Freeze-thaw and solvent-exchange strategy to generate physically cross-linked organogels and hydrogels of curdlan with tunable mechanical properties

Physical gels from natural polysaccharides present the advantage of no toxic cross-linking agents and no chemical modification during preparation. Herein, novel physical gels, transparent organogels and opaque hydrogels from the microorganism-derived (1,3)-beta-D-glucan of curdlan were prepared in dimethyl sulfoxide (DMSO) using the freeze-thaw technique, followed by a solvent-exchange strategy with water. The mechanical and structural properties of these gels were investigated by rheology, scanning electron microscopy, attenuated total reflection infrared spectroscopy, wide-angle X-ray diffraction and small-angle X-ray scattering. Gelation mechanisms and intermolecular interaction models have also been proposed. The good solvent DMSO serves as both a crosslinker and a pore-foaming agent in organogels. The reversible macromolecular conformation changes and phase separation of curdlan endow the gels with reversible transparency, volume change and tunable mechanical strength. The new design strategy of facile preparation and performance tuning provides a platform for developing new organogels and sterile hydrogels of curdlan.

Automated summary

In this study, transparent organogels and opaque hydrogels derived from curdlan were prepared using the freeze-thaw technique and a solvent-exchange strategy. The mechanical and structural properties of these gels were investigated, and the use of DMSO as a crosslinker and pore-foaming agent in organogels was explored. The reversible conformation changes and phase separation of curdlan endowed the gels with reversible transparency and tunable mechanical strength. This design strategy provides a platform for developing new organogels and sterile hydrogels of curdlan.