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PubMed1993

Cytotoxic and cytostatic activity of copper(II) complexes. Importance of the speciation for the correct interpretation of the in vitro biological results.

The cytotoxicity of some copper(II) compounds against the mouse cancer cell line B16, murine L929, human KB cells, and fibroblasts was investigated. All the copper(II) systems tested were shown to have pronounced toxicity against transformed cells and a cytostatic effect against untransformed cells, i.e., human fibroblasts. A careful speciation of the actual in vitro conditions reveals that copper(II) is essentially present as mixed complexes formed with the amino acids of the culture medium, [Cu(glutamine)(histidine)] being the main species. It was found that the cytotoxic activity is related to the amount of copper(II) contained in the tested compounds.

Acetates↗
PubMed1993

Determination of superoxide dismutase-like activity of copper(II) complexes. Relevance of the speciation for the correct interpretation of in vitro O2- scavenger activity.

The superoxide dismutase activity of several copper(II) complexes of linear and cyclic dipeptides has been measured. The results of a classic indirect method (xanthine-xanthine oxidase) have been compared with those obtained by generation of the superoxide radical through 2-(3-benzoylphenyl)propionic acid (ketoprofen) photolysis. A simulation approach, based on the knowledge of the stability constants of the different complex species existing in experimental conditions, has allowed us to obtain the correct speciation and to use these data to calculate the pertinent catalytic constants.

Catalysis↗
PubMed1995

1H and 31P NMR study of speciation in systems containing ADP, Al3+, and fluoride.

It has been proposed that AlF4- can serve as a tetrahedral pseudophosphate bound to guanosine diphosphate (GDP) [or other nucleoside diphosphates (NDP)] in G-protein systems. In a previous paper [D. J. Nelson and R. B. Martin, J. Inorg. Biochem. 43, 37 (1991)], 19F and 1H NMR were used to analyze the ternary system Al(3+)-NDP-F- in aqueous solutions. Ternary complexes (NDP)AlFx (with x = 1-3) were identified, but no (NDP)AlF4 was found. In this paper, the equilibrium constants for ternary complex formation that were obtained in the previous paper were further tested in a more extensive 1H and 31P NMR study of speciation in systems that contained Al3+, F-, and adenosine 5'-diphosphate (ADP). The results of the study are in general support of previously derived constants for ternary complexes and also provide support for the existence at relatively high ADP concentration (approximately 10 mM) of a base-stacked intermolecular dihydroxy-di-Al3+ bridged ADP dimeric structure at an ADP to Al3+ molar ratio of 1:1. 31P NMR of the dimer reveals that each of the two Al3+ ions is bidentately coordinated to the alpha and beta phosphates of a single (but different) ADP molecule. Evidence is also presented for the existence at relatively low ADP concentration (approximately 0.5 mM) of a monomeric species in which a single Al3+ ion is coordinated to alpha and beta phosphates of a single ADP molecule. 1H NMR of the monomeric species reveals the expected "wrong-way chemical shift" of the adenine C8 proton upon Al3+ ion complexation to the phosphate chain.

Adenosine Diphosphate↗
PubMed1996

The speciation of lysine-complexed copper as a bovine nutritional supplement.

Copper deficiencies in ruminants can be corrected by administering either free (inorganic) or complexed (chelated) copper. Chelated forms are thought to be more bioavailable as they are more stable, and may therefore be absorbed intact. Formation constants for the complexes between copper and the different ligands in the digestive tract can be used to predict if the chelate does, in fact, remain intact. Using a gravimetric autotitrator, the various complex formation constants for the copper(II) lysine system were determined at 38 degrees C, the temperature of the rumen environment. Formation constants for copper(II) complexes with the amino acids glycine and histidine were also determined at 25 and 38 degrees C. The formation constants for the copper(II) lysine system were then utilized in computer simulations to determine the fate of the complex prior to arriving at the rumen. The speciation of the copper(II) lysine system was determined in McDougall's solution, a simulated form of bovine saliva. Results suggest that if copper is administered as copper lysine "chelate," this will disintegrate and the copper will be present mainly as carbonate and phosphate complexes.

Animal Feed↗
PubMed1988

Aluminium speciation in surface waters from a Welsh upland area.

The complete aluminium speciation of surface waters from an acidified catchment, during dry weather and during storm episodes, is obtained. For the first time, estimates of adsorbed aluminium (Al(ad)) are reported together with other aluminium species. Al(ad) is calculated from the difference between monomeric aluminium content before and after separation of suspended solids by filtration (0.015 microm pore diameter). This fraction was very significant (Al(ad) >; 40 microg litre(-1)) for samples with high suspended solids content (ss >; 20 mg litre(-1)) collected during storm episodes. Plots of pAl(3+) versus pH for samples collected during dry weather are approximated by a straight line, close to the solubility line of synthetic gibbsite, and have a slope of 2.5, which suggests that these samples were saturated with respect to gibbsite. The cloud of pAl(3+) versus pH points for samples from storm episodes has a near zero slope, and shows a significant degree of undersaturation with respect to synthetic gibbsite. Various mechanisms of aluminium mobilisation are discussed.

Journal Article↗
PubMed1989

Phthalate ester speciation in estuarine water, suspended particulates and sediments.

Following earlier work (Al-Omran & Preston, 1987) in which phthalate ester speciation was examined in laboratory studies, the present paper describes the results of an attempt to validate the results by field measurements in the River Mersey Estuary, Liverpool, UK. Samples of water, suspended solids and sediments were analysed for their phthalate ester content. Solid samples were also analysed for their carbon, organic carbon and lipid content. A comparison of the field and laboratory results confirms the association between diethylhexyl phthalate and small particles and shows that other phthalates tend to be associated with relatively coarse, lipid-rich particles. Partition coefficients between dissolved phthalate esters and suspended particles are calculated and compared with other laboratory studies.

Journal Article↗
PubMed1983

Physicochemical speciation of toxic fractions of wastewaters.

A physicochemical speciation scheme in tandem with bioassays identified the toxic fractions of the wastewater from a base metal refining and fertilizer complex. The toxic fractions were the leachates from suspended solids, purgeables, and bound metals of the dissolved fraction. Most of the metals were bound to macrosolutes of Mr greater than 30,000 and exchangeable by cation- and weak anion-exchange resins. In contrast, total chromium and surfactants were bound strongly to microsolutes of Mr less than 1500, removable only by strong anion-exchange resin.

Animals↗
PubMed1983

Aeromonas species in clinical microbiology: significance, epidemiology, and speciation.

Over a one-year period, 32 strains (31 clinical, 1 environmental) of Aeromonas sp. were recovered. Chief sources of isolation were the gastrointestinal tract (48%), wounds (19%), and blood (13%). Gastrointestinal isolates were most often recovered from young (less than 5 yrs) children with diarrhea; wound or blood isolates were recovered more often from an older (avg. 56 yrs) population with one of several underlying disorders. Regardless of body site of isolation, most strains of Aeromonas appeared to be community acquired and not nosocomially transmitted. Over 70% of all isolates recovered during this year period were isolated during summer or fall months, suggesting a seasonal distribution of this microorganism. Speciation of Aeromonas isolates revealed A. hydrophila to be the predominant species isolated from clinical specimens, although significant percentages of other Aeromonas sp. were also recovered from clinical material.

Adult↗
PubMed1993

Toxicity, bioavailability and metal speciation.

1. Environmental toxicology emphasizes the difference from traditional toxicology in which pure compounds of interest are added to purified diets, or injected into the test animals. When the objective is to study the fate and effects of trace elements in the environment, knowledge of the speciation of the elements and their physico-chemical forms is important. 2. Cadmium salts such as the sulfides, carbonates or oxides, are practically insoluble in water. However, these can be converted to water-soluble salts in nature under the influence of oxygen and acids. Chronic exposure to Cd is associated with renal toxicity in humans once a critical body burden is reached. 3. The solubility of As(III) oxide in water is fairly low, but high in either acid or alkali. In water, arsenic is usually in the form of the arsenate or arsenite. As(III) is systemically more poisonous than the As(V), and As(V) is reduced to the As(III) form before exerting any toxic effects. Organic arsenicals also exert their toxic effects in vivo in animals by first metabolizing to the trivalent arsenoxide form. Some methyl arsenic compounds, such as di- and trimethylarsines, occur naturally as a consequence of biological activity. The toxic effect of arsenite can be potentiated by dithiols, while As has a protective effect against the toxicity of a variety of forms of Se in several species. 4. Selenium occurs in several oxidation states and many selenium analogues of organic sulfur compounds exist in nature. Selenium in selenate form occurs in alkaline soils, where it is soluble and easily available to plants. Selenite binds tightly to iron and aluminum oxides and thus is quite insoluble in soils. Hydrogen selenide is a very toxic gas at room temperature. The methylated forms of Se are much less toxic for the organism than selenite. However, the methylated Se derivatives have strong synergistic toxicity with other minerals such as arsenic. 5. Aquatic organisms absorb and retain Hg in the tissues, as methylmercury, although most of the environmental Hg to which they are exposed is inorganic. The methylmercury in fish arises from the bacterial methylation of inorganic Hg. Methylmercury in the human diet is almost completely absorbed into the bloodstream. The nervous system is the principal target tissue affected by methylmercury in adult human beings, while kidney is the critical organ following the ingestion of Hg(II) salts.

Animals↗
PubMed2004

Bioavailability of silver and its relationship to ionoregulation and silver speciation across a range of salinities in the gulf toadfish (Opsanus beta).

Silver is taken up as a Na(+) analog (Ag(+)) by freshwater organisms, but little is known about its bioavailability in relation to salinity. Adult Opsanus beta were acclimated to 2.5, 5, 10, 20, 40, 60, 80, and 100% seawater (Cl(-)=545 mM) and exposed for 24 h to 2.18 microg L(-1) silver as (110m)Ag-labelled AgNO(3), a concentration close to the U.S. EPA marine criterion and less than 0.1% of the acute 96-h LC50 in seawater. Plasma osmolality, Na(+), and Cl(-) remained approximately constant from 100% down to 20-40% seawater, thereafter declining to 89% (osmolality) and 82% (Na(+), Cl(-)) of seawater values at the lowest salinity (2.5% seawater), while plasma Mg(2+) was invariant. Ionic measurements in intestinal fluids and urine supported the view that above the isosmotic point (about 32% seawater), toadfish drink the medium, absorb Na(+), Cl(-), and water across the gastrointestinal tract, actively excrete Na(+) and Cl(-) across the gills, and secrete Mg(2+) into the urine. Below this point, toadfish appear to stop drinking, actively take up Na(+) and Cl(-) at the gills, and retain ions at the kidney. Silver accumulation varied greatly with salinity, by nine-fold (whole body), 26-fold (gill tissue), and 18-fold (liver), with the maxima occurring in 2.5% seawater, the minima in 40% seawater (close to the isosmotic point), and slightly greater values at higher salinities. Highest silver concentrations occurred in liver, second highest in gills, intermediate concentrations in kidney, spleen, and gastrointestinal tissues, and lowest in swim bladder and white muscle, though patterns changed with salinity. There were substantial biliary but minimal urinary levels of silver. The salinity-dependent pattern of silver accumulation best correlated with the abundance of the neutral complex AgCl(0), though the presence of small amounts of Ag(+) at the lowest salinities may also have been important. In contrast, silver accumulation in the esophagus-stomach was greatest in 100% seawater and least at the isosmotic salinity (five-fold variation), a pattern probably explained by drinking and silver uptake into the blood through the gills. Models of silver bioavailability across salinity must consider the presence of silver-binding ligands on both gills and gastrointestinal tract, changing silver speciation, and the changing ionoregulatory physiology of the organism.

Animals↗
PubMed2005

Evaluation of the speciation status of aluminium(III) ions in isolated osteoarthritic knee-joint synovial fluid.

High field 1H NMR spectroscopy demonstrated that the equilibration of added Al(III) ions in osteoarthritic (OA) knee-joint synovial fluid (SF) resulted in its complexation by citrate and, to a much lesser extent, tyrosine and histidine. The ability of these ligands, together with inorganic phosphate, to compete for the available Al(III) in terms of (1) thermodynamic equilibrium constants for the formation of their complexes and (2) their SF concentrations was probed through the use of computer speciation calculations, which considered low-molecular-mass binary and ternary Al(III) species, the predominant Al(III) plasma transport protein transferrin, and also relevant hydrolysis and precipitation processes. It was found that, at relatively low added Al(III) concentrations, citrate species were more favoured, whilst phosphate species became dominant at higher levels. The significance of these findings with regard to the in vivo corrosion of aluminium-containing metal alloy joint prostheses (e.g., TiAlV alloys) is discussed.

Aluminum↗
PubMed2005

Speciation of phytate ion in aqueous solution. Dimethyltin(IV) interactions in NaCl(aq) at different ionic strengths.

As the introduction of a systematic study on the sequestering ability of phytate (Phy) towards heavy metal and organometal cations, this paper describes the results of an investigation (at t=25 degrees C by potentiometry, ISE-H(+) glass electrode) of its interactions with dimethyltin(IV) cation [(CH(3))(2)Sn(2+), DMT] in NaCl aqueous solutions at different ionic strengths (0.1< or =I (mol L(-1))< or =1), in the pH range 2.5< or =pH< or =8.5 and considering metal to ligand ratios 1:1< or =DMT:Phy< or =4:1. We observed the formation of 18 DMT(i)H(j)Phy((12-2i-j)-) species: with i=1 and 0< or =j< or =7; i=2 and 0< or =j< or =5; i=3 and 0< or =j< or =3. Their complex formation constant values are fairly dependent on ionic strength and this dependence was modeled by a Debye-Hückel type equation. The speciation of phytic acid and dimethyltin(IV) is also dependent on the metal to ligand ratio; the dependence of the stability of phytate-dimethyltin(IV) species on both the phytate protonation step and the number of cations bound to the ligand has been modeled and an empirical predictive relationship is also proposed. From the results obtained it emerged that phytate has very good sequestering ability towards (CH(3))(2)Sn(2+). Comparisons are made with other ligands, such as ethylenediamine-N,N,N',N'-tetraacetic acid (EDTA) and phosphate.

Hydrogen-Ion Concentration↗
PubMed2006

Speciation of phytate ion in aqueous solution. Sequestration of magnesium and calcium by phytate at different temperatures and ionic strengths, in NaCl(aq).

The formation and stability of Mg(2+) and Ca(2+)-phytate complexes was studied potentiometrically using an ISE-H(+) electrode. Measurements were performed at 10 degrees C and 25 degrees C in NaCl(aq) in the ionic strength range 0.1< or =I< or =0.75 mol L(-1). For both magnesium and calcium systems, the formation of ten M(i)PhyH(j)((12-2i-j)-) species was observed in the range 3< or =pH< or =7 with i=1, 2, 3 and j=3, 4, 5 (and i=3, j=2). These species are quite stable; here we report for example some quantitative data for the species Ca(i)PhyH(3)((9-2i)-), i=1, 2, 3 (equilibrium iCa(2+)+H(j)Phy((12-j)-)=Ca(i)PhyH(j)((12-j-2i)-): K(ij)) at I=0.25 mol L(-1) and t=25 degrees C: logK(13)=3.42, logK(23)=6.47 and logK(33)=9.41. The speciation of the Ca(2+)-phytate system was also checked by ISE-Ca(2+) measurements. Dependence on ionic strength was modeled using a simple Debye-Hückel type equation and formation constants were calculated at infinite dilution. The stability constants of complexes formed at pH>7 were estimated using an empirical predictive equation. The sequestering ability of phytate towards Mg(2+) and Ca(2+) was calculated in different experimental conditions and compared with those of other chelating agents.

Calcium↗
PubMed2004

Evaluation and standardisation of a simple HG-AAS method for rapid speciation of As(III) and As(V) in some contaminated groundwater samples of West Bengal, India.

A simple HG-AAS technique has been evaluated and standardised for rapid speciation of As(III) and As(V) in a number of contaminated groundwater samples of West Bengal, India. Citric acid has been used for selective hydride formation of As(III). The sensitivity of the evaluated HG-AAS method is 7.91 mg(-1)l, standard deviation, 0.001 and detection limit, 0.4 microg l(-1). As(III) sensitivity remains constant in the sample pH range of 2.3-10.6. Concomitant mineral matrix of the water samples did not interfere with arsenic determination. Eight out of ten groundwater samples analysed for As(IlI)and As(V) contain more As(III), which lies in the range of 54-350 ppb. As(III) estimation in drinking water along with total arsenic should be invoked as a policy for a realistic risk assessment of the contaminated water.

Arsenic↗
PubMed2004

Speciation of chromium in 12 agricultural soils from Turkey.

The objective of the study was to speciate and to evaluate various soil Cr species in relation to soil properties. Surface soil samples were taken from outskirts of the Cr factory and applied a sequential extraction procedure. Extracts analyzed in atomic absorption spectrophotometry (AAS). Chromium was partitioned into exchangeable Cr, Cr bound to carbonate, Fe-Mn oxide, and organic matter, and residual Cr. The most common form of chromium was in the residual form, followed by the organic form. Very low concentrations of Cr were found in the exchangeable and carbonate forms. Mean values of the extractable forms of Cr, expressed in percentages of total soil contents were: 0.94% exchangeable, 0.80% carbonates, 2.13% oxides, 7.08% organics and 89.81% residual. Multiple regression analysis of analytical data revealed that soil pH, contents of organic matter and calcium carbonate were the most important factor controlling the distribution of Cr forms determined.

Chromium↗
PubMed2005

Speciation and quantification of mercury in Oxisol, Ultisol, and Spodosol from Amazon (Manaus, Brazil).

In order to investigate the content and distribution of Hg in soils from Amazon areas not impacted by gold mining activities, the concentration and granulometric distribution of Hg were determined in three different types of soils. Hg speciation data were obtained by a thermodesorption atomic spectrometry system and the role of physico-chemical and mineralogical characteristics on Hg content were also studied. Hg concentrations found in the soil fraction <2000 microm were similar to values found in other Amazon areas without anthropogenic sources. The fine fraction (<53 microm) of podzolized soils had a higher Hg content than clayey soils. Multivariate analysis shows that there are marking differences between Spodosols of two distinct areas (fine fraction Hg contents up to 10-fold as high) indicating the importance of pedogenic processes. All statistical data analysis indicated that organic matter plays an important role in Hg accumulation in the types of soils studied. Thermodesorption analysis revealed the presence of only Hg2+, and the predominance of organically bound Hg in the majority of the studied samples.

Brazil↗
PubMed2005

Guidelines for routine mercury speciation analysis in seafood by gas chromatography coupled to a home-modified AFS detector. Application to the Andalusian coast (south Spain).

A home-modified atomic fluorescence detector (mAFS) has been employed for mercury and methylmercury determination in bivalves from the Andalusian coast (south Spain). This modification consists on the inclusion of a quartz flow cell into the detector, which increases the concentration of mercury atoms in the detector and therefore enhances sensitivity about two fold. Two analytical approaches for mercury speciation based on the coupling of gas chromatography on-line pyrolysis and mAFS (GC-Pyro-mAFS) have been tested. The first approach (Method 1) is based on aqueous ethylation followed by extraction into an organic solvent, and the second one (Method 2) in the extraction of monoalkylated mercury as chloride. Method 1 is a rapid procedure but not sensitive enough for the analysis of methylmercury in non-polluted sites (detection limit: 20 ng g(-1) as mercury, wet basis). The second one is quite more sensitive (detection limit: 0.2 ng g(-1), wet weight), but sample treatment is cumbersome and time-consuming. The optimum range for mercury determination for both methods are complementary and exhibit an overlapping measurable concentration range (OMCR) in which methylmercury can be indistinctly determined (75-100 ng g(-1) as mercury, wet basis). The suitability of both methods has been assayed with spiking experiences at levels within the OMCR with good recoveries. Both approaches have been validated with two certified reference materials (BCR-463, mercury and methylmercury in tuna fish; and NIST-2977, organic contaminants and trace metals in mussel tissue). Both procedures have been used for the analysis of three species of bivalve molluscs collected along the Andalusian coast (south Spain), all of them employed for human consumption (Chamelea gallina, Donax trunculus and Scrobicularia plana), and their potential use in routine analysis has been established.

Animals↗
PubMed2005

Size fractionated speciation of nitrate and sulfate aerosols in a sub-tropical industrial environment.

Size fractionated chemical speciation of acidic aerosols were performed for ammonium sulfate, other sulfates, ammonium nitrate and other nitrates in a sub-tropical industrial area, Bina, India during December 2003 to November 2004. Analysis of variance (ANOVA) revealed highly significant temporal variations (p > .001) in the concentrations of nitrate and sulfate aerosols in all the three size fractions (fine, mid-size and coarse). Winter demonstrated utmost concentrations of ammonium sulfate, which ranged from 3.2 to 26.4 microg m(-3) in fine particles and 0.20-0.34 microg m(-3) in coarse particles. Ammonium sulfate was chiefly in fine mode (43.77% of total particulate sulfate) as compared to coarse particles (28.60% of total particulate sulfate). The major fraction Ammonium sulfate existed in different forms in atmospheric aerosols, for example NH4Fe(SO4)2, (NH4)2SO4, (NH4)3H(SO4)2 in fine particles, and (NH4)4(NO3)SO4+ in coarse particles. Other sulfate concentrations were also higher during winter ranging from 1.89 to 14.3 microg m(-3) in fine particles and 0.12-0.65microg m(-3) in coarse particles. Ammonium nitrate constituted the major fraction of total particulate nitrate all through the year and was principally in fine particles (the highest concentration in January i.e. 14.2 microg m(-3)). Other nitrates were mainly distributed in the fine particles (highest concentration in January i.e. 11.2 microg m(-3)) All the sulfate and nitrate species were mainly distributed in fine mode and have significant impact on human health.

Aerosols↗