Semi-interpenetrating Polymer Network Research Articles

Regulating electrostatic phenomena by cationic polymer binder for scalable high-areal-capacity Li battery electrodes

Despite the enormous interest in high-areal-capacity Li battery electrodes, their structural instability and nonuniform charge transfer have plagued practical application. Herein, we present a cationic semi-interpenetrating polymer network (c-IPN) binder strategy, with a focus on the regulation of electrostatic phenomena in electrodes. Compared to conventional neutral linear binders, the c-IPN suppresses solvent-drying-induced crack evolution of electrodes and improves the dispersion state of electrode components owing to its surface charge-driven electrostatic repulsion and mechanical toughness. The c-IPN immobilizes anions of liquid electrolytes inside the electrodes via electrostatic attraction, thereby facilitating Li+ conduction and forming stable cathode–electrolyte interphases. Consequently, the c-IPN enables high-areal-capacity (up to 20 mAh cm–2) cathodes with decent cyclability (capacity retention after 100 cycles = 82%) using commercial slurry-cast electrode fabrication, while fully utilizing the theoretical specific capacity of LiNi0.8Co0.1Mn0.1O2. Further, coupling of the c-IPN cathodes with Li-metal anodes yields double-stacked pouch-type cells with high energy content at 25 °C (376 Wh kgcell−1/1043 Wh Lcell–1, estimated including packaging substances), demonstrating practical viability of the c-IPN binder for scalable high-areal-capacity electrodes.

Preparation of a controlled drug release system from semi-interpenetrating polymeric network hydrogel of NaAlg-g-poly(NaA)/PVP

Preparation of a controlled drug release system from semi-interpenetrating polymeric network hydrogel of NaAlg-g-poly(NaA)/PVP

Capsaicin-based silicone antifouling coating with enhanced interlocking adhesion via SIPN

Silicone-based coatings generally exhibit excellent dynamic fouling release due to their low surface energy and elastic modulus. However, the poor adhesion of these coatings at the interface between the coating and the substrate, as well as deficient static antifouling capabilities, severely deteriorate their antifouling properties over extended periods. Herein, an epoxy-poly(dimethylsiloxane)/capsaicin (EP-PDMS/CAP) coating with highly enhanced interfacial adhesion and remarkable antifouling performances was prepared. The coating adhesion strength of the EP-PDMS/CAP has been improved by more than 5 times compared to a PDMS control coating (from 0.4 MPa to 2.04 MPa) by forming a semi-interpenetrating polymer network (SIPN) structure between the epoxy and PDMS layers. The EP-PDMS/CAP coating achieved the superior antifouling effects in both static and dynamic conditions, the anti-bacterial rate was as high as 96.8 %, and the anti-algal adhesion rate to the green algae Chlorella increased by 95.7 %, due to the synergistic effects of the fouling release performance from the PDMS coating and the fouling prevention of capsaicin. Furthermore, the EP-PDMS/CAP coating was proven to be extremely stable in different treatments such as acid/basic solutions, air oven heating test, and cyclic sand abrasion, showing great potential for anti-biofouling under aggressive conditions. This work provides a promising pathway towards the development of high-performance silicone-based composite coatings for efficient marine anti-biofouling.

Characterization of Stimuli-Responsive Acrylamide/Sodium Methacrylate/Kaolin Semi-Interpenetrating Polymer Network Composite Hydrogels

With the advantages of their self-healing, stimuli-response ability, water sorption capacity and shape memory, hydrogels have been commonly utilized. However, new strategies have been developed to enhance mechanical and thermal properties of hydrogels in addition to increase their water sorption. In this study, stimuli-responsive acrylamide/sodium methacrylate based hydrogels were synthesized with the optimization of sodium methacrylate amount by free radical polymerization. With the incorporation of optimum amount of polyethylene glycol 400 (PEG-400) into the hydrogel network, semi-interpenetrating polymer network (semi-IPN) hydrogels were prepared. With the addition of kaolin, swelling properties of the semi-IPN composite hydrogels were investigated in water under the effect of different pH and temperature. Maximum swelling percent of the semi-IPN composite hydrogels was determined as 24214% at pH 7 and 25 °C. Fourier transform infrared spectroscopy (FTIR) analyses revealed that hydrogel samples were successfully synthesized. Morphological structure of hydrogel samples was examined by scanning electron microscopy (SEM) analyses. Both of the water motion through the hydrogel layered structure and water diffusion into the pores made the semi-IPN composite hydrogel more swollen material compared to the acrylamide/sodium methacrylate based hydrogel.

Nitrile-Containing Spiro-Twisted Benzoxazines for All-Solid-State Polymer Electrolytes in Lithium-Ion Batteries

In this study, we developed new cross-linkable benzoxazine molecules comprising a spiro-twisted core and benzyl cyanide or benzonitrile groups to prepare semi-interpenetrating polymer network (s-IPN) electrolytes. The features of spiro-twisted core and cross-linking network derived from the cured benzoxazines play a crucial role in creating a high free volume and inhibiting the crystallinity. In addition, the incorporation of the nitrile group onto the crosslinked spiro-twisted molecular chains by covalent bonding would certainly enhance the miscibility of SPE membranes with lithium salts while maintaining good mechanical properties. On the other hand, the -CN groups would have more space for rotation and vibration to improve lithium migration owing to the presence of a high fractional free volume of spiro-twisted matrix. Along blending with poly (ethylene oxide) (PEO) electrolytes, a new type of CN-containing semi-interpenetrating polymer networks for solid polymer electrolytes (SPEs) has been achieved.

Characterization and swelling behavior of hydrogels from N-isopropylacrylamide, N,N′-diethylacrylamide, acrylic acid, and its use for drug release

Here, a series of semi-interpenetrating polymer network (semi-IPN) hydrogels were synthesized and investigated by combining three materials such as N-isopropylacrylamide (NIPAM), N,N′-diethylacrylamide (DEA), and acrylic acid (AAc). The linear copolymer p(NIPAM-co-AAc) was introduced into DEA solution in the presence of N,N′-methylenebisacrylamide to synthesize p(NIPAM-co-AAc)/pDEA semi-IPN hydrogels using free radical polymerization. Scanning electron microscope images demonstrated the porous morphology of hydrogels with pore sizes in the range of 220–969 µm. The physicochemical properties of polymers were evaluated by various characterization techniques, including gel permeation chromatography, dynamic light scattering, differential scanning calorimetry, rheological measurement, mechanical properties, and swelling behaviors. The results indicated that the introduction of linear copolymers into conventional hydrogels has significantly improved the properties of the hydrogels. Besides, the use of NIPAM has significantly improved the thermal sensitivity of the polymers in this work. Finally, a selected semi-IPN hydrogel was evaluated for its potential for the drug release of paracetamol. The sorption of paracetamol was an exothermic process that obeyed the Freundlich isotherms, with the highest sorption of 119.57 mg/g. The paracetamol release followed the Korsmeyer–Peppas model and was consistent with the Fickian diffusion mechanism.

Laser-direct-writing assisted preparation of flexible humidity sensors based on semi-interpenetrating polymer network for applications in non-contact human-machine interaction

Flexible sensors for non-contact human-machine interaction (HMI) received great attention recently due to increasing requirements for cross-infection of bacteria or virus, which is prominent considering the disaster brought about by COVID-19. Herein, a semi-interpenetrating network of poly(dimethyl diallyl ammonium chloride)/crosslinked poly(vinyl alcohol)/graphene oxide (PDDA/c-PVA/GO) was deposited on polytetrafluoroethylene membrane with interdigital electrodes constructed by reducing GO with laser-direct-writing technology to prepare a flexible humidity sensor (FHS). As-prepared PDDA/c-PVA/GO FHS showed excellent sensing performance, including high response magnitude over wide range of relative humidity (RH) (impedance change of three orders of magnitude between 10 % and 90 % RH), good sensing linearity (R2 = 0.991) on a semi-logarithmic scale, small hysteresis (∼ 4.4 % RH) and resistance to humid environment. Moreover, the FHS exhibited good performance in various scenarios of non-contact HMI, including prompt differentiation of respiration status, speech recognition, accurate measurement of fingertip movement (as small as 2 mm). Specially, a 3 × 3 FHS sensor array could realize accurate non-contact positioning. This work provides a new approach for developing high performance flexible sensors with great application potentials in non-contact HMI.

Evaluation of shape memory effect in PLA/copolymers blends

AbstractIn this work, polylactic acid (PLA)/copolymer blends were prepared by melt blending. Ethylene‐glycidyl methacrylate (E‐GMA) and ethylene‐butyl acrylate‐maleic anhydride (EBA‐MAH) functional block copolymers were used. A ternary blend of PLA/E‐GMA/EBA‐MAH was also studied. FTIR analyses evidenced the occurrence of reactive compatibilization of E‐GMA and EBA‐MAH with PLA in the binary blends due to the reactivity of the GMA and MAH functional groups with the terminal hydroxyl and carboxyl groups of PLA. Rheological measurements evidenced the occurrence of cross‐link reactions between E‐GMA and EBA‐MAH copolymers in the ternary blend. Three distinct morphologies were observed in the blends: PLA/E‐GMA exhibited a sea‐island structure, PLA/EBA‐MAH exhibited a co‐continuous structure, and PLA/E‐GMA/EBA‐MAH exhibited a semi‐interpenetrating polymer network (SIPN) structure. The shape memory effect (SME) of PLA and PLA/copolymers blends was evaluated by three different methods: fold‐deploy, tension, and torsion. Fold‐deploy tests were conducted in a water bath, whereas the tension and torsion tests were conducted using a rheometer. All methods proved to be effective; however, some precautions must be taken to choose the most suitable test for a given purpose, which is thoroughly discussed in this work. The SME of PLA was enhanced through the incorporation of the copolymers. Blending PLA with E‐GMA, EBA‐MAH, and E‐GMA/EBA‐MAH copolymers increased its shape recovery from 32% to 84%, 79.2%, and 80%, respectively, while its shape fixity remained around 100%.

Ecofriendly polysaccharide-based alginate/pluronic F127 semi-IPN hydrogel with magnetic collectability for precise release of pesticides and sustained pest control

Controlled-release systems are crucial for efficient pesticide utilization and environmental protection in agricultural production. The utilization of polysaccharide-based materials derived from biopolymers as carriers for controlling pesticide release holds significant potential. In this work, a reversible near infrared-responsive polysaccharide-based hydrogel (RNPH) was fabricated by employing a semi-interpenetrating polymer network (alginate-FeIII/pluronic F127) as a carrier to encapsulate Fe3O4@polydopamine (FP) and emamectin benzoate (EB)-loaded hollow mesoporous silica. The incorporation of FP into the RNPH introduced a photothermal effect, enabling the precise release of EB through reversible shrinkage of the hydrogel upon NIR irradiation. Additionally, the presence of magnetic Fe3O4 in the system facilitated the rapid removal of remaining RNPH from the environment using a magnet, reducing EB residue. Importantly, RNPH exhibited exceptional controlled-release performance and could be reused for at least 4 cycles. Furthermore, the anti-photolysis ability of EB protected by RNPH was enhanced by 4.8 times compared to EB alone. Moreover, RNPH significantly improved the adhesion of EB to foliar surfaces, thereby reducing the loss of EB while ensuring crop safety. Therefore, the polysaccharide-based hydrogel holds promise as a versatile carrier for the precise release of EB, offering valuable applications in enhancing pesticide bioavailability and promoting environmental safety.

Effective removal of antibiotic resistance genes from wastewater using marine waste-derived novel nanocomposites

Wastewater (WW) has been identified as a major hotspot of microbial emerging contaminants (MECs), such as antibiotic resistant bacteria (ARB) and antibiotic resistance genes (ARGs). Currently used WW treatment methods cannot efficiently eliminate these pollutants, resulting in passive contamination of adjacent environments receiving undertreated discharge. More effective WW treatment strategies are therefore urgently required. In this study, newly developed and well-characterised semi-interpenetrating polymer network (semi-IPN) hydrogels derived from the valorisation of marine wastes (e.g., shrimp shells) were investigated for their ARG removal potential. The results indicated that multiple ARGs prevalent in WW, such as ermB, qrnS, sul1 and tetO, were removed by up to 100% after being treated by novel hydrogels. In terms of horizontal gene transfer-associated genetic elements, such as integron-1 intl1, transposons tnpA1 (IS4 group) and tnpA2 (IS6 group), substantial reduction approaching 99.9% was also achieved. Moreover, up to 97% of efflux pump-associated qacEΔ1 conferring multidrug resistance (MR) was successfully attenuated. To conclude, the semi-INP hydrogels developed exhibited great potential for ARG mitigation towards strengthening WW decontamination, which provides a viable, cost-effective and environmentally friendly novel treatment approach.

Semi-Interpenetrating Network Anion Exchange Membranes by Thiol-Ene Coupling Reaction for Alkaline Fuel Cells and Water Electrolyzers.

In this work, a thiol-ene coupling reaction was employed to prepare the semi-interpenetrating polymer network AEMs. The obtained QP-1/2 membrane exhibits high hydroxide conductivity (162.5 mS cm-1 at 80 °C) with a relatively lower swelling ratio, demonstrating its mechanical strength of 42 MPa. This membrane is noteworthy for its improved alkaline stability, as the semi-interpenetrating network effectively limits the attack of hydroxide. Even after being treated in 2 M NaOH at 80 °C for 600 h, 82.5% of the hydroxide conductivity is maintained. The H2/O2 fuel cell with QP-1/2 membrane displays a peak power density of 521 mW cm-2. Alkaline water electrolyzers based on QP-1/2 membrane demonstrated a current density of 1460 mA cm-2 at a cell voltage of 2.00 V using NiCoFe catalysts in the anode. All the results demonstrate that a semi-interpenetrating structure is a promising way to enhance the mechanical property, ionic conductivity, and alkaline stability of AEMs for the application of alkaline fuel cells and water electrolyzers.

Skin-adhesive lignin-grafted-polyacrylamide/hydroxypropyl cellulose hydrogel sensor for real-time cervical spine bending monitoring in human-machine Interface

Developing a straightforward method to produce conductive hydrogels with excellent mechanical properties, self-adhesion, and biocompatibility remains a significant challenge. While current approaches aim to enhance mechanical performance, they often require additional steps or external forces for fixation, leading to increased production time and limited practicality. A novel lignin-grafted polyacrylamide/hydroxypropyl cellulose hydrogel (L-g-PAM/HPC hydrogel) with a semi-interpenetrating polymer network structure had been developed in this research that boasted exceptional adhesion to the skin (∼68 kPa) and stretchability properties (∼1637 %) compared to PAM-based hydrogels. By incorporating conductive additives such as silver nanowires and carbon nanocages to construct a bridge-like structure within the hydrogel matrix, the resulting AgC@L-g-PAM/HPC hydrogel exhibited impressive electrical conductivity, surpassing that of other PAM-based hydrogels relying on MXene, with a maximum value of 0.76 S/m. Furthermore, the AgC@L-g-PAM/HPC hydrogel retained its efficient electrical signal transmission capability even under mechanical stress. These make it an ideal flexible strain sensor capable of detecting various human motions. In this study, a smart real-time monitoring system was successfully developed for tracking cervical spine bending, serving as an extension for monitoring human activities.

Novel biodegradable nanocomposite hydrogels based on biopolymers and various montmorillonite contents as high-strength coating membranes for efficient slow-release fertilizers

Slow-release fertilizers (SRF) have emerged as a sustainable remedy to the environmental problems caused by conventional water-soluble fertilizers. They have demonstrated their efficacy in reducing fertilizer dosage applications, enhancing fertilizer utilization efficiency, minimizing losses, and ultimately improving crop yield. This study developed biodegradable nanocomposite hydrogels (BHM) as a promising approach by combining cassava starch (Cst), polyacrylamide (PAM), natural rubber (NR), and various montmorillonite (MMT) contents (0–10 wt%) and fabricating via free-radical polymerization and semi-interpenetrating polymer network technology, crosslinked by glutaraldehyde. Notably, the addition of MMT played a crucial role and significantly improved the tensile strength, biodegradability, and N release efficiency of the BHM hydrogels. BHM3 (3 wt% MMT) demonstrated the highest swelling ratio of 7074% and improved N release efficiency, mechanical strength, and biodegradation rate by 39.1%, 260% and 58%, respectively, compared to BHM0. The FWBHM formulations (urea coated with BHM and wax layers) also exhibited good biosafety. Finally, FWBHM3 yielded acceptable growth rates, a greater yield, and a 4-fold lower price than commercial SRF. These findings provide a promising route for developing new nanocomposite hydrogels based on Cst, NR, and MMT components with high swelling and water-retention, high strengths, and excellent biodegradation with greater slow-release duration and sustained environments.

Polyvinyl alcohol composite hydrogels/epoxidized natural rubber composites (CMCS/PVA/CS-ENR) with core-shell structure as biomass coating material for slow-release nitrogen fertilizer

Using natural rubber (NR)/chitosan (CS)/polyvinyl alcohol (PVA) as raw materials, biodegradable semi-IPN (semi-interpenetrating polymer network) composites were prepared by thiol-epoxy click reaction under UV light, which was used as the shell of sustained release preparation. Using polyvinyl alcohol (PVA)/carboxymethyl chitosan (CMCS) as raw material and vanillin as the cross-linking agent, hydrogen-bonded hybrid network hydrogel loaded with urea was prepared by freeze-thaw cycle, which was used as the core of sustained-release preparation. Finally, a green-coated urea fertilizer with core-shell structure was prepared to ameliorate the environmental pollution of slow-release fertilizer (for example, synthetic polymer-coated fertilizers are difficult to biodegrade), as well as to achieve the water retention and the effective slow-release. The high CS/PVA contents and the combination of the hydrogel core and the rubber shell significantly improved the mechanical properties of the coating material (tensile strength above 5 MPa, elongation at break up to 1400 %), hydrophilicity (to promote the degradation rate of the rubber shell) and soil water retention of the coating material (close to pure hydrogel), showing enhanced reaction. In terms of slow-release effect, coated nitrogen fertilizer with 3 % CS content, 5 % PVA content and 10-min coating time (SRP3/10) achieved the best slow-release effect of nitrogen (N) in water (62.7 % at 10 days), which was related to the hydrophilicity, semi-IPN skeleton and the cross-linking structure of the network, and the release conformed to the Korsmeyer-Peppas model with a non-Fickian diffusion release mechanism, indicating that the behavior of N release was mediated by a combination of drug diffusion and skeleton dissolution.

Electrospun Poly(vinyl alcohol)-Based Conductive Semi-interpenetrating Polymer Network Fibrous Hydrogel: A Toolbox for Optimal Cross-Linking

Cross-linking of poly(vinyl alcohol) (PVA) creates a three-dimensional network by bonding adjacent polymer chains. The cross-linked structure, upon immersion in water, turns into a hydrogel, which exhibits unique absorption properties due to the presence of hydrophilic groups within the PVA polymer chains and, simultaneously, ceases to be soluble in water. The properties of PVA can be adjusted by chemical modification or blending with other substances, such as polymers, e.g., conductive poly[3-(potassium-5-butanoate)thiophene-2,5-diyl] (P3KBT). In this work, PVA-based conductive semi-interpenetrating polymer networks (semi-IPNs) are successfully fabricated. The systems are obtained as a result of electrospinning of PVA/P3KBT precursor solutions with different polymer concentrations and then cross-linking using “green”, environmentally safe methods. One approach consists of thermal treatment (H), while the second approach combines stabilization with ethanol and heating (E). The comprehensive characterization allows to evaluate the correlation between the cross-linking methods and properties of nanofibrous hydrogels. While both methods are successful, the cross-linking density is higher in the thermally cross-linked samples, resulting in lower conductivity and swelling ratio compared to the E-treated samples. Moreover, the H-cross-linked systems have better mechanical properties─lower stiffness and greater tensile strength. All the tested systems are biocompatible, and interestingly, due to the presence of P3KBT, they show photoresponsivity to solar radiation generated by the simulator. The results indicate that both methods of PVA cross-linking are highly effective and can be applied to a specific system depending on the target, e.g., biomedical or electronic applications.

Enhancing selective transformation of benzyl alcohol by interface catalysis of a bilayer composite membrane

Facile and environment-friendly preparation of chloride-free benzaldehyde is still a great challenge in industry. Herein, a novel bilayer composite membrane with a top semi-interpenetrating polymer network layer and a lower polyvinylidene fluoride/poly (methacrylic acid) @Pd catalytic layer was prepared for the green preparation of chloride-free benzaldehyde. Results indicated that when the composite membrane was placed between the interface of H2O2/water solution and benzyl alcohol/toluene solution, it could efficiently and conveniently catalyze the oxidation of benzyl alcohol by hydrogen peroxide into chloride-free benzaldehyde. Furthermore, the oil phase and water phase were always separated by the bilayer membrane during the whole process and thus the reaction was operated conveniently. The good result was attributed to the unique structure of the bilayer membrane and the interface reaction technique. Undoubtedly, coupling the bilayer membrane with the interface reaction technique is a new and effective strategy for the green preparation of chloride-free benzaldehyde.

Siloxane-type single-ion conductors enable composite solid polymer electrolyte membranes with fast Li+ transporting networks for dendrite-proof lithium-metal batteries

Solid polymer electrolytes (SPEs) significantly improve the operational safety of lithium-metal batteries (LMBs) by replacing the flammable liquid electrolytes, but still suffer from key limitations including low ionic conductivities, inferior lithium-ion transference numbers (tLi+), and poor mechanical properties. Herein, a novel poly (ethylene oxide) (PEO)-based composite electrolyte, with a semi-interpenetrating polymer network, is fabricated via in-situ cross-linking siloxane-type single-ion conductors (SICs) in PEO SPEs by one-step sol–gel method, enabling they simultaneously achieve the enhanced electrochemical and physicochemical properties. Incorporating a thermodynamically compatible SIC network not only reduces the crystallization of PEO matrix while facilitating the segmental relaxation of polymer chains, but also contributes to dissociating Li-salt and forming a three-dimensional conducting network for fast Li-ion transport. Thus, the resulting composite SPEs exhibit higher ionic conductivities (1.10 × 10−5 S cm−1 at 25 °C and 1.41 × 10−4 S cm−1 at 60 °C), tLi+ (0.52), and electrochemical window stability (4. 59 V) than pure PEO SPEs. Furthermore, this stable SIC networks can also enhance the mechanical performance and thermal stability of the composite SPEs. Thanks to these merits, the composite SPEs show the significant feasibility to regulate Li deposition and suppress the growth of Li dendrites, affording excellent stability and compatibility with Li metal. As a result, the Li/Li symmetrical cells using the composite SPEs show excellent cycling performances without an evident polarization enlargement for more than 900 h. The LiFePO4/Li batteries also achieve a remarkable capacity of 132.8 mA g−1 at 1C and exhibit impressive cycling abilities with 91.9% retention over 250 cycles. This study provides a promising concept for developing advanced composite SPEs for potential application in solid-state dendrite-free LMBs.

Temperature‐Optimized Synthesis of SiO2‐Reinforced N‐(Alkyl)Acrylamide‐Based Semi‐IPN Hybrid Gels Functionalized with Methacrylic Acid Units

Front Cover: In article number 2300006, Nermin Orakdogen and co-workers deal with temperature-optimized synthesis of N-(alkyl)acrylamide-based semi-interpenetrating polymer network reinforced with silica nanoparticles and functionalized with methacrylic acid units by varying the polymerization temperature. The gelation is performed at different temperatures to evaluate the formation mechanism. The mechanical properties, swelling properties and susceptibility to stimuli show a wide dependence on the polymerization temperature.

Sponge-like, semi-interpenetrating self-sensory hydrogel for smart photothermal-responsive soft actuator with biomimetic self-diagnostic intelligence

Actuators based on hydrogels are good candidates for biomimetic soft robots due to their excellent mechanical properties and flexibility. Despite great efforts in hydrogel-based actuators, their actuation process still differs from the “recognition-judgment-execution” process that conscious intelligent beings go through owing to the lack of perceptive capacity. Herein, to imitate the intelligent actuation process of conscious organisms, a fast photo-thermal responsive and self-sensory soft actuator is proposed based on sponge-like hydrogel with semi-interpenetrating (semi-IPN) polymer network of thermosensitive poly (N-isopropylacrylamide) (PNIPAM) and electronically conductive polyaniline (PANI). The proposed actuator exhibits excellent photo-thermal responsiveness enabling remotely triggered actuation controlled by near infrared light (NIR), covering all azimuths with ultrafast response rate (within 2 s) and recover rate (within 1 s). Meanwhile, the conformational transition of PNIPAM networks during the course of actuation also lead to accompanying migration of the interpenetrated PANI chains and significant variation of local conductivity (>15%), endowing the actuator with self-sensing capacity to monitor its deformations. Eventually, a smart self-adaptive actuator is designed inspired by neuromuscular in intelligent organisms, which can actively perceive external environmental stimuli and consciously regulate its own shape transformation by monitoring and analyzing electrical signal. This sensory actuating hydrogel can provide insights into the development of artificial intelligent soft robotics with higher levels of autonomy and complexity.

Development and evaluation of pH sensitive semi-interpenetrating networks: assessing the impact of itaconic acid and aloe vera on network swelling and cetirizine release.

Hydrogels are crosslinked three-dimensional networks, and their properties can be easily tuned to target the various segments of the gastrointestinal tract (GIT). Cetirizine HCl (CTZ HCl) is an antihistaminic drug, which when given orally can upset the stomach. Moreover, this molecule has shown maximum absorption in the intestine. To address these issues, we developed a pH-responsive semi-interpenetrating polymer network (semi-IPN) for the delivery of CTZ HCl to the lower part of the GIT. Initially, 10 different formulations of itaconic acid-grafted-poly (acrylamide)/aloe vera [IA-g-poly (AAm)/aloe vera] semi-IPN were developed by varying the concentration of IA and aloe vera using the free radical polymerization technique. Based on swelling and sol-gel analysis, formulation F5 containing 0.3%w/w aloe vera and 6%w/w IA was chosen as the optimum formulation. The solid-state characterization of the optimized formulation (F5) revealed a successful incorporation of CTZ HCl in semi-IPN without any drug-destabilizing interaction. The in vitro drug release from F5 showed limited release in acidic media followed by a controlled release in the intestinal environment for over 72h. Furthermore, during the in vivo evaluation, formulation F5 did not affect the hematological parameters, kidney, and liver functions. Clinical observations did not reveal any signs of illness in rabbits treated with hydrogels. Histopathological images of vital organs of treated animals showed normal cellular architecture. Thus, the results suggest a non-toxic nature and overall potential of the developed formulation as a targeted drug carrier.