3D printable and mechanically tunable hydrogels achieved through hydrophobic and ionic interactions.

Thermal stiffening materials are commonly applied in the aerospace and automotive industries, among others, since their dimensional stabilities and stiffness characteristics improve at high temperatures. In this study, temperature-triggered modulus-tunable hydrogels were prepared by combining Pluronic F-127 with charged polymers. Pluronic F-127, a triblock copolymer micelle, provided three-dimensional printing capabilities of fine resolution with high viscosity, while hydrophobic and ionic interactions among polymer networks provided thermal stiffening.

Seamless Integration of Conducting Hydrogels in Daily Life: From Preparation to Wearable Application.

Conductive hydrogels (CHs) have received significant attention for use in wearable devices because they retain their softness and flexibility while maintaining high conductivity. CHs are well suited for applications in skin-contact electronics and biomedical devices owing to their high biocompatibility and conformality. Although highly conductive hydrogels for smart wearable devices are extensively researched, a detailed summary of the outstanding results of CHs is required for a comprehensive understanding.

High-Resolution 3D Printing of Mechanically Tough Hydrogels Prepared by Thermo-Responsive Poloxamer Ink Platform.

High-resolution 3D-printable hydrogels with high mechanical strength and biocompatibility are in great demand because of their potential applications in numerous fields. In this study, a material system comprising Pluronic F-127 dimethacrylate (FDMA) is developed to function as a direct ink writing (DIW) hydrogel for 3D printing. FDMA is a triblock copolymer that transforms into micelles at elevated temperatures.

Recent Advances in Design Strategies for Tough and Stretchable Hydrogels.

The development of multifunctional hydrogels with excellent stretchability and toughness is one of the most fascinating subjects in soft matter research. Numerous research efforts have focused on the design of new hydrogel systems with superior mechanical properties because of their potential applications in diverse fields. In this Minireview, we consider the most up-to-date mechanically strong hydrogels and summarize their design strategies based on the formation of double networks and dual physical crosslinking.

Integration of Macro-Cross-Linker and Metal Coordination: A Super Stretchable Hydrogel with High Toughness.

The development of multifunctional hydrogels with high strength and stretchability is one of the most important topics in soft-matter research owing to their potential applications in various fields. In this work, a dual physically cross-linked network was designed for the fabrication of ultrastretchable tough hydrogels. The hydrogels were prepared through polymerization of acrylic acid and acrylamide in the presence of positively charged quaternary poly(ethylene imine) (Q-PEI) and micelle-forming Pluronic F127 diacrylate, thus introducing electrostatic interactions between the positively charged Q-PEI and negatively charged poly(acrylic acid--acrylamide).

Temperature-Controllable Hydrogels in Double-Walled Microtube Structure Prepared by Using a Triple Channel Microfluidic System.

Hydrogels in the shape of double-walled microtubes possess great potential for development into artificial human blood vessels. In this work, we have prepared temperature-responsive tubular hydrogels with selectively controllable wall diameters, by using alginate templated photopolymerization in a triple channel microfluidic device. These tubular hydrogels mimic human blood vessels because of the separate thermally active inner and passive outer walls.

Microfluidic Fabrication of Multistimuli-Responsive Tubular Hydrogels for Cellular Scaffolds.

Stimuli-responsive hydrogel microfibers and microtubes are in great demand for biomedical applications due to their similarity to the native extracellular matrix. In this study, we prepared pH- and temperature-responsive hydrogel microfibers and microtubes using a microfluidic device through alginate-templated photopolymerization. Hydrogel monomer solutions containing N-isopropylacrylamide (NIPAm) and sodium acrylate (SA) or allyl amine (AA) were irradiated with UV light to invoke in situ photopolymerization.