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Tumbic, J.

Publications and source records attributed to Tumbic, J..

2 recordsLinked to original sources

An injectable granular hydrogel stabilized by electrostatic interactions between hyaluronic acid-based microparticles and soluble gelatin exhibits poroelasticity and strain-stiffening

Injectable hydrogels with shear-thinning and self-healing properties are critical for biomedical applications including 3D bioprinting and regenerative medicine. While granular hydrogels inherently exhibit these properties, they often lack post-injection stability. Here, we developed an electrostatically stabilized granular hydrogel system composed of norbornene-modified hyaluronic acid (NorHA) microgels and cationic gelatin ((+) Gel). NorHA microgels (9.91 {+/-} 4.85 m diameter) were synthesized via batch emulsification, while (+) Gel was prepared by modifying gelatin with ethylene diamine to increase zeta potential from 2.08 {+/-} 0.97 mV to 13.76 {+/-} 1.11 mV. The negatively charged NorHA microgels formed stable materials when combined with (+) Gel through electrostatic interactions, confirmed by gel inversion tests and salt sensitivity studies. Rheological characterization revealed that (+) Gel addition produced poroelastic behavior and strain-stiffening properties, with storage modulus and yield onset increasing under compression. Large amplitude oscillatory shear analysis showed strain-stiffening behavior (e3 > 0) that enhanced with both (+) Gel concentration and compression. Confocal microscopy demonstrated tunable porosity through gelatin fraction control, with (+) Gel forming aggregate-like clusters. Extrusion testing showed formulations required low injection pressures (0.47-0.91 kPa) comparable to PBS and significantly lower than Pluronic, while forming robust filaments up to 23 mm in length. The materials exhibited rapid self-healing behavior and maintained structural integrity post-extrusion. This electrostatically stabilized granular hydrogel system offers a promising platform for injectable biomaterials that combine ease of delivery with post-injection stability for wound healing and 3D bioprinting applications.

bioengineering↗

Particle-based hydrogel inks and support matrices for biofabricating structural complexity, soluble gradients, and cell-lined channels in fully granular bioprinted systems

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. The designs of the granular ink and support hydrogels are crucial to achieving complexity. High resolution structures and channels depend on small particles that flow and can be stabilized, and that can be printed and then removed, respectively. Herein, an all-granular system is described that used a granular formulation of an established, tunable hyaluronic acid-based hydrogel as the basis for a support matrix and a small particle gelatin hydrogel as an ink. Towards facilitating stabilization of the printed structure and flow during printing, the support and ink materials included soluble, interstitial components, and all exhibited yield stress behaviors characteristic of granular hydrogel systems. The support matrixs viscoelastic properties were dependent on intraparticle hydrogel network design, and it could be stabilized against flow by photoinitiated crosslinking. The gelatin ink could form fine filaments, as small as 100 {micro}m in testing here, and melted to leave channels within crosslinked support matrices. Channels could support flows introduced by hydrostatic pressure and could be used to rapidly transport soluble factors into the construct, which could be used to establish soluble gradients by diffusion and support cell viability. The all-granular system supported printing of complex, multimaterial structures, with feature resolution on the order of 100 {micro}m and spatial positioning on the order of 10s {micro}m. The process and materials exhibited biocompatibility with respect to cells included within the support matrix during printing or introduced into channels to begin establishing endothelialized bioprinted vessels.

bioengineering↗