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BACKGROUND: Various types of hydrogel compounds have recently been developed for controlling invasive and pest ants in a range of environmental settings including agricultural, urban and natural areas. The current study evaluated the potential of sodium polyacrylate (ACR) hydrogels to effectively deliver liquid baits to Argentine ants. RESULTS: Relative to standard polyacrylamide (PAM) hydrogels, individual ACR hydrogel particles were approximately five-fold heavier; this may affect how ants interact with the bait particles, and further influence bait uptake and efficacy. Additionally, ACR hydrogels had significantly higher water absorption capacity and significantly slower rate of water loss, especially during the first 2 h. The efficacy of ACR hydrogel bait containing 0.005% fipronil and various attractants was evaluated on laboratory colonies. Results demonstrated that ACR hydrogel acceptance is significantly increased by the addition of feeding attractants. In addition, a field trial was performed in a nature reserve invaded by Argentine ants to evaluate the efficacy of ACR hydrogel bait. The field trial demonstrated that ACR hydrogel bait containing 0.005% fipronil with various attractants is highly effective and that ant densities throughout the baited plots declined by >99% within 7 days. CONCLUSIONS: The results of this study demonstrate that: (i) fipronil is highly effective for Argentine ant control in natural areas when used in low concentrations (0.005%); (ii) ACR hydrogels are an effective tool for delivering liquid baits to Argentine ants; and (iii) hydrogel baits augmented with various attractants including salt, protein and pheromone are highly attractive to Argentine ants. © 2024 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

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The effective detoxification and removal of arsenite (As(III)) has been widely concerned because of its strong toxicity and migration ability. In this study, we designed a layered double hydroxide-supported polyacrylate stabilized ferrous sulfide composite (PAA/FeS@LDH) and coupled it with UV excitation to purify As(III)-polluted water. The removal efficiency of As(III) under UV irradiation reached almost 100% in 120 min, and the first-order kinetic constant was 3.12 orders of magnitude higher than under dark. UV irradiation significantly accelerated the oxidation and detoxification of As(III) at the interface of PAA/FeS@LDH and treatment solution. It is attributable to the generation of reactive oxygen species (ROS) intermediates, including .O2-, .OH, and SO4.- under UV irradiation, because of the presence of the photogenerated electron-hole pairs and iron valence states cycles. Importantly, .O2- may be rapidly captured and oxidized to 1O2 on the surface of PAA/FeS@LDH that is also an important contributor to the oxidation removal of As(III). Noticeably, As(III) concentrations in the real water were rapidly reduced to below the guideline limitation of drinking water (10 µg/L) within 20 min under UV irradiation. Our outcomes provide a novel photoexcitation treatment system for the efficient detoxification and removal of As from actual wastewater.

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Mg(OH)2 dissolves slowly and can provide a long-term source of alkalinity, thus a promising alternative reagent for the in situ remediation of heavy metal polluted groundwater. Unfortunately, it exhibits a relatively poor stabilization effect on heavy metal Cd due to the higher solubility of the resulting stabilized product, Cd(OH)2. To overcome this limitation, we investigated the use of MgCO3/Mg(OH)2 colloid modified by sodium polyacrylate (PAAS) to remove Cd from groundwater. Through ultrasonic dispersion, the molecular chains of PAAS are broken, causing a transformation from flocculation to surface modification, resulting in the production of a stable colloid. The colloidal particles of MgCO3/Mg(OH)2 have a smaller size and a negatively charged surface, which significantly enhances their migration ability in aquifers. The combination of MgCO3 and Mg(OH)2 provides a complementary effect, where MgCO3 effectively precipitates Cd in the aquifer while Mg(OH)2 maintains the required pH level for stabilization. The optimal compounding ratio of MgCO3 to Mg(OH)2 for achieving the best stabilization effect on Cd is found to be 1:1. Column experiments demonstrate that the injection of MgCO3/Mg(OH)2 colloid substantially enhances Cd stability, reducing the exchangeable fraction of Cd in aquifer media from 88.61% to a range of 22.50-34.38%. Based on these results, the MgCO3/Mg(OH)2 colloid shows great potential as a reactive medium for remediating Cd-contaminated groundwater.

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This study investigated the interaction of monovalent cations with different sizes on quartz surfaces and the rheological impact that this causes in concentrated suspensions when subjected to the action of a rheological modifier, in this case, sodium polyacrylate (NaPA). Yield stress was determined using a rheometer with a vane-in-cup configuration to establish the relationship between shear stress and strain. Experiments were carried out in LiCl, NaCl, KCl, and CsCl solutions. The results show that the yield stress increases following the order Li < Na < K < Cs in the absence of PAA. However, the addition of NaPA significantly reduced the yield stress in all cases. This reduction was more noticeable in the LiCl and NaCl solutions than in the KCl and CsCl solutions, suggesting a more pronounced effect of PA in maker salts. We conducted molecular dynamics simulations to understand how PA interacts with dissolved salts on the quartz surface. Our results showed that Li had the highest adsorption, followed by Na, K, and Cs. As the salt concentration increased, so did the adsorption. We validated these simulation results with rheological experiments, which helped us understand the observed differences. The molecular interactions indicate that, in the lithium system, cationic bridges and the synergy between hydrogen bridges and hydrophobic bridges predominate mainly. This tendency decreases as the type of cation is changed due to the decrease in the electrical density of the cation in the following order: Li < Na < K < Cs. This reduces bridging with the quartz surface and, therefore, directly impacts the system's rheological properties.

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Dentin bond interface stability is the key issue of dental adhesion in present clinical dentistry. The concept of selective extrafibrillar demineralization has opened a new way to maintain intrafibrillar minerals to prevent interface degradation. Here, using ultra-high-molecular-weight sodium polyacrylate [Carbopol (Carbo) > 40 kDa] as a calcium chelator, we challenge this concept and propose a protocol for reliable dentin dry bonding. The results of high-resolution transmission electron microscopy revealed periodic bands of 67 nm dentin collagen fibrils after Carbo etching, and the hydroxyproline concentration increasing with prolonged chelating time denied the concept of extrafibrillar demineralization. The results that wet and dry bonding with Carbo-based demineralization produced a weaker bond strength than the traditional phosphoric acid wet adhesion suggested that the Carbo-based demineralization is an unreliable adhesion strategy. A novel protocol of Er:YAG laser physical etching followed by Carbo chemical etching for dentin adhesion revealed that a micro-/nano-level rough, rigid, and non-collagen exposed dentin surface was produced, the micro-tensile bond strength was maintained after aging under dry and wet bonding modes, and in situ zymography and nanoleakage within the hybrid layers presented lower signals after aging. Cell culture in vitro and a rabbit deep dentin adhesion model in vivo proved that this protocol is safe and biocompatible. Taken together, the concept of extrafibrillar demineralization is limited and insufficient to use in the clinic. The strategy of Er:YAG laser physical etching followed by Carbo chemical etching for dentin adhesion produces a bonding effect with reliability, durability, and safety.

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With the growing demands of human beings, sanitary landfill, along with the increase in landfill depth and leachate water pressure, has put forward new and higher requirements for the impermeable layer. In particular, it is required to have a certain adsorption capacity of harmful substances from the perspective of environmental protection. Hence, the impermeability of polymer bentonite-sand mixtures (PBTS) at different water pressure and the adsorption properties of polymer bentonite (PBT) on contaminants were investigated through the modification of PBT using betaine compounded with sodium polyacrylate (SPA). It was found that the composite modification of betaine and SPA could reduce the average particle size of PBT dispersed in water (reduced to 106 nm from 201 nm) and enhance the swelling properties. As the content of SPA increased, the hydraulic conductivity of PBTS system decreases and the permeability resistance improves, while the resistance to external water pressure increases. It is proposed a concept of the potential of osmotic pressure in a constrained space to explain the impermeability mechanism of PBTS. The potential of osmotic pressure obtained by linear extrapolation of the trendline of colloidal osmotic pressure versus mass content of PBT could represent the external water pressure that the PBT resist. Additionally, the PBT also has a high adsorption capacity for both organic pollutants and heavy metal ions. The adsorption rate of PBT was up to 99.36% for phenol; up to 99.9% for methylene blue; and 99.89%, 99.9%, and 95.7% for low concentrations of Pb2+, Cd2+, and Hg+, respectively. This work is expected to provide strong technical support for the future development in the field of impermeability and removal of hazardous substances (organic and heavy metals).

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Designing a functional and efficient blood-clotting agent is a major challenge. In this research, hemostatic scaffolds (GSp) were prepared from the superabsorbent, inter-crosslinked polymer sodium polyacrylate (Sp) bound to a natural protein gelatin (G) loaded with thrombin (Th) by a cost-effective freeze-drying method. Five compositions were grafted (GSp0.0, Gsp0.1, GSp0.2, GSp0.3, GSp0.3-Th) where the concentration of Sp varied but the ratios of G remained the same. The fundamental physical characteristics that increased the amounts of Sp with G gave synergistic effects after interacting with thrombin. Due to the presence of superabsorbent polymer (SAP) swelling capacities in GSp0.3 and GSp0.3-Th surge forward 6265% and 6948%, respectively. Pore sizes became uniform and larger (ranging ≤ 300 µm) and well-interconnected. The water-contact angle declined in GSp0.3 and GSp0.3-Th to 75.73 ± 1.097 and 75.33 ± 0.8342 degrees, respectively, thus increasing hydrophilicity. The pH difference was found to be insignificant as well. In addition, an evaluation of the scaffold in in vitro biocompatibility with the L929 cell line showed cell viability >80%, so the samples were nontoxic and produced a favorable environment for cell proliferation. The composite GSp0.3-Th revealed the lowest HR (%) (2.601%), and the in vivo blood-clotting time (s) and blood loss (gm) supported hemostasis. Overall, the results showed that a novel GSp0.3-Th scaffold can be a potential candidate as a hemostatic agent.

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Monitoring sweat rate is vital for estimating sweat loss and accurately measuring biomarkers of interest. Although various optical or electrical sensors have been developed to monitor the sensible sweat rate, the quantification of the insensible sweat rate that is directly related to body thermoregulation and skin barrier functions still remains a challenge. This work introduces a superhydrophobic sweat sensor based on a polyacrylate sodium/MXene composite sandwiched between two superhydrophobic textile layers to continuously measure sweat vapor from insensible sweat with high sensitivity and rapid response. The superhydrophobic textile on a holey thin substrate with reduced stiffness and excellent breathability allows the permeation of sweat vapor, while preventing the sensor from being affected by the external water droplets and internal sensible sweat. Integrating the insensible sweat sensor with a flexible wireless communication and powering module further yields a standalone sensing system to continuously monitor insensible sweat rates at different body locations for diverse application scenarios. Proof-of-concept demonstrations on human subjects showcase the feasibility to continuously evaluate the body's thermoregulation and skin barrier functions for the assessment of thermal comfort, disease conditions, and nervous system activity. The results presented in this work also provide a low-cost device platform to detect other health-relevant biomarkers in the sweat (vapor) as the next-generation sweat sensor for smart healthcare and personalized medicine.

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The influences of sodium polyacrylate (PAAS) at the ratios of 0% (CK), 0.5% (F1), 1.0% (F2), 1.5% (F3), 2.0% (F4) and 2.5% (F5) on nitrogen transformation and bacterial community composition were investigated in the composting of food waste digestate (FWD) and corn straw (CS). PAAS addition increased the thermophilic temperature but had no significant effect on pH values. PAAS exerted significantly effects on the concentration of total nitrogen (TN), ammonia nitrogen (NH4+-N), nitrite-nitrogen (NO2--N) and nitrate-nitrogen (NO3--N). The compost product in 1.0% PAAS treatment was more active in absorbing nutrients. Firmicutes (9.40-83.54%), Actinobacteriota (9.98-51.50%), Proteobacteria (0.20-27.87%) and Bacteroidota (0.11-34.69%) were the dominant phyla in FWD composting. Moreover, relative to CK, PAAS promoted the propagation of dominant bacterial phyla Firmicutes with increment of 30.05-102.06% in the thermophilic phase. Kroppenstedtia, Thermobifida and Saccharomonospora were observed to be dominant at the maturing phase and correlated with NH4+-N, NO2--N, TN and NO3--N. Therefore, they might be regarded as probable biomarkers symbolic for the maturing phase during FWD composting. The compost product had the highest maturity degree in 1.0% PAAS treatment. These results indicated that PAAS addition improved the maturity and nutrient contents of the compost product as well as altered compost bacterial community dynamics.

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Clinoptilolite and sodium polyacrylate (Na-PAA) were used as water-retaining agents to improve the water-holding capacity of compacted clay cover (CCC). The optimum moisture content and Atterberg limits of the CCC modified by clinoptilolite and Na-PAA were studied. The soil-water characteristic curve (SWCC) of the CCC modified by clinoptilolite and Na-PAA was studied. The mesostructure of the CCC was analyzed by polarized light microscopy. The test results show that: (1) the optimum moisture content and liquid limit of the CCC modified by clinoptilolite and Na-PAA increased, while the maximum dry density decreased; (2) the SWCC of the CCC modified by clinoptilolite and Na-PAA shifts to the upper right, and the volume moisture content of modified CCC is higher than that of unmodified CCC under the same matrix suction; (3) compared with the unmodified CCC, the air-entry value (AEV) of the clinoptilolite-modified CCC increased by 65.18% at most, and the AEV of the further modified CCC with Na-PAA in-creased by about two times; and (4) the flocculation structure and porosity of modified CCC decreased, and the porosity was distributed uniformly.

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As an effective way to obtain freshwater resources, atmospheric water harvesting (AWH) technology has been a wide concern of researchers. Therefore, hydrogels gradually become key materials for atmospheric water harvesters due to their high specific surface area and three-dimensional porous structure. Here, we construct a core-shell hydrogel-based atmospheric water harvesting material consisting of a shell sodium polyacrylate (PAAS) hydrogel with an open pore structure and a core thermosensitive poly N-isopropylacrylamide (PNIPAAm) hydrogel with a large pore size. Theoretically, the mutual synergistic hygroscopic effect between the core layer and the shell layer accelerates the capture, transport, and storage of moisture to achieve continuous and high-capacity moisture adsorption. Simultaneously, the integration of polydopamine (PDA) with the hydrogel realizes solar-driven photothermal evaporation. Therefore, the prepared core-shell hydrogel material possesses great advantages in water adsorption capacity and water desorption capacity with an adsorption of 2.76 g g-1 (90% RH) and a desorption of 1.42 kg m-2 h-1. Additionally, the core-shell structure hydrogel collects 1.31 g g-1 day-1 of fresh water in outdoor experiments, which verifies that this core-shell hydrogel with integrated photothermal properties can capture moisture in a wide range of humidity without any external energy consumption, can further sustainably obtain fresh water in remote water-shortage areas.

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Limitations to the scaling of sodium alginate (SA) fibers by wet spinning and for commercial applications are the high spinning dope viscosity and low fiber mechanical performance. In this study, the viscosities of SA spinning dopes dramatically reduced to an order of magnitude lower while the maximum spin draw ratio increased from 1 to 6 as sodium polyacrylate (PAAS) loading increased up to 20 %. However, distinct to a simple plasticizing effect, adding appropriate amount of PAAS strengthens the mechanical properties of fully drawn fibers, through the formation of new physical crosslinks with SA. Fibers having the tenacity of ∼0.6 cN/dtex, modulus of ∼37 cN/dtex, strain at break of ∼7 % and toughness of ∼4 J/g were achieved with 15 % PAAS loading. Therefore, the PAAS addition has dual-effects in SA fiber wet spinning: to modify the rheology of the SA spinning solution and to strengthen the wet-spun SA fibers for textile applications.

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Robots operating in changing underwater environments may be required to adapt to these varying conditions. In tidal estuaries, for example, where the degree of salinity cycles in step with the level of the water, a robot may need to adapt its behaviour depending on the position of the tide. In freshwater bodies, the unexpected presence of a pollutant may also require the robot to respond by altering its behaviour. Embodying this sensing and response in the body of the robot means that adaptivity to the environment can be achieved without resorting to centralised control. This can also allow direct responsivity using 'free' environmental energy, actuating without requiring stored onboard energy. In this work we present a soft artificial muscle, the contraction of which varies in response to the salinity the water surrounding it. The novel actuator uses a super-absorbent polymer gel encapsulated within a series of discrete cells. This gel readily absorbs water through the membrane wall of the actuator, and can swell to over 300 times its initial volume. This swelling generates significant pressure, changing the shape of the cells and driving the contraction of the muscle. The degree of swelling is significantly reduced by the presence of salts and pollutants in the surrounding water, so transitioning from a freshwater to a saltwater environment causes the muscle to relax. In this paper, we discuss the design and fabrication of these superabsorbent polymer-based Bubble Artificial Muscle (SAP-BAM) actuators. The tensile properties of the muscle under actuated (fresh water) and relaxed (salt water) conditions are characterised, showing a maximum generated force of 10.96N. The length response under constant load for a full actuation cycle is given, showing a maximum contraction of 27.5% of the initial length at 1N load, and the performance over repeated actuation and relaxation cycles is shown. The SAP-BAM muscles are straightforward to fabricate and are composed of low-cost, freely-available materials. Many existing pneumatically-actuated muscles can be modified to use the approach taken for this muscle. The muscle presented in this work represents the first example of a new class of super-absorbent polymer-driven environmental soft artificial muscles.

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Hydrogels are a very useful type of polymeric material in several economic sectors, acquiring great importance due to their potential applications; however, this type of material, similarly to all polymers, is susceptible to degradation, which must be studied to improve its use. In this sense, the present work shows the degradation phenomena of commercial hydrogels based on potassium and sodium polyacrylate caused by the intrinsic content of different types of potable waters and aqueous solutions. In this way, a methodology for the analysis of this type of phenomenon is presented, facilitating the understanding of this type of degradation phenomenon. In this context, the hydrogels were characterized through swelling and FTIR to verify their performance and their structural changes. Likewise, the waters and wastewaters used for the swelling process were characterized by turbidity, pH, hardness, metals, total dissolved solids, electrical conductivity, DLS, Z-potential, and UV-vis to determine the changes generated in the types of waters caused by polymeric degradation and which are the most relevant variables in the degradation of the studied materials. The results obtained suggest a polymeric degradation reducing the swelling capacity and the useful life of the hydrogel; in addition, significant physicochemical changes such as the emergence of polymeric nanoparticles are observed in some types of analyzed waters.

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Phosphorus recovery from waste activated sludge (WAS) is expected to alleviate the shortage of phosphate rock and reduce eutrophication. In this study, acid, alkali and sodium polyacrylate (PAAS) were compared to enhance phosphorus release and recovery from WAS. During anaerobic fermentation (AF) stage, the optimal pretreated conditions for ortho-phosphate release were the pH of 4 (AF 12 h), 13 (AF 12 h) and 22.4 g PAAS/L (AF 24 h) with the phosphorus release efficiencies of 40.9%, 62.6% and 31.7%, respectively. Acid, alkali and PAAS addition were beneficial for apatite phosphorus (AP), non-apatite inorganic phosphorus (NAIP) and organic phosphorus (OP) release from WAS, respectively. Strong acidic (pH = 4) and alkaline (pH = 12 and 13) conditions inhibited the release of soluble ammonia, while PAAS would not have a negative impact on the release of soluble ammonia. By means of precipitation crystallization, the ortho-phosphate could be almost recovered after acid/alkali pretreatment compared with PAAS (88.9%) at optimal Mg/P molar ratio of 1.5:1. The XRD, FT-IR and SEM-EDX analyses confirmed the main component in the product was struvite. The purity of the struvite in the product recovered from acid (named PreAC, 78.9%) and alkali (named PreAL, 89.6%) pretreated sludge were higher than that of the PAAS (named PrePA, 72.3%) by elemental analysis. The mercury and chromium content existed in PreAC were above the Control Standards of Pollutants in Sludge for Agricultural Use, whereas detected heavy metal elements level of the PreAL and PrePA were below the standard. By means of cost analysis, acid/alkali pretreatment could obtain economic benefits compared with PAAS. Thus, those discoveries would broaden the phosphorus recovery way to serve in practice.

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Multifunctional composite coatings composed of metal oxide nanoparticles dispersed in polymer matrices are an advanced solution to solve the problem of stone heritage deterioration. Their innovative design is meant to be stable, durable, transparent, easy to apply and remove, non-toxic, hydrophobic, and permeable. Coating formulations for the protection of buildings and monuments have been intensively researched lately. Such formulations are based on multifunctional composite coatings incorporating metal oxides. The present work aims to combine the hydrophobic properties of sodium polyacrylate (NaPAC16) with the antimicrobial effectiveness, with promising antimicrobial results even in the absence of light, and good compatibility of MgO (a safe to use, low cost and environmentally friendly material) and TiO2 (with antibacterial and antifungal properties), in order to develop coatings for stone materials protection. MgO (pure phase periclase) and TiO2 (pure phase anatase) nanopowders were prepared through sol-gel method, specifically routes. Aqueous dispersions of hydrophobically modified polymer (NaPAC16, polyacrylic acid sodium salt) and MgO/TiO2 nanopowders were deposited through layer-by-layer dip coating technique on glass slides and through immersion on stone fragments closely resembling the mosaic stone from the fourth century AD Roman Mosaic Edifice, from Constanta, Romania. The oxide nanopowders were characterized by: Thermal analysis (TG/DTA), scanning electron microscopy (SEM), X-ray diffraction (XRD), BET specific surface area and porosity, and UV-Vis spectroscopy for band gap determination. An aqueous dispersion of modified polyacrylate polymer and oxide nanopowders was deposited on different substrates (glass slides, red bricks, gypsum mortars). Film hydrophobicity was verified by contact angle measurements. The colour parameters were evaluated. Photocatalytic and antimicrobial activity of the powders and composite coatings were tested.

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Upon stimulus by CO2, CO2-switchable viscoelastic fluids experience a deliberate transition between non-viscous and highly viscous solution states. Despite attracting considerable recent attention, most such fluids have not been applied at a large- scale due to their high costs and/or complex synthesis processes. Here, we report the development of CO2-switchable viscoelastic fluids using commercially available sodium polyacrylate (NaPAA) and N,N-dimethyl ethanol amine (DMEA)-based switchable water. Upon bubbling CO2, into the solutions under study, DMEA molecules are protonated to generate quaternary ammonium salts, resulting in pronounced decreases in solutions viscosity and elasticity due to the influence of increased ionic strength on NaPAA molecular conformations. Upon removal of CO2 via introduction of N2, quaternary salts are deprotonated to tertiary amines, allowing recovery of fluid viscosity and elasticity to near the initial state. This work provides a simple approach to fabricating CO2-switchable viscoelastic fluids, widening the potential use of CO2 in stimuli-responsive applications.

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Designing desirable adsorbent for highly efficient removal of heavy metal ions is of practical significance, given the cost-effectiveness, environmental benign, natural abundance and easy-handling collection features. Herein, a bead-like adsorbent with high adsorption capacity was prepared by modifying alginate beads using polyacrylate with high density of carboxyl groups. The developed alginate/polyacrylate beads were collaboratively characterized by FT-IR, TGA, SEM, XPS, etc., and various adsorption conditions were tested including the pH of the solution, contact time and the initial concentration. The experimental data were fitted well by the Freundlich isotherm model, and the maximum adsorption capacity was obtained from the Langmuir model was 611.0 mg/g, and adsorption process followed the Pseudo-second-order kinetic model. The adsorption mechanisms conformed to multi-layer adsorption, and mainly dominated by chemical interactions. The bead-like adsorbent exhibited excellent reusability after eight sequential cycles and displayed higher adsorption capacity towards lead ions. This type of adsorbent might possess promising role in treating heavy metals from water by virtue of degradable, cost-effective component and high adsorption efficiency.

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The Flory-Rehner theoretical description of the free energy in a hydrogel swelling model can be broken into two swelling components: the mixing energy and the ionic energy. Conventionally for ionized gels, the ionic energy is characterized as the main contributor to swelling and, therefore, the mixing energy is assumed negligible. However, this assumption is made at the equilibrium state and ignores the dynamics of gel swelling. Here, the influence of the mixing energy on swelling ionized gels is quantified through numerical simulations on sodium polyacrylate using a Mixed Hybrid Finite Element Method. For univalent and divalent solutions, at initial porosities greater than 0.90, the contribution of the mixing energy is negligible. However, at initial porosities less than 0.90, the total swelling pressure is significantly influenced by the mixing energy. Therefore, both ionic and mixing energies are required for the modeling of sodium polyacrylate ionized gel swelling. The numerical model results are in good agreement with the analytical solution as well as experimental swelling tests.

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ObjectiveThere are many kinds of intestinal cleansing drugs in clinical practice at present, but there is no universal and effective intestinal cleansing program. In this study, sodium polyacrylate was used as a candidate drug for intestinal preparation to explore its feasibility, efficacy and safety for intestinal preparation in mice.Methods24 mice fasted for 12 hours were divided, with random number table method, into 4 groups (6 mice in each): blank group, sodium phosphate group, polyethylene glycol group and sodium polyacrylate solution group. Except that the blank group was given isotonic saline (0.6mL/20g) to fill the stomach, the other groups were given sodium phosphate (0.5mL/20g), polyethylene glycol(0.6mL/20g) and sodium polyacrylate solution (0.6mL/20g) to fill the stomach, and the small intestinal propulsion (carbon powder propulsion), the defecation and intestine volume in mice were observed to explore the effect of sodium polyacrylate on the mice colon cleansing.ResultsAfter administration by gavage for 15min, compared with the blank group [(62.72±6.58) %] and the sodium phosphate group [(66.40±9.53) %], the carbon powder propulsion rate of the sodium polyacrylate solution group [(81.17±4.75) %] significantly increased (P<0.05). The number of fecal excretion [(11.5±2.4) granules] in the sodium polyacrylate solution group after 2 hours of gavage was significantly higher than that in the blank group [(4.5±1.0) granules], the sodium phosphate group [(6.2±2.0) granules] and the polyethylene glycol group [(8.5±1.0) granules] (P<0.05). Compared with the blank group [(39.7±11.60) mg] and the sodium phosphate group [(77.2±15.91) mg], the defecation quality of sodium polyacrylate solution [(162.4±16.69) mg] significantly increased within 2h after gavage (P<0.05). Compared with the blank group [(2.25±0.29)g], the sodium phosphate group [(2.72±0.24)g] and the polyethylene glycol group [(2.95±0.19)g], the intestinal mass of the sodium polyacrylate solution group [(3.30±0.16)g] significantly increased (P<0.05).ConclusionOral administration of sodium polyacrylate solution can accelerate intestinal peristalsis in normal mice, promote defecation in mice, and significantly reduce intestinal absorption of water. As a potential intestinal preparation drug, it has the advantages of small dose, high efficiency, safety and reliability.