The detection of deep‐seated lesions is of great significance for biomedical applications. However, due to the strong photon absorption and scattering of biological tissues, it is challenging to realize in… Click to show full abstract
The detection of deep‐seated lesions is of great significance for biomedical applications. However, due to the strong photon absorption and scattering of biological tissues, it is challenging to realize in vivo deep optical detections, particularly for those using the safe laser irradiance below clinical maximum permissible exposure (MPE). In this work, the combination of ultra‐bright surface‐enhanced Raman scattering (SERS) nanotags and transmission Raman spectroscopy (TRS) is reported to achieve the non‐invasive and photosafe detection of “phantom” lesions deeply hidden in biological tissues, under the guidance of theoretical calculations showing the importance of SERS nanotags’ brightness and the expansion of laser beam size. Using a home‐built TRS system with a laser power density of 0.264 W cm−2 (below the MPE criteria), we successfully demonstrated the detection of SERS nanotags through up to 14‐cm‐thick ex vivo porcine tissues, as well as in vivo imaging of “phantom” lesions labeled by SERS nanotags in a 1.5‐cm‐thick unshaved mouse under MPE. This work highlights the potential of transmission Raman‐guided identification and non‐invasive imaging toward clinically photosafe cancer diagnoses.
               
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