Phase Imaging Microscopy: Beyond Dark-Field, Phase Contrast, and Differential Interference Contrast Microscopy
Chrysanthe Preza, Sharon V. King, Nicoleta Dragomir, Carol J. Cogswell
Abstract
Chrysanthe Preza, Sharon V. King, Nicoleta Dragomir, Carol J. Cogswell
Abstract
Biomedical applications aimed toward understanding livecell dynamics have rekindled an interest in optical microscope modes that may provide additional information beyond the widely used ¦uorescence modalities that include confocal, structured illumination microscopy, multiphoton, and STED imaging. e three microscope modes discussed in this chapter-dark-eld, phase contrast, and dierential interference contrast (DIC) microscopy-are techniques that readily address the challenges of live-cell imaging. eir ability to image cell structure dynamics without having to introduce any chemical probes or dyes can be of great advantage in ensuring that cell function is not being altered. In addition, the ability to observe living cells over time, without introducing the potentially damaging eects of high-intensity light sources, oered by these techniques is o²en desirable for many biological investigations.
OpenAlex reports 6 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Biomedical applications aimed toward understanding livecell dynamics have rekindled an interest in optical microscope modes that may provide additional information beyond the widely used ¦uorescence modalities that include confocal, structured illumination microscopy, multiphoton, and STED imaging. e three microscope modes discussed in this chapter-dark-eld, phase contrast, and dierential interference contrast (DIC) microscopy-are techniques that readily address the challenges of live-cell imaging. eir ability to image cell structure dynamics without having to introduce any chemical probes or dyes can be of great advantage in ensuring that cell function is not being altered. In addition, the ability to observe living cells over time, without introducing the potentially damaging eects of high-intensity light sources, oered by these techniques is o²en desirable for many biological investigations.
Key concepts: Differential interference contrast microscopy, Phase contrast microscopy, Dark field microscopy, Microscopy, Contrast (vision), Bright-field microscopy, Interference microscopy, Phase (matter)