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Integrated laser ablation and computed tomography

Repository of the University of Ljubljana (University of Ljubljana) 2026
Jan Biskupič, Peter Scheer, Jana Hložková, Ahmet Davut AKSU, Lucie Šudomová, Viktória Parobková, Petra Procházková, Tomáš Zikmund, Jozef Kaiser, Gabriela Kalčíková, Michaela Kuchynka

Summary

Scientists developed a new way to find and map tiny plastic particles (microplastics) hiding inside body tissue by combining two techniques: a 3D imaging scan (like a CT scan) and a chemical detection method that spots trace metals found in common plastics like PET (the material in water bottles). This matters because current methods struggle to reliably detect microplastics in our organs, and this proof-of-concept approach—tested in rat tissue—could eventually help researchers better understand how much plastic accumulates in our bodies and where it ends up, an important step toward figuring out what that means for our health.

Polymers
Models

Detecting and characterizing microplastics within biological tissues remains analytically challenging due to their small size, complex composition, and the heterogeneous nature of biological matrices. Existing methods often rely on destructive sample preparation or only provide partial information, highlighting the need for advanced techniques that can simultaneously resolve both the structural and chemical features of microplastics in situ. To address this gap, we introduce a multimodal analytical approach that integrates micro-computed tomography (μCT), which enables non-invasive volumetric imaging of the tissue with laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to detect microplastics based on their metal markers. Rat tissue was spiked with polyethylene terephthalate (PET) microplastics, and results showed that μCT imaging alone was insufficient for definitively determining microplastics. However, PET contained several elements, such as antimony and cobalt, and it was possible to detect PET microplastics using LA-ICP-MS based on those metal markers. Furthermore, the developed workflow combining μCT and LA-ICP-MS enabled volumetric segmentation of microplastic reconstruction based on their 3D distribution and evaluation of their size distribution. The results demonstrate that integrating LA-ICP-MS spatial element mapping of PET metal markers facilitates precise validation and segmentation of microplastic locations within tissue on μCT. The proposed protocol was evaluated against a reference size distribution method, addressing the associated detection limitations. Overall, this dual-modality approach provides a proof of concept for microplastic detection in biological tissues by combining both structural and chemical analyses.

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