Deep-learning-based prediction of living cells mitosis via quantitative phase microscopy

2021 ◽  
Vol 19 (5) ◽  
pp. 051701
Author(s):  
Ying Li ◽  
Jianglei Di ◽  
Li Ren ◽  
Jianlin Zhao
2015 ◽  
Vol 20 (9) ◽  
pp. 096005 ◽  
Author(s):  
Cristina Martinez-Torres ◽  
Bastien Laperrousaz ◽  
Lotfi Berguiga ◽  
Elise Boyer-Provera ◽  
Juan Elezgaray ◽  
...  

2019 ◽  
Vol 8 (1) ◽  
Author(s):  
Yair Rivenson ◽  
Tairan Liu ◽  
Zhensong Wei ◽  
Yibo Zhang ◽  
Kevin de Haan ◽  
...  

2016 ◽  
Author(s):  
C. Martinez Torres ◽  
B. Laperrousaz ◽  
L. Berguiga ◽  
E. Boyer Provera ◽  
J. Elezgaray ◽  
...  

2008 ◽  
Vol 295 (2) ◽  
pp. C538-C544 ◽  
Author(s):  
Gabriel Popescu ◽  
YoungKeun Park ◽  
Niyom Lue ◽  
Catherine Best-Popescu ◽  
Lauren Deflores ◽  
...  

Using novel interferometric quantitative phase microscopy methods, we demonstrate that the surface integral of the optical phase associated with live cells is invariant to cell water content. Thus, we provide an entirely noninvasive method to measure the nonaqueous content or “dry mass” of living cells. Given the extremely high stability of the interferometric microscope and the femtogram sensitivity of the method to changes in cellular dry mass, this new technique is not only ideal for quantifying cell growth but also reveals spatially resolved cellular and subcellular dynamics of living cells over many decades in a temporal scale. Specifically, we present quantitative histograms of individual cell mass characterizing the hypertrophic effect of high glucose in a mesangial cell model. In addition, we show that in an epithelial cell model observed for long periods of time, the mean squared displacement data reveal specific information about cellular and subcellular dynamics at various characteristic length and time scales. Overall, this study shows that interferometeric quantitative phase microscopy represents a noninvasive optical assay for monitoring cell growth, characterizing cellular motility, and investigating the subcellular motions of living cells.


Pharmaceutics ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 590
Author(s):  
Jennifer Cauzzo ◽  
Nikhil Jayakumar ◽  
Balpreet Singh Ahluwalia ◽  
Azeem Ahmad ◽  
Nataša Škalko-Basnet

The rapid development of nanomedicine and drug delivery systems calls for new and effective characterization techniques that can accurately characterize both the properties and the behavior of nanosystems. Standard methods such as dynamic light scattering (DLS) and fluorescent-based assays present challenges in terms of system’s instability, machine sensitivity, and loss of tracking ability, among others. In this study, we explore some of the downsides of batch-mode analyses and fluorescent labeling, while introducing quantitative phase microscopy (QPM) as a label-free complimentary characterization technique. Liposomes were used as a model nanocarrier for their therapeutic relevance and structural versatility. A successful immobilization of liposomes in a non-dried setup allowed for static imaging conditions in an off-axis phase microscope. Image reconstruction was then performed with a phase-shifting algorithm providing high spatial resolution. Our results show the potential of QPM to localize subdiffraction-limited liposomes, estimate their size, and track their integrity over time. Moreover, QPM full-field-of-view images enable the estimation of a single-particle-based size distribution, providing an alternative to the batch mode approach. QPM thus overcomes some of the drawbacks of the conventional methods, serving as a relevant complimentary technique in the characterization of nanosystems.


2017 ◽  
Vol 8 (10) ◽  
pp. 4687 ◽  
Author(s):  
Jiaji Li ◽  
Qian Chen ◽  
Jialin Zhang ◽  
Yan Zhang ◽  
Linpeng Lu ◽  
...  

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