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<p>Magnetic resonance imaging (MRI) is a cornerstone of medical imaging, celebrated for its non-invasiveness, high spatial and temporal resolution, and exceptional soft tissue contrast, with over 100 million clinical procedures performed annually worldwide. In this field, MRI-based nanosensors have garnered significant interest in biomedical research due to their tunable sensing mechanisms, high permeability, rapid kinetics, and surface functionality. Extensive studies in the field have reported the use of superparamagnetic iron oxide nanoparticles (SPIONs) and proteins as a proof-of-concept for sensing critical neurochemicals via MRI. However, the signal change ratio and response rate of our SPION-protein-based in vitro dopamine and in vivo calcium sensors need to be further enhanced to detect the subtle and transient fluctuations in neurochemical levels associated with neural activities, starting from in vitro diagnostics. In this paper, we present an advanced reinforcement-learning-based computational model that treats sensor design as an optimal decision-making problem by choosing sensor performance as a weighted reward objective function. The adjustments of the SPION’s and protein’s three-dimensional configuration and magnetic moment establish a set of actions that can autonomously maximize the cumulative reward in the computational environment. Our new model first elucidates the sensor’s conformation alteration behind the increment in T<sub>2</sub> contrast observed experimentally in MRI in the presence and absence of calcium and dopamine neurochemicals. Additionally, our enhanced machine-learning algorithm can autonomously learn the performance trends of SPION-protein-based sensors and identify their optimal structural parameters. Experimental in vitro validation with TEM and MR relaxometry confirmed the predicted optimal SPION diameters, demonstrating the highest sensing performance at 9&#xa0;nm for calcium and 11&#xa0;nm for dopamine detection. Beginning with in vitro diagnostics, these results demonstrate a versatile modeling platform for the development of MRI-based neurochemical sensors, providing insights into their behavior under operational conditions. This platform also enables the autonomous design of improved sensor sizes and geometries, providing a roadmap for the future optimization of MRI sensors.</p>

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Automatic design and optimization of MRI-based neurochemical sensors via reinforcement learning

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年9月1日

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  • Zulaikha Ali,
  • Aaron Asparin,
  • Yunfei Zhang,
  • Hannah Mettee,
  • Diya Taha,
  • Yuna Ha,
  • Deepika Bhanot,
  • Khaldoon Sarwar,
  • Hamzah Kiran,
  • Shuo Wu,
  • He Wei

摘要

Magnetic resonance imaging (MRI) is a cornerstone of medical imaging, celebrated for its non-invasiveness, high spatial and temporal resolution, and exceptional soft tissue contrast, with over 100 million clinical procedures performed annually worldwide. In this field, MRI-based nanosensors have garnered significant interest in biomedical research due to their tunable sensing mechanisms, high permeability, rapid kinetics, and surface functionality. Extensive studies in the field have reported the use of superparamagnetic iron oxide nanoparticles (SPIONs) and proteins as a proof-of-concept for sensing critical neurochemicals via MRI. However, the signal change ratio and response rate of our SPION-protein-based in vitro dopamine and in vivo calcium sensors need to be further enhanced to detect the subtle and transient fluctuations in neurochemical levels associated with neural activities, starting from in vitro diagnostics. In this paper, we present an advanced reinforcement-learning-based computational model that treats sensor design as an optimal decision-making problem by choosing sensor performance as a weighted reward objective function. The adjustments of the SPION’s and protein’s three-dimensional configuration and magnetic moment establish a set of actions that can autonomously maximize the cumulative reward in the computational environment. Our new model first elucidates the sensor’s conformation alteration behind the increment in T2 contrast observed experimentally in MRI in the presence and absence of calcium and dopamine neurochemicals. Additionally, our enhanced machine-learning algorithm can autonomously learn the performance trends of SPION-protein-based sensors and identify their optimal structural parameters. Experimental in vitro validation with TEM and MR relaxometry confirmed the predicted optimal SPION diameters, demonstrating the highest sensing performance at 9 nm for calcium and 11 nm for dopamine detection. Beginning with in vitro diagnostics, these results demonstrate a versatile modeling platform for the development of MRI-based neurochemical sensors, providing insights into their behavior under operational conditions. This platform also enables the autonomous design of improved sensor sizes and geometries, providing a roadmap for the future optimization of MRI sensors.