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January 20, 2026Analytical Chemistry2 citations

Azo-Enhanced Raman Rotors: Bridging Raman Scattering and Fluorescence for Hyperspectral Imaging of Live-Cell Microviscosity Dynamics

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WXWanyi XieYYYajun YuYPYaping Peng

Key Points

  • The aim is to develop azo-enhanced Raman rotors for hyperspectral imaging to measure microviscosity dynamics in live cells.
  • Designed and fine-tuned azobenzene derivatives for dual-use as Raman reporters and fluorescence emitters.
  • Employed a hyperspectral imaging system to capture both Raman and fluorescence signals.
  • Analyzed the fluorescence-versus-Raman intensity ratio to quantify microviscosity changes in organelles.
  • Successfully demonstrated simultaneous detection of Raman scattering and fluorescence in live cells.
  • Provided self-calibrated readouts for accurate microviscosity visualization within structures like mitochondria and lysosomes.
  • Established a robust methodology for investigating physicochemical heterogeneity in biological systems.

Abstract

Azobenzene derivatives are well-known molecular photoswitches that undergo tunable changes in the geometry, dipole moment, and electronic structure upon light irradiation. While their tunable absorption and fluorescence have inspired diverse applications in sensing various physical and chemical environments, recent advances have shown that azobenzene conjugates also serve as powerful Raman reporters through azo-enhanced Raman scattering. Although Raman scattering, a narrow-band vibrational signature, and fluorescence, a broadband electronic emission, are both valuable photophysical processes, their distinct energy-level transitions pose challenges for simultaneously interpreting both signals in a single measurement, especially for measuring heterogeneous biological systems. In this study, we fine-tuned a class of azo-enhanced Raman rotors for hyperspectral imaging and leveraged their fluorescence-versus-Raman intensity ratio to report microviscosity in live cells. This approach provides self-calibrated readouts, enabling accurate visualization of microviscosity changes within organelles, such as mitochondria, lysosomes, and the endoplasmic reticulum. Our findings demonstrate an effective strategy to bridge the spectral gap between Raman scattering and fluorescence, offering a robust method for probing physicochemical heterogeneity in biological systems. The ability to simultaneously harness both photophysical processes in a single molecular platform opens new avenues for advanced hyperspectral bioimaging, cellular diagnostics, and mechanistic studies of heterogeneous nonbiological interfaces.

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Cite This Study

Xie et al. (2026) studied this question.

synapsesocial.com/papers/696f1a849e64f732b51eec1fhttps://doi.org/10.1021/acs.analchem.5c04681
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