Relevance of light conditions for clinical in situ Raman spectroscopy

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Contributors

Abstract

BACKGROUND: Clinical Raman spectroscopy is a promising optical technology for intraoperative brain tumor delineation and diagnosis. As it exploits weak signals, illumination of the operating room (OR) and OR devices might impact the acquired spectra. The aim of this study was to investigate which optical artifacts can be tolerated during the intraoperative analysis of brain tumors in situ while still allowing the extraction of meaningful Raman spectra.

METHODS: Tissue samples of rat brain and human brain tumors were investigated in an experimental OR, and background signals and Raman spectroscopic datasets were acquired using a fiber-based system. The measurements were performed under various lighting conditions and OR equipment.

RESULTS: Ceiling light intensity increased the background, which could be prevented by manual coverage. Hence, the signal-to-noise-ratio of Raman spectra was not altered by ceiling lights. The intensity of the raw spectra of brain tissue and glioma was determined mainly by tissue autofluorescence and not by OR illumination, but it substantially affected the raw spectra of meningioma having low autofluorescence. Operating (OP) lights lead to saturation of the Raman camera. The exoscope, displays, and optical neuronavigation systems produced spectrally structured artifacts. Correct background subtraction was sufficient for artifact correction and obtaining valid Raman spectra.

CONCLUSIONS: For clinical Raman spectroscopy, it is of utmost importance to be aware of optical disturbances. Intense illumination needs to be avoided but (spectrally structured) disturbances can be corrected by data preprocessing. Rather than external illumination, strong tissue autofluorescence might lead to impaired Raman spectral quality, making tumor tissue recognition difficult.

Details

Original languageEnglish
Article number1850523
JournalFrontiers in Oncology
Volume16
Publication statusPublished - 27 Jul 2026
Peer-reviewedYes

External IDs

ORCID /0000-0001-5084-1180/work/222089373
ORCID /0000-0002-0633-0321/work/222089439
ORCID /0000-0002-6603-5375/work/222089462
unpaywall 10.3389/fonc.2026.1850523
PubMed 42577048

Keywords