Digital holographic microscopy for phase images of cervical cells 3D structure

Author(s):  
M. Mihailescu ◽  
I. A. Paun ◽  
E. I. Scarlat ◽  
I. Grigorescu ◽  
O. T. Nedelcu ◽  
...  
Author(s):  
Kaveh Azartash ◽  
Enrico Gratton

A modified Mach-Zender set-up in reflection is applied to record and reconstruct holographic amplitude and phase images. A charged couple device (CCD) is used to record a hologram and numerical reconstruction algorithms are then applied to rebuild the hologram for obtaining both phase and amplitude information. One could also focus on multiple focal planes from a single hologram, similar to the focusing control of a conventional microscope. The morphology and behavior of mammalian cells is determined by an interaction between signals from the intracellular matrix and the cellular responses. It is important to note that the physical aspect of the extracellular matrix is as significant as the chemical nature of it. Specifically the stresses, mechanical forces, and the profile of the external environment have major effects on cell behavior. The mechanical and physical characteristics of a tissue are greatly dependent on a hierarchical spatial arrangement of its extra-cellular matrix components. A key player in the ECM is collagen which exhibits significant tensile strength on the cellular scale. Digital holographic microscopy (DHM) is applied to study the deformation of collage matrix in response to cell migration.


2018 ◽  
Vol 2018 ◽  
pp. 1-8 ◽  
Author(s):  
Lin Hu ◽  
Yunxiu Shui ◽  
Yaohui Dai ◽  
Haiyu Wu ◽  
Gang Zhu ◽  
...  

A dual-wavelength digital holographic microscopy with premagnification is proposed to obtain the object surface measurements over the large gradient. The quantitative phase images of specimens are captured in high precision by the processing of filtering and phase compensation. The phase images are acquired without phase unwrapping, which is necessary in traditional digital holographic microscopy; thereby the proposed system can greatly increase the speed of reconstruction. The results of numerical simulation and optical experiments demonstrated that the reconstructed speed increased by 37.9 times, and the relative error of measurement is 4% compared with the traditional holographic microscopy system. It means that the proposed system can directly acquire the higher quality quantitative phase distribution for specimens.


2005 ◽  
Author(s):  
Florian Charriere ◽  
Pierre Marquet ◽  
Etienne Cuche ◽  
Christian D. Depeursinge

2014 ◽  
Vol 256 (2) ◽  
pp. 117-125 ◽  
Author(s):  
T. ZIKMUND ◽  
L. KVASNICA ◽  
M. TÝČ ◽  
A. KŘÍŽOVÁ ◽  
J. ČOLLÁKOVÁ ◽  
...  

2021 ◽  
Author(s):  
Sarita Ahlawat ◽  
Purnima Sharma ◽  
Ankita Pandey ◽  
Durga Bisht ◽  
Aanisa Jan ◽  
...  

We summarize a study involving simultaneous imaging of cervical cells from Pap-smear samples using bright-field and quantitative phase microscopy. The optimization approach to phase reconstruction used in our study enables full diffraction limited performance from single-shot holograms and is thus suitable for reducing cost of a quantitative phase microscope system. Over 48000 cervical cells from patient samples obtained from three clinical sites have been imaged in this study. The clinical sites used different sample preparation methodologies and the subjects represented a range of age groups and geographical diversity. Visual examination of quantitative phase images of cervical cell nuclei show distinct morphological features that we believe have not appeared in the prior literature. A PCA based analysis of numerical parameters derived from the bright-field and quantitative phase images of the cervical cells shows good separation of superficial, intermediate and abnormal cells. The distribution of phase based parameters of normal cells is also shown to be highly overlapping among different patients from the same clinical site, patients across different clinical sites and for two age groups (below and above 30 years), thus suggesting robustness and possibility of standardization of quantitative phase as an imaging modality for cell classification in future clinical usage.


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