Traceable and Reproducible 3D Magnetic Field Mapping for Data-Driven Magnetic Drug Targeting

Authors

  • Robert-Leonard BERNAD Faculty of Automation and Computers, Politehnica University Timişoara
  • Radu CARAGIN-CRASOVAN Faculty of Automation and Computers, Politehnica University Timişoara
  • Lăcrimioara STOICU-TIVADAR Faculty of Automation and Computers, Politehnica University Timişoara
  • Mihaela CRISAN-VIDA Faculty of Automation and Computers, Politehnica University Timişoara
  • Sandor Ianos BERNAD Centre for Fundamental and Advanced Technical Research, Romanian Academy Timişoara Branch

Keywords:

Medical informatics, Magnetic drug targeting, Reproducible measurements, Magnetic field mapping, Data quality, Experimental standardization

Abstract

Background: Magnetic Drug Targeting (MDT) aims to localise drugs while minimising systemic toxicity in vascular disease, localised tumours, and site-specific inflammatory conditions. MDT safety and efficacy depend on accurate three-dimensional magnetic-field distributions and gradients governing particle transport, capture efficiency, and off-target exposure. Automated three-dimensional field mapping is often affected by motion-related uncertainties—such as scale errors, drift, misalignment, and load effects—leading to non-deterministic datasets and biased gradients that limit data reuse, interoperability, and reproducibility. Objective: To develop and describe an automated three-dimensional magnetic-field mapping infrastructure serving as a data acquisition and quality-assurance layer for MDT medical informatics workflows, delivering traceable, reproducible, analysis-ready magnetic-field inputs integrable into computational modelling, digital twin frameworks, and data-driven decision support systems. Methods: The workflow implements controlled, high-accuracy three-dimensional magnetic-field acquisition through coordinated motion control, optical referencing, and calibration under operational load. Laser-assisted positioning establishes repeatable spatial registration between the magnetic source and the field sensor, while automated motion execution ensures deterministic sampling over a predefined grid. Motion integrity is monitored through closed-loop feedback to detect scale deviations, tracking errors, and mechanical drift. Prior to acquisition, axis scaling and alignment are calibrated using optical reference markers to compensate for load-dependent uncertainties. Magnetic-field values are acquired at each sampling node via automated optical digitisation of a calibrated digital teslameter, followed by confidence scoring, unit normalisation, and structured logging to ensure traceability. Results: The workflow produces consistent, reproducible volumetric magnetic-field datasets enriched with provenance metadata and systematic quality-control indicators at acquisition. These datasets are suitable for downstream computational analysis and modelling. Conclusions: Data derived from the mapping infrastructure enable the training of deep learning surrogate models that approximate the relationships between magnet position, orientation, and magnetic-field distribution. Such proxy predictors reduce the need for repeated measurement campaigns, supporting efficient estimation of magnetic-field distributions and gradients for data-driven MDT applications.

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Published

29.06.2026

How to Cite

1.
BERNAD R-L, CARAGIN-CRASOVAN R, STOICU-TIVADAR L, CRISAN-VIDA M, BERNAD SI. Traceable and Reproducible 3D Magnetic Field Mapping for Data-Driven Magnetic Drug Targeting. Appl Med Inform [Internet]. 2026 Jun. 29 [cited 2026 Jul. 5];48(Suppl. 1):S14-S15. Available from: https://ami.info.umfcluj.ro/index.php/AMI/article/view/1297

Issue

Section

Special Issue - RoMedINF