Multifocal structured illumination optoacoustic microscopy

Zhenyue Chen; Ali Özbek; Johannes Rebling; Quanyu Zhou; Xosé Luís Deán-Ben; Daniel Razansky

doi:10.1038/s41377-020-00390-9

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Multifocal structured illumination optoacoustic microscopy

Original Articles

- Multifocal structured illumination optoacoustic microscopy
- Multifocal structured illumination optoacoustic microscopy
- LSA 2020年9卷第5期页码：1473-1481
- Affiliations：
  
  Institute for Biomedical Engineering and Institute of Pharmacology and Toxicology, University of Zurich and ETH Zurich, Zurich, Switzerland
- Author bio：
  
  Daniel Razansky (daniel.razansky@uzh.ch)
- Funds：
- DOI：10.1038/s41377-020-00390-9
  中图分类号：
- 纸质出版日期：2020，
  
  网络出版日期：2020-08-31，
  
  收稿日期：2020-04-03，
  
  修回日期：2020-08-15，
  
  录用日期：2020-08-18
- Accepted：
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Multifocal structured illumination optoacoustic microscopy[J]. LSA, 2020,9(5):1473-1481.

Chen, Z. Y. et al. Multifocal structured illumination optoacoustic microscopy. Light: Science & Applications, 9, 1473-1481 (2020).
Multifocal structured illumination optoacoustic microscopy[J]. LSA, 2020,9(5):1473-1481. DOI： 10.1038/s41377-020-00390-9.

Chen, Z. Y. et al. Multifocal structured illumination optoacoustic microscopy. Light: Science & Applications, 9, 1473-1481 (2020). DOI： 10.1038/s41377-020-00390-9.

摘要

Abstract

Optoacoustic (OA) imaging has the capacity to effectively bridge the gap between macroscopic and microscopic realms in biological imaging. High-resolution OA microscopy has so far been performed via point-by-point scanning with a focused laser beam

thus greatly restricting the achievable imaging speed and/or field of view. Herein we introduce multifocal structured illumination OA microscopy (MSIOAM) that attains real-time 3D imaging speeds. For this purpose

the excitation laser beam is shaped to a grid of focused spots at the tissue surface by means of a beamsplitting diffraction grating and a condenser and is then scanned with an acousto-optic deflector operating at kHz rates. In both phantom and in vivo mouse experiments

a 10 mm wide volumetric field of view was imaged with 15 Hz frame rate at 28 μm spatial resolution. The proposed method is expected to greatly aid in biological investigations of dynamic functional

kinetic

and metabolic processes across multiple scales.

关键词

Keywords

references

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