Combining lateral shear interferometry with digital holography for quantitative phase microscopy

2006 ◽  
Author(s):  
P. Ferraro ◽  
D. Alfieri ◽  
S. De Nicola ◽  
L. De Petrocellis ◽  
A. Finizio ◽  
...  
Keyword(s):  
Digital Holography ◽  
Lateral Shear ◽  
Quantitative Phase ◽  
Phase Microscopy ◽  
Quantitative Phase Microscopy ◽  
Lateral Shear Interferometry

Quantitative phase microscopy using dual-plane in-line digital holography

2012 ◽  
Vol 51 (9) ◽  
pp. 1387 ◽  
Author(s):  
Bhargab Das ◽  
Chandra S. Yelleswarapu ◽  
D. V. G. L. N. Rao
Keyword(s):  
Digital Holography ◽  
Dual Plane ◽  
Quantitative Phase ◽  
Phase Microscopy ◽  
Quantitative Phase Microscopy

scholarly journals Quantitative phase microscopy with asynchronous digital holography

2007 ◽  
Vol 15 (6) ◽  
pp. 3047 ◽  
Author(s):  
Kevin J. Chalut ◽  
William J. Brown ◽  
Adam Wax
Keyword(s):  
Digital Holography ◽  
Quantitative Phase ◽  
Phase Microscopy ◽  
Quantitative Phase Microscopy

scholarly journals Characterization of Liposomes Using Quantitative Phase Microscopy (QPM)

Pharmaceutics ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 590
Author(s):  
Jennifer Cauzzo ◽  
Nikhil Jayakumar ◽  
Balpreet Singh Ahluwalia ◽  
Azeem Ahmad ◽  
Nataša Škalko-Basnet
Keyword(s):  
Rapid Development ◽  
Fluorescent Labeling ◽  
Label Free ◽  
Batch Mode ◽  
Full Field ◽  
Quantitative Phase ◽  
Phase Microscopy ◽  
Quantitative Phase Microscopy ◽  
Tracking Ability

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.

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