4.6 Article

A Fast Fluorescence Background Suppression Method for Raman Spectroscopy Based on Stepwise Spectral Reconstruction

Journal

IEEE ACCESS
Volume 6, Issue -, Pages 67709-67717

Publisher

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/ACCESS.2018.2879160

Keywords

Biomedical signal processing; Raman spectroscopy; fluorescence suppression; Raman imaging

Funding

  1. National Natural Science Foundation of China [61605025, 61501101]
  2. Science and Technology Foundation of National Defense Key Laboratory [61424080209]
  3. Program for Innovation Talents in Universities of Liaoning Province [LR2016031]
  4. Fundamental Research Funds for the Central Universities [N171902001]
  5. Ministry of Education in Singapore [MOE2015-T2-2-112]
  6. NTU-AIT-MUV Programme in advanced biomedical imaging [NAM/15004]

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Raman spectroscopy is a rapid and non-destructive technique for detecting unique spectral fingerprints from biological samples. Raw Raman spectra often come with strong fluorescence background that makes spectral interpretation challenging. Although fluorescence background can be suppressed experimentally, this approach requires sophisticated and costly instruments. For convenience and cost-effectiveness, numerical methods have been used frequently to remove fluorescence background. Unfortunately, many of such methods suffer from long computation time. Therefore, a fast numerical method for fluorescence suppression is highly desirable especially in Raman spectroscopic imaging where Raman measurements from many pixels need to be processed rapidly. In response to this demand, we propose a fast numerical method for fluorescence background suppression based on the strategy of stepwise spectral reconstruction that we previously developed. Compared with traditional computational methods, including polynomial fitting, wavelet transform, Fourier transform, and peak detection, our results consistently show significant advantages in both accuracy and computational efficiency when tested on Raman spectra measured from phantoms and cells as well as surfaced enhanced Raman spectra from blood serum samples. In particular, our method yields clean Raman spectra closest to the reference results generated by polynomial fitting while several orders of magnitude faster than others. Therefore, the proposed fast fluorescence suppression method is promising in Raman spectroscopic imaging or related application in which high-computation efficiency is critical and a calibration dataset is available.

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