Broadband backscattering confocal microscopy enables label-free 3D live cell nanoscale sensitive imaging

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Authors: Mark F. Coughlan, Lei Zhang, Rebecca T. Perelman, Umar Khan, Xuejun Zhang, Paul Kumar Upputuri, Yuri N. Zakharov, Le Qiu, Lev T. Perelman
Cited by: 1
References: 44

Abstract

Fluorescence microscopy is a cornerstone of biological research. However, fluorescent labeling is challenging in live cells and is constrained by photobleaching and phototoxicity. Label-free methods allow cells to be studied in their native state, but most techniques have poor contrast, lack 3D capability, rely on complex optics, and fail to provide structural information. We present broadband backscattering confocal microscopy (BBCM), which employs a broadband supercontinuum laser and collects backscattered light in confocal geometry using a photomultiplier tube. Broadband illumination averages out size-dependent oscillations that confound monochromatic backscattering. This eliminates blind spots and intensity ambiguities, allowing all scatterers to be visible, with the signal increasing approximately linearly with scatterer size. BBCM is easy to retrofit to standard confocal microscopes, requires no specialized optics, and is straightforward for nonspecialists. It enables high-contrast, label-free 3D imaging of live cells with size sensitivity to subcellular structures without employing custom optics or complex data processing.

Fields of Study & Subjects

Advanced Fluorescence Microscopy Techniques Random lasers and scattering media Advanced Optical Sensing Technologies

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Publication date
4 February 2026
Language
EN
Document type
Preprint