Controlled release study of carbaryl insecticide from calcium alginate and nickel alginate hydrogel beads

In this study, controlled release formulations for reducing environmental impact of pesticides have been produced by encapsulating as a model pesticide carbaryl (Carb) in the alginate beads. The various hydrogel bead formulations were prepared by the ionotropic crosslinking of sodium alginate (NaAlg) with calcium and nickel ions. The surface morphology of prepared beads was characterized with scanning electron microscopy (SEM). SEM confirmed the spherical nature and surface morphology of the particles. Bead characteristics, such as carbaryl entrapment efficiency, particle size, equilibrium swelling degree, and carbaryl release kinetics, were determined. The effects of the bead preparation conditions such as crosslinker concentration and type, carbaryl/sodium alginate (Carb/NaAlg) ratio and percentage of NaAlg on the carbaryl release from the calcium alginate (Ca‐Alg) and nickel alginate (Ni‐Alg) beads were investigated in distilled water at 25°C. It was observed that carbaryl release from the Ca‐Alg beads was slower than that of Ni‐Alg beads. The release results indicated that carbaryl release from both of the Ca‐Alg and Ni‐Alg beads decreases with the increasing crosslinker concentration, Carb/NaAlg ratio and percentage of NaAlg. The highest carbaryl release was found to be 100% for the Ni‐Alg beads at 3 days whereas the lowest carbaryl release was found to be 67% for the Ca‐Alg beads at 21 days. The swelling measurements of the beads were also in consistent with the carbaryl release results. The carbaryl release from most of the bead formulations followed Case II transport. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Controlled release formulations of carbaryl based on copper alginate,barium alginate,and alginic acid beads

A controlled release system for reducing environmental impact was produced by encapsulating the pesticide carbaryl (Carb) in the alginate beads. The various bead formulations were prepared by using sodium alginate (NaAlg) as a polymer, CuCl₂, BaCl₂ as a crosslinking agent, and HCl as a linking agent. The surface morphology of prepared beads was characterized with scanning electron microscopy (SEM). SEM confirmed the spherical nature and surface morphology of the particles. Bead characteristics, such as Carb entrapment efficiency, particle size, swelling degree, and Carb release kinetics, were determined. The effects of crosslinker or linker concentration, type, and carbaryl/sodium alginate (Carb/NaAlg) ratio on Carb release from the beads were investigated for 20 days at 25°C. It was observed that Carb release from the beads increased with the increase of Carb/NaAlg ratio whereas decreased with the increase of crosslinker concentration. At the end of 20 days, the Carb release from alginic acid beads was found to be higher than that of copper alginate (Cu‐Alg) and barium alginate (Ba‐Alg) beads. The swelling measurements of the beads supported the release results. Release kinetics were described by Fickian and non‐Fickian approaches. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4245–4253, 2006     

Controlled release of naproxen from sodium alginate and poly(vinyl alcohol)/sodium alginate blend beads crosslinked with glutaraldehyde

In this study, polymeric beads of sodium alginate (NaAlg) and its blend with poly(vinyl alcohol) (PVA) were prepared by crosslinking with glutaraldehyde (2.5% v/v) and hydrochloric acid (3% v/v) for the release of naproxen sodium (NS). The prepared beads were characterized with Fourier transform infrared spectroscopy, and pictures of the beads were determined with an optic microscope. The release studies were carried out at three pH values (1.2, 6.8, and 7.4) for 2 h. The effects of the preparation conditions, including the PVA/NaAlg (w/w) ratio, drug/polymer (w/w) ratio, and time of exposure to the crosslinker, on the release of NS were investigated for 10 h at 37°C. The release of NS decreased with the PVA/NaAlg (w/w) ratio and drug/polymer ratio increasing. At the end of 10 h, the highest release of NS was found to be 84% for the 1/2 PVA/NaAlg (w/w) ratio. The swelling measurements of the beads supported the release results. The release kinetics were described with Fickian and non‐Fickian approaches. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Synthesis of crosslinked superabsorbent carboxymethyl cellulose/acrylamide hydrogels through electron‐beam irradiation

A study on the possibility of the preparation of superabsorbent hydrogels based on crosslinked carboxymethyl cellulose polymer and acrylamide monomer through electron‐beam irradiation was carried out. The effects of the irradiation dose and polymer–monomer compositions on the crosslinking density were studied. The hydrophilic properties of the superabsorbent hydrogels were identified by the swelling percentage. The prepared hydrogels had higher swelling in distilled water than in salt solutions. Moreover, the hydrogels exhibited the highest swelling at pH 7. Also, increasing the temperature up to 50°C caused an increase in the swelling. The thermal properties of the hydrogels were characterized with thermogravimetric analysis. The use of the prepared superabsorbent hydrogels for the growth of rice was also investigated through the water‐retention property. The water retention in the soil was enhanced with the hydrogels. Superabsorbent hydrogels based on carboxymethyl cellulose polymer and acrylamide monomer could be considered as water‐managing materials for agriculture and horticulture in desert and drought‐prone areas. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2003–2008, 2007     

Hydrogels of starch/carboxymethyl cellulose crosslinked with sodium trimetaphosphate via reactive extrusion

Hydrogels are materials with advantages in specific applications, such as, retention of food active compounds. This work aims to develop starch (S)/carboxymethyl cellulose (CMC) hydrogels with porous structure, using reactive extrusion to promote crosslinking with sodium trimetaphosphate (STMP). The expansion, porosity, degree of substitution, gel fraction, swelling properties, and FTIR are studied, comparing S, S/CMC, S/STMP, and S/CMC/STMP formulations. Samples containing STMP present the same degree of substitution (0.050 ± 0.001). Higher porosity and percentage of open pores are observed in the mixed hydrogel (S/CMC/STMP). Crosslinking increase the swelling capacity at pH 7, and this property, just like the gel fraction, are sensitive to pH variations. The hydrogel S/CMC present the highest swelling rate compared with the other samples, suggesting strong interaction between components. The reactive extrusion process is efficient to produce starch and starch/CMC hydrogels crosslinked with STMP and the overall results demonstrate the advantages of the mixed hydrogel.     

Characterization of sodium alginate membrane crosslinked with glutaraldehyde in pervaporation separation

Dense sodium alginate (SA) membranes crosslinked with glutaraldehyde (GA) have been prepared by the solution method, wherein a nonsolvent of SA (acetone) was used in a reaction solution instead of an aqueous salt solution. Through infrared radation, X-ray diffractometry, and the swelling measurement, the crosslinking reaction between the hydroxyl groups of SA and the aldehyde groups of GA was characterized. To investigate the selective sorption behavior of the crosslinked SA membranes, swelling measurements of the membranes in ethanol-water mixtures of 70–90 wt % ethanol contents were conducted by equipment that was able to measure precisely the concentration and amount of the liquid absorbed in the membranes. It was observed that the crosslinking could reduce both the solubility of water in the resulting membrane and the permselectivity of the membrane toward water at the expense of membrane stability against water. The pervaporation separation of a ethanol-water mixture was conducted with the membranes prepared at different GA contents in the reaction solution. When the membrane was prepared at a higher GA content, both flux and separation factor to water were found to be reduced, thus resulting from the more crosslinking structure in it. The pervaporation separations of ethanol-water mixtures were also performed at different feed compositions and temperatures ranging from 40 to 80°C. A decline in the pervaporative performance was observed due to the relaxation of polymeric chains taking place during pervaporation, depending on operating temperature and feed composition. The relaxational phenomena were also elucidated through an analysis on experimental data of the membrane performance measured by repeating the operation in the given temperature range. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 67: 209–219, 1998     

丙烯腈接枝改性海藻酸钙水凝胶中水杨酸的释放行为

将海藻酸钙水凝胶与丙烯腈单体进行不同程度的接枝共聚改性,再由FTIR加以分析,并测定包埋了水杨酸模拟药物的改性海藻酸钙水凝胶在不同介质中的药物释放量。实验表明,改性海藻酸钙水凝胶的药物释放量既与介质有关,也取决于接枝率的大小。     

Improvement of physical properties of crosslinked alginate and carboxymethyl konjac glucomannan blend films

Blend films from carboxymethyl konjac glucomannan and sodium alginate in different ratios were prepared by blending 4 wt % sodium alginate aqueous solution with 2 wt % konjac glucomannan aqueous solution. After crosslinking with 5 wt % calcium chloride aqueous solution, the blend films formed a structure of semi‐interpenetrating networks. The structure and physical properties of both uncrosslinked and crosslinked films were characterized by Fourier transformed infrared spectra (FTIR), differential thermal analysis (DTA), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and tensile tests. The results indicated that the mechanical properties and the thermal stability of the films were improved by blending sodium alginate with carboxymethyl konjac glucomannan due to the intermolecular hydrogen bonds between sodium alginate and carboxymethyl konjac glucomannan. The crosslinked blend films with Ca²⁺, compared with uncrosslinked blend films, exhibited further improved physical properties due to the formation of a semi‐IPN structure. Furthermore, the degree of swelling of the crosslinked films was also investigated. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2554–2560, 2002     

Controlled release of diclofenac sodium and ibuprofen through beads of sodium alginate and hydroxy ethyl cellulose blends

Controlled release of diclofenac sodium (DS) and ibuprofen (IB) drugs through sodium alginate (NaAlg)‐hydroxy ethyl cellulose (HEC) blend polymeric beads has been investigated. Beads were prepared by precipitating the viscous solution of NaAlg and HEC blend in alcohol followed by crosslinking with calcium chloride. Different formulations were developed in bead form by varying the amount of HEC, crosslinking agent, and drug concentration. Swelling studies in water, percent encapsulation of drugs, and release studies were carried out. The DS‐loaded beads have shown better release performance than the IB‐loaded beads. Diffusion parameters were evaluated from the Fickian diffusion theory. Mathematical modeling studies and drug release characteristics through bead matrices were studied by solving Fick's diffusion equation. The results are discussed in terms of drug release patterns and theoretical concentration profiles generated through matrices, considering spherical geometry of the beads. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5708–5718, 2006     

PVA/TEOS crosslinked membranes incorporating zinc oxide nanoparticles and sodium alginate to improve reverse osmosis performance for desalination

Pure water is becoming less available with increases in world population, so seawater desalination is becoming more important. For efficient seawater desalination, this paper proposes a novel mixed matrix membrane (MMM) based on the deposition of a poly(vinyl alcohol) (PVA) nanofibrous active layer on a 3-triethoxysilylpropylamine-functionalized cellulose acetate substrate. The active layer is fabricated by utilizing a tetraethyl orthosilicate–crosslinked PVA incorporating zinc oxide nanoparticles (ZnO-NPs) and sodium alginate (NaAlg). The overall reverse osmosis performance of the MMMs is enhanced by the infusion of ZnO-NPs and NaAlg in PVA; we find the optimum concentration for the best performance to be ZnO-NPs at 0.1 wt % and NaAlg at 0.01 wt %. In terms of permeation flux, salt rejection, salt passage, stability, long-term rejection, membrane antifouling, reusability, and chlorine resistance, the proposed MMMs are examined using a dead-end reverse osmosis filtration setup. The results show that the active layer achieves an optimal permeation flux of 34.6 L/m² h, a natural sea salt rejection of 97%, and a chlorine resistance of 93%, suggesting that the proposed MMMs can be useful for seawater desalination. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47559.     

MWCNTs reinforced conductive,self-healing polyvinyl alcohol/carboxymethyl chitosan/oxidized sodium alginate hydrogel as the strain sensor

The preparation and application of hydrogel has been a hot research field in recent years. Here in, a composite hydrogel based on poly(vinyl alcohol) (PVA), carboxymethyl chitosan (CMCS), oxidized sodium alginate (OSA), and oxidized multiwall carbon nanotubes (OMWCNTs) was successfully prepared. Hydrogen and imine bonds of the hydrogel endowed the composite hydrogel with self-healing property and pH sensitivity. The fracture strength of the hydrogel was enhanced to about 0.8 MPa with the help of OMWCNTs, which was about 2.5 times compared with the one without OMWCNTs. Meanwhile, a new conductive network inside the hydrogel was constructed by OMWCNTs, which improved the conductivity of the hydrogel from 1.75 × 10⁻⁴ to 7.02 × 10⁻⁴ S/cm. The sensing test of the hydrogel showed that it could produce profound feedback signals for the deformation caused by external force and response to human body movements, such as finger bending, swallowing, and speaking.     

Synthesis and characterization of bacterial cellulose/alginate blend membranes

Bacterial cellulose and alginate in an aqueous NaOH/urea solution were used as substrate materials for the fabrication of a novel blend membrane. The blend solution was cast onto a Teflon plate, coagulated in a 5 wt % CaCl₂ aqueous solution, and then treated with a 1% HCl solution. Supercritical carbon dioxide drying was then applied for the formation of a nanoporous structure. The physical properties and morphology of the regenerated bacterial cellulose and blend membranes were characterized. The blend membrane with 80% bacterial cellulose/20 wt % alginate displayed a homogeneous structure and exhibited a better water adsorption capacity and water vapor transmission rate. However, the tensile strength and elongation at break of the film with a thickness of 0.09 mm slightly decreased to 3.38 MPa and 31.60%, respectively. The average pore size of the blend membrane was 10.60 Å with a 19.50 m²/g surface area. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Preparation and properties of alginate superabsorbent filament fibers crosslinked with glutaraldehyde

Superabsorbent filament fibers based on sodium alginate were prepared using glutaraldehyde as a crosslinking agent. Alginate was extruded into an aqueous hydrochloric acid coagulation bath to form continuous alginic acid gel fibers via a wet‐spinning method. The alginic acid gel fibers were dehydrated by exchanging water with dioxane, crosslinked, then neutralized for better absorbency. Crosslinked alginate filaments exhibited a high saline solution and synthetic urine absorbencies, maintaining the integrity of the fiber structure. Maximum synthetic urine absorbency was obtained with the fiber crosslinked at a lower glutaraldehyde concentration compared with that required for maximum saline solution absorbency. This appears to be due to the crosslinking effect of calcium ions in the synthetic urine solution being absorbed. Strain and tenacity of the crosslinked alginate fibers decreased with an increasing amount of glutaraldehyde used in the crosslinking reaction. The decrease in tenacity was not significant while the strain showed an extensive decrease. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 1797–1804, 2000     

Syntheses and characterization of blend membranes of sodium alginate and poly(vinyl alcohol) for the pervaporation separation of water + isopropanol mixtures

The blend membranes of sodium alginate and poly(vinyl alcohol) have been prepared by physical mixing in different ratios (75, 50, and 25%) of sodium alginate with poly(vinyl alcohol). The membranes were crosslinked with glutaraldehyde and used in the pervaporation separation of water + isopropanol mixtures at 30°C. The crosslinking reaction was confirmed by Fourier transform infrared spectra. Permeation flux increased with an increase in mass % of water in the feed mixture as well as with an increase in the amount of poly(vinyl alcohol) in the blend, but separation selectivity decreased. Diffusion coefficients of water + isopropanol mixtures have been calculated using the Fick's equation from the sorption data. Arrhenius activation parameters were calculated for 10 mass % of water in the feed mixture using the values of flux and diffusion coefficients obtained at 30, 40, and 50°C. The diffusion and pervaporation results have been explained on the basis of solution‐diffusion principles. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 3642–3651, 2002     

Effect of postcrosslinking modification with glutaraldehyde on the properties of thermoplastic starch/poly(vinyl alcohol) blend films

Thermoplastic starch (TPS)/poly(vinyl alcohol) (PVA) blend films were modified by crosslinking through soaking the films in glutaraldehyde aqueous solution and then heating in an oven. The effects of the concentration of the glutaraldehyde aqueous solution, soaking time, reaction temperature, and time on the crosslinking reaction were investigated. The moisture absorption and mechanical properties of the films were measured to characterize the influence of the crosslinking modification. It was found that the crosslinking modification significantly reduced the moisture sensitivity of the TPS/PVA blend films and increased the tensile strength and Young's modulus but decreased the elongation at break of the TPS/PVA blend films. The described method could be used for posttreating TPS/PVA‐based products to optimize their properties. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Electrically modulated transport of diclofenac salts through hydrogels of sodium alginate,carbopol, and their blend polymers

The electrically modulated transdermal migration of diclofenac sodium (DS), diclofenac potassium (DP), and diclofenac diethylammonium (DD) drugs from the hydrogels of sodium alginate (NaAlg), carbopol (CP), and blends of NaAlg with CP prepared in 2:1, 2:1.5, and 2:2 ratios was investigated. The release of DS, DP, and DD was investigated through excised rat skin to study the effects of viscosity, pH, and the ionic strength of the receptor medium under the influence of an electrical current in a switch‐on and switch‐off mode. A pulsatile pattern of transport was observed that depended on the presence or absence of an electrical current. Drug transport was dependent on the electrical current, the ionic nature of drugs, and the ionic strength of the diffusion medium. Drug transport followed the sequence DS > DP > DD. A decrease in viscosity and an increase in the pH of the hydrogel were observed when an electrical current was applied. CP was more responsive to an electrical stimulus, but the rate of transport was higher for NaAlg. Increasing the amount of CP in the blends increased the electrical responsiveness. The blend hydrogel with a high CP content showed the highest enhancement in drug transport, whereas the NaAlg hydrogel showed the least. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 301–311, 2005     

Novel physically crosslinked hydrogels of carboxymethyl chitosan and cellulose ethers: Structure and controlled drug release behavior

Novel hydrogels, physically crosslinked by hydrogen bonding of component polymers, were obtained by mixing aqueous solutions of carboxymethylchitosan (CMCS) with cellulose ethers including hydroxyethylcellulose (HEC) and methylcellulose (MC). The hydrogels were characterized by IR, XPS, WAXD, and SEM. The swelling and controlled drug release behaviors of hydrogels were also studied. The results indicate that intermacromolecular hydrogen bonding in CMCS/HEC is stronger than that in CMCS/MC. The swelling and drug release rate of hydrogels decrease as the interaction of component polymers increases. Both the swelling and drug release from hydrogels can be controlled by component polymer ratio. The hydrogels may be potential candidates for biomedical applications. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Preparation and characterization of alginate/gelatin blend fibers

Alginate and gelatin blend fibers were prepared by spinning their solution through a viscose‐type spinneret into a coagulating bath containing aqueous CaCl₂ and ethanol. The structure and properties of the blend fibers were studied with the aid of infrared spectra, scanning electron micrography, X‐ray diffraction, and thermogravimetric analysis. Mechanical properties and water‐retention properties were measured. The best values of the tensile strength and breaking elongation of blend fibers were obtained when gelatin content was 30 wt %. The water‐retention values of blend fibers increase as the amount of gelatin is raised. The structural analysis indicated that there was strong interaction and good miscibility between alginate and gelatin molecules resulted from intermolecular hydrogen bonds. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1625–1629, 2005     

Effects of pH and temperature on the sorption of sodium dodecyl sulfate by cellulose acetate/polyaniline blend membranes

Cellulose acetate/polyaniline (PANi) blends show a selective response to the presence of sodium dodecyl sulfate (SDS). Such detection can be monitored by visible absorption spectroscopy. In this article, we show how this is dependent on the pH and temperature. At pH 2, the redshift of the maximum absorbance wavelength of blend films is essentially dependent on hydrochloric acid; however, at pH 3, this effect clearly decreases, and at pH values between 4 and 6, the alteration of the blend color depends only on SDS. The selective detection of SDS is faster with a higher percentage of PANi in the blend. At 25°C, the mechanism of sorption is essentially Fickian for short times, but this changes at higher temperatures, and at temperatures of 40°C and higher, the sorption kinetics show an initial time lag in which no visible response from the blend to SDS is detected. The response rate of blends to SDS detection increases with the temperature and PANi content. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Preparation,characterization and preliminary calcium release study of floating sodium alginate/dextran‐based hydrogel beads: part I

Ionically crosslinked calcium alginate/dextran‐based floating beads were prepared using NaHCO₃ as porogen. Various micrometric properties such as tapped density, apparent density, compressibility index, etc., were determined for beads with different compositions. The beads were also evaluated for their mechanical strength. The percent buoyancy of the beads was measured as a function of time in simulated gastric fluid (pH = 1.2 at 37 °C). The beads prepared with higher concentrations of NaHCO₃ porogen and CaCl₂ crosslinker possessed 100% buoyancy and remained buoyant for nearly 20 h, or even more. Finally, the release of calcium from the beads was observed to follow diffusion‐controlled Higuchi kinetics. Copyright © 2007 Society of Chemical Industry