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  • 1
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 40 (1992), S. 2488-2492 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 39 (1991), S. 797-800 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 107 (1976), S. 1391-1411 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The mass, IR- and NMR-spectra of 18 compounds were interpreted; one of these compounds has been15N-labelled. Fragmentation processes give evidence that azo- and hydrazone-tautomeres are present in the gaseous state. IR-and NMR-spectroscopic investigations show, that the phenyl-hydrazones as solids and in solution exist as bis chelated (Z)-isomers only. An approximately linear relationship is given between the chemical shifts of NH-Protons and pK B-and Hammett σ-values resp.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1436-5073
    Keywords: Preconcentration ; third phase ; trace elements ; ICP-AES
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A preconcentration method based on third phase extraction has been developed and combined with inductively coupled plasma atomic emission spectrometry (ICP-AES) for determination of Sb, Pb, Tl at trace levels in water samples. The reagents diantipyrylmethane and potassium iodide were applied for complexing Sb, Pb, Tl and producing a third phase extraction system. This third phase system produces relatively large enrichment factors and complete isolation of trace elements from high salt-containing matrices which influence strongly the plasma condition. Experimental parameters of the extraction, such as concentrations of complexing reagents, pH and extraction time have been optimized. Under the selected conditions, this third phase ICP-AES combination procedure gave multielemental detection limits for Sb, Pb, Tl which are superior by an order of magnitude or more to those obtained by ICP-AES alone without preconcentration. Precision of the technique is better than 10% at the 10 μg/l level. The accuracy of this approach is demonstrated by its application to tapwater, artificial seawater and reference seawater samples.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A method for the determination of hydrogen peroxide and several organic peroxides by high-performance liquid chromatography with post-column UV irradiation, derivatization and fluorescence detection is described. By means of post-column UV irradiation in the presence of water organic peroxides are converted into hydrogen peroxide and organic hydroperoxides, which react rapidly with the post-column derivatization agent p-hydroxyphenylacetic acid (PHPAA) under catalysis of horseradish peroxidase to yield the fluorescent PHPAA dimer that is detected at excitation and emission wavelengths of 285 and 400 nm, respectively. The detection limit for hydrogen peroxide is 14 ng/mL, for organic peroxides between 34 ng/mL and 5 μg/mL. No interference by other compounds was observed when their concentrations were below 10 mg/mL except ethers and phenols.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract None of the reaction products of ozone and DNPH immobilized on solid phase support have been identified yet. However, they can interfere with the determination of carbonyl compounds in ozone containing air when analysis is performed by sampling and derivatization with DNPH coated silica cartridges. To elucidate the structure of these compounds, DNPH silica cartridges were treated with synthetic air containing defined concentrations of ozone and eluted with acetonitrile. The products were characterized by HPLC-UV/Vis and nuclear magnetic resonance (NMR) spectroscopy. Three of the degradation products were identified as 2,4-dinitrophenol, 2,4-dinitroaniline and 1,3-dinitrobenzene. The identification was confirmed by comparison with commercially available standard compounds. The other elutable products were characterized as substituted aromatic compounds. The formation of all characterized products is consistent with a radical mechanism which has been previously discussed in the literature.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The quality of the aquatic and marine environment can be monitored by the determination of pollutants in organisms living in this environment. Certified reference materials and well-organised proficiency tests are powerful means of ensuring a constant level of quality and verifying the correct application of standardised methods. The preparation of a tuna fish proficiency testing material for the evaluation of quality of As and Hg monitoring in seafood is described. Preparation and characterisation of the material as well as studies on its homogeneity and stability are described. Concentrations of 3.4 ± 0.2 mg/kg total arsenic and 2.91 ± 0.09 mg/kg total mercury have been determined as target values. Moreover indicative values for some trace elements (Cd, Cu, Ni, Pb, Sr) and some major constituents (Al, Br, C, Ca, Cl, Fe, H, K, Mg, N, Na, P, S, Si, Zn) have also been measured.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Archives of toxicology 66 (1992), S. 471-477 
    ISSN: 1432-0738
    Keywords: 2,3,7,8-Tetrachlorodibenzo-p-dioxin ; 1,2,3,7,8-Pentachlorodibenzo-p-dioxin ; 1,2,3,4,7,8-hex achlorodibenzo-p-dioxin ; 1,2,3,4,6,7,8-Heptachlorodibenzo-p-dioxin ; Acute toxicity ; Mixture ; Structure-activity relationship ; Toxic equivalency factor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract There is presently no scientifically proven method to assess the toxicity of environmental samples containing complex mixtures of chlorinated dibenzo-p-dioxins (CDDs) of known composition. Their risk assessment is currently based on the interim concept of toxicity equivalency factors (TEFs), with the unproven assumption that all interactions of CDDs are additive. To address this problem we conducted acute toxicity studies with four different CDDs, viz 2,3,7,8-tetrachlorodibenzo-p-dioxin (tetra-CDD), 1,2,3,7,8-pentachlorodibenzo-p-dioxin (penta-CDD), 1,2,3,4,7,8-hexachlorodibenzo-p-dioxin (hexa-CDD) and 1,2,3,4,6,7,8-heptachlorodibenzo-p-dioxin (hepta-CDD), all containing chlorine substituents in the crucial 2,3,7,8-positions. The homologues, dissolved in corn oil/acetone, were administered to groups of five male Sprague Dawley rats at several doses (at least three) by gastric intubation. The obtained mortality data were employed to calculate the LD20,50 and80 for each homologue. These data were subsequently used to prepare equipotent doses (expected mortality of 20, 50 and 80%) of a mixture containing all four homologues, each of them contributing one fourth of the toxicity, under the assumption of additive toxicity. The obtained LD50 value and (TEF) was for tetra-CDD 43 μg/kg (1), penta-CDD 206 μg/kg (0.2) hexa-CDD 887 μg/kg (0.05) and hepta-CDD 6325 μg/kg (0.007), respectively. The dose-response to the mixture confirmed the hypothesis of strict additivity in the acute toxicity of the four CDD homologues.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-0738
    Keywords: 2,3,7,8-Tetrachlorodibenzo-p-dioxin ; 1,2,3,7,8-Pentachlorodibenzo-p-dioxin ; 1,2,3,4,7,8-Hexachlorodibenzo-p-dioxin ; 1,2,3,4,6,7,8-Heptachlorodibenzo-p-dioxin ; Mixture ; Structure-activity relationship ; Acute toxicity ; Phosphoenolpyruvate carboxykinase ; Pyruvate carboxylase ; γ-Glutamyl transpeptidase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Male Sprague-Dawley rats were treated with an LD20, LD50 and LD80 respectively, of tetra-, penta-, hexa-,hepta-CDD and a mixture of the four CDDs, all carrying chlorine substituents in the biologically crucial 2, 3, 7, and 8 positions. Specific activities of two key enzymes of gluconeogenesis, viz, phosphoenolpyruvate carboxykinase (PEPCK) and pyruvate carboxylase (PC), as well as the activity of the preneoplastic marker enzyme γ-glutamyl transpeptidase (γ-GT), were determined in livers of CDD-treated and ad libitum-fed control animals. PEPCK activity showed evidence for dose-related inhibition on the second day after dosing; PC activity was slightly reduced, whereas γ-GT activity was dose-dependently inhibited. By 8 days after dosing PEPCK activities were dose-dependently decreased after administration of all four CDDs and their mixture. PC activities were significantly reduced, but no dose-response was evident. The activity of γ-GT was dosedependently inhibited, but only to a value of 25% below control activities. It is concluded that CDDs share a common mechanism of acute toxicity, viz, inhibition of glucocorticoid-dependent enzymes which results in a derailment of intermediary metabolism not compatible with survival of the animals.
    Type of Medium: Electronic Resource
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