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Updated: Jan 26, 2026

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Measurement of Vacuolar and Cytosolic pH In Vivo in Yeast Cell Suspensions
Published on: April 19, 2013
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Deep-penetration fluorescence imaging through dense yeast cells suspensions using Airy beams
Optics Letters
|April 16, 2019
Summary
We developed a novel Airy beam scanning method to image fluorescent objects in scattering media. This technique offers higher resolution and signal-to-noise ratio compared to confocal imaging, even providing depth information.
Area of Science:
- Optics and Photonics
- Biomedical Imaging
- Microscopy
Background:
- Imaging through turbid media is challenging due to light scattering.
- Confocal microscopy suffers from reduced resolution and signal in scattering environments.
- Non-diffractive beams offer potential for deep tissue imaging.
Purpose of the Study:
- To introduce a new method for imaging fluorescent objects in turbid media using Airy beam scanning.
- To demonstrate the advantages of Airy beam scanning over conventional techniques like confocal imaging.
- To showcase the capability of depth information retrieval without additional sectioning.
Main Methods:
- Utilizing the non-diffractive property of Airy beams for light penetration.
- Employing Airy beam scanning for fluorescence imaging.
- Experimental validation using fluorescent microbeads in a yeast cell suspension.
Main Results:
- Achieved higher resolution and signal-to-noise ratio compared to confocal imaging.
- Successfully imaged 1 μm fluorescent beads at a depth of 90 μm in a scattering medium (51 cm-1).
- Demonstrated intrinsic depth localization capability of the technique.
Conclusions:
- Airy beam scanning is a promising technique for high-resolution fluorescence imaging in scattering biological tissues.
- The method overcomes limitations of traditional imaging techniques in turbid environments.
- This approach offers a new tool for in-situ depth-resolved imaging of fluorescent targets.
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