As a new class of high-strength hydrogels, we designed a tetra-PEG gel by combining two symmetrical tetrahedron-like macromonomers of the same size. Because the nanostructural unit of the gel network was defined by the length of the tetrahedral PEG arm, the gel had a homogeneous structure and resultant high mechanical strength comparable to that of native articular cartilage. Furthermore, since the gel was formed by mixing two biocompatible macromonomer solutions, the gelation reaction itself and the resultant gel were also biocompatible. The breaking strength had local maxima at the overlap concentration of the macromonomers (C*) and at 2C*. Dynamic light scattering measurement indicated the near absence of inhomogeneities in the network at C*. Thus, we successfully designed and fabricated a high-strength hydrogel by controlling the homogeneity of network structure for the first time, which will lead to multiplied effects, i.e., contributing to the understanding of ideal networks, providing a universal strategy for designing high-strength gels, and opening up the biomedical application of hydrogels.

Hydrogels are three-dimensional polymer networks that contain a large amount of water inside. Certain hydrogels can be injected in solution and transformed into the gel state with the required shape. Despite their potential biomedical applications, the use of hydrogels has been severely limited because all the conventional hydrogels inevitably "swell" under physiological conditions, which drastically degrades their mechanical properties. We report the synthesis of injectable "nonswellable" hydrogels from hydrophilic and thermoresponsive polymers, in which two independently occurring effects (swelling and shrinking) oppose each other. The hydrogels can endure a compressive stress up to 60 megapascals and can be stretched more than sevenfold without hysteresis. Our results demonstrate that the suppression of swelling helps retain the mechanical properties of hydrogels under physiological conditions.

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The structure of Tetra-PEG gel, a new class of biocompatible, easy-made, and high-strength hydrogel consisting of a four-arm polyethylene glycol (PEG) network, has been investigated by means of small-angle neutron scattering (SANS). Since the Tetra-PEG gel is prepared by cross-end-coupling two kinds of four-arm PEG macromers having different functional groups at the ends, i.e., amine group and succinimidyl ester group respectively, the coupling reaction occurs exclusively between PEG chains carrying different functional groups. SANS results showed that the four-arm PEG macromer aqueous solutions and Tetra-PEG gels were successfully described by the theoretical scattering function for multiarm Gaussian chains and the Ornstein-Zernike function, respectively. Surprisingly, no noticeable excess scattering that originated from cross-linking was observed in Tetra-PEG gels, suggesting that its network structure is extremely uniform. Investigations on nonstoichiometric Tetra-PEG gels showed weakening of the mechanical properties as well as an increase of dangling chains (defects) in the network. It is concluded that Tetra-PEG gels have an extremely uniform network structure, probably mimicking a diamond-like structure, and this is one of the reasons for the advanced mechanical properties of Tetra-PEG gels.