Sodium Phosphate Salts Research Articles

Elucidating the individual effects of calcium and phosphate ions on hMSCs by using composite materials

The biological performance of bone graft substitutes based on calcium phosphate bioceramics is dependent on a number of properties including chemical composition, porosity and surface micro- and nanoscale structure. However, in contemporary bioceramics these properties are interlinked, therefore making it difficult to investigate the individual effects of each property on cell behavior. In this study we have attempted to investigate the effects of calcium and inorganic phosphate ions independent from one another by preparing composite materials with polylactic acid (PLA) as a polymeric matrix and calcium carbonate or sodium phosphate salts as fillers. Clinically relevant bone marrow derived human mesenchymal stromal cells (hMSCs) were cultured on these composites and proliferation, osteogenic differentiation and ECM mineralization were investigated with time and were compared to plain PLA control particles. In parallel, cells were also cultured on conventional cell culture plates in media supplemented with calcium or inorganic phosphate to study the effect of these ions independent of the 3D environment created by the particles. Calcium was shown to increase proliferation of cells, whereas both calcium and phosphate positively affected alkaline phosphatase enzyme production. QPCR analysis revealed positive effects of calcium and of inorganic phosphate on the expression of osteogenic markers, in particular bone morphogenetic protein-2 and osteopontin. Higher levels of mineralization were also observed upon exposure to either ion. Effects were similar for cells cultured on composite materials and those cultured in supplemented media, although ion concentrations in the composite cultures were lower. The approach presented here may be a valuable tool for studying the individual effects of a variety of soluble compounds, including bioinorganics, without interference from other material properties.

Injectable in situ forming chitosan-based hydrogels for curcumin delivery

In this paper, a series of injectable in situ forming chitosan-based hydrogels were prepared by chemical crosslinking of chitosan and genipin with the cooperation of ionic bonds between chitosan and sodium salts at room temperature. Four hydrogels (A, B, C, and D) were obtained by mixing chitosan, genipin and a sodium salt of trisodium phosphate (Na3PO4·12H2O), sodium sulfate (Na2SO4), sodium sulfite (Na2SO3), or sodium bicarbonate (NaHCO3) and examined for their characteristics, morphology, and rheological properties. Their cell viability assays exhibited low toxicity and the localized in situ gel formation was detected after subcutaneous injections in rat. Curcumin which possesses many pharmaceutical potentials but has low bioavailability, was chosen as a drug model. In vitro curcumin release profiles exhibit sustained release properties with initial burst release for all hydrogels with about 3 to 6 times higher cumulative release than other gel controls. The results of this study demonstrate that our hydrogels have a potential as local curcumin carriers.

Solid‐State Characterization and Transformation of Various Creatine Phosphate Sodium Hydrates

Creatine phosphate sodium (CPS) salt is a first-line cardiovascular drug for severe diastolic heart failure. The drug exists in different hydrate forms. The marketed drug form was determined as CPS·4.5H2 O (H1); however, the reference standard was supplied as CPS·6H2 O (H2). In this work, we present two newly identified hydrate forms: a thermodynamically stable low hydrate form, CPS·1.5H2 O (H3), and a pressure-sensitive transit form, CPS·7H2 O (H4). The hydrate forms were discovered through a comprehensive solid-state screening experiment and fully characterized using a range of analytical techniques including X-ray powder diffraction (XRPD), FTIR, Raman spectroscopy, hot-stage microscopy (HSM), thermogravimetric analysis, and differential scanning calorimetry. Stability tests revealed that H3 was the most stable hydrate under thermal stimulation. H4 is a pressure-sensitive hydrate and easily transforms to H2 and then H1 upon grinding. The form transformation process was closely monitored using the HSM, variable-temperature XRPD (VT-XRPD), and VT-Raman spectroscopy techniques. Specifically, the transformation of H4 to H1 is characterized in a single-crystal-to-single-crystal transformation process. The newly discovered hydrate form H3 has superior physicochemical properties than the marketed forms and is worthy of further development.

Aluminum Contamination in Parenteral Nutrition Admixtures for Low-Birth-Weight Preterm Infants in Mexico.

Aluminum contamination from intravenous solutions still represents an unsolved clinical and biochemical problem. Increased aluminum intake constitutes a risk factor for the development to metabolic bone disease, anemia, cholestasis, and neurocognitive alterations. Low-birth-weight preterm infants (LBWPIs) are one of the most exposed populations for aluminum toxicity. To determine the presence of aluminum in components employed in the preparation of parenteral nutrition (PN) admixtures in Mexico and compare with the maximal aluminum recommended intake from the Food and Drug Administration. Cysteine, trace elements, levocarnitine, phosphate, and calcium salts tested positive for aluminum contamination. All components analyzed were contained in glass vials. Total aluminum intake for 2 sample PN admixtures were calculated in basis to cover nutrition requirements of 2 hypothetical LBWPIs. Aluminum contents, stratified in micrograms per kilogram of weight, exceeded maximal aluminum recommendations, particularly for the very LBWPIs. Substituting sodium phosphate for potassium phosphate salts reduced aluminum intake by 52.7%. Calcium gluconate was the leading aluminum contamination source and confers the greatest risk for aluminum overdose, even with the salt substitution of potassium phosphate by sodium phosphate salts. Adding cysteine and trace elements might increase aluminum content in PN admixtures. Cysteine, trace elements, phosphate, and gluconate salts are the main sources of aluminum in PN prepared in Mexico. Substituting sodium phosphate for potassium phosphate salts reduces aluminum intake but does not resolve aluminum contamination risk. Mineral salts contained in plastic vials should be explored as an additional measure to reduce aluminum contamination.

A new enantioselective CE method for determination of oxcarbazepine and licarbazepine after fungal biotransformation.

The present work describes, for the first time, the simultaneous separation of oxcarbazepine (OXC) and its active metabolite 10-hydroxy-10,11-dihydrocarbamazepine (licarbazepine, Lic) by chiral CE. The developed method was employed to monitor the enantioselective biotransformation of OXC into its active metabolite by fungi. The electrophoretic separations were performed using 10 mmol/L of a Tris-phosphate buffer solution (pH 2.5) containing 1% w/v of β-CD phosphate sodium salt (P-β-CD) as running electrolyte, -20 kV of applied voltage and a 15°C capillary temperature. The method was linear over the concentration range of 1000-30 000 ng/mL for OXC and 75-900 ng/mL for each Lic enantiomer (r ≥ 0.9952). Within-day precision and accuracy evaluated by RSD and relative errors, respectively, were lower than 15% for all analytes. The validated method was used to evaluate the enantioselective biotransformation of OXC, mediated by fungi, into its active metabolite Lic. This study showed that the fungi Glomerella cingulata (VA1) and Beuveria bassiana were able to enantioselectively metabolize the OXC into Lic after 360 h of incubation. Biotransformation by the fungus Beuveria bassiana showed 79% enantiomeric excess for (S)-(+)-Lic, while VA1 gave an enantiomeric excess of 100% for (S)-(+)-Lic. This study opens a new route to the drug (S)-(+)-licarbazepine.

Enhanced enamel benefits from a novel toothpaste and dual phase gel containing calcium silicate and sodium phosphate salts

To investigate the enamel health benefits of a novel toothpaste and a dual phase gel containing calcium silicate, sodium phosphate and fluoride. Enamel demineralisation was assessed using two pH cycling protocols with either lactic acid or citric acid as the acid challenge. Remineralisation of lactic acid softened and citric acid softened enamel was assessed using a number of protocols. All demineralisation and remineralisation evaluation was by surface microhardness measurements. The novel calcium silicate/phosphate fluoride toothpaste inhibited enamel demineralisation to a significantly (p<0.05) greater extent than control formulations, including a fluoride control. The novel calcium silicate/phosphate fluoride toothpaste also showed significant (p<0.05) remineralisation of lactic acid and citric acid softened enamel compared to fluoride and non-fluoride controls. The addition of the novel calcium silicate/phosphate fluoride dual phase gel provided enhanced remineralisation of citric acid softened enamel compared to fluoride and non-fluoride controls. These studies show that formulations containing calcium silicate, sodium phosphate salts and fluoride provide enhanced enamel demineralisation and remineralisation in vitro benefits. The novel oral care formulations containing calcium silicate, sodium phosphate salts and fluoride is a new approach to the protection of enamel from acid attacks and the repair of demineralised enamel, leading to increased dental hard tissue benefits.

Mode of action studies on the formation of enamel minerals from a novel toothpaste containing calcium silicate and sodium phosphate salts

To investigate in vitro and in situ the deposition and formation of hydroxyapatite (HAP) on enamel surfaces following brushing with a novel toothpaste containing calcium silicate (CaSi), sodium phosphate salts and fluoride. Polished enamel blocks were brushed in vitro with a slurry of the CaSi toothpaste. After one brush and four weeks simulated brushing the enamel surfaces were analysed. In an in situ protocol, enamel blocks were attached to first or second molar teeth of healthy subjects, exposed to 4 weeks twice per day brushing with the CaSi toothpaste and then analysed. The surface deposits were analysed using scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and selected area electron diffraction (SAED). In addition, the CaSi toothpaste was slurried in simulated oral fluid (SOF) over a 3 hour period and the solids were isolated and analysed by Fourier transform infrared spectroscopy (FTIR). The FTIR study demonstrated that calcium phosphate phases had formed and these became increasingly crystalline over 3 hours. CaSi was deposited onto enamel surfaces following one brushing with the toothpaste in vitro.The deposited particles showed evidence of HAP crystalline phases associated with the CaSi. Following 4 weeks brushing in vitro, the deposition increased and analyses showed that the deposited material was HAP. These results were confirmed by the in situ study. Calcium silicate can be deposited onto enamel surfaces from a novel toothpaste formulation where it can form the enamel mineral HAP. A novel toothpaste formulation containing CaSi can form HAP on enamel surfaces. The potential of this technology is for a novel approach to the repair of demineralised enamel and the protection of enamel during acid exposure.

Remineralisation effect of a dual-phase calcium silicate/phosphate gel combined with calcium silicate/phosphate toothpaste on acid-challenged enamel in situ

To test if a novel dual-phase gel system (calcium silicate and phosphate with 1450 ppmF, as NaF/MFP; TG) combined with a toothpaste (calcium silicate and sodium phosphate with 1450 ppmF, as MFP; TG) was able to re-harden previously acid-challenged enamel to a greater extent than other toothpastes. The study consisted of a double-blind, randomised, cross-over design with four 7-day treatment legs. In each leg, subjects wearing a partial denture holding four demineralised enamel specimens (25 min in 0.3% citric acid, pH3.8) used either the test regimen (TG+TP) or one of the three controls. (placebo TG+TP; Positive Control - placebo TG+marketed 1450 ppmF toothpaste; Negative Control - placebo TG+placebo TP). Enamel specimens were removed after 1, 2, 3 and 7 days. The gel systems were applied once per day for the first three days during which subjects also brushed with the corresponding toothpaste; this was followed by four days use of the toothpastes only. Toothpastes were used in the conventional way brushing twice per day throughout the seven days. The outcome variable was %Surface Microhardness Recovery calculated after three and seven days of in situ treatment. The results showed a statistically significant (p<0.001) re-hardening effect for all treatments compared to pre-treatment hardness. After three days and after seven days of in situ treatment significantly greater hardening (p<0.05) was found in the samples treated with calcium silicate/phosphate gel system plus calcium silicate/phosphate toothpaste than in the control groups. It is concluded that the test regimen based on the novel dual-phase gel system combined with toothpaste was able to re-harden acid-challenged tooth enamel to a greater extent than a normal fluoride toothpaste. The novel oral care products containing calcium silicate, sodium phosphate salts and fluoride is a new approach to the repair of demineralised enamel.

Introduction of an interproximal mineralisation model to measure remineralisation caused by novel formulations containing calcium silicate, sodium phosphate salts and fluoride

To introduce a new interproximal mineralisation model and to investigate the effectiveness of novel toothpaste and dual phase gel formulations to remineralise acid softened enamel in a simulated interproximal environment. Specimens were positioned opposite each other with an approximately 100 μm space between enamel surfaces to simulate an interproximal environment. Target specimens were demineralised in 1% (w/v) citric acid, pH3.75. Specimens were daily immersed in artificial saliva (AS) for 1h, treated with formulations, re-immersed in AS for 6h, re-treated and re-immersed in AS for a further 1h. Study 1 evaluated prototype calcium silicate/phosphate fluoride toothpaste formulations. Study 2 evaluated novel calcium silicate/phosphate fluoride toothpaste and dual phase gel formulations. Both studies contained fluoridated and non-fluoridated controls. The surface microhardness of each target enamel block was measured following demineralisation and following days three, seven and fourteen for study one and after days one, three and seven for study two. This new mineralisation model was able to show increased remineralisation from calcium silicate/phosphate fluoride prototype formulations over fluoridated formulations alone, after three and seven days of treatment. Using this new model, the combined application of novel calcium silicate/phosphate fluoride toothpaste and novel calcium silicate/phosphate fluoride dual phase gel showed the greatest amount of remineralisation, which was significantly greater than sodium fluoride and non-fluoride controls. Employing a new interproximal mineralisation model successfully determined the remineralisation potential of novel calcium silicate/phosphate fluoride oral healthcare formulations. Modifying a mineralisation model to include specimens positioned in an interproximal environment allows us to better understand the remineralisation potential of oral healthcare products. It is important to minimise mineral loss at interproximal sites as the enamel within these areas is thinner than the rest of the crown.

A disposable alkaline phosphatase-based biosensor for vanadium chronoamperometric determination.

A chronoamperometric method for vanadium ion determination, based on the inhibition of the enzyme alkaline phosphatase, is reported. Screen-printed carbon electrodes modified with gold nanoparticles were used as transducers for the immobilization of the enzyme. The enzymatic activity over 4-nitrophenyl phosphate sodium salt is affected by vanadium ions, which results in a decrease in the chronoamperometric current registered. The developed method has a detection limit of 0.39 ± 0.06 μM, a repeatability of 7.7% (n = 4) and a reproducibility of 8% (n = 3). A study of the possible interferences shows that the presence of Mo(VI), Cr(III), Ca(II) and W(VI), may affect vanadium determination at concentration higher than 1.0 mM. The method was successfully applied to the determination of vanadium in spiked tap water.

A thixotropic supramolecular hydrogel of adenine and riboflavin-5′-phosphate sodium salt showing enhanced fluorescence properties

An equimolar mixture of riboflavin-5′-phosphate sodium salt (RP) and adenine (AD) dissolved in a phosphate buffer (pH 4.0, 1.0% w/v) produces a red coloured transparent thixotropic hydrogel at 30 °C. The gelation of the RPAD system occurs in the pH range of 2–5. FTIR spectra and WAXS patterns indicate self-assembly via H-bonding between the >C=O group of RP and the amino/imino group of AD followed by supramolecular organization through a π-stacking process producing a fibrillar network structure. FESEM images clearly indicate that the nanofibres are produced from the intertwining of helical fibrils. The dynamic frequency sweep experiment of the supramolecular gel at a constant strain of 1% exhibits a wide linear viscoelastic region and a considerably higher G′ value (460 Pa) than that of G′′ (21 Pa) confirming the gel nature of the RPAD system. The hydrogel shows high stiffness (G′/G′′ = 3.3), a high yield stress (σ*) (79.5 Pa) and a moderate critical strain (γ = 17.5%). Time sweep experiments at both low (0.1%) and high strain (100%) indicate the thixotropic property of the gel. The RPAD hydrogel shows non-Newtonian viscosity in the shear rate region (0.1–158 s(−1)) and after that there is a sudden fall of viscosity. The gel melting point obtained by the falling ball method is 6° higher than that obtained by the DSC method probably due to the presence of the thixotropic property of the gel. The UV-vis spectra indicate a red shift of the π–π* transition band of RP in the RPAD xerogel. On excitation of the RPAD hydrogel at 373 nm it shows twelve times enhancement of emission intensity with a 7 nm red shift of the emission peak. This has been attributed to the enhancement of lifetime from 2.2 ns in RP to 3.4 ns in the RPAD hydrogel. With increase of temperature, the fluorescence intensity of the RPAD hydrogel at first increases till 40 °C, then decreases up to 55 °C and it again increases after 60 °C.

Effects of Detergent β-Octylglucoside and Phosphate Salt Solutions on Phase Behavior of Monoolein Mesophases

Using small-angle x-ray scattering (SAXS), we investigated the phase behavior of mesophases of monoolein (MO) mixed with additives commonly used for the crystallization of membrane proteins from lipidic mesophases. In particular, we examined the effect of sodium and potassium phosphate salts and the detergent β-octylglucoside (βOG) over a wide range of compositions relevant for the crystallization of membrane proteins in lipidic mesophases. We studied two types of systems: 1), ternary mixtures of MO with salt solutions above the hydration boundary; and 2), quaternary mixtures of MO with βOG and salt solutions over a wide range of hydration conditions. All quaternary mixtures showed highly regular lyotropic phase behavior with the same sequence of phases (Lα, Ia3d, and Pn3m) as MO/water mixtures at similar temperatures. The effects of additives in quaternary systems agreed qualitatively with those found in ternary mixtures in which only one additive is present. However, quantitative differences in the effects of additives on the lattice parameters of fully hydrated mesophases were found between ternary and quaternary mixtures. We discuss the implications of these findings for mechanistic investigations of membrane protein crystallization in lipidic mesophases and for studies of the suitability of precipitants for mesophase-based crystallization methods.

Stability studies for titanium dioxide nanoparticles upon adsorption of Suwannee River humic and fulvic acids and natural organic matter

In many studies humic acid, fulvic acid, or natural organic matter is used interchangeably to model the effect of naturally derived organic matter on geochemical processes in the environment. In this study, the term NOOM (naturally occurring organic matter) is used to include both humic and fulvic acids as well as natural organic matter and compares the effect of NOOM type on NOOM removal onto nano-TiO2. In general, regardless of variations in solution chemistry, the order of the percentage of removal of NOOM onto nano-TiO2 was humic acid>natural organic matter>fulvic acid. The order of adsorption constant values of NOOM onto nano-TiO2 was also found to be humic acid>natural organic matter>fulvic acid under all conditions studied. The extent of NOOM removal by nano-TiO2 was enhanced in the presence of the divalent ions, magnesium and calcium, at pH7.8 when compared to the presence of the monovalent ions, sodium and potassium. Also, lower NOOM removal by nano-TiO2 in the presence of sodium salts of dihydrogen phosphate, bicarbonate and nitrate relative to chloride was observed and was likely due to the competition between polyatomic anions and NOOM adsorption onto the surface of nano-TiO2 indicating an anionic effect. Low concentrations of NOOM (10–20mgL−1) destabilized nano-TiO2 in solution, however, the stability of nano-TiO2 increased as the amount of NOOM adsorbed onto nano-TiO2 increased at higher dissolved NOOM concentrations and significant stabilization was seen at 25mgL−1 NOOM. Thus, the three fractions of NOOM, humic and fulvic acids and natural organic matter and their concentrations were found to affect nano-TiO2 stability to different degrees although pH dependent trends in cation and anion effects had similar patterns. While the effects of adsorption of these three commonly used types of NOOM onto nanoparticles are similar, there are important differences that can be related to structural differences.

The effect of sulphate, phosphate, nitrate and acetate on the corrosion behaviour of ZnAl-Mg hot-dip galvanised steel

In this work the hot-dip galvanising coating ZnAl2Mg2 was tested against the reference material ZnAl0.2 in nonstandardised salt spray test. In those tests the samples were exposed to the sodium salts of sulphate, nitrate, phosphate and acetate. The corrosion products formed on the alloys were analysed with XRD. Additionally the corrosion behaviour of the samples was investigated by studying cross-section cuts with SEM. With this information the corrosivity of the different anions in relation to chloride ions and their corrosion behaviour could be determined.

English

The effects of different nutrient sources (nitrogen, phosphorus and carbon) on the growth status and glycogen reserves in Synechocystis sp. strain PCC 6803 and Anabaena sp. strain PCC 7120 were studied. The two cyanobacteria grew well on suitable nutrient sources, for example, nitrate (sodium nitrate), phosphate (two potassium hydrogen phosphate) or inorganic (sodium carbonate, dicarbonate) and organic (sodium acetate, glucose) carbon. On the contrary, the growth rate decreased markedly when grown on ill-suited nutrient sources, for example, ammonium (ammonium chloride), organic nitrogen (urea), pyrophosphate (sodium pyrophosphate) and organophosphate (D-Glucose,6-(dihydrogen phosphate) sodium salt (1:2), adenosine-triphosphate). The yield of phycocyanin and chlorophyll a was higher when grown on suitable than ill-suited nutrient sources, whereas, the activities of superoxide dismutase (SOD) and peroxidase (POD) were higher on ill-suited than suitable nutrient sources, and the glycogen reserves presented the same variation tendences as peroxidase. These results indicate that the nutrient sources used in this study were involved in regulation of (1) the contents of pigments and glycogen, (2) energy and electron transport efficiencies of photosynthesis, and (3) activity level of SOD and POD in Synechocystis sp. PCC 6803 and Anabaena sp. PCC 7120. Key words: Nitrogen, phosphorus, carbon, growth, glycogen reserves.

Spectroscopic and microscopic analyses of rod‐shaped gold nanoparticles interacting with single‐stranded DNA oligonucleotides

The application of rod-shaped gold nanoparticles as probes and carriers in biological systems have recently attracted great interest. UV-vis spectroscopy, circular dichroism, Fourier transform infrared spectroscopy, scanning electron microscopy and atomic force microscopy were used to study optical and structural properties of rod-shaped gold nanoparticles when interacting with DNA oligomers in phosphate sodium salt buffer. The morphological transformation process of rod-shaped gold nanoparticles resulting from the interaction with single-stranded DNA (ssDNA) showed the role of hexadecyltrimethylammonium bromide (CTAB) in nanostructures as the main interacting agent. The obtained results confirmed that the CTAB coat of rod-shaped gold nanoparticles have powerful positive charges for conjugations with surface negative charges of phosphate groups on ssDNA oligomers. The CTAB also inhibit the formation of covalent sulphide bonds between the gold core of rod-shaped nanoparticles and alkanethiol oligonucleotides. The authors found that when the nanorods were exposed to ssDNA oligonucleotides, the gold nanorods changed their shapes and sizes, and exposed some microscopic malformations which could be used in the development of colorimetric assays of nucleic acids.

Kinetics of phosphate absorption in lactating dairy cows after enteral administration of sodium phosphate or calcium phosphate salts

Hypophosphataemia is frequently encountered in dairy cows during early lactation. Although supplementation of P is generally recommended, controversy exists over the suitability of oral P supplementation in animals with decreased or absent rumen motility. Since the effects of transruminal P absorption and the reticular groove reflex on the absorption kinetics of P are not well understood, it is unclear in how far treatment efficacy of oral P supplementation is affected by decreased rumen motility. Phosphate absorption was studied in six phosphate-depleted dairy cows fitted with rumen cannulas and treated with test solutions containing either NaH2PO4 or CaHPO4 with acetaminophen. Each animal was treated orally, intraruminally and intra-abomasally in randomised order. Absorption kinetics of P were studied and compared with the absorption kinetics of acetaminophen, a marker substance only absorbed from the small intestine. Intra-abomasal treatment with NaH2PO4 resulted in the most rapid and highest peaks in plasma inorganic P (Pi) concentration. Oral and intraruminal administration of NaH2PO4 resulted in similar increases in plasma Pi concentration from 4 to 7 h in both groups. Treatment with NaH2PO4 caused more pronounced peaks in plasma Pi concentration compared with CaHPO4. Neither transruminal P absorption nor the reticular groove reflex affected P absorption kinetics as determined by comparing plasma concentration–time curves of P and acetaminophen after administration of 1M-phosphate salt solutions. It is concluded that oral treatment with NaH2PO4 but not CaHPO4 is effective in supplementing P in hypophosphataemic cows with adequate rumen motility. Decreased rumen motility is likely to hamper the efficacy of oral phosphate treatment.

Studies of Monolayer and Mixed Micelle Formation of Anionic and Nonionic Surfactants in the Presence of Adenosine-5-monophosphate

The interactions between the anionic surfactant di-(2-ethylhexyl) phosphate sodium salt (DEP) and two nonionic surfactants, dimethyldecyl phosphineoxide (DDPO) and dimethyltetradecyl phosphineoxide (DTPO), at the interface and in the micellar phases were investigated in the absence and presence of adenosine-5-monophosphoric acid disodium salt (AMP). The mixed systems were DEP–DDPO, DEP–DDPO/AMP (0.001 mol⋅L−1), DEP–DTPO, and DEP–DTPO/AMP (0.001 mol⋅L−1) at different bulk mole fractions of the anionic component (α 1=0.9,0.8,0.6,0.4,0.2). The mixed systems studied were investigated based on the theoretical models of Rubingh and Clint. The results showed surface tension reduction efficiency. The adsorbed mixed monolayer demonstrated stronger interactions than the mixed micelles, whereas AMP increased the interfacial interactions more than those in the micellar phase. The Gibbs energy of mixing suggests that the stability of the mixed micellar phase is greater than that of the micellar phases of the individual components. The synergism that occurred in the different mixed phases is discussed.

Comparison of anion removal capacities of Octolig® and Cuprilig

Mixtures of sodium salts of phosphate, arsenate, and fluoride were used in chromatography and batch experiments to compare the capacity of two immobilized ligands (IMLIGs) to remove these anions: Octolig® and its copper (II)-based metallolig, Cuprilig. The focus of this study was twofold. First, to find out which material, Octolig® or Cuprilig, would remove these anions most effectively; and secondly to determine the optimal capacity for removal of representative anions. Removal capacity was evaluated by two methods: by chromatography and by a batch method. The methods gave identical results, but the batch method was more convenient. Cuprilig had a lower capacity for removal of phosphate than Octolig®. The capability of Octolig® for removing anions was: phosphate > arsenate > fluoride >>>chloride >>>>bromide. Replication of phosphate removal was good for a given batch of Octolig®. Of three different samples of Octolig®, two seemed to be alike based on the phosphate- removal capacity; the third was different on the basis of a Student's t-test. This distinction indicates the batch procedure could serve as a quality control/assurance technique.

Optical detection of sodium salts of fluoride, acetate and phosphate by a diacylhydrazine ligand by the formation of a colour alkali metal complex

A solution of N, N’-diacylhydrazine ligand in organic solvent is potential for colourimetric detection of F − /AcO − /PO\(_{4}^{3-}\) via -NH deprotonation, tautomerization and its stabilization as a colour alkali metal complex. Colourimetric detection of fluoride, acetate and phosphate in a semi-aqueous solvent system via deprotonation, tautomerization followed by complex formation which is established by single crystal X-ray structural analysis.