiltration of Individual Nanoparticles from a Colloidal Solution in Track Membranes

2018 ◽  
Vol 85 (5) ◽  
pp. 916-922 ◽  
Author(s):  
S. I. Kulik ◽  
I. Yu. Eremchev ◽  
P. Yu. Apel ◽  
D. L. Zagorski ◽  
A. V. Naumova
2020 ◽  
Vol 8 ◽  
Author(s):  
Sergey V. Gudkov ◽  
Ilya V. Baimler ◽  
Oleg V. Uvarov ◽  
Veronika V. Smirnova ◽  
Mikhail Yu Volkov ◽  
...  

The evolution of the size distribution of nanoparticles depending on the concentration of nanoparticles in a colloidal solution is investigated. The formation of new stable distributions shifted relative to the initial distribution is directly related to the processes of agglomeration of nanoparticles. Using successive two-fold dilutions of nanoparticles by 2–32 times, it was shown that the maximum of the nanoparticle size distribution shifts toward smaller sizes with a decrease in the concentration of nanoparticles, both for distributions by the number of nanoparticles and for distributions by mass of nanoparticles. Thus, with dilutions, the relative concentration of individual nanoparticles increases, while the number of particles in one aggregate decreases. A mathematical model has been created that predicts a change in distribution with a change in the concentration of nanoparticles in a colloid.


Author(s):  
C J R Sheppard

The confocal microscope is now widely used in both biomedical and industrial applications for imaging, in three dimensions, objects with appreciable depth. There are now a range of different microscopes on the market, which have adopted a variety of different designs. The aim of this paper is to explore the effects on imaging performance of design parameters including the method of scanning, the type of detector, and the size and shape of the confocal aperture.It is becoming apparent that there is no such thing as an ideal confocal microscope: all systems have limitations and the best compromise depends on what the microscope is used for and how it is used. The most important compromise at present is between image quality and speed of scanning, which is particularly apparent when imaging with very weak signals. If great speed is not of importance, then the fundamental limitation for fluorescence imaging is the detection of sufficient numbers of photons before the fluorochrome bleaches.


Author(s):  
Byunghee Hwang ◽  
Tae-Il Kim ◽  
Hyunjin Kim ◽  
Sungjin Jeon ◽  
Yongdoo Choi ◽  
...  

A ubiquinone-BODIPY photosensitizer self-assembles into nanoparticles (PS-Q-NPs) and undergoes selective activation within the highly reductive intracellular environment of tumors, resulting in “turn-on” fluorescence and photosensitizing activities.


2003 ◽  
Vol 773 ◽  
Author(s):  
Xiaohu Gao ◽  
Shuming Nie ◽  
Wallace H. Coulter

AbstractLuminescent quantum dots (QDs) are emerging as a new class of biological labels with unique properties and applications that are not available from traditional organic dyes and fluorescent proteins. Here we report new developments in using semiconductor quantum dots for quantitative imaging and spectroscopy of single cancer cells. We show that both live and fixed cells can be labeled with multicolor QDs, and that single cells can be analyzed by fluorescence imaging and wavelength-resolved spectroscopy. These results raise new possibilities in cancer imaging, molecular profiling, and disease staging.


Author(s):  
Tytus Bernas ◽  
Elikplimi K. Asem ◽  
J. Paul Robinson ◽  
Peter R. Cook ◽  
Jurek W. Dobrucki

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