科研之友
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摘要
Within the last years Zr-89 has attracted considerable attention as long-lived radionuclide for positron emission tomography (PET) applications. So far desferrioxamine B (DFO) has been mainly used as bifunctional chelating system. Fusarinine C (FSC), having complexing properties comparable to DFO, was expected to be an alternative with potentially higher stability due to its cyclic structure. In this study, as proof of principle, various FSC-RGD conjugates targeting alpha(v)beta(3) integrins were synthesized using different conjugation strategies and labeled with Zr-89. In vitro stability, biodistribution, and microPET/CT imaging were evaluated using [Zr-89]FSC-RGD conjugates or [Zr-89]triacetylfusarinine C (TAFC). Quantitative Zr-89 labeling was achieved within 90 min at room temperature. The distribution coefficients of the different radioligands indicate hydrophilic character. Compared to [Zr-89]DFO, [Zr-89]FSC derivatives showed excellent in vitro stability and resistance against transchelation in phosphate buffered saline (PBS), ethylenediaminetetraacetic acid solution (EDTA), and human serum for up to 7 days. Cell binding studies and biodistribution as well as microPET/CT imaging experiments showed efficient receptor-specific targeting of [Zr-89]FSC-RGD conjugates. No bone uptake was observed analyzing PET images indicating high in vivo stability. These findings indicate that FSC is a highly promising chelator for the development of Zr-89-based PET imaging agents.
