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Diffusion Model-Based Design of Bionic Bone Scaffolds with Tunable Microstructures.

Authors

Chen J,Shen S,Xu L,Zheng Z,Zou X,Ye M,Zhang C,Liu H,Yao P,Xu RX

Affiliations (11)

  • Division of Life Sciences and Medicine, School of Biomedical Engineering, University of Science and Technology of China, Hefei, 230026, Anhui, China.
  • Suzhou Institute for Advanced Research, University of Science and Technology of China, Suzhou, 215123, Jiangsu, China.
  • Division of Life Sciences and Medicine, School of Biomedical Engineering, University of Science and Technology of China, Hefei, 230026, Anhui, China. [email protected].
  • Suzhou Institute for Advanced Research, University of Science and Technology of China, Suzhou, 215123, Jiangsu, China. [email protected].
  • Department of Precision Machinery and Precision Instrument, University of Science and Technology of China, Hefei, 230026, China.
  • School of Nano Science and Technology, University of Science and Technology of China, Suzhou, 215123, China.
  • First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230001, China.
  • School of Microelectronics, University of Science and Technology of China, Hefei, 230026, China. [email protected].
  • Division of Life Sciences and Medicine, School of Biomedical Engineering, University of Science and Technology of China, Hefei, 230026, Anhui, China. [email protected].
  • Suzhou Institute for Advanced Research, University of Science and Technology of China, Suzhou, 215123, Jiangsu, China. [email protected].
  • Department of Precision Machinery and Precision Instrument, University of Science and Technology of China, Hefei, 230026, China. [email protected].

Abstract

In the clinical treatment of bone defects that exceed the critical size threshold, traditional methods using metal fixation devices, autografts, and allografts exhibit significant limitations. Meanwhile, bone scaffolds with minimal risks of secondary injury, low immune rejection are emerging as a promising alternative. The effective design of porosity, pore size, and trabecular thickness in bone scaffolds is critical; however, current strategies often struggle to optimally balance these parameters. Here, we propose a bionic bone scaffold design method that mimics multiple properties of natural cancellous bone using a diffusion model. First, we develop a classifier-free conditional diffusion model and train it on a Micro-CT (μCT) image dataset of porcine vertebral cancellous bone. The training model can produce personalized 2-dimensional images of natural-like bone with tunable microstructures. Subsequently, we stack images layer by layer to form 3-dimensional scaffolds, mimicking the CT/μCT image reconstruction process. Finally, computational fluid dynamics analysis is conducted to validate the scaffold models' fluid properties, while bioresin bone scaffold samples are 3D-printed for mechanical testing and biocompatibility assessment. The three key morphological parameters of the generated images-porosity (50-70%), pore size (468-936 μm), and trabecular thickness (156-312 μm)-can be precisely and independently controlled. Fluid simulation and mechanical testing confirm scaffolds' robust performance in permeability (10⁻⁹ to 10⁻⁸ m<sup>2</sup>), average fluid shear stress (0.1-0.3 Pa), Young's modulus (14-fold adjustable range), compressive strength (9-fold adjustable range), and viscoelastic properties. The scaffolds also exhibit good biocompatibility, meeting the basic requirements for clinical implantation. These promising results highlight the potential of our method for the personalized design of scaffolds to effectively repair large bone defects.

Topics

Journal Article

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