Evidence map›Paper›PMID 40459854›Full record

ArticleAnalytical chemistry2025

A Novel Spectral Barcoding and Classification Approach for Complex Biological Samples Using Multiexcitation Raman Spectroscopy (MX-Raman).

George Devitt, Niall Hanrahan, Miguel Ramírez Moreno, Amrit Mudher, Sumeet Mahajan

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Article in Analytical chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

George DevittSchool of Biological Sciences, University of Southampton, Highfield Campus, SO17 1BJ Southampton, U.K.ORCID 0000-0001-7179-4459
Niall HanrahanSchool of Chemistry and Chemical Engineering, University of Southampton, Highfield Campus, SO17 1BJ Southampton, U.K.ORCID 0000-0002-3596-7049
Miguel Ramírez MorenoSchool of Biological Sciences, University of Southampton, Highfield Campus, SO17 1BJ Southampton, U.K.ORCID 0000-0003-1559-8976
Amrit MudherSchool of Biological Sciences, University of Southampton, Highfield Campus, SO17 1BJ Southampton, U.K.
Sumeet MahajanSchool of Chemistry and Chemical Engineering, University of Southampton, Highfield Campus, SO17 1BJ Southampton, U.K.ORCID 0000-0001-8923-6666

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the development and application of a novel spectral barcoding approach that exploits our multiexcitation (MX) Raman spectroscopy-based methodology for improved label-free detection and classification of complex biological samples. To develop our improved MX-Raman methodology, we utilized post-mortem brain tissue from several neurodegenerative diseases (NDDs) that have considerable clinical overlap. For improving our methodology we used three sources of spectral information arising from distinct physical phenomena to assess which was most important for NDD classification. Spectral measurements utilized combinations of data from multiple, distinct excitation laser wavelengths and polarization states to differentially probe molecular vibrations and autofluorescence signals. We demonstrate that the more informative MX-Raman (532 nm-785 nm) spectra are classified with 96.7% accuracy on average, compared to conventional single-excitation Raman spectroscopy that resulted in 78.5% accuracy (532 nm) or 85.6% accuracy (785 nm) using linear discriminant analysis (LDA) on 5 NDD classes. By combining information from distinct laser polarizations we observed a nonsignificant increase in classification accuracy without the need of a second laser (785 nm-785 nm polarized), whereas combining Raman spectra with autofluorescence signals did not increase classification accuracy. Finally, by filtering out spectral features that were redundant for classification or not descriptive of disease class, we engineered spectral barcodes consisting of a minimal subset of highly disease-specific MX-Raman features that improved the unsupervised and cross-validated clustering of MX-Raman spectra. The results demonstrate that increasing spectral information content using our optical MX-Raman methodology enables enhanced identification and distinction of complex biological samples but only when that information is independent and descriptive of class. The future translation of such technology to biofluids could support diagnosis and stratification of patients living with dementia and potentially other clinical conditions such as cancer and infectious disease.

Indexed as

Neurodegenerative DiseasesSpectrum Analysis, RamanBrainDiscriminant AnalysisHumans

Identifiers

PMID40459854
PMCPMC12177875

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.