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Bioinspired Nanoscale 3D Printing of Calcium Phosphates Using Bone Prenucleation Clusters.
Iman Roohani1,2, Shuning Wang1, Chaohui Xu1
1School of Biomedical Engineering, University of Sydney, Sydney, NSW, 2006, Australia.
Advanced Materials (Deerfield Beach, Fla.)
|February 28, 2025
Summary
Researchers developed a novel 3D printing method using bioinspired chemistry to create nanoscale calcium phosphate (CaP) structures with high precision. This breakthrough enables finer control over material microstructure for advanced biomedical applications.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Bioinspired Chemistry
Background:
- Calcium phosphates (CaPs) are vital in biological systems (bones, teeth) and biomedical uses.
- Current 3D printing methods struggle to fabricate CaPs at the nanoscale with high resolution.
- Existing techniques like two-photon polymerization (2pp) are unsuitable for CaP nanostructure fabrication.
Purpose of the Study:
- To present a novel 3D printing approach for fabricating nanoscale calcium phosphate structures.
- To achieve unprecedented resolution in 3D printed CaP materials.
- To overcome limitations of current nanofabrication techniques for CaPs.
Main Methods:
- Utilized bioinspired chemistry, specifically bone prenucleation nanoclusters (PNCs, ~5 nm).
- Incorporated PNCs into a photosensitive resin to create a transparent photoresist.
- Leveraged the transparent photoresist for high-resolution 3D nanopatterning of CaPs.
Main Results:
- Achieved 3D printing of CaP structures with ≈300 nm resolution, three orders of magnitude finer than existing methods.
- Overcame light-scattering issues common with larger CaP nanoparticles.
- Enabled precise control over CaP microstructure down to submicron grain levels.
Conclusions:
- The novel method allows for nanopatterning of CaPs on various substrates.
- This advancement opens possibilities for bioinspired metamaterials and precision coatings.
- The technique facilitates the development of damage-tolerant materials and cell-modulating interfaces.

