Polyacrylamide Research Articles

A high temperature-resistant, strong, and self-healing double-network hydrogel for profile control in oil recovery

Hydrogels are widely used in profile control to plug high-permeability zones in oil recovery. In this study, a novel double-network (DN) hydrogel is developed for profile control. The two networks of the prepared hydrogel are polyacrylamide (PAAm) crosslinked by N,N’-Methylenebisacrylamide (MBAA) and konjac glucomannan (KGM) crosslinked by borax (B), respectively. The two networks are interconnected by their interpenetrating structures and hydrogen bonds. Based on the results of a series of evaluation experiments, the AAm/KGM DN hydrogels developed in this study exhibit a strong mechanical strength with their fracture stresses exceeding 0.137 MPa. Meanwhile, the AAm/KGM DN hydrogels can remain thermally stable after being heated at 130 °C for 24 h, indicating the good high-temperature resistance of the new sample. Moreover, the prepared AAm/KGM DN hydrogels present excellent self-healing performance due to the abundant hydrogen bonds in their structures, which helps form stable and long-term plugging in porous media. In addition, the pure PAAm hydrogel and the AAm/KGM DN hydrogel are sheared into two dispersed particle gel (DPG) suspensions to investigate their plugging performances. The results demonstrate that the AAm/KGM DN DPG can effectively plug a high-permeability sandpack with a plugging efficiency of 93.2 %, while the pure AAm DPG can only provide a much lower plugging efficiency of 60.5 %. The AAm/KGM DN hydrogel developed in this study, with its high mechanical strength, high-temperature resistance, and self-healing capability, offers a promising new candidate for profile control in oil recovery.

The influence of polyacrylamide gel substrate elasticity on primary cultures of rat retinal ganglion cells

In vitro primary cell culture models of retinal ganglion cells (RGC) are widely used to study pathomechanisms of diseases such as glaucoma. The biomechanic interaction with the culture substrate is known to influence core cellular functions. RGC cultures, however, are usually grown on rigid plastic or glass substrates. We hypothesized that soft polyacrylamide gel substrates may alter survival and neurite outgrowth of primary cultured RGC.Primary retinal cultures from postnatal (day 1-6) Wistar rats were grown on glass coverslips or polyacrylamide (PA) gel substrate with different Young’s elastic moduli (0.75, 10 or 30 kPa). Substrates were coated with Poly-l-lysine and / or laminin. RGC were immunostained with anti-beta-III-tubulin. Total neurite length, growth cone morphology, RGC density, mitochondrial morphology and transport as well as pro-survival pathways (Erk1/2, Akt, CREB) were assessed.PA gel substrates of E = 10 kPa significantly increased the total neurite length by factor 1.5 compared to glass (p = 0.02). The growth cone area was significantly larger by factor 5.3 on 30 kPa gels (p = 0.01). The presence of a substrate coating was more important for neurite outgrowth and RGC survival on PA gels (poly-l-lysine > laminin) than on glass. Neither mitochondrial morphology and motility nor the activation of pro-survival pathways significantly differed between the four substrates.PA gel substrates significantly enhanced RGC neurite outgrowth. The signaling cascades mediating this effect remain to be determined.

Loofah-based self-powered triboelectric nanogenerator-supercapacitor for an integrated self-charging energy system

New urbanization is ushering in a surge in construction and amplifying a substantial demand for urban road development, simultaneously spurring innovation and development of environmentally sustainable power sources. Triboelectric nanogenerator (TENG), a revolutionary technology of energy conversion, efficiently capturing high-entropy energy from the environment and offering the advantages of self-powered and immediacy. Recognizing the critical need to store the energy harvested by TENGs, we present an integrated energy conversion and storage system that combines a loofah-based self-powered rotating TENG (LS-TENG) with a supercapacitor. The maximum instantaneous output power and the corresponding instantaneous power density of the LS-TENG are 0.75mW and 202.69mW/m2 at 30rpm. The supercapacitor, featuring carbon nanotube (CNT) interdigitated electrodes created through microelectronic printing technology, utilizes polyacrylamide (PAM)-lithium chloride (LiCl) as a gel electrolyte (adhesion strength of 16.69 kPa). The supercapacitor is seamlessly integrated onto the back of the LS-TENG’s stator, which effectively simplified the energy conversion and storage system. At a current density of 0.01mA/cm2, the supercapacitor achieves a high volumetric capacitance of 341.47 mF/cm3, an energy density of 17.07mWh/cm3, and a power density of 257.07 mW/cm3, with a remarkable capacitance retention rate of 99.12% after 30000 cycles at a current density of 0.02mA/cm2. Furthermore, a concept demonstration of an integrated self-charging energy system is implemented, in which the supercapacitor can be charged at wind speed rate of 3.0m/s. The proposed integrated energy storage and conversion system makes it ideal for converting and storing wind energy.

An adhesive, highly stretchable and low-hysteresis alginate-based conductive hydrogel strain sensing system for motion capture

A strain sensor stands as an indispensable tool for capturing intricate motions in various applications, ranging from human motion monitoring to electronic skin and soft robotics. However, existing strain sensors still face difficulties in simultaneously achieving superior sensing performance sufficing for practical applications like high stretchability and low hysteresis, as well as seamless device fabrication like desirable interfacial adhesion and system-level integration. Herein, we develop a highly stretchable and low-hysteresis strain sensor with adhesive poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/polyacrylamide (PAAm)‑sodium alginate (SA) composite hydrogel, allowing the successful construction of a wireless motion capture sensing system that can provide precise data collection within a large deformation range. The resultant composite hydrogel displays favorable interfacial adhesion and robust mechanical stability, and the fabricated strain sensor demonstrates a wide working strain range (up to 500 %) with high sensitivity (gauge factor = 11) and ultra-low hysteresis (1.52 %), outperforming previous PEDOT-based hydrogel strain sensors. Enabled by the intriguing material properties and high sensing performance, we further demonstrate the fabrication and integration of a wireless motion capture sensing system for diverse applications like human motion monitoring, gesture recognition, and interactive communication.

High-strength, super-hydrophilic alginate electrospun nanofibrous membranes for rapid oil-water emulsion separation

Ultrafiltration membrane separation technology is considered an effective method for separating oil-water emulsions. However, oil droplets can easily deposit on the surface of the membranes, leading to severe fouling and a decrease in flux. In this study, poly (ethylene oxide)/acrylamide/sodium alginate (PEO/AM/NaAlg) hydrogel nanofibers were deposited on a poly (hydroxybutyric acid) (PHB) electrospun nanofibrous membrane. Subsequently, superhydrophilic (ethylene oxide)-poly(acrylamide)/calcium alginate hydrogel nanofiber composite filtration membranes (PEO/PAM/CaAlg-PHB) were prepared by polymerization and Ca2+ cross-linking using a PHB electrospun nanofibrous membrane as the matrix. The morphology, tensile strength, water contact angle, and oil–water emulsion separation properties of the PEO/PAM/CaAlg-PHB hydrogel filtration membrane were investigated. The results showed that the PEO/PAM/CaAlg-PHB membrane had good anti-fouling performance, with a tensile strength of 1.95 MPa. After 3 h of the filtration operation, the stable flux and oil–water emulsion rejection of the membrane reached 2925.2 L m−2 h−1 bar−1 and 98.66 %, respectively. The preparation method was simple, cost effective, and environmentally friendly, without introducing any organic pollutants. The PEO/PAM/CaAlg-PHB hydrogel filtration membrane shows promise for separating oil–water emulsions.

Synergistic Effect Between 0D CQDs and 2D MXene to Enhance the Photothermal Conversion of Hydrogel Evaporators for Efficient Solar Water Evaporation, Photothermal Sensing and Electricity Generation.

Solar-powered interfacial water evaporation is a promising technique for alleviating freshwater stress. However, the evaporation performance of solar evaporators is still constrained by low photothermal conversion efficiency and high water evaporation enthalpy. Herein, 0D carbon quantum dots (CQDs) are combined with 2D MXene to serve as a hybrid photothermal material to enhance the light absorption and photothermal conversion ability, meanwhile sodium carboxymethyl cellulose (CMC)/polyacrylamide (PAM) hydrogels are used as a substrate material for water transport to reduce the enthalpy of water evaporation. The synergistic effect in 0D CQDs/2D MXene hybrid photothermal materials accelerate the carrier transfer, inducing efficient localized surface plasmon resonance (LSPR) effect. This results in the enhanced photothermal conversion efficiency. The integrated hydrogel evaporators demonstrate a high evaporation rate (1.93 and 2.86kgm-2h-1 under 1 and 2 sunlights, respectively) and low evaporation enthalpy (1485Jg-1). In addition, the hydrogel evaporators are applied for photothermal sensing and temperature difference power generation (TEG). The TEG device presents an efficient output power density (230.7mWm-2) under 1 sunlight. This work provides a feasible approach for regulating and controlling the evaporation performances of hydrogel evaporators, and gives a proof-of-concept for the design of multipurpose solar evaporation systems.

Composite Hydrogel of Polyacrylamide/Starch/Gelatin as a Novel Amoxicillin Delivery System.

This study investigates the development and characterization of a novel composite hydrogel composed of polyacrylamide (PAAm), starch, and gelatin for use as an amoxicillin delivery system. The optical properties, swelling behavior, and drug release profile of the composite hydrogel's were studied to evaluate its efficacy and potential applications. UV-visible spectroscopy was employed to determine the optical properties, revealing significant transparency in the visible range, which is essential for biomedical applications. The incorporation of starch and gelatin into the polyacrylamide matrix significantly enhanced the hydrogel's swelling capacity and biocompatibility. Studies on drug delivery demonstrated a sustained release profile of amoxicillin in simulated gastrointestinal fluids, which is essential for maintaining therapeutic levels for a prolonged amount of time. The results indicate that the composite hydrogel of PAAm/starch/gelatin has good swelling behavior, appealing optical characteristics, and a promising controlled drug release mechanism. These results point to this hydrogel's considerable potential as a drug delivery method, providing a viable path toward enhancing the medicinal effectiveness of amoxicillin and maybe other medications.

Strength characteristics of cement stabilized construction waste slurry modified by polyacrylamide with different moisture contents

Waste slurry is a major component of construction waste, and its resource utilization can effectively reduce its environmental impact. The effect of polyacrylamide (PAM) content and moisture content on the strength characteristics of PAM modified cement stabilized construction waste slurry (PCMS) was studied using unconfined compressive strength (UCS) and triaxial tests. It can be concluded that, 1) The UCS of PCMS increases with the increase of curing age and significantly decreases with the increase of moisture content. As the content of PAM increases, it first increases and then decreases, with UCS reaching its maximum at a PAM content of 0.5%. 2) When the moisture content is 50%, PAM can increase the elastic modulus of PCMS. When the content of PAM is 0.5%, the elastic modulus reaches its maximum value. When the moisture content is 80% and 100%, the effect of PAM on the elastic modulus of PCMS is not significant. 3) The addition of PAM can improve the shear strength of PCMS. Under the same confining pressure, the shear strength of PCMS increases first and then decreases with the increase of PAM content, and the optimal content is 0.5%. 4) The variation pattern of PCMS cohesion is basically consistent with the shear strength. PAM improves the shear strength of PCMS by enhancing its cohesion. The addition of PAM has a relatively small impact on the internal friction angle of PCMS. These findings provide valuable insights for research into modification technology and the resource utilization of construction waste slurry.

A Bio-Inspired Multifunctional Hydrogel Network with Toughly Interfacial Chemistry for Dendrite-Free Flexible Zinc Ion Battery.

Flexible and high-performance aqueous zinc-ion batteries (ZIBs), coupled with low cost and safe, are considered as one of the most promising energy storage candidates for wearable electronics. Hydrogel electrolytes present a compelling alternative to liquid electrolytes due to their remarkable flexibility and clear advantages in mitigating parasitic side reactions. However, hydrogel electrolytes suffer from poor mechanical properties and interfacial chemistry, which limits them to suppressed performance levels in flexible ZIBs, especially under harsh mechanical strains. Herein, a bio-inspired multifunctional hydrogel electrolyte network (polyacrylamide (PAM)/trehalose) with improved mechanical and adhesive properties was developed via a simple trehalose network-repairing strategy to stabilize the interfacial chemistry for dendrite-free and long-life flexible ZIBs. As a result, the trehalose-modified PAM hydrogel exhibits a superior strength and stretchability up to 100 kPa and 5338 %, respectively, as well as strong adhesive properties to various substrates. Also, the PAM/trehalose hydrogel electrolyte provides superior anti-corrosion capability for Zn anode and regulates Zn nucleation/growth, resulting in achieving a high Coulombic efficiency of 98.8 %, and long-term stability over 2400 h. Importantly, the flexible Zn//MnO2 pouch cell exhibits excellent cycling performance under different bending conditions, which offers a great potential in flexible energy-related applications and beyond.

Preparation and motion-sensing properties of ion/electron mixed conductive hydrogels fabricated by carbon-coated sepiolite nanofibers

Hydrogels have experienced significant advancements owing to their versatile applications in biomedicine, wound care, food packaging, and smart devices. The pursuit of environmentally sustainable and scalable hydrogel production methods remains a primary research objective. This study introduces an innovative hydrogel fabrication technique involving the integration of surface-modified sepiolite nanofibers with polyacrylamide (PAM), resulting in the formation of sepiolite-based composite hydrogels (PASSC). These hydrogels exhibit both ionic and electronic conductivity, along with improved mechanical properties and rheological behavior. PASSC hydrogels demonstrate remarkable fatigue resistance, maintaining mechanical integrity over 10,000 stress cycles, thereby indicating their potential for long-term applications. Additionally, these hydrogels exhibit distinctive mixed conductivity, which enhances their strain sensitivity and efficacy in strain sensing. The ability of PASSC hydrogels to accurately detect a range of movements underscores their versatility and reliability in monitoring strain changes across diverse applications.

Development of levamlodipine long-acting patches based on an ion-pair strategy: Investigation of the mechanism for reducing skin irritation

The aim of this study was to develop a long-acting transdermal patch of levamlodipine (LAM) using an ion-pair strategy to reduce the skin irritation induced by topical application of LAM and explore the mechanism underlying the improvement of skin irritation. The formulation was optimized through porcine in vitro transdermal experiments and rabbit in vivo skin irritation tests. The obtained formulation consisted of poly (2-Ethylhexyl acrylate-co-N-Vinyl-2-pyrrolidone-co-N-(2-Hydroxyethyl) acrylamide) (PENH) as the adhesive matrix, 13.00 % levamlodipine-sorbic acid ion-pair complex (LAM-SA) (w/w), and 10 % isopropyl myristate (IPM) (w/w), with a patch thickness of 70 μm, achieving an erythema index of 188 for rabbit skin and 117–187 for human skin (264 for rabbit skin and 110–260 for human skin in the absence of sorbic acid (SA)). In vivo rabbit and human skin erythema analysis and H&E staining verified that the optimized ion-pair patch effectively reduced skin irritation. Drug distribution experiments in the skin, ATR-FTIR, and molecular simulation were used to characterize the mechanism by which the ion-pair reduced skin irritation. Excessive accumulation of LAM in the epidermis induced secondary structural changes in keratin, resulting in skin barrier damage and inflammatory response. The formation of the LAM-SA ion pair altered physicochemical properties of LAM, reducing drug retention in the epidermis and, thereby, reducing skin irritation. This study demonstrated the potential of the ion-pair strategy to improve the safety of transdermal drug delivery system (TDDS) and provided a means for reducing skin irritation caused by the active pharmaceutical ingredient (API) itself.

Comprehensive analysis of the relationship between yield stress and dewatering performance in sludge conditioning: Insights from various treatment methods

Understanding the relationship between sludge yield stress (σy) and dewatering performance is essential for optimizing sludge conditioning processes. This study systematically investigates the effects of various conditioning methods—including thermal hydrolysis (TH), freezing/thawing (FT), anaerobic digestion (AD), polyaluminum chloride (PAC), polyacrylamide (PAM), and Fenton treatment (Fenton)—on sludge yield stress and its correlation with dewatering efficiency. Using linear regression, partial least squares regression (PLSR), and correlation heatmap analyses, we reveal significant variations in the correlation between σy and dewatering indexes, including moisture content (Mc), capillary suction time (CST), and bound water proportion (Wb/Wt), depending on the conditioning method and intensity. Under FT and PAM conditioning, σy shows a strong negative linear correlation with dewatering performance, with Pearson's r values exceeding −0.880, indicating that a decrease in σy corresponds to improved dewatering efficiency. Conversely, AD conditioning exhibits a positive linear correlation, with r values up to 0.993, suggesting that an increase in σy correlates with reduced dewatering efficiency. For TH, PAC, and Fenton treatments, the correlation between σy and dewatering metrics is highly sensitive to changes in treatment intensity. In the PLSR analysis, the VIP values, which quantify the importance of each predictor variable, indicate that Wb/Wt in TH conditioning (VIP = 1.649) and CST in PAC (VIP = 1.309) and Fenton (VIP = 1.299) conditioning strongly influence σy. This study highlights the significant impact of conditioning methods and intensities on the correlation between σy and dewatering performance. While σy provides valuable insights as a predictive indicator, its predictive power is limited in more complex conditioning scenarios. Therefore, optimizing conditioning intensity and incorporating multiple rheological parameters are essential for achieving superior sludge dewatering outcomes.

Mechanical properties and micro-mechanism of seawater cementitious materials reinforced by in-situ polymerization

Understanding the potential mechanism of in-situ polymerization of acrylamide (AM) for modifying seawater cementitious materials is crucial for designing high-strength and durable marine concrete. Herein, the acrylamide (AM) in-situ polymerization was investigated for its effects on the hydration behavior, micro-morphology, and pore structure of cementitious materials mixed with seawater and freshwater through a series of elaborately designed microscopic characterization methods. The results reveal that the hydration process of cementitious materials proceeds simultaneously with in-situ polymerization. However, compared with freshwater mixtures, seawater provides a large number of metal ions and SO42- ions, which can cross-link with the generated polyacrylamide (PAM) during in-situ polymerization to form a three-dimensional network structure. The synergistic effect of the hydration, in-situ polymerization, and cross-linking processes of cementitious materials can improve the pore structure of seawater-mixed paste, enhance erosion resistance, and improve the stability and toughness of microstructure. These findings were further confirmed by comparing infrared spectroscopy results, hydration products, pore size, and micro-morphology analysis as well as flexural performance tests. This is of great significance to guide the design of novel materials in marine infrastructure.

Experimental study on surface optimization of dosage in magnetic coagulation process for enhancing primary treatment of urban sewage

This work aims to investigate the minimum dosage required to achieve optimal removal of carbon, nitrogen, and phosphorus in the Chemical Enhanced Primary Treatment (CEPT) process using magnetic coagulation technology. A response surface methodology was adopted to generate multiple regression models to optimize the dosages of three types of coagulation, i.e., polyaluminum chloride (PAC), polyacrylamide (PAM), and magnetic medium Fe3O4 particles (MP), based on the removal rates of chemical oxygen demand (COD), ammonia nitrogen (NH3-N), and total phosphorus (TP). The results showed that the regression models could predict results well with actual engineering results. Compared to the traditional coagulation process, the synergistic enhancement of PAC+PAM+MP in the CEPT process significantly improved the treatment effects. Based on the COD removal rates, PAC performed better than MP, followed by PAM; likewise, for the NH3-N and TP removal rates, PAC outperformed PAM, followed by MP. The optimized PAC, PAM, and MP dosages were 135.87, 1.51, and 108.36 mg/L, respectively, reaching 92.27 % COD, 71.98 % NH3-N, and 91.33 % TP removal rates with less than 5 % errors compared to the experimental verification results. These optimization models offer a practical and cost-saving reference for enhancing the primary treatment effect on carbon, nitrogen, and phosphorus removal using PAC+PAM+MP.

A robust low-friction triple network hydrogel based on multiple synergistic enhancement mechanisms

Hydrogels exhibit promising applications, particularly due to their high water content and excellent biocompatibility. Despite notable progress in hydrogel technology, the concurrent enhancement of water content, mechanical strength, and low friction poses substantial challenges to practical utilization. In this study, employing molecular and network design guided based on multiple synergistic enhancement mechanisms, we have developed a robust polyvinyl alcohol (PVA)–polyacrylic acid (PAA)–polyacrylamide (PAAm) three-network (TN) hydrogel exhibiting high water content, enhanced strength, low friction, and fatigue resistance. The hydrogel manifests a water content of 63.7%, compression strength of 6.3 MPa, compression modulus of 2.68 MPa, tensile strength reaching 7.3 MPa, and a tensile modulus of 10.27 MPa. Remarkably, even after one million cycles of dynamic loading, the hydrogel exhibits no signs of fatigue failure, with a minimal strain difference of only 1.15%. Furthermore, it boasts a low sliding coefficient of friction (COF) of 0.043 and excellent biocompatibility. This advancement extends the applications of hydrogels in emerging fields within biomedicine and soft bio-devices, including load-bearing artificial tissues, artificial blood vessels, tissue scaffolds, robust hydrogel coatings for medical devices, and joint parts of soft robots.

Effects of graphene reinforcement on morphology, thermophysical, and mechanical properties of polyvinyl alcohol and polyacrylamide in condensed phases

The subtle interplay of noncovalent interaction in enhancing the compatibility between the graphene-based material and the oligomers of polyvinyl alcohol (PVA) and polyacrylamide (PAM) in the solvent phase is unraveled within the framework of all-atom classical force field-based molecular dynamics (MD) simulations. The decomposition of binding free energy analysis demonstrates that the interaction between polymer segments and graphene (G)-surface crucially emanates from the van der Waals (vdW) interactions, while the adsorption of polymer chains on the graphene oxide (GO)-surface is influenced by vdW and electrostatic interactions. The influence of diverse factors including the strain rate, the size of the nanofiller, the number of oligomers, and the thermal quenching rate on controlling the morphology, mechanical, and thermophysical properties of the graphene-reinforced polymer nanocomposites are further explored. The uniaxial deformation simulations of the graphene-reinforced PVA and PAM matrices show that the interfacial mechanical strength is escalated for the G-PVA nanocomposite. The inclusion of graphene nanofiller reduces the polymer chain mobility and increases the intermolecular interaction, which in turn enhances the toughness of the graphene-polymer composites. Increasing the strain rate raises the yield strength and modulus, making the composites appear stronger and stiffer. As evidenced by the predicted glass transition temperature, the thermal stability of the PVA and PAM matrices is significantly improved by the graphene reinforcement.

Unraveling the synergistic mechanisms of coagulation combined with oxidation for the treatment of sewer overflow: The interaction between iron species and NaClO

During wet weather, sewer overflow pollution can pose a serious threat to surface water. In order to reduce the impact of overflow discharge on receiving waters, ferric chloride (Fe(Ⅲ))/potassium ferrate (Fe(Ⅵ))/polyacrylamide (PAM) coagulation (Fe(Ⅲ)/Fe(Ⅵ)/PAM) combined with sodium hypochlorite (NaClO) oxidation was proposed. Different combinations were constructed, including pre-oxidation coagulation (NaClO-Fe(Ⅲ)/Fe(Ⅵ)/PAM), pre-coagulation oxidation (Fe(Ⅲ)/Fe(Ⅵ)/PAM-NaClO), and synchronous coagulation oxidation (NaClO+Fe(Ⅲ)/Fe(Ⅵ)/PAM). The combined processes achieved efficient removal of conventional contaminants, and the produced byproducts were controlled, especially in the NaClO-Fe(Ⅲ)/Fe(Ⅵ)/PAM. The obvious discrepancy in the sulfamethoxazole (SMX) removal was observed in different processes. NaClO affected the distribution of hydrolyzed iron species, and the proportion of active iron in the NaClO-Fe(Ⅲ)/Fe(Ⅵ)/PAM significantly increased. More complexation sites were generated in the NaClO-Fe(Ⅲ)/Fe(Ⅵ)/PAM, which can complex with the coagulant and then effectively transfer to the flocs. The composition of the flocs further confirmed the differences in coagulation characteristics. The generated·OH played a crucial role in SMX removal in the NaClO+Fe(Ⅲ)/Fe(Ⅵ)/PAM, and ClO·was responsible for partial removal of ammonia nitrogen (NH4+-N). The contribution of high-valent iron species was confirmed, and the introduction of NaClO promoted the generation of iron species. This study may provide an ideal for overflow treatment to improve the urban water environment.

Study of cell migration trajectory on two-dimensional continuous stiffness gradient surface edited by grayscale photopolymerization

In native tissues, cells encounter a diverse range of stiffness, which can significantly affect their behavior and function. The ability of cells to sense and respond to these mechanical cues is essential for various physiological processes, including cell migration. Cell migration is a complex process influenced by multiple factors, with substrate stiffness emerging as a critical determinant. This study developed a technique to edit the stiffness of polyacrylamide (PAA) hydrogel substrates by adjusting the grayscale level of a photomask during photopolymerization. By analyzing cell morphologies on the hydrogel, we confirmed the development of a single PAA hydrogel substrate with continuous stiffness gradients. This method was used to explore the correlation between substrate stiffness and cell migration dynamics. The study found that cells typically migrated from softer to stiffer surfaces. When the cells initially located on stiffer surfaces, they were able to travel longer distances. Additionally, a continuous 2D stiffness gradient surface was fabricated to explore how cells migrate on smoother versus steeper stiffness gradients. The results showed that cells tended to migrate more readily on smoother stiffness gradient surfaces compared to steeper ones. This study provides valuable insights into cell migration dynamics on substrates with varying stiffness gradients. The results underscore the importance of the mechanical environment in cancer cell migration and offer promising directions for developing interventions to prevent cancer spread.

Carboxymethyl chitosan/polyacrylamide double network hydrogels based on hydrogen bond cross-linking as potential wound dressings for skin repair

An ideal biomedical hydrogel should imitate natural tissues with high water absorption, high toughness and superior biocompatibility. However, hydrogels constructed from biomolecules such as polysaccharides have low mechanical strength and limited applications. Based on carboxymethyl chitosan (CMCS) and polyacrylamide (PAM), a facile process is presented for preparing double network hydrogels (CMCS/PAM) with improved mechanical properties. According to the systematic characterization, carboxymethyl chitosan and polyacrylamide form a double network hydrogel through hydrogen bonding. The introduction of carboxymethyl chitosan alters the microscopic structure of PAM hydrogel, resulting in a consistent porosity pattern. Hydrogels with double networks exhibit high tensile properties, high stiffness, and good energy dissipation. Furthermore, the hydrogel exhibits effective adhesion to other hydrophilic surfaces. The CMCS/PAM network hydrogels possess excellent properties such as high swelling capacity, injectability, and cellular biocompatibility, making them potentially valuable for biomedical applications.

Heterogeneous micro-architectonic integration of SU-8 and highly entangled polyacrylamide hydrogel to realize cut-resistant soft superhydrophobic surfaces

This paper presents a novel idea to create cut-resistant superhydrophobic (SHPo) surfaces by integrating an array of SU-8 micropillars on a highly entangled polyacrylamide (PAAm) hydrogel substrate. We begin by demonstrating that this highly entangled PAAm hydrogel exhibits superior resistance to cutting while being as transparent, flexible, and stretchable as other polymeric substrates like polydimethylsiloxane (PDMS). Currently, there are no well-known methods or chemicals to directly integrate SU-8 and PAAm with a covalent bond. To overcome this challenge, we introduce a thin layer of chemically modified PDMS between the SU-8 and PAAm so that covalent bonds can be formed between both the SU-8/PDMS interface and the PDMS/PAAm interface. After validating the reliability of the bonding in our experiments, we develop a heterogeneous integration process to fabricate the desired SHPo surface. To demonstrate the critical role of PAAm hydrogel in achieving the cut-resistant SHPo surface, we contrast this new SHPo surface with a reference version that uses a PDMS substrate instead. We conduct microscopic inspections using scanning electron microscopy (SEM) and a contact angle goniometer before and after cutting the two surfaces. These evaluations show significant differences in their structural integrity and behavior in water interaction.