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Updated: Feb 26, 2026

High Spatial Resolution Chemical Imaging of Implant-Associated Infections with X-ray Excited Luminescence Chemical Imaging Through Tissue
Published on: September 30, 2022
Sensitivity evaluation and selective plane imaging geometry for x-ray-induced luminescence imaging
Bryan P Quigley1, Corey D Smith1, Shih-Hsun Cheng1
1Department of Radiology, The University of Chicago, Chicago, IL, 60637, USA.
Selective plane X-ray-induced luminescence (SPXIL) improves deep tissue imaging of nanophosphors for radiotherapy. This novel geometry and imaging model accurately reconstruct nanophosphor distributions, enhancing potential theranostic applications.
Area of Science:
- Hybrid imaging modalities
- Nanoparticle-based theranostics
- Optical imaging in scattering media
Background:
- X-ray-induced luminescence (XIL) uses nanophosphors for imaging and potential radiotherapy applications.
- Current XIL methods face limitations in determining deep nanophosphor distributions due to signal attenuation in scattering tissues.
- Developing robust imaging models is crucial for extracting clinical information from XIL signals.
Purpose of the Study:
- To introduce and validate a novel imaging geometry, selective plane XIL (SPXIL), for improved depth sensitivity.
- To develop and calibrate an imaging model for determining nanophosphor distributions from surface radiance measurements.
- To assess the dose-dependent sensitivity and depth limitations of XIL in diffuse optical environments.
Main Methods:
- An analytical imaging model based on selective plane geometry was developed for homogeneous, semi-infinite media.
- Y₂O₃:Eu³⁺ nanophosphors were synthesized and characterized for luminescent properties and response to X-ray dose.
- SPXIL imaging was performed on optical gel phantoms, and nanophosphor distributions were reconstructed using Richardson-Lucy deconvolution.
Main Results:
- Y₂O₃:Eu³⁺ nanophosphors exhibited optimal emission at 611 nm with linear and quadratic responses to X-ray current/voltage and concentration.
- Luminescence efficiency was determined to be 1.06 photons per keV of absorbed X-ray radiation per g/mL of nanophosphor.
- SPXIL imaging successfully resolved sources 1 cm apart up to 1.75 cm depth, with sensitivity simulations indicating detection at 2-4 cm depth for 1 mg/mL concentration and 1 cGy dose.
Conclusions:
- The novel SPXIL geometry and associated imaging model provide a robust method for XIL in diffuse optical environments.
- Experimental validation in phantoms and sensitivity simulations demonstrate the potential of SPXIL for deep-tissue imaging.
- SPXIL shows promise for advancing nanophosphor-based applications in radiotherapy, such as theranostics and nanodosimetry.
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