This study provides a practical framework for creating intrafilamentary porosity into 3D-printed PCL scaffolds with improved surface-mediated biological performance.
Abstract
Extrusion-based three-dimensional printing enables the fabrication of patient-specific scaffolds. Polycaprolactone (PCL)-based scaffolds have been widely used for the treatment of bone defects. However, extruded filaments are typically nonporous, which can prolong their degradation, limit cell adhesion and infiltration, and therefore interrupt normal tissue regeneration. Here, we present a simple and scalable method to generate polymeric scaffolds with hierarchical porosity by incorporating sacrificial sugar particles in a printable PCL ink. Microstructural analysis by SEM demonstrates an average pore size of around 10 μm with increased pore density at higher porogen fractions. Porous PCL improved apparent wettability and protein adsorption, accelerated hydrolytic degradation by more than five-fold, and enabled tunable mechanical properties. Printability testing shows improved filament stability and reduced fusion at higher porogen loading, enabling significantly higher printing resolution. In vitro evaluation demonstrates enhanced early preosteoblast attachment on porous scaffolds (>three-fold), without loss of cytocompatibility. Importantly, porous scaffolds support osteogenic differentiation of the cells and mineralization. This study provides a practical framework for creating intrafilamentary porosity into 3D-printed PCL scaffolds with improved surface-mediated biological performance.
Three‐dimensional, interconnected hydrogel networks are central to tissue engineering and disease modeling, where tailored pore architecture and mechanical robustness are essential for supporting cellular functions. However, the limited ability to engineer microstructural features in vat polymerization 3D‐printed natur...
Liwei Liu, Liwen Zhang, Xumin Huang et al.· Small Methods· 0 citations
A strong negative relationship between pH and mass loss indicates that pH is a major mechanistic marker of deterioration, and highlights the importance of scaffold design and nanoparticle incorporation in controlling scaffold biodegradation.
Improved scaffold architecture and introduced hydroxyl groups enabled outstanding cell viability and proliferation, as evidenced by abundant live cells, uniform distribution, and minimal cell death.
Overall, the developed Alg/MP/OPLA/CaP scaffold provides a bioactive environment for bone regeneration, thus serving as a potential alternative for the repair of critical-sized bone defects.
Overall, PTB4 achieved the best balance among printability, mechanical compatibility, cytocompatibility, angiogenesis-related activity, and osteogenic performance, supporting low-dose BT modification as a promising strategy for safe, printable scaffolds for critical-size craniofacial and oral bone defect repair.
This review highlights recent progress in 3D‑printed Alg-based scaffolds for BTE, emphasizing how advanced fabrication techniques and BGs incorporation contribute to improved biological performance and structural reinforcement.
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A new machine-learning framework aims to improve the success rate of computational protein design while moving away from results that reproduce sequences found in nature.