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February 22, 2026Journal of Synchrotron Radiation0 citationsOpen Access

Multifunctional bending magnet beamline with a capillary optic for X-ray fluorescence studies of metals in tissue sections

BRBenjamin RoterACAndrew M. CrawfordQJQi Jin

Key Points

  • The research aims to describe a multifunctional beamline for improved X-ray fluorescence imaging of metals in biological tissues.
  • Utilized the bending magnet beamline 8-BM-B at the Advanced Photon Source.
  • Incorporated two microscopy stations: one with Kirkpatrick–Baez optics and a prototype with capillary optic.
  • Estimated spatial resolution and analyzed fluorescence spectral data.
  • Achieved spatial resolution of 10.5 µm for the KB station at 100 ms dwell time.
  • Achieved 6.5 µm spatial resolution for the capillary optic station at 50 ms dwell time.
  • Fluence rates were similar, indicating efficiency of both stations for imaging.

Abstract

Scanning fluorescence X-ray microscopy lets one non-destructively and quantitatively map the distribution of most biologically important metals in cells and tissues. For studies on large-scale tissues and organs, a spatial resolution of several micrometres is often sufficient; in this case, bending magnets at synchrotron light sources provide abundant X-ray flux. We describe here the use of bending magnet beamline 8-BM-B at the Advanced Photon Source with two distinct microscopy stations: a pre-existing one with Kirkpatrick–Baez (KB) mirror optics for slightly higher throughput and the ability to accommodate samples tens of centimetres across, and a new prototype station with an axially symmetric, single-bounce, capillary optic with slightly less flux, but finer resolution at similar fluence per time. The KB station provides δ res = 10.5 µm spatial resolution at a per-pixel exposure time of t dwell = 100 ms and a fluence per time of 5.8 × 10 7 photons µm −2 s −1 , while the prototype capillary station provides δ res = 6.5 µm at t dwell = 50 ms and a fluence per time of 5.6 × 10 7 photons µm −2 s −1 . We used image power spectral density to estimate the achieved spatial resolution δ res from individually acquired images, with δ res depending on the optic, the fluorescence signal strength of the sample being imaged, and the method used to process raw fluorescence spectral data.

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Cite This Study

Roter et al. (2026) studied this question.

synapsesocial.com/papers/699a9ceb482488d673cd299ahttps://doi.org/10.1107/s1600577526000925
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