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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 8 (1994), S. 463-471 
    ISSN: 0268-2605
    Keywords: Arsenic ; organic arsenic ; C. roseus ; cells ; NMR ; biomolecules ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H spin-echo NMR spectroscopy of intact cells of C. roseus facilitates monitoring changes inside the cells on treatment with arsenicals. This in situ detection method is non-invasive and non-destructive in comparison to other available biochemical methods. Short term uptake of the arsinicals, methylarsinate MMA and dimethylarsenate DMA, by C. roseus cells that have reached stationary phase in 1-B5 medium, is followed by using NMR spectroscopy, and in particular, the Carr-Purcell-Meiboom-Gill pulse sequence. An increase in the peak height of the methylarsenic resonance over a period of 11 h is indicative of uptake of each arsenical. However, there is no evidence of any biotransformation products in the 1H NMR spectra. The accumulation site of DMA is probably the vacuole as is seen from the change in the chemical shift of DMA as it moves into a compartment of lower pH. Biochemical changes associated with the presence of arsenicals are evident in the 1H NMR spectra of C. roseus cells isolated at different stages in the growth cycle. Although uptake has been demonstrated by other analytical techniques, the resonances corresponding to both MMA and DMA are not observed in the 1H NMR spectra of cells growing in media containing each arsenical. The association of these arsenicals with large biomolecules in the cell may account for these absences. In this event, the spins-spin relaxation time of the arsenic species would shorten and the signals would not be seen in the spin-echo NMR spectrum. In cells growing in the presence of MMA, a new resonance is observed at a chemical shift position 2.2 ppm after 15 days of growth. The shift in position of the resonance, from 1.75 ppm expected at physiological pH, may indicate an altered environment around the arsenic species such as high intracellular acidity.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 2 (1988), S. 1-7 
    ISSN: 0268-2605
    Keywords: Organoarsenic ; analysis ; hydride generation ; photo-oxidation ; marine clams ; HPLC ; GFAA ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The separation of arylarsonic acids by HPLC on a reverse-phase C18 column is described. Solutions containing these arsenicals and others such as arsenobetaine are photo-oxidized to arsenate by ultraviolet (UV) radiation (1200 W, 1 h exposure). This allows the analysis of the solution for arsenic by hydride generation techniques. The method, UV HGAA, is developed and applied to the determination of arsenic in the methanol extracts of the Manila clam (Verupis japonica) and the Horse clam (Schizothoerus nutalli).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 369-379 
    ISSN: 0268-2605
    Keywords: efflux ; liposomes ; dimethylarsinic acid ; membrane modification ; egg phosphatidylcholine ; bilayer ; tributyltin chloride ; monobutyltin trichloride ; facilitated diffusion ; NMR ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The efflux of dimethylarsinic acid (DMA) from liposomes formed from egg phosphatidylcholine (EPC) is increased when tributyltin chloride (TBT) is added to the extraliposomal compartment; however the addition of monobutyltin trichloride (MBT) slows down the efflux. When the liposomes are prepared from EPC and organotin compounds, different mechanisms for DMA efflux seem to operate: TBT-EPC liposomes show a mixture of facilitated and passive diffusion; MBT-EPC liposomes show only passive diffusion. The facilitated diffusion of DMA- seems to be stopped by the addition of TBT to the extraliposomal compartment. © 1997 by John Wiley & Sons, Ltd.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 6 (1992), S. 207-211 
    ISSN: 0268-2605
    Keywords: Dimethylantimony ; trimethylantimony ; analysis ; hydride generation ; aquatic speciation ; GCAA ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reports in the literature that the compounds MeSb(O)(OH)2 and Me2Sb(O)(OH) are present in marine and fresh-waters need to be re-examined. The results of several synthetic strategies suggest that these methylantimony(V) compounds are either environmentally inaccessible or polymeric in nature. Pure samples of various di- and tri- methylated antimony(V) species were prepared and found to undergo molecular rearrangement reactions when subjected to hydride generation procedures typically used for aquatic speciation.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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