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Antoine M. Snijders

Publications and source records attributed to Antoine M. Snijders.

3 recordsLinked to original sources

Radiation damage to normal mammalian tissue in vivo with laser-driven protons at ultra-high instantaneous dose rate

The differential sparing of normal tissues relative to tumor control observed at ultra-high dose rates, referred to as the FLASH effect, has recently gained considerable attention. The therapeutic advantages of FLASH radiotherapy are expected to be further amplified through the use of protons and ions, which enable precise dose deposition at tumor depth while minimizing irradiation of healthy tissues proximal and distal to the target. Nevertheless, the mechanism underlying this sparing effect remains poorly understood. Laser-driven proton accelerators are capable of delivering uniquely high instantaneous dose rates in ultrashort bunches. Here, we report the first in vivo investigation of normal tissue response to laser-driven proton irradiation, with exposures to 8 MeV protons, delivering total doses up to 50 Gy at 2 Gy per laser shot. Our findings reveal a reduction in tissue swelling following laser-driven proton treatment compared with X-ray irradiations at conventional dose rates. RNA sequencing identified differential gene expression associated with immune and epidermal programs following laser-driven proton irradiations at two different dose levels.

physics.med-ph↗

Design Optimization of Permanent-Magnet Based Compact Transport Systems for Laser-Driven Proton Beams

Laser-driven (LD) ion acceleration has been explored in a newly constructed short focal length beamline at the BELLA petawatt facility (interaction point 2, iP2). For applications utilizing such LD ion beams, a beam transport system is required, which for reasons of compactness be ideally contained within 3 m. The large divergence and energy spread of LD ion beams present a unique challenge to transporting them compared to beams from conventional accelerators. This work gives an overview of proposed compact transport designs that can satisfy different requirements depending on the application for the iP2 proton beamline such as radiation biology, material science, and high energy density science. These designs are optimized for different parameters such as energy spread and peak proton density according to an application's need. The various designs consist solely of permanent magnet elements, which can provide high magnetic field gradients on a small footprint. While the field strengths are fixed, we have shown that the beam size and energy can be tuned effectively by varying the placement of the magnets. The performance of each design was evaluated based on high order particle tracking simulations of typical LD proton beams. A more detailed investigation was carried out for a design to deliver 10 MeV LD accelerated ions for radiation biology applications. With these transport system designs, the iP2 beamline is ready to house various application experiments.

physics.acc-ph↗

Union of Intersections (UoI) for Interpretable Data Driven Discovery and Prediction

The increasing size and complexity of scientific data could dramatically enhance discovery and prediction for basic scientific applications. Realizing this potential, however, requires novel statistical analysis methods that are both interpretable and predictive. We introduce Union of Intersections (UoI), a flexible, modular, and scalable framework for enhanced model selection and estimation. Methods based on UoI perform model selection and model estimation through intersection and union operations, respectively. We show that UoI-based methods achieve low-variance and nearly unbiased estimation of a small number of interpretable features, while maintaining high-quality prediction accuracy. We perform extensive numerical investigation to evaluate a UoI algorithm ($UoI_{Lasso}$) on synthetic and real data. In doing so, we demonstrate the extraction of interpretable functional networks from human electrophysiology recordings as well as accurate prediction of phenotypes from genotype-phenotype data with reduced features. We also show (with the $UoI_{L1Logistic}$ and $UoI_{CUR}$ variants of the basic framework) improved prediction parsimony for classification and matrix factorization on several benchmark biomedical data sets. These results suggest that methods based on the UoI framework could improve interpretation and prediction in data-driven discovery across scientific fields.

stat.ML↗