Acrylamide Research Articles

Synthesis and Application of Biodegradable Cellulose Hydrogels From Sunflower Husks as a Water‐Retaining Material in Agriculture

ABSTRACTThe water shortage is currently a major problem for agriculture around the world, and this, in turn, can negatively impact food safety. Therefore, in this article, acrylamide monomer (AAm) was bound by the cross‐linking agent N, N′‐methylene‐bis‐acrylamide (MBA) in amounts of 10, 15, and 20 mg along with microcrystalline cellulose (MCC) obtained from sunflower seed husk (SFH) and a biodegradable hydrogel in the soil layer with high sorption capacity was synthesized. As a result of the study, the AAm monomer found to be attached to the MCC matrix via intermolecular hydrogen bonds. The kinetics of swelling of the obtained hydrogels in aqueous, electrolytic and water‐ethanol, water‐acetone binary solutions at various amounts of cross‐linking agent were comparatively studied, and it was found that the water sorption potential of the natural polymer—MCC‐based hydrogel (MCC hydrogel)—is high at pH = 6.5 and corresponds to the pH of the soil environment. The study showed that the synthesized hydrogel is optimal when using 10 mg of a cross‐linking agent, has mechanical strength, withstands pressure up to 27 MPa, completely decomposes at 796°C, and has good thermal stability. It has been established that the pore sizes of hydrogel with 10 mg of cross‐linking agent lie within the range of 313.9 nm‐den 3.41 μm and belong to mesoporous materials, where the degree of swelling is 1176%. The MCC hydrogel was saturated with water from the soil within 5 days and collapsed within 35 days, releasing the absorbed water back into the soil, losing 66% of its mass and undergoing biological decomposition. These properties of MCC hydrogel allow it to be used as a “water‐retaining material” in agriculture.

100 μs Luminescence Lifetime Boosts the Excited State Reactivity of a Ruthenium(II)-Anthracene Complex in Photon Upconversion and Photocatalytic Polymerizations with Red Light.

The triplet excited state lifetime of a photosensitizer is an essential parameter for diffusion-controlled energy- and electron-transfer, which occurs usually in a competitive manner to the intrinsic decay of a triplet excited state. Here we show the decisive role of luminescence lifetime in the triplet excited state reactivity toward energy- and electron transfer. Anchoring two phenyl anthracene chromophores to a ruthenium(II) polypyridyl complex (RuII ref) leads to a RuII triad with a luminescence lifetime above 100 μs, which is more than 40 times longer than that of the prototypical complex. The obtained RuII triad sensitizes energy transfer to anthracene-based annihilators more efficiently than RuII ref and enables red-to-blue photon upconversion with a pseudo anti-Stokes shift of 0.94 eV and a moderate upconversion efficiency near 1 % in aerated solution. Particularly, RuII triad allows rapid photoredox catalytic polymerizations of acrylate and acrylamide monomers under aerobic condition with red light, which are kinetically hindered for RuII ref. Our work shows that excited state lifetime of a photosensitizer governs the dynamics of the excited state reactions, which seems an overlooked but important aspect for photochemistry.

Computational and experimental investigation on functional monomer selection for a novel molecularly imprinting polymer of remdesivir

Molecularly-imprinted polymers (MIPs) are a sample preparation technique with a functional cavity that can rebind the same or similar analyte to the template. It also can increase the selectivity of the analytical method. Computational approaches are capable of making predictions about the most optimal synthesis conditions, including the most appropriate monomers and solvents. This study used the DFT method, GFN2-xTB, and molecular dynamics simulation to predict MIP synthesis’s best functional monomer, solvent, and stoichiometric ratio. Remdesivir (RMD), used as a template, has also never been developed to be made as MIP. The monomers were acrylic acid (AA), 2-hydroxyethyl methacrylate (HEMA), and acrylamide (AM). Laboratory testing, association constant, and Job plot analysis are carried out to confirm the results of computational tests. The polymer was synthesized using precipitation and characterized using SEM, FTIR, and TGA. The adsorption capacity was evaluated in two different solvents, i.e. acetonitrile (ACN) and water: ACN=9: 1 (v/v). Computational study results identified acrylamide as the most interactive ligand with RMD as a template. The results of molecular dynamics simulations identify that the RMD: AM=1: 1 complex is the most stable in terms of the radial distribution function, hydrogen bond occupancy, and Gibbs bond free energy. The adsorption ability test results show that MIP 1 and MIP 2 have imprinting factor values of 1.36 and 1.15, respectively.

Preparation of phosphorus-nitrogen synergistic flame retardant cellulose composite aerogel from waste cotton/phytic acid/acrylamide

Cellulose aerogel is a green and biodegradable material, but the high flammability of cellulose aerogel hinders its development. In order to expand the application range of cellulose aerogel, it is necessary to improve the flame retardancy of cellulose aerogel. In this paper, cellulose hydrogels were prepared by decolorizing waste cotton fabrics (WCF) and dissolving them in 1-butyl-3-methylimidazole chloride salt ([Bmim]Cl)/DMSO. The cellulose hydrogels were impregnated in aqueous phytic acid (PA)/acrylamide (AM) solution for a period of time and then heated and treated. A cellulose composite aerogel with excellent flame retardant properties was successfully prepared by using in situ polymerization. The results show that the cellulose composite aerogel has a porous structure and good thermal stability, and the residual carbon content in the air at 800 °C is >2.86 %. At the same time, it has excellent flame retardancy, the ultimate oxygen index (LOL) is >40, and the vertical combustion carbon length is <3.5 cm. The thermal insulation performance has also been improved, and the composite aerogel with a height of 1 cm has a temperature difference of 40.2 °C between the upper and lower surfaces on the 80 °C heating table.

Research and Application of Thermally Activated Gel for Control of Lost Circulations

Summary Thermally activated gel (TAG) for control of lost circulations was evaluated, which is based on acrylamide (AM) and N-vinylpyrrolidone (NVP) copolymers crosslinked by polyethyleneimine (PEI). Viscoelasticity, pumpable time, breakthrough pressures, thermal tolerance, and fluid compatibility were tested in this paper, and then field applications in Missan Oilfield, Iraq, were introduced. Laboratory results showed that the strain limit in the linear viscoelastic region was 169% and storage modulus was 870 Pa. Pumpable time of TAG varies with pH values, so pumpable time can be controlled above 60 minutes by adjusting pH values in the temperature ranges of 100°C to 140°C. Breakthrough pressures were tested in 5-mm (inner diameter) and 10-mm (inner diameter) simulating pipes.The breakthrough pressure gradients were 1.172 psi/cm and 1.200 psi/cm at 0.5 mL/min and 1.0 mL/min, respectively, for 10-mm simulating pipes, 1.872 psi/cm and 2.200 psi/cm for 5-mm simulating pipes. TAG maintained morphologies completely and dehydrated slightly after 30 days of aging at 140°C, transformed into a degraded and low-viscosity fluid after 45 days of aging. Tests proved that invasions of inorganic electrolytes, drilling fluid additives, and drilling fluids can lengthen the pumpable time of TAG, so flash settings due to invasions could not occur. Applications in Missan Oilfield verified the performances of TAG mentioned above.

A hydrogel sensor based on conic baston structure

AbstractResistive flexible pressure sensors are extensively employed in wearable devices owing to their wide operational range and straightforward construction. This study presents a conic bastion‐structured sensor microunit to improve the sensor sensitivity. The base hydrogel is synthesized using acrylamide (AM), with Mg2+ and Na+ acting as conductive ions. The sensor is fabricated using digital light processing (DLP) 3D printing technology and is subjected to experimental evaluation. The findings indicate that the hydrogel sensor with a 50 wt% AM composition demonstrates enhanced mechanical strength and conductive properties, achieving a peak sensitivity of 0.534 kPa−1 within a pressure range of 0–0.8 kPa. Furthermore, the sensor exhibits favorable response characteristics (30 ms) and recovery characteristics (40 ms), along with stability. The proposed sensor is suitable for wearable devices and live joint angle detection. Additionally, the “handwriting fingerprint” pattern recognition and document verification proposed in this article make it applicable in scenarios, such as banking, notarization, and other handwriting and seal verification contexts.

Photocatalysis coupled electro-Fenton process for treatment of acrylamide wastewater: an optimised study

ABSTRACT Electro-Fenton is a commonly used approach for pollutant removal from different wastewater that requires high energy consumption. Coupling electro-Fenton with solar energy could potentially overcome high power consumption. Thus, this study combined photocatalysis with three-dimensional electro-Fenton to treat acrylamide (AM) wastewater. The removal efficiencies of chemical oxygen demand (COD), ammonia nitrogen (NH3−N), and total organic carbon (TOC) in photocatalysis-coupled electro-Fenton were studied. The effects of current density, iron powder dosage, plate spacing, and photocatalyst dosage on COD and NH3−N removal were also optimised using response surface methodology (RSM). The photocatalysis coupled three-dimensional electro-Fenton reduced energy consumption compared to single photocatalysis or electro-Fenton technology. The COD and NH3−N removal rates were 82.444% and 92.810%, respectively, at the current density of 16.000 mA/cm2, iron powder dosage of 1.330 g, plate spacing of 16.643 mm, photocatalyst dosage of 0.2 g. This study demonstrated that organic pollutants can be degraded efficiently at a low concentration of catalysts coupled with the electro-Fenton process, offering a low-energy consumption treatment of wastewater.

Facile and green preparation of carbonaceous material-based wood bio-adhesives using hydrochar from hydrothermal carbonization of glucose with or without acrylic acid/acrylamide

To address the issues of formaldehyde emission, mildew, and easy combustion of traditional wood adhesives, this paper, for the first time, reported formaldehyde-free plywood bio-adhesives using carbonaceous material (hydrochar) generated from hydrothermal carbonization (HTC) of glucose with or without acrylic acid (AA) and acrylamide (AM). The highest wet shear strength of bio-adhesives (BD-G/AA-180) was 1.32 MPa, which meets the Chinese national standard GB/T 9846-2015 (≥0.7 MPa). It was found that functional groups (–NH2 and –COOH) were abundant on the surface of hydrochar from co-HTC of glucose with AM or AA. The formation of covalent bonds (between components of bio-adhesives; between bio-adhesives and wood) via dehydration or esterification reaction was a key factor in improving wet shear strength during hot-press treatment. Unlike bio-adhesives developed from polysaccharides and proteins, these hydrochar carbonaceous material-derived bio-adhesives had excellent anti-mildew properties and flame resistance with help from ammonium polyphosphate. This work paves a new road to prepare green formaldehyde-free plywood bio-adhesives.

Detoxification of Acrylamide by Potentially Probiotic Strains of Lactic Acid Bacteria and Yeast.

Some potentially probiotic strains of lactic acid bacteria (LAB) and yeast that inhabit the digestive tract of humans are known to detoxify xenobiotics, including acrylamide (AA). The objective of the subsequent research was to evaluate the AA-detoxification capability of LAB and yeast isolated from various sources. Namely, the effect of AA was tested on the growth of LAB and yeast strains, as well in the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Subsequently, the AA-binding ability of LAB and yeast was investigated in various environments, including the pH, incubation temperature, cell density, and with inanimate cells. The ability of selected LAB and yeast to reduce the genotoxicity of AA was tested on Caco-2 and Hep-G2 cell lines. The results showed that all tested strains exhibited strong resistance to AA at concentrations of 5, 10, and 50 µg/mL. Also, AA was detected in the intracellular and membrane extracts of tested strains. The most effective binding strain was Pediococcus acidilactici 16 at pH = 5, cell density = 109 CFU/mL, and incubation temperature = 37 °C (87.6% of AA removed). Additionally, all tested strains reduced the genotoxicity of AA, with the greatest reduction observed at the highest concentration of 50 µg/mL. The phenomena of detoxification by potentially probiotic strains could reduce the toxic and harmful effects of AA exposure to humans every day.

Purification Processes for Generating Cationic Lignin-Acrylamide Polymers.

Purification is an essential step in many polymerization processes for fabricating highly pure polymers. This study considered various purification methods for purifying the product of lignin, acrylamide (AM), and diallyl dimethylammonium chloride (DADMAC) copolymerization reactions at a laboratory scale. The charge density, yield, molecular weight, and solubility analyses confirmed that ethanol extraction and membrane filtration were the most effective processes for producing lignin-p(AM)-p(DADMAC). The 1H NMR analysis revealed that the membrane dialysis effectively removed unreacted AM and DADMAC monomers from the reaction medium. The produced samples of the ethanol-extraction and dialysis processes had higher solubility and yield compared to the product of the acidification process. Thermogravimetric studies confirmed that the ethanol-extracted and dialyzed samples had a degradation temperature (220 °C) higher than that of the acidified samples (160 °C). The rheological studies confirmed that the viscosities of the polymer solutions were influenced more by the solubility than by the molecular weight of the generated polymers within the molecular weight range examined in this study. The flocculation studies confirmed that the ethanol-extracted and dialyzed polymers were more effective flocculants than the acidified samples for the particles of a kaolinite suspension. Based on the above results, membrane filtration with a larger pore size could be an environmentally friendly method for effectively purifying lignin-p(AM)-p(DADMAC).

Preparation and characterization of functional dual network hydrogel for motion monitoring in smart bra

The smart bra is a kind of sports underwear with providing health monitoring and comfort protection for women breast in sports. Developing smart sensing materials that combine comfort and functionality for sensing breast condition remains a challenge. Here, natural polysaccharide sodium alginate (SA), acrylamide (AM) monomer and chitosan (CS) and polypyrrole (PPy) in-situ polymerized from pyrole (Py) monomer were used as raw materials to successfully synthesize double network conductive hydrogel by two-step method. The results show that in the hydrogels, the entanglement and interpenetration of macromolecules produce toughness (tensile/compressive strength is ∼0.248 MPa/∼2.836 MPa), elasticity (tensile/compression elastic recovery rate is∼94.06 %/∼98.41 %) and durability (after 30 tensile/compression cycles conducting at 25 %, 50 % and 100 % constant strain keep at high recovery rate). The rich moisture content provides its adhesion (adhesion strength ∼4.7557 kPa) and flexibility (bending stiffness 1.0843 cN cm∼), presenting sufficient adhesion reliability and robustness to different substrates. The addition of PPy enables the hydrogel to have conductivity (6.77 × 10−2 S cm−1) and sensing performance (tensile/compression sensitivity is ∼1.94/∼1.43). The conductive hydrogel, as a flexible strain sensor, shows good adhesion, flexibility, elasticity and sensitivity in application of sports smart bra, can detect both the tensile behavior of skin and the compression state of tissue through its mechano-electricity, and accurately sense the changes of physiological parameters during movement. The conductive hydrogel with high elasticity and strength has broad application prospects in smart bra.

An Electrochemical Bioplatform Based on Acrylamide‐Induced Inhibition of DNA‐RNA Hybridization for the Determination of Acrylamide

AbstractThis study reports the development of an innovative electrochemical bioplatform for the indirect determination of acrylamide (AM) based on its inhibitory effect on the hybridization of nucleic acids through the formation of AM‐guanine single‐stranded (ssDNA) adducts. The method combines the advantages of the formation and selective immunorecognition of DNA/RNA heteroduplex, with the use of MBs and amperometric transduction using disposable SPCEs. Increasing concentrations of acrylamide prevented the efficient hybridization of a synthetic biotinylated DNA probe immobilized on streptavidin‐coated magnetic beads with its complementary RNA target and the as‐formed heteroduplex recognition with a specific antibody and a secondary HRP‐labeled antibody used for electrochemical readout. The resulting magnetic bioconjugates were magnetically trapped on the surface of the working electrode of a SPCE and the amperometric transduction was carried out in the presence of the H2O2/HQ system, recording a cathodic response inversely proportional to the AM concentration. The developed bioplatform is more competitive with other reported methods in terms of simplicity and assay time, allowing the selective detection of 1 nM AM in 60 min. In addition, the bioplatform was applied to the analysis of potato crisp water extracts.

Synthesis of Polyacrylamide Nanomicrospheres Modified with a Reactive Carbamate Surfactant for Efficient Profile Control and Blocking

Urethane surfactants (REQ) were synthesized with octadecanol ethoxylate (AEO) and isocyanate methacrylate (IEM). Subsequently, reactive-carbamate-surfactant-modified nanomicrospheres (PER) were prepared via two-phase aqueous dispersion polymerization using acrylamide (AM), 2-acrylamido-2-methylpropanesulfonic acid (AMPS) and ethylene glycol dimethacrylate (EGDMA). The microstructures and properties of the nanomicrospheres were characterized and examined via infrared spectroscopy, nano-laser particle size analysis, scanning electron microscopy, and in-house simulated exfoliation experiments. The results showed that the synthesized PER nanomicrospheres had a uniform particle size distribution, with an average size of 336 nm. The thermal decomposition temperature of the nanomicrospheres was 278 °C, and the nanomicrospheres had good thermal stability. At the same time, the nanomicrospheres maintained good swelling properties at mineralization &lt; 10,000 mg/L and temperature &lt; 90 °C. Under the condition of certain permeability, the blocking rate and drag coefficient gradually increased with increasing polymer microsphere concentration. Furthermore, at certain polymer microsphere concentrations, the blocking rate and drag coefficient gradually decreased with increasing core permeability. The experimental results indicate that nanomicrospheres used in the artificial core simulation drive have a better ability to drive oil recovery. Compared with AM microspheres (without REQ modification), nanomicrospheres exert a more considerable effect on recovery improvement. Compared with the water drive stage, the final recovery rate after the drive increases by 23.53%. This improvement is attributed to the unique structural design of the nanorods, which can form a thin film at the oil–water–rock interface and promote oil emulsification and stripping. In conclusion, PER nanomicrospheres can effectively control the fluid dynamics within the reservoir, reduce the loss of oil and gas resources, and improve the economic benefits of oil and gas fields, giving them a good application prospect.

Synthesis and characterization of allyl mannitol cross-linker based novel hydrogel for capturing of toxic metal ions from aqueous solution

ABSTRACT Three grades of allyl-mannitol cross-linker-based hydrogel (AMCLHs hydrogel) have been synthesized with the help of acrylic acid and acrylamide monomers using a free radical co-polymerization technique. The three prepared grades of AMCLHs hydrogel have been referred to as AMCLHs-1, AMCLHs-2, and AMCLHs-3, respectively. The prepared AMCLHs hydrogels have been characterized by several analytical techniques viz. Fourier transform infrared (FTIR) spectroscopy, thermogravimetric (TG) analysis, point of zero charge (ΔpHPZC), analysis, and scanning electron microscope (SEM) analysis, respectively. The synthesized hydrogels have been utilized for the elimination of Cu2+ and Co2+ ions from wastewater. The properties of prepared AMCLHs hydrogels, i.e. swelling and water retention ratio have been studied in distilled water under optimized conditions. The maximum swelling ratio of the best grade of hydrogel (AMCLHs-1) has been found to be 400.5 g/g with the water retention ratio of 75.09% during 24 h. These findings indicate the AMCLHs-1 hydrogel has remarkable swelling and water retention capacity. The maximum metal ion removal efficiency of AMCLHs-1 hydrogel from aqueous solutions has been found to be 96.6% for Cu2+ and 94.2% for Co2+ ions under optimum conditions. The experimental data fitted well with the Langmuir and Freundlich adsorption models, revealing maximum adsorption capacities of 431.03 mg/g for Cu2+ ions and 414.93 mg/g for Co2+ ions, respectively. In addition, the rate for the adsorption of Cu2+ and Co2+ ions onto AMCLHs-1 hydrogel follows both Pseudo first and second-order kinetic models. The negative ΔG values indicate that the adsorption process occurs spontaneously, while positive ΔH values suggest that the adsorption process is exothermic in nature. The prepared AMCLHs hydrogel is reusable and exhibits high desorption efficiency with 87.63% for Cu2+ and 85.21% for Co2+ metal ions even after the fourth cycle. Overall, AMCLHs hydrogel is a cost-effective and reusable adsorbent that possesses a significant potential for heavy metal ion removal from aqueous solutions.

Bidirectional Temperature‐Responsive Thermochromic Hydrogels With Adjustable Light Transmission Interval for Smart Windows

AbstractThermochromic smart windows have been widely developed for solar regulation to save building energy. However, most current smart windows still exhibit a single responsiveness to a specific temperature, which is not conducive to daytime energy saving or nighttime privacy protection. Herein, a low‐temperature response is achieved by pre‐initiation of the monomer acrylamide (AAm) and acrylic acid (AA) in the synthesis of P(AAm‐co‐AA). Then, N‐isopropyl acrylamide and AAm are introduced into P(AAm‐co‐AA) to form a pre‐polymerized precursor solution. The liquid precursor solution can be encapsulated within two quartz glasses and synthesized in situ to prepare smart windows, which exhibit a high visible light transmittance of 84.4%, excellent solar modulation of 69.5%, and bidirectional temperature responsiveness (cold and hot). In addition, the upper critical solution temperature and the lower critical solution temperature of the hydrogel and the light transmission interval between the two temperatures can be flexibly adjusted to adapt to different climates and individual user needs. The designed smart window maintains a high light transmission within the human body's comfort temperature range. The bidirectional temperature response window achieves the dual functions of energy saving and privacy protection, making it an ideal smart window candidate with good prospects for practical applications.

Synthesis and Polymerization of Poly Acryl Imide and One of Their Derivatives Then Curing the Product with Alkyl Halide

The present work involved four steps: First step include reaction of acrylamide ,N-?-Methylen-bis(acryl amide) and N-tert Butyl acryl amide with poly acryloyl chloride in the presence of triethyl amine (Et3N) as catalyst, the second step include homopolymerization of all products of the first step by using benzoyl peroxide(BPO) as initiator in (80-90)Co in the presence of Nitrogen gas(N2). In the third step the poly acrylimide which prepare in second step was convert into potassium salt by using alcoholic potassium hydroxide solution. Fourth step include Alkylation of the prepared polymeric salts in third step by react it with different alkyl halides(benzyl chloride, allylbromide , methyl iodide) by using DMF as solvent for(10-12) hours. Structure Confirmation of all prepared polymers were proved using FT-IR, 1H-NMR and C13-NMR spectroscopy for some polymers. Other physical properties including softening and melting points of the polymers were also measured.

Lnc-Pim1 Promotes Neurite Outgrowth and Regeneration of Neuron-Like Cells Following ACR-Induced Neuronal Injury.

Decreased regenerative capacity of central nervous system neurons is the main cause for failure of damaged neuron regeneration and functional recovery. Long noncoding RNAs (lncRNAs) are abundant in mammalian transcriptomes, and many time- and tissue-specific lncRNAs are thought to be closely related to specific biological functions. The promoting effect of Pim-1 gene on neural differentiation and regeneration has been documented, but the effect and mechanism of its neighbor gene Lnc-Pim1 in regulating the response of central neurons to injury remain unclear. RT-PCR in this study demonstrated that the expression of Lnc-Pim1 was upregulated in acrylamide (ACR)-induced neuronal injury. FISH and nucleus-cytoplasmic assay demonstrated that Lnc-Pim1 was mainly expressed in the neuron cytoplasm, with a small amount in the nucleus. Western blot analysis proved that Lnc-Pim1 overexpression induced by the lentivirus vector could promote neurite outgrowth in Neuro-2a cells by activating the Erk1/2 signal pathway, and improve neurite regeneration of injured neurons by upregulating GAP-43 and β-Ⅲ tubulin protein expression. However, silencing Lnc-Pim1 expression by interfering RNA could effectively downregulate the GAP-43 and β-Ⅲ tubulin protein expression, and inhibit neurite growth of neurons. In addition, CHIRP-MS was performed to identify several potential targets of Lnc-Pim1 involved in the regulation of neurite regeneration of injured neurons. In conclusion, our study demonstrated that Lnc-Pim1 is a potential lnc-RNA, playing an important role in regulating central nerve regeneration.

Protective effect of aspirin and gentisic acid, a plant-derived phenolic acid, on acrylamide-induced neurotoxicity by inhibiting apoptosis and autophagy.

Acrylamide (ACR) is a toxic agent for humans and animals. Gentisic acid, anaspirinmetabolite, has antioxidant activity. Therefore, the present study investigated the probable protective effects of aspirin and gentisic acid on ACR-induced neurotoxicity in PC12 cells and rats. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay was used to assess the effects of aspirin and gentisic acid (1.25, 2.5, 5 µM) on ACR (5 mM) toxicity. Male Wistar rats were randomly divided into 13 groups: (1) Control group, (2) ACR (50 mg/kg, 11 days, i.p.), (3-5) ACR + aspirin (25, 50, 75 mg/kg, 11 days, p.o.), (6-8) ACR + gentisic acid (25, 50, 75 mg/kg, 11 days, p.o.), (9) ACR + vitamin E (200 mg/kg, every other day, i.p.), (10, 11) Aspirin (75, 100 mg/kg, 11 days, p.o.), (12, 13) Gentisic acid (75, 100 mg/kg, 11 days, p.o.). Behavioral tests were assessed on the final day of the study. In the cerebral cortex, malondialdehyde (MDA), glutathione (GSH), cleaved-caspase-3, and microtubule-associated protein 1A/1B-light chain 3 (LC3) protein levels were evaluated. When compared with the ACR group, aspirin (2.5, 5 µM) and gentisic acid (2.5 µM) significantly enhanced cell viability. In comparison to the control group, ACR induced severe motor impairment, elevated MDA, cleaved-caspase-3, LC3 II/I ratio, and decreased GSH levels in the cerebral cortex of rats. ACR-induced changes were significantly reversed by aspirin and gentisic acid (25 mg/kg). Oxidative stress, apoptosis, and autophagy play important roles in the neurotoxicity of ACR. Aspirin and gentisic acid significantly reduced ACR-induced toxicity by inhibiting the mentioned mechanisms.

Preparation and performance study of thermo-responsive P(NIPAM-AM-ABP)/keratin composite nanofiber membrane for bio-application

This paper describes a temperature-responsive composite nanofibrous membrane by blending of the P(NIPAM-AM-ABP) (PNAA) nanofiber and the wool keratin (WK) nanofiber. The photo crosslinkable PNAA with the LCST value of 38.1 °C was obtained by free radical copolymerization of the temperature sensitive N-Isopropylacrylamide (NIPAM) monomer, the hydrophilic monomer Acrylamide (AM), and the photo crosslinkable monomer 4-Acryloyloxybenzophenone (ABP). Keratin was extracted from waste wool fiber by reduction method. The PNAA nanofiber (PNAA-NF) and the keratin nanofiber (WK-NF) were electoral spun separately by two-needle parallel spinning, and the obtained composite nanofiber membrane was then crosslinked by UV irradiation and heat treatments to prepare the PNAA/WK nanofiber membrane (PNAA/WK-NFM) with good water tolerance. The result indicated that the photo cross-linkable temperature sensitive PNAA with the LCST of 38.1 °C was successfully synthesized. The obtained PNAA/WK-NFM has a good fibrous morphology and excellent water tolerance. The composite nanofiber membrane showed good reversible temperature sensitivity and temperature responsive drug releasing property due to the PNAA. By combining of the PNAA-NF and WK-NF, the mechanical property of the PNAA/WK-NFM was greatly enhanced in both dry and wet states, and the slow drug releasing property of the membrane was further improved. In-vitro cell culture experiments indicated that the PNAA/WK-NFM has a good biocompatibility with no cytotoxicity. These findings suggested that the PNAA/WK-NFM has a potential application in temperature responsive drug releasing biomaterials.

Phase-changing NIPAM-AM/ATO hydrogels for thermochromic smart windows with highly adaptive solar modulation

Improving the solar regulation and reducing the response temperature of thermochromic smart windows are pivotal importance for energy-saving buildings. However, these two strategies are challenging to be integrated into one window. Herein, a novel composite hydrogel based on N-isopropylacrylamide (NIPAM) doped with antimony-doped tin oxide (ATO) nanoparticles and acrylamide (AM) was developed for producing a high-performance smart window, which successfully achieved enhanced solar energy regulation and reduced response temperature. This smart window was fabricated by combining a reversible thermoresponsive hydrogel (TAH) that acted as a thermochromic material with a ATO multilayer film that performed as a transparent heater. The as-prepared smart window could modulate solar light over a range from ultraviolet (UV) to infrared (IR) radiation and achieved active responses to high-temperature weather. The smart window showed high luminous transmittance (Tlum, 82.92 %) together with an excellent solar modulation performance (ΔTlum = 73.31 %, ΔTIR = 38.26 %, and ΔTsol = 60.74 %), and a lower critical solution temperature of 32 °C. Even after 120 high- and low-temperature cyclic durability tests, the smart windows still exhibited a high solar modulation capability. In outdoor demonstrations, the as-prepared smart window exhibited a promising temperature regulation ability under strong solar irradiation. Therefore, the present universal modification framework provided some insights for the future design of energy-saving windows.