Replicating the nonlinear, strain-dependent mechanics of soft biological tissues remains a central challenge in scaffold engineering, implantable devices and tissue-mimicking phantom development. Current approaches lack a systematic, experimentally validated framework that quantitatively links unit cell characteristics to macroscopic mechanical response across clinically relevant stiffness ranges. Here, we introduce a geometry-driven design strategy for 3D-printed adipose-inspired soft metamaterials, systematically varying unit cell diameter, shell thickness, orientation angle, and base material across multiple architectures. Compression experiments reveal that shell thickness governs initial stiffness and buckling onset, cell diameter controls the extent of the progressive instability plateau, and orientation angle switches the deformation mode from instability-driven buckling to progressive compaction. Finite element simulations capture these mechanisms quantitatively, while a multivariate regression model predicts effective modulus, buckling stress, and energy absorption (R2adj > 0.86). The resulting design space spans elastic moduli from units to hundreds of kPa, covering the mechanical ranges of multiple soft biological tissues, demonstrating that a single geometric framework can be systematically tuned to target diverse soft-tissue mechanical environments. This integrated experimental–computational–statistical platform establishes a mechanistic and geometry-driven design foundation that can inform the rational development of programmable soft metamaterials for regenerative scaffolds, tissue-mimicking phantoms, and soft implantable devices.

From Geometry to Function: Programmable Mechanical Response in 3D‐Printed Adipose‐Inspired Soft Metamaterials

Berardo, Alice;Carniel, Emanuele Luigi
2026

Abstract

Replicating the nonlinear, strain-dependent mechanics of soft biological tissues remains a central challenge in scaffold engineering, implantable devices and tissue-mimicking phantom development. Current approaches lack a systematic, experimentally validated framework that quantitatively links unit cell characteristics to macroscopic mechanical response across clinically relevant stiffness ranges. Here, we introduce a geometry-driven design strategy for 3D-printed adipose-inspired soft metamaterials, systematically varying unit cell diameter, shell thickness, orientation angle, and base material across multiple architectures. Compression experiments reveal that shell thickness governs initial stiffness and buckling onset, cell diameter controls the extent of the progressive instability plateau, and orientation angle switches the deformation mode from instability-driven buckling to progressive compaction. Finite element simulations capture these mechanisms quantitatively, while a multivariate regression model predicts effective modulus, buckling stress, and energy absorption (R2adj > 0.86). The resulting design space spans elastic moduli from units to hundreds of kPa, covering the mechanical ranges of multiple soft biological tissues, demonstrating that a single geometric framework can be systematically tuned to target diverse soft-tissue mechanical environments. This integrated experimental–computational–statistical platform establishes a mechanistic and geometry-driven design foundation that can inform the rational development of programmable soft metamaterials for regenerative scaffolds, tissue-mimicking phantoms, and soft implantable devices.
2026
   Elastomeric scaffolds for soft tissue Repair, Replacement and Augmentation
   ERRA
   University of Padova - DII
File in questo prodotto:
File Dimensione Formato  
Adv Funct Materials - 2026 - Berardo - From Geometry to Function Programmable Mechanical Response in 3D‐Printed.pdf

accesso aperto

Descrizione: paper
Tipologia: Published (Publisher's Version of Record)
Licenza: Creative commons
Dimensione 14.36 MB
Formato Adobe PDF
14.36 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/3606739
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
  • OpenAlex ND
social impact