Nanocomposite Hydrogels Research Articles

Sustained Ampicillin Loading and Releasing Ability of Novel In-Situ Ca2+ Functionalized Ternary GO/PVP/CMC Nanocomposite Hydrogel

Sustained Ampicillin Loading and Releasing Ability of Novel In-Situ Ca2+ Functionalized Ternary GO/PVP/CMC Nanocomposite Hydrogel

Spreadable thermosensitive nanocomposite hydrogel dressing with ultrasound-responsive bactericidal/repair-promoting regulation and cascade antioxidantion for infected burn wound repair

Treating severe burn wounds poses significant challenges, including considerable cell loss, excessive inflammation, and a high susceptibility to bacterial infections. Ideal burn dressings should exhibit excellent antibacterial properties, anti-inflammatory effects, and promote cell proliferation. Additionally, they need facilitate painless dressing changes and be user-friendly. Herein, we synthesized a thermosensitive hydrogel by crosslinking poly (N-isopropylacrylamide-co-allyloxybenzaldehyde) (PNA) and amino-terminated Pluronic F127 (APF) through a Schiff base reaction. It exhibited reversible gel-sol transition and spreadability. By incorporating piezoelectric gold nanoparticle-modified barium titanate (Au@BaTiO3) and cascade antioxidant MOF-818, a nanocomposite hydrogel dressing with diverse bioactive functionalities was developed. Results demonstrated that the nanocomposite hydrogel possessed gel-sol transition properties, maintained a stable gel state within a broad temperature range, and desirable self-healing property. Au@BaTiO3 exhibited good piezoelectric properties and ROS generation upon ultrasound stimulation, while MOF-818 displayed highly efficient cascade nanozyme activity. The combination of Au@BaTiO3 and MOF-818 promoted fibroblast proliferation and migration, reduced intracellular ROS levels, and induced anti-inflammatory polarization of macrophages under ultrasound stimulation. In vitro and in vivo antibacterial results disclosed that the nanocomposite hydrogel had excellent antibacterial activity under high-intensity ultrasound stimulation. When applied to infected burn wounds, the nanocomposite hydrogel can rapidly sterilize the wound upon initial high-intensity ultrasound, and then reduce inflammation and promote M2 macrophage polarization by the following low-intensity ultrasound stimulation, and thus accelerating the healing by improving granulation tissue formation, angiogenesis, and collagen deposition.

Fabrication of multi-responsive dynamic poly(ethylene glycol)-iron oxide nanoparticle nanocomposite hydrogels through interfacial boronate-catechol crosslinking

Poly(ethylene glycol) (PEG)-based nanocomposite (NC) hydrogel with multiple advantageous properties such as high mechanical strength and stimuli-responsiveness have been demonstrated as promising materials across various fields. Here, an innovative type of PEG-based NC hydrogels is fabricated using phenylboronic acid-polyethyleneimine (PBA-PEI)-functionalized iron oxide nanoparticles (PP-IOPs) to crosslink the dopamine-modified 4arm-PEG (DA-4APEG) through boronate-catechol crosslinking. DA-4APEG/PP-IOP NC hydrogels exhibit tunable microstructures (i.e., pore size) and properties (i.e., rheological, mechanical, and swelling behaviors) by changing the number of PP-IOPs in the hydrogel network. With the dynamic crosslinks and magnetic nanoparticles in the network, DA-4APEG/PP-IOP NC hydrogels are self-healable and also responsive to various stimuli, including temperature, pH, glucose, dopamine, hydrogen peroxide, magnetic field, and near-infrared light. Therefore, a versatile PEG-based hydrogel platform has been developed, featuring customizable properties, multiple stimuli-responsiveness, and dynamic characteristics, making it suitable for advanced applications.

Green NiO nanoparticle-integrated PVA-alginate hydrogel: potent nanocatalyst for efficient reduction of anthropogenic water pollutants.

Hydrogel nanocatalyst composed of nickel oxide (NiO) nanoparticles embedded in PVA-alginate hydrogels were potentially explored toward the reduction of anthropogenic water pollutants. The NiO nanoparticleswas accomplished via green method using waste pineapple peel extract. The formation of the nanoparticles was affirmed from different analytical techniques such as UV-Vis, FTIR, XRD, TGA, FESEM, and EDS. Spherical NiO nanoparticles were obtained having an average size of 11.5nm. The nano NiO were then integrated into PVA-alginate hydrogel matrix forming a nanocomposite hydrogel (PVALg@ NiO). The integration of nano NiO rendered an improved thermal stability to the parent hydrogel. The PVALg@ NiO hydrogel was utilized as a catalyst in the reduction of 4-nitrophenol (4-NP), potassium hexacyanoferrate (III), rhodamine B (RhB), methyl orange (MO), and malachite green (MG) in the presence of a reducing agent, i.e., NaBH4. Under optimized conditions, the reduction reactions were completed by 4.0min and 3.0min for 4-NP and potassium hexacyanoferrate (III), respectively, and the rate constant was estimated to be 1.14min-1 and 2.15min-1. The rate of reduction was found to be faster for the dyes and the respective rate constants were be 0.17s-1 for RhB, MG and 0.05s-1 for MO. The PVALg@ NiO hydrogel nanocatalyst demonstrated a recyclability of four runs without any perceptible diminution in its catalytic mettle. The efficacy of the PVALg@ NiO hydrogel nanocatalyst was further examined for the reduction of dyes in real water samples collected from different sources and the results affirm its high catalytic potential. Thus, this study paves the path for the development of a sustainable hydrogel nanocatalyst for reduction of hazardous pollutants in wastewater treatment.

Optimizing biomaterial inks: A study on the printability of Carboxymethyl cellulose-Laponite nanocomposite hydrogels and dental pulp stem cells bioprinting

Tissue engineering approaches require biocompatible materials with precise pre-designed geometry, shape fidelity, and promote cellular functions. Addressing these requirements, our study focused on developing an optimized bioink formulation using carboxymethyl cellulose (CMC) and Laponite hydrogels tailored for extrusion-based three-dimensional bioprinting. To this, we investigated the rheological properties and filament behavior before and during printing. As Laponite concentration increased in CMC solutions, it improved shear-thinning behavior, viscosity, and storage modulus, resulting in well-defined filament characteristics with lower diffusion rates, excellent shape fidelity, and robust printability. Thus, we achieved a suitable biomaterial ink formulation with concentrations of 1 wt% of CMC and 4 wt% of Laponite (1C4L). Subsequently, a statistical analysis guided us to select the optimal parameters for large-scale construct printing: a nozzle speed of 5 mm/s, a print distance of 0.41 mm, and an extrusion multiplier of 1.35. After that, we enhanced the structural integrity of printed hydrogels through ionic crosslinking with calcium chloride (CaCl2) and citric acid (CA), revealing higher-strength hydrogels at higher concentrations of CaCl2. Finally, we have confirmed the groundbreaking potential of our bioink by integrating dental pulp mesenchymal stem cells (DPSC) into the 1C4L ink. Our bioprinted constructs showed optimized swelling, non-toxic effects, and retained excellent shape fidelity, crucial for creating anatomically accurate tissues. Our findings provide crucial insights linking the rheological analysis, the bioprinting process, and the biological properties of hydrogels, paving the way for their use for tissue engineering and other biomedical applications.

An NIR-responsive hydrogel loaded with polydeoxyribonucleotide nano-vectors for enhanced chronic wound healing

Chronic diabetic wounds are difficult to treat due to imbalanced inflammatory responses, high blood glucose levels, and bacterial infections. Novel therapeutic approaches based on nucleic acid analogues have been proposed, with unique advantages in improving angiogenesis, increasing collagen synthesis, and exerting anti-inflammatory effects. However, the inherent electronegativity of nucleic acids makes them less susceptible to cellular uptake. In this paper, a kind of near infrared (NIR)-responsive nanocomposite hydrogel loaded with nucleic acid vectors was proposed for promoting wound healing. The redox system composed of molybdenum disulphide nanosheets (MoS2 NSs) initiated the copolymerization of quaternized chitosan containing double bonds and N-isopropylacrylamide (NIPAAm) to form the matrix. In addition, MoS2 NSs with photothermal conversion performance endow the nanocomposite hydrogel to have NIR-response property and act as physical crosslinking points in the matrix. Polydeoxyribonucleotides (PDRN), which have the effect of promoting wound healing, were made into nucleic acid vectors, and loaded into the NIR-responsive hydrogel. MoS2 NSs can convert NIR irradiation into heat, causing phase transitions of temperature-sensitive segments that trigger volume contraction of the hydrogel to extrude the nucleic acid vector. Promoting angiogenesis, slowing inflammation, and guiding tissue regeneration were demonstrated in the diabetic wound model treated with the NIR-responsive nanocomposite hydrogel.

Evaluation of scarless wound healing through nanohydrogel infused with selected plant extracts

In this study, a CMC-based hydrogel nanocomposite was prepared and loaded with bioactive components along with silver nanoparticles. For aesthetic reasons, an alternative was found that can result in scar-free wound healing. To accelerate scar-free wound healing, bioactive phytoproducts such as aloe vera, curcumin, and peel of plantain were blended along with the nanocomposite hydrogel that contained silver nanoparticles (CMC + Ag + P). The prepared hydrogels proved to have good antibacterial activity against both Gram-positive (S.aureus) and Gram-negative (E.coli) non-pathogenic bacteria. The prepared hydrogel had an excellent wound-healing ability which was studied using in vitro scratch assay against A375 cell line. The biocompatibility of the hydrogels was proved using an MTT assay. The scar free wound healing was established in Wistar rat model where burn wounds were healed using CMC + Ag + P. The wound healed were compared with only silver (CMC + Ag) and saline treated animals and the histopathological studies, VEGF and PDGF analysis confirmed that the wound healing was scar free after CMC + Ag + P treatment. We could conclude that the presence of plantain peel extract which is a source of ascorbic acid and is rich in vitamin C can aid in scar-free wound healing.

Highly Reusable Nano Adsorbent Based on Clay-Incorporated Hydrogel Nanocomposite for Cationic Dye Adsorption

Highly Reusable Nano Adsorbent Based on Clay-Incorporated Hydrogel Nanocomposite for Cationic Dye Adsorption

Self‐healing, adhesive, photothermal responsive, stretchable, and strain‐sensitive supramolecular nanocomposite hydrogels based on host–guest interactions

AbstractThe development of multifunctional supramolecular nanocomposite hydrogels remains challenging. Here, the dynamic host–guest interactions involving the host molecule CB[8] and guest units were utilized to prepare Fe3O4 hybrid supramolecular nanocomposite hydrogels. The results showed that the hydrogels obtained possessed a porous structure. The CB[8]‐modified Fe3O4 (Fe3O4@CB[8]) nanoparticles served as cross‐linkers in forming the network of hydrogels. By adjusting the Fe3O4@CB[8] content, the mechanical properties of the hydrogels could be controlled. The tensile stress was measured at 160 kPa with a fracture strain of 1380%, while the compression stress was 230 kPa at 70% compression strain. The self‐healing efficiency of the hydrogels at room temperature reached 95% after 24 h. The as‐obtained hydrogels show strain sensitivity and have the potential for applications in detecting elbow and finger movements. Our supramolecular nanocomposite hydrogels exhibit multiple functions, including self‐healing, injectability, photothermal responsiveness, and conductivity, making them suitable for integration into flexible electronics.Highlights Fe3O4@CB[8] nanoparticles serve as cross‐linkers for the nanocomposite hydrogels. CB[8] based host–guest interactions enable hydrogels to self‐heal. Fe3O4@CB[8] endow hydrogels with stretchability and photothermal responsiveness. Hydrogels exhibit injectability, NIR responsiveness, and conductive ability.

Facile design of biofunctionalized nanocomposite hydrogel to potentiate angiogenesis and osteogenesis for the skull regeneration

The clinical treatment of cranial defect reconstruction using hydrogels faces challenges such as inadequate biomechanical strength and limited biofunctional effects. In this study, we have addressed these issues by developing a novel hydrogel. This hydrogel composes desferrioxamine-modified laponite nanoplatelets (LAP/DFO) combined with tannin-modified poly(vinyl alcohol) (PVA/TA), aiming to closely emulate the natural organic-inorganic bony matrix. Our results indicated that the multifunctional hydrogel system, particularly when incorporating LAP/DFO (referred to as PL10), could form a highly ordered porous structure, achieve appropriate biomechanical strength, and release bioactive factors as expected. This system enhanced the adhesion and proliferation of human umbilical vein endothelial cells (HUVECs) for angiogenesis and promoted mesenchymal stem cells (MSCs) osteogenic differentiation for osteogenesis in vitro. Moreover, in vivo investigations confirmed the efficacy of the multifunctional hydrogels, particularly PL10, in enhancing bone regeneration compared to blank PVA. Collectively, this study contributes valuable insights into the design of bioactive factor delivery systems and offers efficient therapeutic strategies for promoting the repair of cranial defects.

Rational design of self-assembling ultrashort peptides for the shape- and size-tunable synthesis of metal nanostructures.

Peptides have attracted great interest as platforms for the design of nanocomposite hydrogels due to their distinct bioactivity, biofunctionality and biocompatibility. Previously, we have reported on a family of peptides that self-assembled to form stabilised three-dimensional hydrogel networks, displaying potent antimicrobial activity. In this paper, we report on the use of these hydrogelator sequences and their analogues as stabilisers and growth controllers to synthesise anisotropic gold nanoparticles (AuNPs) of different sizes and shapes. In particular, hollow spherical nanoparticles were obtained for HG2.81-AuNPs, whereas hexagonal nanoparticles were observed for TOH_1N-AuNPs and PentaOH-AuNPs in their respective hydrogel networks. The PentaOH-AuNPs' hydrogel exhibited excellent results with high antimicrobial potency against Staphylococcus aureus and Pseudomonas aeruginosa ATCC 27853 and negligible cytotoxicity. On the other hand, TOH_1N-AuNPs showed no antibacterial activity and no cytotoxicity, demonstrating the versatility of these peptides. This work gives credence towards the development of these materials towards further applications such as in tissue culture technology and wound dressing materials.

Synthesis and biological applications of nanocomposite hydrogels based on the methacrylation of hydroxypropyl methylcellulose and lignin loaded with alpha-pinene

Oral conditions, such as recurrent aphthous stomatitis, are chronic inflammatory disorders that significantly affect the life quality. This study aims to develop a novel buccal mucoadhesive based on methacrylate hydroxypropyl methylcellulose (M-HPMC) and methacrylate lignin (M-SLS) encapsulated with nanostructured lipid carriers (NLCs) for controlled release of alpha-pinene (α-pinene). NLCs with particle sizes of 152 ± 3 nm were prepared by using stearic acid and oleic acid as solid and liquid lipids, respectively. Following the successful synthesis of M-HPMC and M-SLS, various concentrations of α-pinene loaded NLCs (0, 18, 38, and 50 wt%) were encapsulated in M-HPMC/M-SLS hydrogel. It was demonstrated that the physiological and mechanical performances of hydrogels were changed, depending on the NLC content. Remarkably, the incorporation of 18 wt% NLC improved the compressive strength (143 ± 14 kPa) and toughness (17 ± 1 kJ/m3) of M-HPMC/M-SLS hydrogel. This nanocomposite hydrogel considerably decreased dissipated energy from 1.64 kJ/m3 to 0.99 kJ/m3, after a five-cycle compression test. The nanocomposite hydrogel exhibited controlled α-pinene release for up to 96 h which could significantly improve the antioxidant activity of M-HPMC/M-SLS matrix. Moreover, the reinforcing M-HPMC/M-SLS hydrogel with α-pinene-loaded NLCs resulted in increased adhesive strength (113.5 ± 7.5 kPa) to bovine buccal mucosa and cytocompatibility in contact with fibroblasts.

Hierarchical Chitin Nanocrystal-Based 3D Printed Dual-Layer Membranes Hydrogels: A Dual Drug Delivery Nano-Platform for Periodontal Tissue Regeneration.

Periodontitis, a prevalent chronic inflammatory disease caused by bacteria, poses a significant challenge to current treatments by merely slowing their progression. Herein, we propose an innovative solution in the form of hierarchical nanostructured 3D printed bilayer membranes that serve as dual-drug delivery nanoplatforms and provide scaffold function for the regeneration of periodontal tissue. Nanocomposite hydrogels were prepared by combining lipid nanoparticle-loaded grape seed extract and simvastatin, as well as chitin nanocrystals, which were then 3D printed into a bilayer membrane that possesses antimicrobial properties and multiscale porosity for periodontal tissue regeneration. The constructs exhibited excellent mechanical properties by adding chitin nanocrystals and provided a sustained release of distinct drugs over 24 days. We demonstrated that the bilayer membranes are cytocompatible and have the ability to induce bone-forming markers in human mesenchymal stem cells, while showing potent antibacterial activity against pathogens associated with periodontitis. In vivo studies further confirmed the efficacy of bilayer membranes in enhancing alveolar bone regeneration and reducing inflammation in a periodontal defect model. This approach suggests promising avenues for the development of implantable constructs that not only combat infections, but also promote the regeneration of periodontal tissue, providing valuable insights into advanced periodontitis treatment strategies.

Injectable Carrageenan/Green Graphene Oxide Hydrogel: A Comprehensive Analysis of Mechanical, Rheological, and Biocompatibility Properties.

In this work, physically crosslinked injectable hydrogels based on carrageenan, locust bean gum, and gelatin, and mechanically nano-reinforced with green graphene oxide (GO), were developed to address the challenge of finding materials with a good balance between injectability and mechanical properties. The effect of GO content on the rheological and mechanical properties, injectability, swelling behavior, and biocompatibility of the nanocomposite hydrogels was studied. The hydrogels' morphology, assessed by FE-SEM, showed a homogeneous porous architecture separated by thin walls for all the GO loadings investigated. The rheology measurements evidence that G' > G″ over the whole frequency range, indicating the dominant elastic nature of the hydrogels and the difference between G' over G″ depends on the GO content. The GO incorporation into the biopolymer network enhanced the mechanical properties (ca. 20%) without appreciable change in the injectability of the nanocomposite hydrogels, demonstrating the success of the approach described in this work. In addition, the injectable hydrogels with GO loadings ≤0.05% w/v exhibit negligible toxicity for 3T3-L1 fibroblasts. However, it is noted that loadings over 0.25% w/v may affect the cell proliferation rate. Therefore, the nano-reinforced injectable hybrid hydrogels reported here, developed with a fully sustainable approach, have a promising future as potential materials for use in tissue repair.

Enhanced methylene blue adsorption using single-walled carbon nanotubes/chitosan-graft-gelatin nanocomposite hydrogels

In the present study, single-walled carbon nanotubes (SWCNTs) incorporating chitosan-graft-gelatin (CS-g-GEL/SWCNTs) hydrogels were fabricated with multiple advantages, including cost-effectiveness, high efficiency, biodegradability, and ease of separation for methylene blue (MB) dye from aqueous solution. To verify the successful formulation of the prepared hydrogels, various characterization methods such as NMR, FTIR, XRD, FE-SEM, TGA, BET, and EDX were employed. The removal efficiency of CS-g-GEL/SWCNTs nanocomposite hydrogel increased significantly to 98.87% when the SWCNTs percentage was increased to 20%. The highest adsorption was observed for pH = 9, an adsorbent dose = 1.5 g L−1, a temperature = 25 °C, a contact time = 60 min, and a contaminant concentration = 20 mg L−1. Based on the thermodynamic results, spontaneous adsorption occurred from a negative Gibbs free energy (ΔG°). In addition, the thermodynamic analysis of the adsorption process revealed an average enthalpy of − 21.869 kJ mol−1 for the adsorption process at a temperature range of 25–45 °C, which indicates its spontaneous and exothermic behavior. The Langmuir isotherm model was successfully used to describe the equilibrium behavior of adsorption. The pseudo-first-order model better described adsorption kinetics compared to the pseudo-second-order, intra-particle, and Elovich models. CS-g-GEL/SWCNTs hydrogels have improved reusability for five consecutive cycles, suggesting that they may be effective for removing anionic dyes from aquatic environments.

Development of banana pseudo stem cellulose fiber based magnetic nanocomposite as an adsorbent for dye removal

A hybrid hydrogel nanocomposite derived from cellulose fiber extracted from Banana Pseudo Stem (BPS) was developed as an adsorbent material for wastewater treatment. The hydrogel was developed by graft copolymerization of N-hydroxyethylacrylamide on Cellulose Fiber (BPSCF-g-PHEAAm) with potassium peroxodisulphate (KPS) as an initiator and N, N′-methylene bisacrylamide (MBA) as a crosslinker using microwave irradiation. Magnetic nanoparticles generated by an in-situ method were incorporated into the network structure. Fourier Transform Infrared Spectroscopy (FTIR), Powder X-ray Diffraction (XRD), Thermogravimetric analysis (TGA), Vibrating Sample Magnetometer (VSM), Brunauer-Emmett-Teller analysis (BET), Field Emission Scanning Electron Microscopy (FESEM), and Energy Dispersive Spectrometer (EDS) were employed. The adsorption capacities of hydrogel and its nanocomposite were evaluated using Methylene Blue (MB) and Crystal Violet (CV) as model dyes. The parent gel exhibited the maximum absorption capacity of 235, and 219 mg g−1 towards MB and CV respectively which was enhanced to 320 and 303 mg g−1 for the nanocomposite. Adsorption data were best fitted with the pseudo-second-order kinetic model and the Freundlich isotherm model. Negative ΔG° and positive ΔH° indicated spontaneous and endothermic adsorption. Desorption was effective to an extent of 99 % in the HCl medium suggesting high reusability potential of the developed adsorbent material.

DNA Aptamer Integrated Hydrogel Nanocomposites on Screen Printed Gold Electrodes for Point-of-Care Detection of Testosterone in Human Serum.

This work describes the development and evaluation of a novel electrochemical aptasensor for testosterone detection. The sensor utilizes a specifically designed DNA immobilized on a screen-printed gold electrode (SPGE) modified with a conductive hydrogel and gold nanoparticles (HG/NP) composite. The aptasensor exhibited a dose-dependent response to testosterone (0.05 to 50 ng/mL) with a detection limit of 0.14 ng/mL and a good sensitivity of 0.23 μA ng-1 mL cm-2. The sensor displayed excellent selectivity towards testosterone compared to structurally similar steroid hormones. Importantly, the incorporation of HG/NP not only improved the sensor's conductivity but also acted as an antifouling layer, minimizing signal interference from non-specific biomolecule interactions in complex biological samples like human serum. The results obtained from the aptasensor showed good correlation with a standard ELISA method, demonstrating its effectiveness in real-world scenarios.

Evaluation of the synergistic effect of nanocomposite hydrogel based on imidazolium nitrate ionic liquids for enhanced oil recovery

A comprehensive research study was conducted to examine the synergistic properties of ionic liquids, and hydrogels. Two nanocomposite hydrogel samples were created: one with ionic liquid and the other without. The samples were made using hydrogel with acrylamide (AM) backbone, Al2O3 nanoparticles, and ionic liquid [C8mim][NO3]. The effectiveness of a nanocomposite hydrogel containing an ionic liquid was tested to improve the wettability alteration and sweeping efficiency of reservoirs. Various tests were performed including IFT, electroconductivity, micromodel, SEM, and equilibrium swelling tests. The tests showed that the presence of the ionic liquid increased the swelling up to 102 %. IL increased conductivity by 124.24 % and 44.86 % at ambient temperature and 90 °C respectively. In the strain sweep test, the maximum elastic modulus for NCH-IL was recorded as 40,350 Pa, while for the sample without ionic liquid, it was 27,100 Pa. The frequency sweep test confirmed the three-dimensional structure of the gel. IL increased the maximum elastic modulus from 13,200 Pa to 27,400 Pa. The critical frequency value also increased by 87.5 %. Moreover, the suspension, which contains 1 wt% of Nanocomposite Hydrogel based on Imidazolium Nitrate Ionic Liquids, has shear-thinning properties, making it easy to inject into reservoirs. The reduction of the contact angle from 109° to 14.2° demonstrated the ability of IL to alter the wettability of NCHs. This result stemmed from the release of part of the ionic liquid within the hydrogel structure, as confirmed by the UV test. During the emulsion stability test, it was observed that the NCH-IL sample created a stable emulsion and a more complete two-phase separation than the sample without the ionic liquid. The sample that contained IL recorded 85 % and 78.4 % oil recovery in homogeneous and heterogeneous micromodels, respectively. Whereas, the sample without IL recorded 71.27 % and 60.73 % in the same micromodels.

Bionic light-responsive hydrogel actuators with multiple-freedom motions in water environments

Soft actuators with biomimetic behavior have widely been utilized in intelligent robotics and artificial muscles. Herein, tannic acid (TA) non-covalently modified and γ-methacrylic trimethoxysilane (MPS) covalently modified MXene (MPS-TA-MXene) are incorporated into a poly(n-isopropylacrylamide-polyacrylamide) (PNIPAM-PAM) copolymer hydrogel to yield a light-responsive hydrogel nanocomposite, denoted as MNA. TA effectively preserves the surface characteristics of MXene while the double bonds in MPS form covalent bonding between MXene and PNIPAM-PAM copolymer, ensuring uniform dispersion of MPS-TA-MXene in MNA hydrogel. Under exposure to ultraviolet light, the resulting MNA hydrogel actuators with nematode- or starfish-shaped exhibit not only bending capabilities in various directions and angles but also demonstrate remarkable multiple-freedom rolling behavior in water environments due to their volume shrinkage induced by the phase transition of MNA hydrogel. Overall, the proposed simply assembled MNA hydrogel actuators with multiple and continuous bionic motions, distinguishing them from conventional single soft actuators limited to bending in one specific direction or performing a simple singular action of rolling, look promising for use in underwater exploration.

Percutaneous Delivery of Oncogel for Targeted Liver Tumor Ablation and Controlled Release of Therapeutics.

Advanced-stage liver cancers are associated with poor prognosis and have limited treatment options, often leading the patient to hospice care. Percutaneous intratumoral injection of anticancer agents has emerged as a potential alternative to systemic therapy to overcome tumor barriers, increase bioavailability, potentiate immunotherapy, and avoid systemic toxicity, which advanced-stage cancer patients cannot tolerate. Here, an injectable OncoGel (OG) comprising of a nanocomposite hydrogel loaded with an ionic liquid (IL) is developed for achieving a predictable and uniform tumor ablation and long-term slow release of anticancer agents into the ablation zone. Rigorous mechanical, physiochemical, drug release, cytotoxicity experiments, and ex vivo human tissue testing identify an injectable version of the OG with bactericidal properties against highly resistant bacteria. Intratumoral injection of OG loaded with Nivolumab (Nivo) and doxorubicin (Dox) into highly malignant tumor models in mice, rats, and rabbits demonstrates enhanced survival and tumor regression associated with robust tissue ablation and drug distribution throughout the tumor. Mass cytometry and proteomic studies in a mouse model of colorectal cancer that often metastasizes to the liver indicate an enhanced anticancer immune response following the intratumoral injection of OG. OG may augment immunotherapy and potentially improve outcomes in liver cancer patients.