Počet záznamů: 1  

Intracellular retention of iodine-125 and astatine-211 labelled epidermal growth factor (EGF) in cultured A431 carcinoma cells

  1. 1.
    0185194 - UJF-V 20000368 RIV GB eng J - Článek v odborném periodiku
    Orlova, A. - Sjöström, A. - Lebeda, Ondřej - Lundquist, H. - Tolmachev, V.
    Intracellular retention of iodine-125 and astatine-211 labelled epidermal growth factor (EGF) in cultured A431 carcinoma cells.
    Nuclear Medicine Communications. Roč. 21, - (2000), s. 577. ISSN 0143-3636. E-ISSN 1473-5628
    Výzkumný záměr: CEZ:AV0Z1048901
    Kód oboru RIV: BG - Jaderná, atomová a mol. fyzika, urychlovače
    Impakt faktor: 1.039, rok: 2000

    The fact, that many tumours over-express receptors to epidermal growth factor (EGF), has led us to considered this molecule in targeted radionuclide therapy. In this study different radiohalogens and labelling methods were applied, the binding pattern and the intracellular retention in carcinoma A431 cells of .sup.125I-EGF, .sup.125I-para-iodo-benzoate-EGF (.sup.125I-PIB-EGF), and .sup.211 At-para-astato-benzoate-EGF (.sup.211At-PAB-EGF), were studied. All labelled molecules bound specifically to the A431 cells. The intracellular retention of radioactivity, after pulse labelling, was found to be about the same for the two iodine labels with biological half-life of 1.5-2h. The astatine label gave a prolonged intracellular retention (biological half-life about 3.5 h) in comparison with radioiodine. Whenthe cells where incubated continuously with the labelled ligands, maximum accumulation was obtained later for the astatine label (about 6h) than for both iodine labels (2-4h).=Since the maximum accumulation is reached when the rate ofbinding is equal to the rate of efflux of degraded conjugate, the shift of the maximum position indicates that the excretion of astatine is slower than iodine labels. In conclusion, the use of non-phenolic linker did not improve intracellular retention of radioactivity. The improved intracellular retention of the astatine might be attributed to binding of radioactive catabolites to cellular proteins.
    Trvalý link: http://hdl.handle.net/11104/0081605

     
     

Počet záznamů: 1  

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