Sorption of wheat seed lectin by polyelectrolyte complexes of chitosan

The possible application of polyelectrolyte complexes (PEC) of chitosan and copolymers of maleic acid with N-vinylpyrrolidone, styrene, and ethylene and/or chitin cross-linked sorbents (CCLS) synthesized on the basis of PEC for sorption of wheat germ agglutinin (WGA) was studied. The synthesis of spherically granulated sorbents was shown. Compared to unmodified chitosan, there was a significant increase in sorption of WGA by the PEC: PEC, 2.5-fold, and CCLS, from 3.5-fold to 7-fold.     

Uptake of fluoride by nano-hydroxyapatite/chitosan, a bioinorganic composite

A bioinorganic composite namely nano-hydroxyapatite/chitosan (n-HApC) composite which could be employed for technology development was prepared and studied for its defluoridation efficiency. It has been observed that there was a slight enhancement in the defluoridation capacity (DC) of n-HApC composite (1560mgF(-)/kg) than nano-hydroxyapatite (n-HAp) which has a DC of 1296mgF(-)/kg. The sorbents were characterized with XRD and TEM studies. The fluoride sorption was explained with Freundlich and Langmuir isotherms. Thermodynamic parameters such as DeltaG degrees , DeltaH degrees , DeltaS degrees and E(a) were calculated in order to understand the nature of sorption. The sorption process was found to be controlled by pseudo-second-order and pore diffusion models. Field studies were carried out with the fluoride containing water sample collected from a fluoride-endemic area in order to test the suitability of the sorbents at field conditions.     

Removal of copper(II) using chitin/chitosan nano-hydroxyapatite composite

Polymeric composites made up of nano-hydroxyapatite (n-HAp) with chitin and chitosan have been prepared and studied for the removal of Cu(II) ions from the aqueous solution. The sorption capacity (SC) of n-HAp, n-HAp/chitin (n-HApC) composite and n-HAp/chitosan (n-HApCs) composite were found to be 4.7, 5.4 and 6.2 mg/g respectively with a minimum contact time of 30 min. Batch adsorption studies were conducted to optimize various equilibrating conditions like contact time, pH and selectivity of metal ion. The sorbents were characterized by FTIR, TEM, XRD and SEM with EDAX analysis. The sorption process was explained with Freundlich and Langmuir isotherms respectively. Thermodynamic parameters such as ΔG°, ΔH° and ΔS° were calculated to understand the nature of sorption. A suitable mechanism for copper sorption was established and the selectivity of the metal ions for the composites was identified.     

Polyelectrolyte complexes of gum kondagogu and chitosan,as diclofenac carriers

Polyelectrolyte complexes (PEC) of gum kondagogu (GKG) and chitosan were prepared by mixing polymeric solutions of different concentrations (0.02–0.18% w/v). The complex formed were loaded with diclofenac sodium, and the release of the drug was measured in vitro and in vivo, along with the measurement of particle size, zeta potential, complex formation, flow properties, and loading efficiency. Maximum yield of PEC was observed at gum kondagogu concentrations above 80%. The PEC showed lower release of diclofenac sodium in 0.1 N HCl as compared to phosphate buffer (pH 6.8). Increasing the concentration of gum kondagogu in PEC led to an increase in drug release. However, PEC 1:3 (gum kondagogu: chitosan) with higher concentration of chitosan showed 98% release with in 4.5 h, owing to the fact that chitosan has a higher degree of swelling in acidic medium. PEC 5:1 and 3:1 showed a 5.3- and 5.8-fold increase in relative bioavailability compared to the free drug when administered orally to the rats.     

Study of lipoprotein sorption by some sulfoderivatives of chitosan

The possibility of deposition of lipoproteins from blood plasma by different chitosan sulfoderivatives has been demonstrated. The influence of structure, substitution degree and molecular weight of chitosan sulfates on lipoprotein sorption was studied as well as the influence of composition of chitosan interpolymer complexes with dextransulfate. Affinic sorbents based on the silica matrixes and sulfoderivatives of chitosan as a ligand can reveal high specificity in relation to low density lipoprotein, but do not cause essential changes in blood count during contact with blood.     

Equilibrium and kinetics studies of adsorption of copper (II) on chitosan and chitosan/PVA beads

The adsorption of Cu(II) ions from aqueous solution by chitosan and chitosan/PVA beads was studied in a batch adsorption system. Chitosan solution was blended with poly(vinyl alcohol) (PVA) in order to obtain sorbents that are insoluble in aqueous acidic and basic solution. The adsorption capacities and rates of Cu(II) ions onto chitosan and chitosan/PVA beads were evaluated. The Langmuir, Freundlich and BET adsorption models were applied to describe the isotherms and isotherm constants. Adsorption isothermal data could be well interpreted by the Langmuir model. The kinetic experimental data properly correlated with the second-order kinetic model, which indicates that the chemical sorption is the rate-limiting step. The Cu(II) ions can be removed from the chitosan and chitosan/PVA beads rapidly by treatment with an aqueous EDTA solution. Results also showed that chitosan and chitosan/PVA beads are favourable adsorbers.     

Comparative studies on the adsorption of Cr(VI) ions on to various sorbents

The adsorption of Cr(VI) ions onto various sorbents (chitin, chitosan, ion exchangers; Purolite CT-275 (Purolite I), Purolite MN-500 (Purolite II) and Amberlite XAD-7) was investigated. Batch adsorption experiments were carried out as a function of pH, agitation period and concentration of Cr(VI) ions. The optimum pH for Cr(VI) adsorption was found as 3.0 for chitin and chitosan. The Cr(VI) uptake by ion exchangers was not very sensitive to changes in the pH of the adsorption medium. The maximum chromium sorption occurred at approximately 50 min for chitin, 40 min for Purolite II and 30 min for chitosan, Purolite I and Amberlite XAD-7. The suitability of the Freundlich and Langmuir adsorption models were also investigated for each chromium-sorbent system. Adsorption isothermal data could be accurately interpreted by the Langmuir equation for chitosan, chitin, Purolite I and Purolite II and by the Freundlich equation for chitosan, chitin and Amberlite XAD-7. The chromium(VI) ions could be removed from the sorbents rapidly by treatment with an aqueous EDTA solution and at the same time the sorbent regenerated and also could be used again to adsorb by heavy metal ions. The results showed that, chitosan, which is a readily available, economic sorbent, was found suitable for removing chromium from aqueous solution.     

Electrosprayed polyelectrolyte complexes between mucoadhesive N,N,N,-trimethylchitosan-homocysteine thiolactone and alginate/carrageenan for camptothecin delivery

Novel hydrogel polyelectrolyte complexes (PECs) between the N,N,N,-trimethylchitosan-homocysteine thiolactone (TM-HT-chitosan) and two anionic polymers were investigated. The particles of pure thiolated chitosan and its PECs with alginate and carrageenan were fabricated using the electrospray ionization technique. The hydrogel PEC particles were characterized by scanning electron microscopy, dynamic light scattering, Fourier transform infrared microscopy, thermogravimetric analysis, encapsulation efficiency (EE), mucoadhesive property and in vitro drug release behavior. TM-HT-chitosan/alginate particles could be loaded with camptothecin (CPT), employed as a model anti-cancer drug, at an over 70% EE, and revealed both a reduced burst effect and a prolonged release of CPT over 3 days. The resultant TM-HT-chitosan/alginate PEC particles displayed a 5.60-, 1.86- and 1.55-fold stronger mucoadhesive property compared to that of the unmodified chitosan/alginate PEC at pH 1.2, 4.0 and 6.4, respectively, and this was not affected by the CPT loading level.     

Study of molybdate ion sorption on chitosan gel beads by different spectrometric analyses

Molybdate ion uptake both by raw chitosan and by glutaraldehyde cross-linked chitosan beads was investigated. This study focused on the identification of sorption mechanisms by means of several analytical procedures such as infra-red and reflectance spectrophotometries and CP-MAS 13C NMR analyses. Although the amine functions of glucosamine residues remain the major sites of interaction with the metal species, other functional groups can also be involved. It is certainly the case with carbonyl functions provided by the glutaraldehyde structure in cross-linked sorbents. Due to the large size of the polynuclear hydrolysed molybdate species, the sorption may involve several monomer units, resulting in additional linkages between the polymer chains. This behaviour can be confirmed by the chemical shifts of the carbon atoms observed by CP-MAS 13C NMR on raw chitosan beads, showing that the carbon atoms supporting the amino sites are not the only atoms affected by molybdate ion sorption. Moreover, cross-linking promotes a partial reduction of molybdenum species in the presence of some unreacted aldehyde groups.     

Composite fluorine polymer-containing sorbents for isolation and purification of biopolymers

Composite fluoropolymer-containing sorbents based on porous silicas were synthesized for the isolation and purification of biopolymers under nondenaturing conditions. Examples of the application of these sorbents in the separation of various mixtures of peptides and proteins and purification of nucleic acids from various sources (plasmid DNA and DNA from nucleated human blood cells) using the cartridge, column, and batch (sorption in a stirred volume) methods are presented. It was shown that the sorbents can be used in laboratory practice because they are selective to nucleic acids (DNA and RNA) and proteins. These materials combine the mechanical properties of the inorganic matrix with the specific sorption properties of the polymer phase and exhibit enhanced stability to alkaline hydrolysis. Alternative methods of preparing sorbents containing polytetrafluoroethylene, polytrifluorostyrene, and polyfluorobutadiene are described. By the example of polyfluorobutadiene-containing sorbents, a completely new method for obtaining fluorinated polymer phases was developed: the polymer phase was preliminarily formed on the surface of porous disperse carriers and was fluorinated with xenon difluoride.     

Sorption of lysine by molecularly imprinted carboxyl sorbents

Tuned (molecularly imprinted) and nontuned, with respect to lysine amino acid, carboxylic heteroreticular sorbents based on methacrylic acid and ethylene glycol dimethacrylate, were synthesized. Study of sorption of lysine within wide pH range and ionic strength indicated significant dissimilarities in amino acid sorption by tuned sorbents, which were expressed as an increase in the contribution of nonionic interaction, and resulted in a decrease in the ionic strength effect on the sorption capacity, as well as an increase in amino acid sorption selectivity.     

A number of sorbents useful for the sorption of cephalosporin C

The physicochemical and sorption properties of a number of sorbents made in the USSR and abroad were studied with respect to the recovery of cephalosporin C from a model solution. It was shown that the sorption capacity of a sorbent depended on its specific surface. The macroporous styrene divinylbenzene sorbents with a specific surface of more than 500 m2/g had the best sorption properties.     

Removal of basic (Methylene Blue) and acid (Egacid Orange) dyes from waters by sorption on chemically treated wood shavings

Spruce wood shavings from Picea abies were used for an adsorptive removal of both basic as well as acid dyes from waters. The sorption properties of the sorbents were modified with HCl, Na(2)CO(3) and Na(2)HPO(4). The treatment of the wood sorbents with alkaline carbonate solution as well as with phosphate solution increased the sorption ability for the basic dye (Methylene Blue), whereas the treatment with mineral acid decreased the sorption ability for Methylene Blue to some extent. The opposite is true for the sorption of the acid dye--Egacid Orange. The maximum sorption capacities estimated from the Langmuir-Freundlich isotherms ranged from 0.060 to 0.165 mmol g(-1) for Methylene Blue, and from 0.045 to 0.513 mmol g(-1) for Egacid Orange. The basic dye sorption decreased at low pH values in accordance with a presupposed ion-exchange mechanism of the sorption. The sorption of acid dye, on the other hand, decreased with increasing pH. The presence of inorganic salts as well as surfactants exhibited only minor effects on the dye sorption.     

Protein sorption with mineral colloids]

A study was made of the effect on sorption of the molecular weight of model proteins (ribonuclease with a molecular weight of 12 10(3), trypsin with a molecular weight of 24-10(3), bovine albumin with a molecular weight of 64-10(3) and gamma-globulin with a molecular weight of 160-10(3)) and dispersity of suspensions of aluminium hydroxide, aluminum phosphate and calcium phosphate used as biopreparation sorbents. The expediency of using phosphate and calcium phosphate used as biopreparation sorbents. The expediency of using for effective sorption of a definite area of sorption surface necessary and adequate for the distribution of protein macromolecules with the best degree of conformational liberty was revealed.     

Sorption of tartrate, citrate, and EDTA onto chitosan and its regeneration applying electrolysis

The equilibrium isotherm data obtained by the sorption of tartrate, citrate, and EDTA onto chitosan were analyzed using Langmuir and Freundlich equations. The process fits best the Langmuir equation. Kinetic investigations showed that the sorption process obeys the pseudo-second-order kinetic equation. Sorption and desorption peculiarities, FTIR investigations, and measurements of molecular weight enable one to hypothesize that sorption proceeds along with the electrostatic interaction between the positively charged -NH3+ groups of chitosan and the negatively charged -COO(-) of carboxylic acids in the formation of amide bonds between the -NH(2) groups of chitosan and the -COOH groups of the carboxylic acid. Electrolysis under galvanostatic conditions in a mixture of chitosan with a 0.1 mol L(-1) Na(2)SO(4) solution enables one to destroy the amide bonds in the cathode compartment of the electrochemical cell and to anodize organics in the anodic compartment. The choosing of relevant conditions of electrolysis enables one to obtain chitosan with properties (deacetylation degree, molecular weight, and sorption ability) similar to those of initial chitosan. After electrolysis the regenerated chitosan possesses the same or even higher ability for sorption of the carboxylic acids as the initial chitosan.     

Equilibrium and Kinetic Studies on the Removal of Basic Violet 10 from Aqueous Solutions Using Activated Carbons Prepared from Industrial Wastes

Low-cost adsorbents prepared from industrial wastes such as sugarcane bagasse (BC), rice husk (RC), and textile waste cloth (TC) are identified as suitable sorbents for removing basic violet 10 (BV). Fourier transform infrared (FTIR) and scanning electron microscopic (SEM) studies were carried out to characterize the prepared sorbents. The effects of dosage, time, and pH on dye removal were examined. It was observed that BV sorption takes place in acidic, neutral, and alkaline aqueous solutions. The work discussed the best-fit sorption isotherms among Freundlich and Langmuir, in addition to the reaction- and diffusion-based kinetic models. Based on the data obtained, it was found that the BV sorption took place in acidic, neutral, and alkaline aqueous solutions and sorption kinetics found to be controlled by pseudo-second-order and pore diffusion models. Also, thermodynamic parameters such as ΔG ^o, ΔH ^o, ΔS ^o, and E _a were calculated in order to understand the nature of the sorption process. The maximum dye removal capacity (DRC) was found to be 5608, 1244, and 27,495 mg/kg for BC, RC, and TC, respectively. Collectively, it can be concluded that the activated carbon sorbents, prepared from the named wastes, can used to adequately remove the basic violet dye from its aqueous waste solution.     

Preparation and use of magnetic sorbents for studying microorganism antigens

In this work simple techniques for obtaining polyacrylamide sorbents with magnetic properties are described. These techniques have permitted obtaining block and microgranulated sorbents with the immobilization of antibodies from plague antiserum in the cellular gel structure for the specific sorption of killed and live Yersinia pestis cells and their first fraction; pig brain gangliosides have also been incorporated into the gel structure with a view to the sorption of cholera toxin from the filtrate of Vibrio cholerae culture. The magnetic properties of sorbents, obtained by the copolymerization of powdered magnetic ferric oxides in gel, have made it possible to increase the effectiveness of specific sorption due to mixing and rapid separation in different magnetic fields, as well as to facilitate and accelerate manipulations with the sorbent at all stages. The capacity of different types of sorbents and the time of sorption have been determined.     

Harvesting of Microalgae Biomass with Polyethylenimine-Based Sorbents

The purpose of this work was to investigate the sorbents on the basis of polyethylenimine (PEI) intended for collecting biomass of microalgae (MA). For this purpose, a series of porous and insoluble polymeric materials were synthesized by cross-linking of PEI with epichlorohydrine. The analysis of kinetics and efficiency of immobilization assessed for the model culture Chlorella vulgaris, revealed that already within 3 h of incubation, 39–75% of MA cells attached to the surface of tested sorbents. It was shown that on the initial stage of immobilization the sorption activity of polymeric materials depended on the “PEI:crosslinker” ratio. One of the tested sorbents was additionally quartenized by alkylation with dimethyl sulphate resulting in sharp increase of its sorption activity. The estimation of the MA desorption from polymeric surface showed that most Ch. vulgaris cells were practically irreversibly immobilized on all tested sorbents based on the PEI cross-linked with epichlorohydrine.     

Removal of perfluorooctane sulfonate from aqueous solution by crosslinked chitosan beads: sorption kinetics and uptake mechanism

The crosslinked chitosan beads were used as an efficient biosorbent to remove perfluorooctane sulfonate (PFOS) from aqueous solution. The chitosan biosorbent had a sorption capacity up to 5.5 mmol/g for PFOS at the equilibrium concentration of 0.33 mmol/L, much higher than some conventional adsorbents. The sorption kinetics indicated that the sorption equilibrium was reached quickly at high pH and low PFOS concentrations, and the adsorbent size also affected the sorption rate to some extent. The double-exponential model described the kinetic data well, and the sorption of PFOS on the chitosan beads was a diffusion-controlled process. Based on the sorption kinetics and adsorbent characterization, the uptake mechanisms including electrostatic and hydrophobic interactions were identified to be responsible for PFOS sorption, and the hemi-micelles and micelles may form in the porous structure due to high PFOS concentrations within the adsorbent, which had the main contribution to the high sorption capacity.     

Protecting effect of chitin and chitosan on experimentally induced murine candidiasis

Chitin and chitosan were found to exhibit a protective effect on mice administered these polysaccharides intraperitoneally against infection of the viable cells of Candida albicans NIH A-207 strain. A significant difference was observed between the protective effects of chitin and chitosan, i.e., chitin was much more effective than chitosan when the C. albicans cells were challenged via the intravenous route. In intraperitoneal inoculations of C. albicans cells, however, chitosan provided stronger resistance for mice than chitin. It has also been revealed that the number of polymorphonuclear leukocytes from circulating blood of chitin-administered mice increased remarkably compared with that of untreated and chitosan-treated mice, and that the increase of active oxygen-generating phagocytic cells was significant. On the other hand, the number of peritoneal exudate cells (PEC) and the amounts of active oxygen generated from these cells in chitosan-treated mice were larger than those of chitin-treated mice. However, candidacidal activities of PEC per fixed cell number in mice treated with chitin or with chitosan were almost the same and greater than those of untreated mice.