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Cellulose nanofibers (CNFs) are renewable bionanomaterials with great utilization potential in future biomedicals. However, conventional CNF hydrogels are limited by low structural flexibility and insufficiently tunable mechanical properties, restricting their use in 3D cell culture systems. To address these limitations, we developed granular hydrogel platforms using photocurable and ionically crosslinkable methacrylated CNFs (CNFMAs) and their copolymers with polyacrylamide a dual cross-linking mechanism. By employing this bottom-up approach, mechanically fragmented microgels were reassembled into granular hydrogels calcium ion crosslinking. This assembly of methacrylated CNF-based microgels successfully supported long-term 3D cell culture and demonstrated the capability to provide biomechanical cues that facilitate different cellular responses. The granular hydrogel of CNFMA alone promoted clustering and migration of human pancreatic cancer cells (PANC-1), while the copolymerization of CNFMA with polyacrylamide introduced stiffness variations into the hybrid granular hydrogel system that enhanced the spreading of preosteoblasts (MC3T3-E1) and facilitated spheroid formation in the culture of PANC-1. These findings underscore the versatility of photocurable nanocellulose in constructing biomaterial platforms. Overall, this study establishes a foundation for advancing models for tissue engineering and cancer research using CNFMA-derived microgel systems.
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http://dx.doi.org/10.1039/d5nr00583c | DOI Listing |
Angiogenesis
September 2025
Division of Plastic Surgery, Department of Surgery, Penn State Health Milton S. Hershey Medical Center, Hershey, PA, 17033, USA.
Vascularization of implanted biomaterials is critical to reconstructive surgery and tissue engineering. Ultimately, the goal is to promote a rapidly perfusable hierarchical microvasculature that persists with time and can meet underlying tissue needs. We have previously shown that using a microsurgical technique, termed micropuncture (MP), in combination with porous granular hydrogel scaffolds (GHS) fabricated via interlinking hydrogel microparticles (microgels) results in a rapidly perfusable patterned microvasculature.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Department of Materials Science and Engineering, College of Engineering, Texas A&M University, College Station, Texas 77843, United States.
Hydrogel-based bioinks are widely adopted in digital light processing (DLP) 3D printing. Modulating their mechanical properties is especially beneficial in biomedical applications, such as directing cell activity toward tissue regeneration and healing. However, in both monolithic and granular hydrogels, the tunability of mechanical properties is limited to parameters such as cross-linking or packing density.
View Article and Find Full Text PDFAdv Healthc Mater
September 2025
Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, MD, 21218, USA.
Hydrogels are widely employed in tissue engineering for their biomimetic microenvironments. However, the dense crosslink network of hydrogels with matching mechanical properties of soft tissues often restricts cell infiltration and tissue integration. While granular hydrogels enhance host integration through the formation of porous channels between particles, they self-anneal in vivo, thereby limiting porosity and interconnectivity.
View Article and Find Full Text PDFMater Today Bio
October 2025
Institute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, Eindhoven, 5600, MB, the Netherlands.
Compared to bulk hydrogels, microgels offer distinct advantages for biomedical applications. Their increased modularity and heterogeneity compared to hydrogels, combined with their small size and reversible dynamic bonding, enhance their suitability for minimally invasive cell delivery. Additionally, microgels offer greater control over porosity, resulting in the formation of intricate porous microstructures.
View Article and Find Full Text PDFBiofabrication
August 2025
Biomedical and Chemical Engineering, University of Virginia, 102 Engineer's Way, Charlottesville, Virginia, 22903-1738, UNITED STATES.
Towards achieving biomimetic complexity in biofabricated systems, an all-granular bioprinting system might use particle-based hydrogel inks to establish structures within a particle-based support matrix. In such a system, the granular support matrix can be designed to persist in the final construct and include cells incorporated prior to printing. To biofabricate complexity, bioprinting can introduce high-resolution heterogeneous structures that guide cell behaviors.
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