Which structure-property-process relationships govern semi-solid extrusion 3D printing? A stepwise and multi-parametric optimization protocol for pharmaceutical applications

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Authors: Sara Bom, Matilde Carvalho, Pedro Henrique Dias Moura Prazeres, Catarina Ferreira Santos, Ana Margarida Martins, Helena Margarida Ribeiro, Joana Marques Marto
Cited by: 1
References: 35

Abstract

Semi-solid extrusion 3D printing (SSE-3DP) emerges as a powerful technology for producing customized soft-matter pharmaceutical products. However, its implementation is limited by the lack of standardized, mechanistically grounded optimization strategies that address the multifactorial nature of printability. Herein, a stepwise and multi-parametric protocol is proposed to streamline the optimization of materials printed via SSE-3DP through a comprehensive structure–property–performance framework. Two gelatin-based model inks, differing in the content of PEG-40 hydrogenated castor oil (PEG40 HCO), were used to validate the approach. Rheology, texture, thermal-imaging and contact angle measurements were performed as part of the pre-printing workflow to elucidate ink structure and interfacial behavior, while width, length, collapse, pentagram and z-stack assays were carried out to optimize the 3DP quality in-process, and macro and scanning electron microscopy (SEM) imaging were introduced as post-characterization validation tools. Rheological analysis revealed that PEG40 HCO lowers the Sol–Gel crossover temperature, increases viscoelastic moduli and reduces creep compliance, indicating enhanced resistance to deformation during extrusion. These property changes translated into higher extrusion forces and increased susceptibility to clogging, quantitatively predicted by texture analysis (R² ≥ 0.94). Interfacial studies identified acrylic as the optimal printing bed. Line fidelity was primarily governed by print speed, while controlled porosity emerged from the coupled optimization of filament spacing and printing path design. SEM confirmed that PEG40 HCO induces mesoscale reorganization of the gelatin network, yielding improved mechanical stability and geometric fidelity. Overall, this work provides a comprehensive and adaptable framework for SSE-3DP, advancing material-process-design optimization in 13 steps.

Fields of Study & Subjects

3D Printing in Biomedical Research Additive Manufacturing and 3D Printing Technologies Polymer Foaming and Composites

Publication details

Journal / source
Colloids and Surfaces A Physicochemical and Engineering Aspects
Publisher
Elsevier BV
Volume
737
Pages
139780–139780
Publication date
30 January 2026
Language
EN