Nanohybrid Hydrogels Research Articles

Tailoring electrochemical properties of hydrogel by different types of graphene oxide

In this study, different concentrations of graphene oxides prepared according to Brodie’s and Hummers’ method (GOB and GOH, respectively) were integrated with mixture of citric acid and hydroxyethyl cellulose (HEC-CA). This three-component solution could be easily coated on glassy carbon electrode surface and thermally crosslinked, forming solid films of nanohybrid hydrogels (HEC-CA-GOB and HEC-CA-GOH). The coated electrodes were characterized by different electrochemical techniques, which revealed that, compared to GOB, GOH significantly hindered diffusion of electroactive species to the electrode surface. Furthermore, application of the electrodes coated with HEC-CA-GOB and HEC-CA-GOH as voltammetric detectors of toxic metals and histamine was investigated. For the former, a low amount (0.075 mg mL−1) of GOB in HEC-CA enhanced the voltammetric response towards Pb2+ and Cu2+ up to 6.5 and 10 times, respectively while effect of GOH was less sound. In histamine detection, 1 mg mL−1 GOB or GOH in HEC-CA improved the response of the electrodes towards the histamine by approximately 25 % and improved antifouling properties of the sensors. As a conclusion, adjusting of GO content in the hydrogel was shown as an interesting and facile tool for preparation of electrodes with wide range of properties adjustable such as to meet requirements of various applications.

Recent advances in near-infrared stimulated nanohybrid hydrogels for cancer photothermal therapy.

Nanomedicine has emerged as a promising avenue for advancing cancer treatment, but the challenge of mitigating its in vivo side effects necessitates the development of innovative structures and materials. Recent investigation has unveiled nanogels as particularly compelling candidates, characterized by a porous, three-dimensional network architecture that exhibits exceptional drug loading capacity. Beyond this, nanogels boast a substantial specific surface area and can be tailored with specific chemical functionalities. Consequently, nanogels are frequently engineered as a multi-modal synergistic platform for combating cancer, wherein photothermal therapy stands out due to its capacity to penetrate deep tissues and achieve localized tumor eradication through the application of elevated temperatures. In this review, we delve into the synthesis of diverse varieties of photothermal nanogels capable of controlled drug release triggered by either chemical or physical stimuli. It also summarizes their potential for synergistic integration with photothermal therapy alongside other therapeutic modalities to realize effective tumor ablation. Moreover, we analyze the primary mechanisms underlying the contribution of photothermal nanogels to cancer treatment while underscoring their adeptness in regulating therapeutic temperatures for repairing bone defects resulting from tumor-associated trauma. Envisioned as an auspicious strategy in the realm of cancer therapy, photothermal nanogels hold promise for furnishing controlled drug delivery and precise thermal ablation capabilities.

Engineered Highly Porous Polyvinyl Alcohol Hydrogels with Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) and Graphene Nanosheets for Musculoskeletal Tissue Engineering: Morphology, Water Sorption, Thermal, Mechanical, Electrical Properties, and Biocompatibility.

Electroactive composite materials are very promising for musculoskeletal tissue engineering because they can be applied in combination with electrostimulation. In this context, novel graphene-based poly(3-hydroxybutyrate-co-3-hydroxyvalerate)/polyvinyl alcohol (PHBV/PVA) semi-interpenetrated networks (semi-IPN) hydrogels were engineered with low amounts of graphene (G) nanosheets dispersed within the polymer matrix to endow them with electroactive properties. The nanohybrid hydrogels, obtained by applying a hybrid solvent casting-freeze-drying method, show an interconnected porous structure and a high water-absorption capacity (swelling degree > 1200%). The thermal characterization indicates that the structure presents microphase separation, with PHBV microdomains located between the PVA network. The PHBV chains located in the microdomains are able to crystallize; even more after the addition of G nanosheets, which act as a nucleating agent. Thermogravimetric analysis indicates that the degradation profile of the semi-IPN is located between those of the neat components, with an improved thermal stability at high temperatures (>450 °C) after the addition of G nanosheets. The mechanical (complex modulus) and electrical properties (surface conductivity) significantly increase in the nanohybrid hydrogels with 0.2% of G nanosheets. Nevertheless, when the amount of G nanoparticles increases fourfold (0.8%), the mechanical properties diminish and the electrical conductivity does not increase proportionally, suggesting the presence of G aggregates. The biological assessment (C2C12 murine myoblasts) indicates a good biocompatibility and proliferative behavior. These results reveal a new conductive and biocompatible semi-IPN with remarkable values of electrical conductivity and ability to induce myoblast proliferation, indicating its great potential for musculoskeletal tissue engineering.

Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release.

A poloxamer 407 (P407)-Casein hydrogel was chosen to carry polycaprolactone nanoparticles carrying terbinafine (PCL-TBH-NP). In this study, terbinafine hydrochloride (TBH) was encapsulated into polycaprolactone (PCL) nanoparticles, which were further incorporated into a poloxamer-casein hydrogel in a different addition order to evaluate the effect of gel formation. Nanoparticles were prepared by the nanoprecipitation technique and characterized by evaluating their physicochemical characteristics and morphology. The nanoparticles had a mean diameter of 196.7 ± 0.7 nm, PDI of 0.07, negative ζ potential (-0.713 mV), high encapsulation efficiency (>98%), and did not show cytotoxic effects in primary human keratinocytes. PCL-NP modulated terbinafine was released in artificial sweat. Rheological properties were analyzed by temperature sweep tests at different addition orders of nanoparticles into hydrogel formation. The rheological behavior of nanohybrid hydrogels showed the influence of TBH-PCL nanoparticles addition in the mechanical properties of the hydrogel and a long-term release of the nanoparticles from it.

Electroactive calcium-alginate/polycaprolactone/reduced graphene oxide nanohybrid hydrogels for skeletal muscle tissue engineering

Graphene derivatives such as reduced graphene oxide (rGO) are used as components of novel biomaterials for their unique electrical properties. Electrical conductivity is a crucial factor for muscle cells, which are electrically active. This study reports the development of a new type of semi-interpenetrated polymer network based on two biodegradable FDA-approved biomaterials, sodium alginate (SA) and polycaprolactone (PCL), with Ca2+ ions as SA crosslinker. Several drawbacks such as the low cell adhesion of SA and weak structural stability can be improved with the incorporation of PCL. Furthermore, this study demonstrates how this semi-IPN can be engineered with rGO nanosheets (0.5% and 2% wt/wt rGO nanosheets) to produce electroactive nanohybrid composite biomaterials. The study focuses on the microstructure and the enhancement of physical and biological properties of these advanced materials, including water sorption, surface wettability, thermal behavior and thermal degradation, mechanical properties, electrical conductivity, cell adhesion and myogenic differentiation. The results suggest the formation of a complex nano-network with different interactions between the components: bonds between SA chains induced by Ca2+ ions (egg-box model), links between rGO nanosheets and SA chains as well as between rGO nanosheets themselves through Ca2+ ions, and strong hydrogen bonding between rGO nanosheets and SA chains. The incorporation of rGO significantly increases the electrical conductivity of the nanohybrid hydrogels, with values in the range of muscle tissue. In vitro cultures with C2C12 murine myoblasts revealed that the conductive nanohybrid hydrogels are not cytotoxic and can greatly enhance myoblast adhesion and myogenic differentiation. These results indicate that these novel electroactive nanohybrid hydrogels have great potential for biomedical applications related to the regeneration of electroactive tissues, particularly in skeletal muscle tissue engineering.

Topical delivery of chemotherapeutic drugs using nano-hybrid hydrogels to inhibit post-surgical tumour recurrence.

Residual microtumours after surgical resection leading to tumour relapse is one of the major challenges for cancer therapy. Herein, we developed a nano-hybrid oligopeptide hydrogel for topical delivery of a chemotherapeutic drug, docetaxel (DTX), to inhibit the post-surgical tumour recurrence. This nano-hybrid hydrogel (DTX-CTs/Gel) was prepared by encapsulating DTX in cell-penetrating peptide-modified transfersomes followed by embedment in an oligopeptide hydrogel. The obtained DTX-CTs/Gel showed paintable and injectable properties, and could support prolonged retention at the administrated sites after topical administration. DTX-CTs released from the hydrogel presented high skin and tumour penetration capabilities, and increased the accumulation of DTX in the cancer cells leading to enhanced cell death. We showed that the topical delivery of DTX using DTX-CTs/Gel efficiently slowed down the tumour relapse in post-surgical mouse melanoma and breast tumour models.

Electrospun nanohybrid hydrogels for enhanced differentiation of myoblasts

Enhancement of myogenic differentiation was accomplished with nanohybrid hydrogels composed of fragmented electrospun nanofibrils (NFs) and gelatin/alginate hydrogels. Electrospun nanofibrous meshes were fragmented and hydrolyzed to short fragments of NFs and subsequently embedded in gelatin/alginate hydrogels and further crosslinked with C2C12 cells. Cell-incorporated NF-embedded hydrogels exhibited a lower swelling ratio and higher mechanical properties as compared to hydrogels without NF due to the rigidity of NF and increased matrix-to-cell interaction. Viability of C2C12 cells in the hydrogels gradually increased in proportion to the amount of NF in the hydrogels. Both confocal microscopy and myogenic gene expression analysis indicated that the formation and maturation of myotubes and the expression of muscle motor proteins were significantly accelerated when NF-embedded hydrogels were employed. Contraction behavior of matured myotubes under electrical stimulation revealed that myotubes in NF-embedded hydrogels exhibited a longer contraction length than that of myotubes in hydrogels without NF. Thus, the nanohybrid matrix demonstrates the potential of nanofiber-embedded hydrogels for engineering myotube formation with topographical cues.

Synergic formulation of onion peel quercetin loaded chitosan-cellulose hydrogel with green zinc oxide nanoparticles towards controlled release, biocompatibility, antimicrobial and anticancer activity.

The therapeutic prospective of a novel carrier based delivery of phyto-derived quercetin (QE) extracted from onion peel waste was studied in the present work. Dialdehyde cellulose (DAC) developed from sugarcane bagasse (SCB) cellulose effectively crosslinked chitosan hydrogel. The hydrogel matrices were embedded with green zinc oxide nanoparticles (ZnO NPs), phyto-synthesized using musk melon seeds. The hybrid carrier formulation was characterised using analytical techniques such as XRD, FTIR and SEM analysis. The onion peel drug (OPD) analysed for its bioactive components using HPLC was reported as a potential source of QE. Taguchi optimization for the QE drug loading in the nanohybrid hydrogel indicated a remarkable improvement by 39% in comparison to drug loading in hydrogel without ZnO NPs. The maximum QE release was obtained at an optimal drug loading condition with pH 5.0, which favoured the anticancer applications. The drug release revealed a Fickian diffusion mechanism by adopting various kinetic models. The commercial QE and QE in OPD (QE/OPD) loaded nanohybrid hydrogels were found to inhibit the growth of Staphylococcus aureus and Trichophyton rubrum strains. The biocompatibility and anticancer properties of the QE/OPD loaded nanohybrid hydrogels were established against normal L929 murine fibroblast cells and A431 human skin carcinoma cell lines respectively.

Nanoparticle-Induced Controlled Drug Delivery Using Chitosan-Based Hydrogel and Scaffold: Application to Bone Regeneration.

The novel chitosan nanohybrid hydrogel and scaffold have been developed with high mechanical strength and tailor the drug release ability for their applications in the biomedical arena. Nanohybrid hydrogels are prepared in dilute acetic acid medium using two different types of two-dimensional-layered nanoparticles. Scaffolds are prepared through lyophilization of hydrogels. Highly porous, open, and 3D interconnected morphologies are observed in the nanohybrid scaffolds, as opposed to the thick wall, smaller pore dimension in pure chitosan. The interaction between the nanoparticles and chitosan chains are elucidated using different spectroscopic techniques, which in turn are responsible for the uniform distribution of the nanoparticle in the chitosan matrix. Nanohybrids are found to be highly mechanically stable in both states (hydrogel and scaffold), as compared to pure chitosan because of the good reinforcing ability of 2D nanoparticles. Sustained drug release has been achieved in nanohybrid in vitro, as compared to the pure chitosan hydrogel/scaffold, mainly due to greater interactions between the components and the better barrier effect of 2D nanoparticles. Cytotoxicity of the nanohybrids is verified using NIH 3T3 mouse embryonic fibroblast cells for their possible use as controlled drug delivery vehicles. Nanohybrids are found to be nontoxic in nature and more biocompatible as compared to pure chitosan, as observed through cell viability and cell imaging studies. Interestingly, cell growth occurs within the pores of the nanohybrid scaffold, vis-à-vis the surface proliferation noticed in the pure chitosan scaffold. Better biocompatibility, hydrophilic nature, and sustained delivery with location specific cell growth make this nanohybrid hydrogel unique for biomedical uses. The bone regeneration rate is found to be significantly higher for the nanohybrid scaffold as compared to blank/pure chitosan without any side effect, suggesting nanohybrid systems are superior biomaterials.

Nanohybrid hydrogels designed for transbuccal anesthesia.

BackgroundLocal anesthesia in dentistry is by far the most terrifying procedure for patients, causing treatment interruption. None of the commercially available topical formulations is effective in eliminating the pain and phobia associated to the needle insertion and injection.Materials and methodsIn this work we prepared a nanostructured lipid-biopolymer hydrogel for the sustained delivery of lidocaine–prilocaine (LDC-PLC) for transbuccal pre-anesthesia. The lipid was composed of optimized nanostructured lipid carriers (NLC) loaded with 5% LDC-PLC (NLC/LDC-PLC). The biopolymer counterpart was selected among alginate, xanthan (XAN), and chitosan matrices. The XAN-NLC hydrogel presented the most uniform aspect and pseudoplastic rheological profile, as required for topical use; therefore, it was selected for subsequent analyses. Accelerated stability tests under critical conditions (40°C; 75% relative humidity) were conducted for 6 months, in terms of drug content (mg/g), weight loss (%), and pH.ResultsIn vitro LDC-PLC release profile through Franz diffusion cells revealed a bimodal kinetics with a burst effect followed by the sustained release of both anesthetics, for 24 hours. Structural analyses (fourier transform infrared spectroscopy, differential scanning calorimetry and scanning electron microscopy) gave details on the molecular organization of the hybrid hydrogel, confirming the synergic interaction between the components. Safety and efficacy were evaluated through in vitro cell viability (3T3, HaCat, and VERO cells) and in vivo antinociceptive (tail-flick, in mice) tests, respectively. In comparison to a control hydrogel and the eutectic mixture of 5% LDC-PLC cream (EMLA®), the XAN-NLC/LDC-PLC hybrid hydrogel doubled and quadrupled the anesthetic effect (8 hours), respectively.ConclusionConsidering such exciting results, this multifaceted nanohybrid system is now ready to be further tested in clinical trials.

Strategy for Preparing Mechanically Strong Hyaluronic Acid–Silica Nanohybrid Hydrogels via In Situ Sol–Gel Process

AbstractA hybridization method to prepare a hyaluronic acid (HA)‐based nanohybrid hydrogel is proposed that introduces an additional inorganic silica network via an in situ sol–gel process. HA hydrogels have been extensively studied because of their excellent biocompatibility and biological functions; however, their poor mechanical strength hinders their use in tissue engineering applications. In the present work, the sol–gel technique is employed to achieve the formation of a structurally organized silica network in the HA hydrogel matrix rather than mixing of discrete particles with the HA polymer matrix. Importantly, the silica densification process results in significant enhancement of the mechanical properties. In addition, the nanohybrid hydrogels exhibit great degradation resistance and bioactivity on both fibroblast and pre‐osteoblast cells. Moreover, the physical characteristics and biological properties can be modulated by varying the silica content; these materials thus show great potential for a wide range of applications for soft and hard tissues.

POSS nanocrosslinked poly (ethylene glycol) hydrogel as hybrid material support for silver nanocatalyst

Silver nanoparticles supported on polyhedral oligomeric silsesquioxane (OA‐POSS) nanocrosslinked poly (ethylene glycol)‐based hydrogels (PEG600‐POSS/Ag NPs) as novel nanohybrid catalysts were synthesized for the first time. The as‐prepared nanohybrid hydrogels were fully characterized by FT‐IR, SEM, EDX, XRD, TEM and TGA. PEG600‐POSS/Ag NPs exhibited excellent catalytic performance for the reduction of 4‐nitrophenol (4‐NP) to 4‐aminophenol (4‐AP) in water at room temperature in the presence of borohydride.

Mechanically robust dual responsive water dispersible-graphene based conductive elastomeric hydrogel for tunable pulsatile drug release

Nanohybrid hydrogels based on pristine graphene with enhanced toughness and dual responsive drug delivery feature is opening a new era for smart materials. Here pristine graphene hydrogels are synthesized by in situ free radical polymerization where graphene platelets are the nanobuiliding blocks to withstand external stress and shows reversible ductility. Such uniqueness is a mere reflection of rubber-like elasticity on the hydrogels. These nanobuilding blocks serve also the extensive physisorption which enhances the physical crosslinking inside the gel matrix. Besides the pH-responsive drug release features, these hydrogels are also implemented as a pulsatile drug delivery device. The electric responsive drug release behaviours are noticed and hypothesized by the formation of conducting network in the polyelectrolytic hydrogel matrix. The hydrogels are also tested as good biocompatibility and feasible cell-attachment during live-dead cell adhesion study. The drug release characteristics can also be tuned by adjusting the conducting filler loading into the gel matrix. As of our knowledge, this type of hydrogels with rubber-like consistency, high mechanical property, tunable and dual responsive drug delivery feature and very good human cell compatible is the first to report.

Nanohybrid hydrogels of laponite: PVA-Alginate as a potential wound healing material

The aim of this study was to develop a novel nanohybrid interpenetrating network hydrogel composed of laponite:polyvinyl alcohol (PVA)-alginate (LAP:PVA-Alginate) with adjustable mechanical, physical and biological properties for wound healing application. Results demonstrated that compared to PVA-Alginate, mechanical strength of LAP:PVA-Alginate significantly enhanced (upon 2 times). Moreover, incorporation of 2wt.% laponite reduced swelling ability (3 times) and degradation ratio (1.2 times) originating from effective enhancement of crosslinking density in the nanohybrid hydrogels. Furthermore, nanohybrid hydrogels revealed admirable biocompatibility against MG63 and fibroblast cells. Noticeably, MTT assay demonstrated that fibroblast proliferation significantly enhanced on 0.5wt.% LAP:PVA-alginate compared to PVA-alginate. Moreover, hemolysis and clotting tests indicated that the nanohybrid hydrogels promoted hemostasis which could be helpful in the wound dressing. Therefore, the synergistic effects of the nanohybrid hydrogels such as superior mechanical properties, adjustable degradation rate and admirable biocompatibility and hemolysis make them a desirable candidate for wound healing process.

Novel temperature and pH dual-sensitive PNIPAM/CMCS/MWCNT semi-IPN nanohybrid hydrogels: Synthesis, characterization, and DOX drug release

ABSTRACTNovel poly(N-isopropylacrylamide)/carboxymethyl chitosan/multiwalled carbon nanotube semi-interpenetrating nanohybrid hydrogels were prepared, and the chemical structure and morphology were characterized. The prepared hydrogels showed temperature and pH dual-responsiveness, and the one containing multiwalled carbon nanotubes (MWCNTs)–COOH possessed high maximal swelling ratios. The phase transition produced at pH of 6.8–7.4 and temperature of 35–40°C, hinging on the system compositions and charge ratios. The hydrogels were used to load hydrophilic anticancer drug, with high entrapped efficiency of about 44%. The drug release changed with temperature, pH, and MWCNTs–COOH contents. The designed hydrogels can be used for site-specific target delivery of protein or hydrophilic anticancer drug.

Structure investigation of nanohybrid PDMA/silica hydrogels at rest and under uniaxial deformation.

Nano-hybrid hydrogels were prepared by cross-linking polymerization of N,N-dimethylacrylamide (DMA) within a dispersion of silica nano-particles. Working at constant polymer/water ratio, the mechanical properties of hydrogels can be finely tuned by changing either the level of covalent cross-linker and/or the amount of particles that act as physical cross-linkers through specific adsorption of PDMA chains. Whatever is the cross-linking ratio (from 0 to 1 mol%), the introduction of silica nano-particles dramatically improves the mechanical behavior of hydrogels with a concomitant increase of stiffness and nominal strain at failure. The physical interactions being reversible in nature, the dynamics of the adsorption/desorption process of PDMA chains directly controls the time-dependence of the mechanical properties. Small angle neutron scattering experiments, performed in contrast matching conditions, show that silica particles, which repel themselves at short range, remain randomly dispersed during the formation of the PDMA network. Although PDMA chains readily interact with silica particles, no significant variation of the polymer concentration was observed in the vicinity of silica surfaces. Together with the time dependence of physical interactions pointed out by mechanical analyses, this result is attributed to the moderate adsorption energy of PDMA chains with silica surfaces at pH 9. From 2D SANS experiments, it was shown that strain rapidly gives rise to a non affine deformation of the hybrid network with shearing due to the transverse compression of the particles. After loading at intermediate deformation, the particles recover their initial distribution due to the covalent network that is not damaged in these conditions. That is no longer true at high deformation where residual anisotropy is observed.

Research on Polymer Materials in Bio Medical and its Application

Intelligent hydrogels is as drug carrier, and it has a good application prospect. There are some changes factors in the human environment, such as temperature, pH. Therefore, the temperature sensitive hydrogels and pH sensitive hydrogels can release system for drugs in the body. So the paper detailed descripts a novel MWCNTs good dispersion of PMAA/MWCNTs nanohybrid hydrogels. The introduction of MWCNTs significantly increased the hydrogel pH response and mechanical strength, and depends on the MWCNTs component ratio, particle size and concentration of cross-linking agent. The study found, swelling rate of hybrid hydrogels was faster than the pure PMAA hydrogel, and the swelling behavior were explained. The compression stress-strain experiments should be found, MWCNTs load transfer plays an important role in improving the mechanical properties of the hybrid hydrogels network compression.

Research on Polymeric Biomedical Materials

The article are outlined the medicinal use of polymer materials and characteristics and described its preparation method and application for controlled drug release from polymer, polymer drugs, pharmaceutical formulations and packaging polymer materials three aspects. Meanwhile elaborates a novel well dispersed MWCNTs PMAA/MWCNTs nanohybrid hydrogels. The introduction of MWCNTs significantly improved pH-responsive hydrogels and mechanical strength, and which depending on the composition ratio of MWCNTs, particle size and concentration of crosslinker. Study found that hybrid hydrogel swelling rate significantly faster than the pure PMAA hydrogel swelling behavior and this is explained. Compressive stress - strain was found, MWCNTs load transfer heterozygous for improving mechanical properties of the hydrogel network compression plays an important role. MTT cell compatibility evaluation proves that this astute hydrogel biomedical research in particular has potential application value.

Hyaluronic Acid–Silica Nanohybrid Gels

Excessive water sorption and low mechanical properties are a severe drawback in some biomedical applications of hyaluronic acid (HA). A way to improve these properties is here explored through the novel concept of nanohybrid hydrogels consisting of a HA matrix including different amounts of silica-derived species. This inorganic filler phase controls the mechanical and swelling properties of HA cross-linked matrices. Below a 2 wt % of silica in the systems, nanoparticle aggregates of tens of nanometers and silica oligomers are distributed more or less homogeneously throughout the organic matrix, without percolating. This morphology of the silica phase is accompanied by an increased swelling degree of the composite when compared with pure HA. For higher silica mass ratios in the composites the inorganic counterpart coalesces, leading to a continuous inorganic silica network interpenetrated with the organic HA network, which coexists with a dispersed phase of silica-nanoparticle aggregates. Silica oligomers originating in the exposition of the nanoparticles to reactives during the composite preparation procedure contribute to the continuity of the silica network. For these compositions, swelling is reduced three times when compared with pure HA, and a significant improvement of the mechanical properties occurs. Water-containing samples of these materials exhibited a glass transition, which pure dry HA does not. None of the compositions studied showed any cytotoxicity. Thus, the materials could be of use in tissue engineering applications where these properties of HA need to be modulated.

Time Dependence of Dissipative and Recovery Processes in Nanohybrid Hydrogels

The strain rate effect on large strain dissipation and behavior recovery are presented to understand the toughening effect of silica nanoparticles in nanohybrid hydrogels. Such nanohybrid gels combine a poly(N,N-dimethylacrylamide) (PDMA) covalent network and physical interactions by adsorption of polymer chains at the silica nanoparticle surface. A series of model nanohybrid gels has been designed to obtain a well-controlled architecture. First insights on the structure (SANS) demonstrated that silica nanoparticles were well-dispersed in the gel, including after cyclic mechanical loading. The characteristic times involved in the nanoparticle/polymer association were investigated by large strain mechanical cycling varying the strain rate from 3 × 10–4 s–1 to 0.6 s–1. The mechanical behavior of the hybrid hydrogel varies tremendously over a relatively small range of strain rates, ranging from almost non dissipative (at slow strain rates) to highly dissipative at high strain rates. However, upon cycling ove...