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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 9 (1995), S. 327-334 
    ISSN: 0268-2605
    Keywords: mercury ; methylmercury ; tin ; tributyltin ; bioconcentration ; distribution ; kinetics ; starfish ; Leptasterias polaris ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Starfish, Leptasterias polaris, were exposed between 30 min and 48 h to seawater containing 0.25 nmol dm-3 of radiolabelled methylmercury (Me203HgCI), tributyltin [(C4H9)3113SnCI], and inorganic 203HgCI2 and 113SnCI4, with the objectives of comparing the uptake and distribution kinetics of these metal species in organs and tissues of treated organisms. Some starfish exposed to metals for 48 h were allowed to depurate for 24 h in clean seawater. Whole-body autoradiography was used to locate radiotracers very precisely within starfish tissues. The total amount of methylmercury (MeHg) accumulated in the whole animal after 48 h reached 0.53 nmol compared with 0.09 nmol for inorganic mercury, while tributyltin (TBT) reached 0.72 nmol compared with 0.017 nmol for inorganic tin. No significant reduction of body burdens occurred during the depuration period. The first-order rate constant characterizing the uptake of metals by whole animals, k1, ranged from 0.102 h-1 for MeHg to 3.6 × 10-3h-1 for inorganic mercury(II) and to 8.4 × 10-4 h-1 for inorganic tin(IV). The first-order rate constant characterizing the translocation of metals from seawater-exposed tissues toward internal organs, k3, was available for inorganic Hg and Sn and had values similar to k1. Concentration ratios between external tissues and internal organs after a 48 h exposure were 11.5 and 25.4 for MeHg and TBT, respectively, and 2.1 and 6.1 for inorganic mercury and tin. Furthermore, autoradiograms showed that MeHg and TBT were accumulated only on the external surface of the body wall and podia. This finding indicates a much slower translocation process for organometallic species than inorganic species, a process which seems to be related to the binding mode of MeHg and TBT to the organic matrix of external tissues of starfish.
    Additional Material: 4 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 12 (1998), S. 435-438 
    ISSN: 0268-2605
    Keywords: tributyltin ; radiolabelling ; 113Sn ; synthesis ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method of synthesis of tributyl[113Sn]tin,­(n/C4H9)3113Sn(IV), from commercially avail-­able inorganic 113Sn(IV) is presented. Inorganic tin is first extracted in diethyl ether and reacted with C4H9MgCl to produce tetrabutyltin, (C4H9)4113Sn, which is then debutylated with HgCl2. The resulting tributyl[113Sn]tin chloride is isolated from the reaction mixture by successive extractions with hexane and aqueous Na2S2O3. The yield is 40-60% and the product obtained is 〉98% pure. It has the same specific activity as the starting 113Sn(IV), i.e. up to 550 MBq mg-1 Sn, making it suitable for use in environmental fate and toxicology studies at concentrations relevant of those found in the aquatic environment. © 1998 John Wiley & Sons, Ltd.
    Additional Material: 2 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. 751-753 
    ISSN: 0268-2605
    Keywords: methylmercury ; radioactive ; synthesis ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple and fast synthesis of radioactive methylmercury is presented. It is based on the methylation of inorganic 203Hg(II) by methylcobalamin and isolation of resulting CH3203Hg(II) in a single extraction step. Time required is less than 4 hours and the final yield is ≥90%. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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