Abstract

Coherent anti-Stokes Raman microscopy (CARS) is a quantitative, chemically specific, and label-free optical imaging technique for studying inhomogeneous systems. However, the complicating influence of the nonresonant response on the CARS signal severely limits its sensitivity and specificity and especially limits the extent to which CARS microscopy has been used as a fully quantitative imaging technique. On the basis of spectral focusing mechanism, we establish a dual-soliton Stokes based CARS microspectroscopy and microscopy scheme capable of quantifying the spatial information of densities and chemical composition within inhomogeneous samples, using a single fiber laser. Dual-soliton Stokes scheme not only removes the nonresonant background but also allows robust acquisition of multiple characteristic vibrational frequencies. This all-fiber based laser source can cover the entire fingerprint (800-2200 cm-1) region with a spectral resolution of 15 cm-1. We demonstrate that quantitative degree determination of lipid-chain unsaturation in the fatty acids mixture can be achieved by the characterization of C = C stretching and CH2 deformation vibrations. For microscopy purposes, we show that the spatially inhomogeneous distribution of lipid droplets can be further quantitatively visualized using this quantified degree of lipid unsaturation in the acyl chain for contrast in the hyperspectral CARS images. The combination of compact excitation source and background-free capability to facilitate extraction of quantitative composition information with multiplex spectral peaks will enable wider applications of quantitative chemical imaging in studying biological and material systems.

Highlights

  • Raman microscopy has been extremely successful in visualizing the chemical changes and distribution of species within soft and complex materials, including polymeric and biological samples, as a powerful label-free technique [1,2]

  • DSCARS spectra of polyethylene glycol terephthalate (PET) is almost identical to its spontaneous counterparts except for relative intensity differences at low and high wavenumbers due to decreased pulse overlap [10]

  • The realization of such a powerful combination is obtained through dual-soliton pulses based on a single fiber laser source under the spectral focusing mechanism

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Summary

Introduction

Raman microscopy has been extremely successful in visualizing the chemical changes and distribution of species within soft and complex materials, including polymeric and biological samples, as a powerful label-free technique [1,2]. Successful techniques for microscopy include coherent anti-Stoke Raman scattering (CARS) microscopy [5] and stimulated Raman scattering (SRS) microscopy [6] In both cases, video-rate imaging of single Raman bands can be achieved with narrow spectral bandwidth [7,8], but suffers from limitations in breadth and speed of laser tuning rates. With respect to the multiplex or broadband CARS or SRS spectroscopy and imaging, there is considerably more information contained throughout an entire spectrum than at just a single frequency within that spectrum [9,10] This advantage is more useful for qualitative discrimination of many overlapping peaks, in general, and more amenable to quantitative analysis of variations in the spatial distribution of different molecules in the sample

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