# Deformation Behaviour of Optimised Three-Dimensional Axisymmetric Chiral Auxetic Structures

**Authors:** Nejc Novak, Alen Grebo, Matej Borovinšek, Lovre Krstulović-Opara, Zoran Ren, Matej Vesenjak

PMC · DOI: 10.3390/biomedicines13112816 · 2025-11-18

## TL;DR

This paper introduces optimized 3D chiral structures with unique mechanical properties that could improve biomedical scaffolds and stents.

## Contribution

A novel fabrication method for auxetic axisymmetric chiral structures with enhanced mechanical performance is introduced.

## Key findings

- Optimized ACS structures show superior mechanical properties compared to non-optimized ones.
- Both structures exhibit auxetic behavior with a Poisson’s ratio of about −0.1 up to 40% strain.
- The auxetic capability is promising for biomedical applications like stents and tissue scaffolds.

## Abstract

Background/Objectives: Developing functional tissue constructs via 3D bioprinting relies heavily on scaffold architecture, demanding precise mechanical tunability and high-resolution feature fidelity. Methods: This paper presents a novel approach utilising photocurable resins and resin 3D printing to fabricate auxetic axisymmetric chiral structures (ACSs), which can be used for advanced scaffold engineering. Results: The experimental tests showed that the optimised ACS (optACS) possess superior mechanical properties compared to their non-optimised counterpart. Both analysed structures possess an auxetic behaviour up to 40% longitudinal strain, with a Poisson’s ratio of about −0.1. Conclusions: This auxetic capability is promising for biomedical applications, particularly in developing enhanced stents or tissue scaffolds.

## Full-text entities

- **Genes:** ACCS (1-aminocyclopropane-1-carboxylate synthase homolog (inactive)) [NCBI Gene 84680] {aka ACS, PHACS}
- **Diseases:** DIC (MESH:C564543), injury to (MESH:D014947)
- **Chemicals:** optACS (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12650214/full.md

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Source: https://tomesphere.com/paper/PMC12650214