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A CMOS active pixel sensor system for laboratory- based x-ray diffraction studies of biological tissue
Sarah E Bohndiek1, Emily J Cook, Costas D Arvanitis
1Department of Medical Physics and Bioengineering, University College London, London, UK. bohndiek@medphys.ucl.ac.uk
Physics in Medicine and Biology
|January 18, 2008
Summary
A novel CMOS active pixel sensor (APS) demonstrates feasibility for X-ray diffraction, offering a promising digital detector for material-specific biological tissue analysis. This technology could advance medical imaging applications.
Area of Science:
- Medical Imaging
- Materials Science
- Biophysics
Background:
- X-ray diffraction (XRD) provides crucial material-specific data for biological tissues.
- Current digital X-ray detectors often lack the required large area, low noise, and wide dynamic range for laboratory XRD.
- Advancements in detector technology are needed for enhanced laboratory-based XRD applications.
Purpose of the Study:
- To introduce and demonstrate the feasibility of CMOS active pixel sensor (APS) technology for coherent scatter imaging.
- To evaluate the potential of APS as a digital X-ray detector for material-specific biological tissue analysis.
- To assess APS performance in angle dispersive X-ray diffraction (ADXRD) for medical applications.
Main Methods:
- A prototype CMOS APS was integrated into an X-ray diffraction system utilizing an industrial X-ray source and beam filtration.
- Experimental setup, including collimator options and detector parameters, was optimized for ADXRD.
- Scatter signatures were measured for 11 materials relevant to breast cancer diagnosis, kidney stone identification, and bone mineral density.
Main Results:
- The APS successfully recorded biologically relevant coherent scatter signatures for various materials and mixed samples.
- Experimental results were validated against two independent predictive models (linear systems model and linear superposition integral).
- Coherent scatter signatures demonstrated sensitivity to sample composition, enabling quantification.
Conclusions:
- CMOS APS technology shows significant potential for fulfilling the requirements of laboratory-based X-ray diffraction studies.
- The ability to quantify sample composition using coherent scatter signatures opens new diagnostic avenues.
- Future development of bespoke APS imagers could facilitate clinical translation of coherent scatter X-ray diffraction.

