This review addresses the potential development of polymer hydrogels in terms of fast stimuli responsiveness and superior mechanical properties. The slow response and mechanical weakness of stimuli-sensitive hydrogels have been considered as the main barriers for their further development and practical application. It has been a dream of scientists to have fast stimuli-responsive hydrogels with superior mechanical performance. In this review, the principal reasons behind the poor stimulus sensitivity and mechanical strength of polymer gels are highlighted, and we present some pioneering physical and chemical efforts aimed at fabricating hydrogels with high stimuli sensitivities and/or superior mechanical properties.
Polymer hydrogels (hereafter called ‘hydrogels’) are three-dimensional polymer networks in which the voids are filled with water. These hydrogels are widely used in a variety of industrial and consumer products such as oil dewatering systems, mechanical absorbers, diapers and contact lenses. One of the most remarkable areas of research on hydrogels in the past few decades has been their stimulus sensitivity. Hydrogels composed of stimuli-responsive polymers reversibly alter their shape and volume in response to small variations in the environment, such as pH, temperature, light and electric and magnetic fields, thereby changing their physico-chemical characteristics.1 Among all of the available environmentally responsive hydrogels, temperature-responsive hydrogels have attracted the most attention because of the facile tuning of their properties. In particular, poly(N-isopropylacrylamide) (poly(NIPA)) hydrogels have been widely investigated as thermosensitive hydrogels. Poly(NIPA) has a low critical solution temperature (LCST) at around 32 °C in water. The flexible coil of poly(NIPA) (soluble) converts into a compact globular state (insoluble) at the LCST, and this conformational change is reversible.2 Thus, hydrogels composed of poly(NIPA) undergo a reversible volume change at a similar transition temperature in water. Poly(NIPA) hydrogels have potential applications in drug delivery systems, therapeutic agents, diagnostic devices, biomaterials, cell cultivation, biocatalysts, sensors, microfluidic devices, actuators, optical devices and size-selective separation among others.3, 4, 5
A recent subject that has attracted much attention in the field of gel science is the fabrication of hydrogels with the rapid stimuli responsiveness and superior mechanical properties required for many applications of stimuli-responsive hydrogels. The creation of durable hydrogels that exhibit reversible and rapid changes in shape or volume, the likes of which are found in living organisms such as muscle, has been a challenge for materials chemists. Hydrogels synthesized from monomer solutions by radical polymerization, a general-purpose method for making synthetic hydrogels, however, face several constraints. The inherently weak mechanical properties caused by underlying spatial inhomogeneity during polymerization and extremely slow responsiveness caused by critical slowing down and vitrification during the shrinking process restrict the widespread use of these hydrogels.6 Although some approaches have been developed to improve the stimuli sensitivities and mechanical properties of hydrogels, it remains a challenge to design ideal gel networks with a combination of desired properties.
In this review, we will begin by introducing some pioneering work in the synthesis of hydrogels with fast stimuli responsiveness specifically attributed to chemical modifications. Work based on thermosensitive NIPA as a monomer has been the main focus of attention. Although hydrogels synthesized through these techniques improve stimuli sensitivity to a greater extent, in most cases, not enough attention has been given to the mechanical properties of these hydrogels, and these properties have not been improved. We will therefore review some recently developed novel methods to improve the mechanical properties of hydrogels and discuss the application of these methods for preparing stimuli-responsive hydrogels with superior mechanical performance.
Fast stimuli-sensitive hydrogels
The volume phase transition7, 8, 9 of hydrogels between the swollen state and collapsed state in response to various types of stimuli indicates that hydrogels can be used as smart materials. Here, the term ‘smart’ refers to materials that are sensitive to changes in the environment. Unfortunately, however, the slow response of hydrogels, which is an inherent characteristic of the volume phase transition phenomenon caused by a critical slowing down, has prevented them from being developed for new technologies. Moreover, vitrification during the shrinking process also contributes to the slow change in volume. After a temperature jump, a dense skin layer forms on the surface of poly(NIPA) hydrogels that inhibits water loss from the inner portion and, consequently, slows down the volume change.10 Without the volume phase transition, in which the volume change of hydrogels is drastic but continuous, the characteristic duration of the volume change can be much shorter than in a discontinuous system. The relaxation time of the volume change of hydrogels, however, is highly dependent on the size of the hydrogel, as the swelling and deswelling of hydrogels is a diffusion process. According to the Tanaka-Fillmore theory, the shrinking rate is inversely proportional to the square of the smallest spatial dimension of the hydrogel. As a result, large, bulky hydrogels typically exhibit slow changes in volume.6
To date, many physical processes have been developed to obtain high thermosensitivity in poly(NIPA) hydrogels, including the following: preparations of phase-separated heterogeneous structures11, 12 and macroporous or mesoporous structures,13, 14, 15 gel formation via vacuum synthesis,16 as well as freezing techniques.17, 18 As an example, a poly(NIPA) hydrogel with a phase-separated heterogeneous network structure can be prepared by polymerization at a temperature above the LCST or in particular mixed solvents, including solvents composed of H2O and an organic solvent such as acetone, phenol or tetrahydrofuran. A pore-forming component such as sodium chloride, glucose, poly(ethylene glycol) (PEG), SiO2 or a hydrophilic or hydrophobic additive can be introduced into the pregel solution. The subsequent removal of this pore-forming component from the hydrogel network provides a macroporous network with fast thermoresponsiveness. The basic mechanism of all these processes involves the effect of micro- or macro-level manipulated structures, which are much larger than molecular level structures, on the quick volume change by the expulsion or absorption of water molecules from or into the hydrogel network. These processes, however, are not suited for some practical applications, as the hydrogels lose their mechanical strength, toughness and optical transparency because of their spongy structures. We will not further discuss such porous hydrogels; rather, we will primarily focus on the strategies used to obtain fast thermoresponsive hydrogels using chemical techniques by which the gel networks are modified at the molecular level. Some of the basic techniques used are mentioned below.
Comb-type poly(NIPA)-grafted gels
Yoshida et al. prepared comb-type poly(NIPA)-grafted gels as follows. First, a chain transfer agent was used to synthesize various linear poly(NIPA)s with different molecular weights and one amino end group. Next, the amino group was converted into an acrylate group that could polymerize with other vinyl monomers. Finally, the semitelechelic linear poly(NIPA)s with acrylate end groups were polymerized with NIPA and small amounts of a crosslinker. Poly(NIPA) chains with one freely mobile side end were thereby grafted onto the polymer networks (Figure 1a).19, 20 These grafted polymer chains can respond faster than crosslinked poly(NIPA) chains and form hydrophobic nuclei in response to a rise in temperature (Figure 1b). The aggregated nuclei then form many channels for the diffusion of water to enhance the shrinking rate of the crosslinked segment of the hydrogel with respect to non-grafted traditional poly(NIPA) hydrogels.
Similarly, the application of a living radical polymerization method to prepare a comb-type grafted polymer network significantly enhances the deswelling response of poly(NIPA) gels.21, 22 Liu et al.21 used reversible addition-fragmentation chain transfer polymerization to synthesize a functional poly(NIPA) hydrogel (Figure 2). This hydrogel consisted of dangling chains, mainly caused by a chain transfer reagent that markedly retarded the crosslinking reaction and showed accelerated shrinking kinetics and higher swelling ratios compared with conventional hydrogels.
Poly(NIPA) hydrogels with micellar structures for water pathways
Noguchi et al.23 grafted surfactants capable of micelle formation on the polymer network of a poly(NIPA) gel (Figure 3a). These grafted surfactants form micelle structures at temperatures above the LCST (Figure 3b). In the shrinking process, trapped water molecules are quickly squeezed out through the hydrophilic channels between the hydrophilic outer shells of the micelles; consequently, the hydrogel shrinks rapidly. A pendant micelle structure can also be introduced into the polymer chains to improve their thermosensitivity.24
Interpenetrating polymer network gels with low skin layer formation
Gil and Hudson25 developed an interpenetrating polymer network (IPN) of silk fibronin/poly(NIPA). The silk fibronin reduces skin layer formation; consequently, a fast deswelling rate is observed for the hydrogel (Figure 4). Poly(NIPA) hydrogels with an IPN structure exhibit slightly improved mechanical strength: The compression modulus and tensile modulus of IPN-poly(NIPA) hydrogels are, respectively, 3.5 and 16.8 times higher than those of conventional poly(NIPA) hydrogels.26 A semi-IPN created by combining poly (acrylic acid) and a porous poly(NIPA) hydrogel also shows fast responses to both temperature and pH changes.27 If a small amount of hydrophilic moieties is introduced into the hydrogel network, hydrophobic aggregation on the hydrogel surface decreases; consequently, the formation of a thick, impermeable skin layer is protected to give fast thermoresponsiveness.28, 29 When large amounts of hydrophilic moieties are used, however, the hydrogel drastically loses its deswelling kinetics.
As mentioned above, the formation of stimuli-sensitive water pathways and the inhibition of skin layer formation during the contraction of hydrogels are the primary ways used to obtain fast stimuli-responsive hydrogels. All of the fast stimuli-responsive hydrogels discussed above have the potential to be smart hydrogels, but their mechanical properties, homogeneity, biocompatibility and reversibility need to be improved for applications that require mechanical durability.
Hydrogels with strong mechanical properties
Free-radical polymerization of a random crosslink between monomers and crosslinkers results in both lightly and heavily crosslinked regions in gel networks, and these different types of regions introduce spatial inhomogeneity into hydrogels. Chemical crosslinks fix the polymer chains to different segments with different lengths. Under deformation, most of the stress is thereby localized on the shortest polymer chains, and soon the crosslinked polymer networks split into several pieces. This mechanical weakness at the molecular level is also sustained at the macro level; thus, conventional hydrogels are mechanically fragile by nature. Recently, various research groups have reported mechanically superior hydrogels. In this section, these mechanically superior hydrogels will be reviewed briefly.
A polymer network in which the polymer chains are tied together by slide-ring pulleys is considered to show unique mechanical properties, as the elasticity of the gel is a consequence of only the chain's topology. Ito and co-workers30, 31, 32, 33 prepared such a ‘slide-ring’ (SR) gel and showed its unique properties. SR gels can be prepared from a polyrotaxane architecture consisting of a number of cyclic molecules (α-cyclodextrin, α-CD) threaded onto a long linear polymer chain (PEG), followed by trapping the cyclic molecules by capping with bulky end groups (Figure 5). Some of the cyclic molecules are then chemically attached to form a figure-eight structure and form the SR gel. The figure-eight crosslinks can move along the long polymer axis to minimize local stress in the gel, similar to pulleys, and this sliding motion gives rise to remarkable physical properties in SR gels (Figure 6). SR gels are considered an intermediate between physical gels and chemical gels, as the polymer network is not formed by either covalent crosslinks, as in chemical gels, or attractive interactions, as in physical gels. This pulley effect has been confirmed through analysis of the static structure of SR gels under uniaxial deformation using small-angle neutron scattering34, 35 and small-angle X-ray scattering.36 A prolate pattern perpendicular to the deformation direction, which is known as a normal butterfly pattern or an almost isotropic pattern, has been reported for SR gels. This pattern is evidence of the pulley effect in SR gels and represents the first observation of a normal butterfly pattern in any polymeric gel. The sliding mode of α-CD in polyrotaxanes and that of crosslinking junctions in SR gels have also been observed in quasi-elastic light scattering studies37 and dynamic light scattering studies.38 SR gels have high stretchability, reaching up to 24 times their original length without hysteresis. In the stress–strain curve of SR gels, a J-shaped curve without any hysteresis loop has been reported, which is completely different from the stress–strain curves of both physical and chemical gels (Figure 7).39, 40 The mechanical strength of SR gels has been reported to be similar to that of mammalian skin, vessels and tissues. SR gels become stiffer as the extension ratio reaches the fracture point; therefore, they could be used as a substitute for various types of biomaterials. Koga and Tanaka41 reported a molecular simulation of Brownian dynamics using a simple model of a polymer network with trifunctional sliding junctions to study the elastic properties of SR gels compared with conventional polymer gels. SR gels exhibit a huge transient overshoot in the swelling and shrinking process at a stepwise change in solvent from 0.1 M NaCl aqueous solution to water and from water to acetone, respectively. This overshoot occurs approximately 20 min after changing the solvent and is assumed to be closely related to the pulley effect. Depending on solvent composition, the volume change of SR gels has been used to prepare stimuli-responsive photonic band gap materials using a closely packed colloidal crystal as a template in which the structural color changes.42 Furthermore, the modification of α-CD by some stimuli-sensitive groups can provide SR gels with stimuli sensitivity. For example, a new type of photoresponsive polymer gel has been developed by introducing an azobenzene moiety on the α-CD of polyrotaxane.43 This azobenzene-modified SR gel exhibits enormous photo-induced deformation and characteristic transient overshoot behavior during expansion.
Solving the inherent inhomogeneity of hydrogel network structures is one of the best ways to improve the mechanical properties of hydrogels. A novel hydrogel named a ‘tetra-PEG gel’ was reported by Sakai et al.,44, 45 in which the combination of two symmetrical tetrahedron-like macromers of the same size resulted in a homogeneous, almost ideal network structure. In that study, four-armed PEG was used to prepare two types of macromers with a tetrahedron-like structure: tetra-amine-terminated PEG and tetra-succinimidyl ester-terminated PEG (Figure 8). Mixing two macromer solutions under controlled pH forms amide bonds between the terminal amino groups and the succinimidyl ester groups; thus, a highly homogeneous, symmetrical, tough tetra-PEG hydrogel network is formed (Figure 9a). Unlike conventional hydrogels, the formation of topological inhomogeneities such as dangling chains, entanglements and loops is negligible in tetra-PEG gels. Dynamic light scattering results suggest that tetrahedral macromers connect to each other alternately to form a network with a characteristic length corresponding to a two-arm length. Tetra-PEG gels can be well fitted to available theoretical scattering functions (the Ornstein–Zernike function), and no observable excess scattering appears in the small-angle neutron scattering results.46 Young’s modulus of tetra-PEG gels is proportionally correlated to polymer volume fractions, indicating the absence of entanglements in the network.47 It has been observed that the compressive strength of tetra-PEG gels is on the order of a few to tens of MPa for a 120 mg ml−1 gel made from a macromer with Mw=10 000. This strength is as high as that of articular cartilage (Figure 9b). The technique to prepare the homogeneous structure of tetra-PEG gels could be used to prepare stimuli-sensitive hydrogels composed of other functional polymers.
Homogenous hydrogels by a click reaction
Malkoch et al. used click chemistry to prepare a well-defined, PEG-based homogeneous hydrogel network with superior mechanical strength.48, 49 In that approach, copper (I)-catalyzed 1,2,3-triazoles formed from azides and terminal acetylene were used for a specific click reaction (Figure 10).50 The unreacted azide and/or acetylene groups allow the incorporation of various additives and functional groups in the hydrogel network without affecting network formation, and the gelation can be performed under mild conditions at room temperature. The click technique forms a gel network via controlled crosslinking, providing an ideal gel network and resulting in improved swelling and mechanical behaviors. Hydrogels prepared by a click reaction using long PEG (Mn=10 000) have true stress of ∼2390 kPa and elongation at a break of ∼1550%. No studies have yet reported the stimuli sensitivity of click gels, but we believe that these gels will exhibit interesting stimuli sensitivity because of their well-defined and homogeneous gel network.
Creative crosslinker structures such as those found in SR gels are also a good way to improve the mechanical properties of hydrogels. Haraguchi and Takehisa51 used various types of clay particles as crosslinkers to prepare nanocomposite hydrogels (NC gels). They first reported NC gels prepared by in situ free-radical polymerization of NIPA in the presence of uniformly dispersed inorganic exfoliated clay particles (clay platelets) in aqueous media (Figure 11). The clay platelets function as multifunctional crosslinkers: the ends of the polymer chains adsorb strongly on the surface of the clay platelets by ionic and coordination interactions.52 The intercrosslinking distance is equivalent to the distance between neighboring clay particles and is very large. In the elongated state of NC gels, these large, flexible polymer chains are capable of being highly and reversibly elongated without breaking the short polymer chains, giving superior mechanical strength to NC gels. NC gels also exhibit high levels of deformation on elongation, compression, tearing, bending, twisting and knotting.53, 54 Depending on the kind of clay particles and monomer used for NC gels, these gels can generally be elongated to more than 1000% of their original length (Figure 12). The modulus value and the fracture energy of NC gels are also much higher than those of conventional poly(NIPA) gels.55 By increasing concentration of clay platelets (Cclay) up to 25 mol%, NC gels exhibit noteworthy increases in strength, modulus and fracture energy without sacrificing elongation at break.56 Irrespective of the nature of polymer and clay content, NC gels are generally very transparent, indicating the formation of uniform network structures with fewer spatial inhomogeneities, unlike that found in conventional hydrogels. The static and dynamic structures of NC gels as a function of the Cclay have been reported by studies using small-angle neutron scattering, small-angle X-ray scattering and dynamic light scattering.57, 58, 59 NC gels using NIPA with small amounts of clay platelets exhibit higher swelling ratios and faster deswelling compared with conventional poly(NIPA) gels.60, 61 In contrast, with increasing Cclay, the mobility of poly(NIPA) chains gradually decreases because of the high crosslinking density; consequently, the deswelling rate also decreases. Moreover, when a large amount of clay is used, the thermosensitivity of NC gels is completely lost.55 However, given that NC gels are essentially a kind of physical gel, their network structure can be dissolved in certain environments. Even so, NC gels are very useful for many applications.
Double network gels
Gong et al. prepared double network (DN) gels, previously known as IPN gels, with superior mechanical strength and toughness.62 DN gels can be synthesized by two kinds of crosslinked polymer networks, in which one network is made from heavily crosslinked rigid polyelectrolyte polymer and the other is made from lightly crosslinked or, in some cases, an uncrosslinked, flexible uncharged polymer (Figure 13). At first, a moderately tight crosslinked gel is formed. After swelling, this first network in a solution of a second monomer with little or no crosslinking agent is used to prepare the second network. Given that the first network is highly swollen in the second monomer solution, the second network is effectively entangled with the first network to form a very strong DN gel.62, 63, 64, 65, 66, 67 The first network contributes to an increase in elastic stress, whereas the second network contributes to an increase in strain. Numerous polymer pairs have been used to optimize the characteristic behaviors of DN gels, and the methyl-propane sulfonate polymer/acrylamide polymer pair has been found to be the most promising. Methyl-propane sulfonate polymer/acrylamide polymer-based DN gels exhibit both hardness (elastic modulus of 0.3 MPa) and toughness (compressive strength of ∼20 MPa) (Figure 14). The tearing fracture energy of methyl-propane sulfonate polymer/acrylamide polymer-based DN gels under optimized conditions can be as high as 103 Jm−2, much higher than that of acrylamide polymer (∼10 Jm−2) and methyl-propane sulfonate polymer gels (∼0.1 Jm−2) alone.68, 69
The structure and property relationships of DN gels have been studied by small-angle neutron scattering,70 dynamic light scattering,71 molecular dynamics simulations,72, 73 modeling of crack formation74 and void formation.71 Entanglements between two polymer networks are a prerequisite condition in all cases for the toughness of DN gels.75 After the innovation of DN gels, some research groups began studying various avenues of research with DN gels, but no detailed observations of stimuli sensitivity have been reported thus far, except in the work of Liang et al.76 Recently, they reported a fast and high solvent-triggered force generation considering their mechanical toughness for very thin DN gels. As high-level inhomogeneities are the origin of superior toughness of DN gels, the stimuli sensitivity of bulk DN gels could be very complex. Moreover, in such IPNs, the stimuli sensitivities for each polymer become seriously impaired because of interactions between the polymers. Thus, it might be considerably difficult to design a stimuli-sensitive hydrogel with good mechanical properties simply using a DN gel. As the mechanical properties of DN gels are substantially superior, however, these gels should have broad applications.
Our approach for making hydrogels with fast stimuli sensitivity and superior mechanical performance
Here, we report a facile and universal approach to introduce the slide-ring phenomenon into conventional hydrogels in order to obtain highly mechanically stable and fast stimuli-responsive hydrogels. We focused on the exploitation of the intriguing properties of polyrotaxanes as crosslinkers in the synthesis of stimuli-sensitive hydrogels. A sparsely dispersed polyrotaxane was used, consisting of larger numbers of α-CD and long PEG (Mw=35 000) molecules in the presence of bulky-end 1-adamantanamine groups in the polymer axis, which prevented the dethreading of α-CD. The hydroxyl groups of α-CD or α-CD derivatives of polyrotaxanes were modified by isocyanate monomer (2-acryloyloxyethylisocyanate) through the formation of a stable carbamate bond, resulting in the hydrophobic polyrotaxane crosslinker, MPR and hydrophilic polyrotaxane crosslinker, MHPR, respectively.77, 78, 79 The solubility and degree of substitution (DS) (0≤DS≤18), that is, the average number of substituted hydroxyl groups per α-CD molecule, could be tuned by changing the derivatives of α-CD or the amount of isocyanate monomer. Hydrogels were fabricated using conventional free-radical polymerization of thermosensitive NIPA monomer or using several types of ionic comonomers in the presence of MPRs or MHPRs as crosslinkers (Figure 15). As a result, we obtained mechanically superior poly (NIPA) hydrogels: rotaxane-NIPA (RN) gels or ionic rotaxane-NIPA (iRN) gels. Moreover, these new types of crosslinkers could easily be applied to a wide range of monomers to synthesize hydrogels by free-radical polymerization and improve their stimuli responsiveness and mechanical properties. RN gels exhibit irregular swelling behavior and resemble graft or block copolymer gels in that the volume phase transition temperature of RN gels is similar to that of conventional poly(NIPA) hydrogels.
In water, RN gels exhibit a sharp volume phase change around the LCST of poly(NIPA). After a sudden temperature jump, RN gels shrink isotropically without creating any deformation on their surface, and the rate of deswelling is very fast. Two stages of relaxation of the volume change have been observed in RN gels during the shrinking process, but most of the change occurs in the first stage. The first-stage relaxation time τ1 for RwiN gels (MPR-based gels) and RwsN (MHPR-based gels) gels is 1.26 × 102 and 2.11 × 102 s, respectively, whereas the second-stage relaxation time τ2 is 1.27 × 104 and 6.1 × 103 s, respectively (Figure 16).78 The second-stage relaxation for RN gels might be derived from the final rearrangement of aggregated nuclei to reach equilibrium-shrunken states. Above the LCST, the crosslinked poly (NIPA) chains of conventional poly(NIPA) gels form a phase-separated insoluble globular structure and the fixed crosslinking facilitates the formation of an insoluble skin layer on the surface. Water molecules cannot pass through this impermeable skin layer. On the other hand, the dynamic nature of the crosslink points may help to aggregate polymer networks to reach the complete collapsed state before forming any impermeable skin layer on the surfaces of RN gels. The micro- and macro-level spatial inhomogeneities and local stresses inside the polymer networks of RN gels can automatically be homogenized and relaxed by movement of the mobile crosslink points. Thus, RN gels shrink by the growth of nucleation without going through the unstable spinodal decomposition mechanism, resulting in very fast shrinking rates. Although RwiN gels reach an equilibrium-shrunken state very quickly and isotropically, hydrophobic aggregation of the water-insoluble MPR gives the gel permanent opacity in the collapsed state. To overcome this problem, the hydrophilic polyrotaxane crosslinker MHPR has been used to prepare RwsN gels. The hydrophilicity of the crosslinker retains the homogeneity of the RwsN gel network and restricts the formation of aggregated globules, permitting the poly(NIPA) chains inside the gel network to move and rotate freely along the long polymer axis under deformation. RN gels exhibit much smaller storage moduli E′ and loss moduli E″ than do conventional poly(NIPA) hydrogels in the frequency ranges studied, indicating the very soft nature of RN gels. When a frequency is applied to RN gels, the poly(NIPA) chains inside the gel network squeeze enough. Because of the sliding and rotating ability of the crosslinks in the RN gels, however, the poly(NIPA) chains can gradually equalize this tension. These movable crosslinks allow the poly(NIPA) chains to relax under deformation, whereas the fixed crosslink networks of conventional poly(NIPA) hydrogels cannot avoid localization of the stress to short poly(NIPA) chains and soon lose their mechanical integrity. An increase in the amount of crosslinker or temperature results in increases in both E′ and E″ in both water and dimethylsulfoxide. Thus, the softness or hardness of RN gels seems to be well controlled. Although RN gels prepared by hydrophobic and hydrophilic polyrotaxane crosslinkers show significant improvements in various respects, they do not show appreciable tensile strength under deformation. The shrinkage of the crosslinkers in water may obstruct the fluid movement of α-CD, which could prevent improvement of the mechanical properties of RN gels.
When a small amount of ionic comonomer (for example, sodium acrylate) is introduced into RN gel networks, the electrostatic repulsion between the ionic groups and the osmotic pressure due to the presence of the counter ions increases the dispersity of the polymer chains attached to α-CD through the long PEG chains, thereby, enhancing the mechanical strength of the hydrogel (A Bin Imran et al., in preparation). The discontinuous volume changes of iRN gels with temperatures could be changed to continuous ones only by changing the pH of the aqueous medium from acidic to basic. iRN gels show normal butterfly patterns in their small-angle X-ray scattering profiles, strongly suggesting the presence of sliding crosslinks that effectively reduce spatial inhomogeneities. The polymer chains in conventional hydrogels are stretched and organized in the stretching, and the frozen structures are displaced along the stretching direction without any notable changes in shape, indicating that spatial inhomogeneity increases in the stretching direction and gives an abnormal butterfly pattern in the scattering pattern. In contrast, the spatial inhomogeneities of iRN gels do not increase in the stretching direction because of the presence of movable crosslinks; consequently, normal butterfly patterns appear in the scattering profile. iRN gels exhibit high levels of deformation with elongation, compression, tearing, bending and twisting and do not readily tear at any cut or notch. The elongation at the break of iRN gels is very high (∼1000% strain) and decreases with increasing amounts of crosslinker. Interestingly, the tensile strength of iRN gels is similar to that of SR gels. The high mechanical integrity of iRN gels suggests that iRN gels could potentially be used as biomaterials, as the softness of the gels would reduce the mechanical and frictional irritation to surrounding tissues. The phenomena observed in iRN gels could successfully be exploited for the development of materials with diverse applications, such as photosensitive materials, biomedical applications, drug delivery systems, smart actuators, contact lenses, artificial cartilage/joints, artificial blood vessels, wound healing materials, shock-absorption materials and adhesives.
The techniques described in this review are very promising for improvement of the stimuli sensitivity and mechanical properties of hydrogels. If a hydrogel can be developed that combines high-quality mechanical performance with fast stimuli responsiveness, it could be widely used for applications ranging from biomedical to commercial. Advanced techniques to improve the mechanical properties and fast stimuli sensitivity of hydrogels simultaneously are expected to expand the range of applications for hydrogels. Among all the hydrogels described, only NC gels and RN gels have been reported to have both fast deswelling kinetics and superior mechanical strength. Research in this area is still in its rudimentary stage and must go further to significantly improve the applications of hydrogels in diverse areas.
This work was partially supported by a Grant-in-Aid for Scientific Research on Innovative Area of ‘Fusion Materials: Creative Development of Materials and Exploration of Their Function through Molecular Control’ (no. 2206) from the Ministry of Education, Culture, Sports, Science, and Technology.
About this article
Colloid and Polymer Science (2019)