Methacryloyl gelatin (GelMA) is a versatile material for bioprinting because of its tunable physical properties and inherent bioactivity. Bioprinting of GelMA is often met with challenges such as lower viscosity of GelMA inks due to higher methacryloyl substitution and longer physical gelation time at room temperature. In this study, a tunable interpenetrating polymer network (IPN) hydrogel was prepared from gelatin-hyaluronan dialdehyde (Gel-HDA) Schiff’s polymer, and 100% methacrylamide substituted GelMA for biofabrication through extrusion based bioprinting. Temperature sweep rheology measurements show a higher sol-gel transition temperature for IPN (30 °C) compared to gold standard GelMA (27 °C). Furthermore, to determine the tunability of the IPN hydrogel, several IPN samples were prepared by combining different ratios of Gel-HDA and GelMA achieving a compressive modulus ranging from 20.6 ± 2.48 KPa to 116.7 ± 14.80 KPa. Our results showed that the mechanical properties and printability at room temperature could be tuned by adjusting the ratios of GelMA and Gel-HDA. To evaluate cell response to the material, MC3T3-E1 mouse pre-osteoblast cells were embedded in hydrogels and 3D-printed, demonstrating excellent cell viability and proliferation after 10 d of 3D in vitro culture, making the IPN an interesting bioink for the fabrication of 3D constructs for tissue engineering applications.

Calcium carbonate (CaCO₃) nanoparticles could have great potential for contrast-enhanced ultrasound imaging (CEUS) due to their gas-generating properties and sensitivity to physiological conditions. However, the use of nano CaCO₃ for biomedical applications requires the assistance of stabilizers to control the size and avoid the fast dissolution/recrystallization of the particles when exposed to aqueous conditions. Herein, we report the stabilization of nano CaCO₃ using lignin, and synthesized core-shell amorphous CaCO₃-lignin nanoparticles (LigCC NPs) with a diameter below 100 nm. We have then investigated the echogenicity of the LigCC NPs by monitoring the consequent generation of contrast in vitro for 90 min in linear and non-linear B-mode imaging. This research explores how lignin type and structure affect stabilization efficiency, lignin structuration around CaCO₃ cores, and particle echogenicity. Interestingly, by employing lignin as the stabilizer, it becomes possible to maintain the echogenic properties of CaCO₃, whereas the use of lipid coatings prevents the production of signal generation in ultrasound imaging. This work opens new avenue for CEUS imaging of the vascular and extravascular space using CaCO₃, as it highlights the potential to generate contrast for extended durations at physiological pH by utilizing the amorphous phase of CaCO₃.

Cryogels, a subset of hydrogels, have recently drawn attention for cartilage tissue engineering due to its inherent microporous architecture and good mechanical properties. In this study a dual crosslinked pullulan–gelatin cryogel (PDAG) scaffold was synthesized by crosslinking gelatin with oxidized pullulan by Schiff’s base reaction followed by cryogelation. Chondrocytes seeded within the PDAG scaffolds and cultured for 21 d in vitro demonstrated enhanced cell proliferation, enhanced production of cartilage-specific extracellular matrix and up-regulated sulfated glycosaminoglycan without altering the articular chondrocyte phenotype. Quantitative reverse transcription-polymerase chain reaction-based gene expression studies, immunofluorescence, and histological studies demonstrated that the PDAG scaffold significantly enhanced the expression of chondrogenic marker genes such as type II collagen, aggrecan, and SOX9. Taken together, these results demonstrated that PDAG scaffold prepared by sequential Schiff’s base reaction and cryogelation would be a promising cell-responsive scaffold for cartilage tissue engineering applications.

Materials with antimicrobial properties and high adsorption capabilities are crucial for managing exudate in post-surgical cases. However, achieving both properties simultaneously remains a challenge. In this study, we first synthesized curcumin-loaded organosolv lignin nanoparticles (Lig-Cur Nps) using a solvent-shifting approach in a continuous flow reactor. These Lig-Cur NPs were then dispersed in a polyvinyl alcohol (PVA) solution. The PVA-Lig-Cur NP colloidal suspension was further crosslinked with tannic acid (TA) through hydrogen bonding interactions. A simple freeze–thaw cycle of the PVA-Lig-Cur NP suspension with TA resulted in the formation of a stable gel, which was then lyophilized to fabricate the PVA-Lig-Cur-TA hydrogel scaffold. This scaffold features an interconnected microporous network with a swelling percentage of 800%, enabling the rapid adsorption of exudates. Its excellent properties and antimicrobial efficacy against Staphylococcus aureus, a bacterium commonly found on the skin, and Pseudomonas aeruginosa highlight its potential to effectively remove exudates while preventing bacterial colonization.