Multi‐modal biomicroscopic system for the characterization of cells with high spatial phase sensitivity and sub‐pixel accuracy

Author(s):  
Shilpa Tayal ◽  
Veena Singh ◽  
Tejinder Kaur ◽  
Neetu Singh ◽  
Dalip Singh Mehta
2019 ◽  
Vol 21 (8) ◽  
pp. 085602 ◽  
Author(s):  
Daryoush Abdollahpour ◽  
Morteza Lotfollahi ◽  
Mohammad Yeganeh ◽  
Saifollah Rasouli

2005 ◽  
Vol 15 (11) ◽  
pp. 1697-1702 ◽  
Author(s):  
Wei-Feng Xu ◽  
Zhi-Ming Shen ◽  
Chao-Yi Li

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Azeem Ahmad ◽  
Vishesh Dubey ◽  
Nikhil Jayakumar ◽  
Anowarul Habib ◽  
Ankit Butola ◽  
...  

AbstractHigh space-bandwidth product with high spatial phase sensitivity is indispensable for a single-shot quantitative phase microscopy (QPM) system. It opens avenue for widespread applications of QPM in the field of biomedical imaging. Temporally low coherence light sources are implemented to achieve high spatial phase sensitivity in QPM at the cost of either reduced temporal resolution or smaller field of view (FOV). In addition, such light sources have low photon degeneracy. On the contrary, high temporal coherence light sources like lasers are capable of exploiting the full FOV of the QPM systems at the expense of less spatial phase sensitivity. In the present work, we demonstrated that use of narrowband partially spatially coherent light source also called pseudo-thermal light source (PTLS) in QPM overcomes the limitations of conventional light sources. The performance of PTLS is compared with conventional light sources in terms of space bandwidth product, phase sensitivity and optical imaging quality. The capabilities of PTLS are demonstrated on both amplitude (USAF resolution chart) and phase (thin optical waveguide, height ~ 8 nm) objects. The spatial phase sensitivity of QPM using PTLS is measured to be equivalent to that for white light source and supports the FOV (18 times more) equivalent to that of laser light source. The high-speed capabilities of PTLS based QPM is demonstrated by imaging live sperm cells that is limited by the camera speed and large FOV is demonstrated by imaging histopathology human placenta tissue samples. Minimal invasive, high-throughput, spatially sensitive and single-shot QPM based on PTLS will enable wider penetration of QPM in life sciences and clinical applications.


2015 ◽  
Vol 114 (6) ◽  
pp. 3326-3338 ◽  
Author(s):  
H. Meffin ◽  
M. A. Hietanen ◽  
S. L. Cloherty ◽  
M. R. Ibbotson

Neurons in primary visual cortex are classified as simple, which are phase sensitive, or complex, which are significantly less phase sensitive. Previously, we have used drifting gratings to show that the phase sensitivity of complex cells increases at low contrast and after contrast adaptation while that of simple cells remains the same at all contrasts (Cloherty SL, Ibbotson MR. J Neurophysiol 113: 434–444, 2015; Crowder NA, van Kleef J, Dreher B, Ibbotson MR. J Neurophysiol 98: 1155–1166, 2007; van Kleef JP, Cloherty SL, Ibbotson MR. J Physiol 588: 3457–3470, 2010). However, drifting gratings confound the influence of spatial and temporal summation, so here we have stimulated complex cells with gratings that are spatially stationary but continuously reverse the polarity of the contrast over time (contrast-reversing gratings). By varying the spatial phase and contrast of the gratings we aimed to establish whether the contrast-dependent phase sensitivity of complex cells results from changes in spatial or temporal processing or both. We found that most of the increase in phase sensitivity at low contrasts could be attributed to changes in the spatial phase sensitivities of complex cells. However, at low contrasts the complex cells did not develop the spatiotemporal response characteristics of simple cells, in which paired response peaks occur 180° out of phase in time and space. Complex cells that increased their spatial phase sensitivity at low contrasts were significantly overrepresented in the supragranular layers of cortex. We conclude that complex cells in supragranular layers of cat cortex have dynamic spatial summation properties and that the mechanisms underlying complex cell receptive fields differ between cortical layers.


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