1064 nm Raman Microscopy Using a Multifocal Excitation Pattern

摘要

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