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Updated: Jun 30, 2026

Non-contact, Label-free Monitoring of Cells and Extracellular Matrix using Raman Spectroscopy
Published on: May 29, 2012
Integrating Artificial Intelligence with Ramanomics for Label-Free Monitoring of Biochemical Environment in Live
Varun Chandola1, Andrey N Kuzmin2, Artem Pliss3
1Department of Computer Science and Engineering, University at Buffalo, State University of New York, Buffalo, New York 14260-3000, United States.
Abstract:
Raman spectrometry, with its capability to noninvasively characterize the molecular composition of microscopic subcellular volumes, including single organelles in live cells, has revolutionized cell biology research. Being introduced as a label-free approach for biochemical imaging, the practical applications of Raman spectrometry still often include the fluorescence probes for the localization of organelles and other subcellular domains of interest. Aiming to overcome this limitation, we report on the development of an artificial intelligence/machine learning approach for true label-free identification of different types of subcellular structures. Here, we explore the application of machine learning (ML) to learn the relationship between a set of biochemical parameters in single organelles of live cells. The biochemical parameters are extracted by Ramanomics, an optical Omics technology, from Raman spectra of single organelles of live cells of different cell lines. Several classification algorithms, such as neural networks, Random Forests, support vector machines, logistic regression, and Gaussian process classification, are evaluated. We report the performance of the best classifier, a shallow neural network, to classify the type of organelle using the biochemical parameters. Evaluation is done using k-fold cross-validation (k = 10), and the final output classification is compared against the ground truth. The k-fold cross-validation shows that the NN-based classifier has significant accuracy (∼90%) to distinguish between different organelles using Ramanomics measurements. Our approach allows us to identify the precise location of separate organelles by local Raman measurement without labeling.
