1064 nm Raman microscopy using a multifocal excitation pattern

Haojie Ji, Marcos Oliveira, Che Wei Chang, James W. Chan

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Abstract

Raman microscopy is well recognized as a nondestructive, label-free biomedical imaging method that provides abundant chemical information of the specimen. Excitation wavelengths in deep near-infrared (e.g., 1064 nm) are used in certain situations, such as when analyzing photosensitive/photolabile specimens to suppress the strong fluorescence and to avoid photodamage. However, the speed and quality of 1064 nm Raman imaging suffers from the low scattering efficiency at this long excitation wavelength and the high noise level of InGaAs detectors. In this study, we investigated a multifocal patterned approach for 1064 nm Raman imaging. A 2-D Hadamard-coded multifocal array generated with X-Y scanning galvomirrors is used to excite and collect multiple Raman spectra simultaneously. The individual spectrum at each focus is retrieved and reconstructed from the superimposed spectra of the multifocal patterns. We demonstrate that the multifocal approach improves both the signal-to-noise ratio (SNR) and the imaging speed of Raman microscopy. Compared to the traditional point scan, at optimal detector conditions, the multifocal approach can be two-times faster for achieving the same image quality and SNR, or provides spectra with three-times higher SNR while applying the same energy dose at the focus. Such improvements of imaging speed and SNR increase up to one or two orders of magnitude under higher noise conditions, such as higher readout rate and higher detector temperatures. The multifocal approach presents advantages for certain imaging situations, such as when heating related damage limits the excitation energy dose that can be applied to the sample.

Original languageEnglish (US)
Title of host publicationLabel-Free Biomedical Imaging and Sensing (LBIS) 2020
EditorsNatan T. Shaked, Oliver Hayden
PublisherSPIE
ISBN (Electronic)9781510632653
DOIs
StatePublished - Jan 1 2020
EventLabel-Free Biomedical Imaging and Sensing ,LBIS 2020 - San Francisco, United States
Duration: Feb 1 2020Feb 4 2020

Publication series

NameProgress in Biomedical Optics and Imaging - Proceedings of SPIE
Volume11251
ISSN (Print)1605-7422

Conference

ConferenceLabel-Free Biomedical Imaging and Sensing ,LBIS 2020
CountryUnited States
CitySan Francisco
Period2/1/202/4/20

Keywords

  • Deep near-infrared
  • Multifocal
  • Raman microscopy

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Biomaterials
  • Atomic and Molecular Physics, and Optics
  • Radiology Nuclear Medicine and imaging

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  • Cite this

    Ji, H., Oliveira, M., Chang, C. W., & Chan, J. W. (2020). 1064 nm Raman microscopy using a multifocal excitation pattern. In N. T. Shaked, & O. Hayden (Eds.), Label-Free Biomedical Imaging and Sensing (LBIS) 2020 [1125104] (Progress in Biomedical Optics and Imaging - Proceedings of SPIE; Vol. 11251). SPIE. https://doi.org/10.1117/12.2546771