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Multimodal 3D Printing of Phantoms to Simulate Biological Tissue
Published on: January 11, 2020
An open source heterogeneous 3D printed mouse phantom utilising a novel bone representative thermoplastic.
Gareth Price1,2,3, Emma R Biglin1,2, Sean Collins4,5
1University of Manchester, Manchester Academic Health Science Centre, The Christie NHS Foundation Trust, Wilmslow Road, Manchester M20 4BX, United Kingdom.
Researchers developed an open-source, anatomically accurate 3D-printed mouse model to improve quality control in small animal radiation therapy. By using custom materials that mimic bone and soft tissue, this phantom allows scientists to test radiation delivery systems with high precision. This tool helps standardize pre-clinical research by providing a reliable, reproducible way to calibrate imaging and treatment equipment.
Area of Science:
- Radiation oncology physics and pre-clinical dosimetry
- Advanced manufacturing and 3D printed mouse phantom development
Background:
Current pre-clinical radiation research lacks standardized quality control protocols for verifying dose delivery accuracy. This deficiency complicates comparisons across different laboratories and experimental setups. Researchers often struggle to replicate complex anatomical structures using conventional calibration tools. That uncertainty drove the need for highly customizable, anthropomorphic models that mimic small animal physiology. Prior research has shown that existing commercial options are often expensive or lack the necessary tissue heterogeneity. No prior work had resolved the challenge of creating accessible, open-source designs for high-resolution anatomical phantoms. This gap motivated the creation of a new fabrication framework for small animal models. Scientists now seek reliable methods to ensure that radiation beams align precisely with target tissues in vivo.
Purpose Of The Study:
The aim of this work is to present a complete methodology for producing high-resolution, anthropomorphic phantoms for pre-clinical radiation research. Researchers sought to address the lack of rigorous quality standards in small animal dosimetry. They identified a need for accessible, customizable models that accurately reflect complex biological structures. This project focuses on developing tissue-equivalent materials that can be easily manufactured using additive fabrication. The authors intended to provide a transparent, open-source design to facilitate widespread adoption within the scientific community. By creating a bone-equivalent filament, they addressed the difficulty of replicating skeletal density in synthetic models. The study also explores how these phantoms can be validated through CT imaging comparisons. Ultimately, the team aimed to establish a common quality assurance standard for pre-clinical radiobiology experiments.
Main Methods:
The team designed a comprehensive fabrication workflow for creating heterogeneous, anatomically realistic models. They employed high-resolution additive manufacturing techniques to construct the internal skeletal and external body structures. A novel thermoplastic was formulated to mimic the specific attenuation properties of bone tissue. Researchers integrated soft-tissue mimicking filaments to complete the structural assembly based on CT scan data. Air gaps were strategically incorporated to represent the lungs within the thoracic region. The review approach involved comparing the geometric fidelity of the printed model against reference animal images. Investigators evaluated x-ray attenuation profiles to ensure the materials behaved predictably under various beam energies. Finally, they assessed the voxel intensity distribution to confirm the phantom matched the biological reference standard.
Main Results:
The strongest finding shows that the phantom achieves sub-millimetre geometric reproduction of the skeleton and body surface. Specifically, the skeletal Distance-To-Agreement is 0.5 mm ± 0.4 mm, while the body surface is 0.7 mm ± 0.5 mm. Key findings from the literature indicate a 6.6% difference in attenuation for the bone-equivalent material in softer beams. This discrepancy rapidly decreases as the radiation beam is hardened, confirming material suitability. Histograms of voxel intensity profiles demonstrate high similarity between the phantom and actual animal images. The results confirm that the model effectively replicates the complex tissue heterogeneity required for pre-clinical dosimetry. These data suggest that the fabrication approach provides a reliable tool for quality assurance. The study confirms that the printed structure maintains anatomical realism across the evaluated imaging parameters.
Conclusions:
The authors demonstrate a viable pathway for producing customizable, high-resolution anthropomorphic models for radiation quality assurance. This synthesis suggests that open-source designs can effectively standardize pre-clinical dosimetry across the radiobiology community. The findings indicate that the bone-equivalent material provides sufficient attenuation characteristics for accurate imaging verification. Researchers highlight that the sub-millimetre geometric precision achieved supports rigorous treatment planning and delivery validation. The study implies that utilizing these phantoms reduces variability in experimental radiation outcomes. Authors emphasize that the provided methodology enables laboratories to replicate complex tissue structures without proprietary constraints. The evidence confirms that the voxel intensity profiles closely match actual animal subjects. This work establishes a framework for future improvements in pre-clinical radiotherapy quality standards.
Frequently Asked Questions
The researchers propose a method using a novel bone-equivalent thermoplastic combined with ABS plastic to replicate mouse anatomy. This approach utilizes CT scan data to guide the 3D printing process, ensuring that the final model accurately reflects the internal structure and density of a real mouse.
The design incorporates a specialized bone-representative filament alongside soft-tissue mimicking Acrylonitrile Butadiene Styrene (ABS) plastic. These materials are chosen to replicate the specific x-ray attenuation properties of skeletal and soft tissues found in a living mouse.
Air gaps are integrated into the design to simulate the low-density environment of the lungs. This technical necessity ensures that the phantom correctly mimics the radiation attenuation profile of the thoracic cavity, which is vital for accurate pre-clinical radiotherapy planning.
The researchers utilize CT image data to define the geometry and density of the phantom. This data type is crucial for validating the model, as it allows for a direct comparison between the phantom's x-ray attenuation and that of a real animal.
The team measured the Distance-To-Agreement for the skeleton at 0.5 mm ± 0.4 mm and the body surface at 0.7 mm ± 0.5 mm. These measurements demonstrate the sub-millimetre accuracy of the 3D printing process in reproducing complex anatomical features.
The authors propose that sharing these designs as open-source resources will encourage the radiobiology community to adopt a common quality assurance standard. They suggest this will lead to more consistent and reliable pre-clinical radiation research outcomes globally.

