Optical diffraction tomography techniques for the study of cell pathophysiology
arXiv:1603.00592
Abstract
Three-dimensional imaging of biological cells is crucial for the investigation of cell biology, provide valuable information to reveal the mechanisms behind pathophysiology of cells and tissues. Recent advances in optical diffraction tomography (ODT) have demonstrated the potential for the study of various cells with its unique advantages of quantitative and label-free imaging capability. To provide insight on this rapidly growing field of research and to discuss its applications in biology and medicine, we present the summary of the ODT principle and highlight recent studies utilizing ODT with the emphasis on the applications to the pathophysiology of cells.
References in corpus (10)
- Measuring the Transmission Matrix in Optics : An Approach to the Study and Control of Light Propagation in Disordered Media
- Recent advances in wavefront shaping techniques for biomedical applications
- Active illumination using a digital micromirror device for quantitative phase imaging
- Optical diffraction tomography using a digital micromirror device for stable measurements of 4-D refractive index tomography of cells
- Diffraction microtomography with sample rotation: influence of a missing apple core in the recorded frequency space
- 3-D refractive index tomograms and deformability of individual human red blood cells from cord blood of newborn infants and maternal blood
- The Theory of Diffraction Tomography
- Single-cell diffraction tomography with optofluidic rotation about a tilted axis
- Alterations in cell surface area and deformability of individual human red blood cells in stored blood
- Diffraction tomography with Fourier ptychography
Cited by in corpus (3)
- Tomographic active optical trapping of arbitrarily shaped objects by exploiting 3-D refractive index maps
- Deep learning-enabled image quality control in tomographic reconstruction: Robust optical diffraction tomography
- Three-dimensional label-free imaging and quantification of lipid droplets in live hepatocytes