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Bis-conjugation of Bioactive Molecules to Cisplatin-like Complexes through (2,2 '-Bipyridine)-4,4 '-Dicarboxylic Acid with Optimal Cytotoxicity Profile Provided by the Combination Ethacrynic Acid/Flurbiprofen

Title
Bis-conjugation of Bioactive Molecules to Cisplatin-like Complexes through (2,2 '-Bipyridine)-4,4 '-Dicarboxylic Acid with Optimal Cytotoxicity Profile Provided by the Combination Ethacrynic Acid/Flurbiprofen
Type
Article in International Scientific Journal
Year
2020
Authors
Biancalana, L
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Batchelor, LK
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Pereira, SAP
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Tseng, PJ
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Zacchini, S
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Pampaloni, G
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Lucia L M F S Saraiva
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Dyson, PJ
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Marchetti, F
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Journal
ISSN: 0947-6539
Publisher: Wiley-Blackwell
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Authenticus ID: P-00T-32H
Abstract (EN): A facile route to Pt-II complexes doubly functionalized with bioactive molecules through a bipyridine-type ligand is described. Initially, ligands L-EE (containing two ethacrynic acid units), L-EF (ethacrynic acid+flurbiprofen) and L-EB (ethacrynic acid+biotin) were obtained in moderate to good yields from 2,2 '-bipyridine-4,4 '-dicarboxylic acid. Subsequent reaction of the ligands with [PtCl2(DMSO)(2)] afforded complexes [PtCl2(L-EE)] (2), [PtCl2(L-EF)] (3) and [PtCl2(L-EB)] (4) in high yields. All compounds were fully characterized by analytical and spectroscopic methods. Complexes 2-4 are highly stable in water/DMSO solution at 37 degrees C after 72 h, whereas progressive release of the bioactive fragments was detected in a cell culture medium. The compounds were assessed for their in vitro antiproliferative activity towards tumorigenic A2780, A2780cisR and Y79 cells and non-tumourigenic HEK293 cells. In particular, the combination of ethacrynic acid and flurbiprofen in 3 overcomes cisplatin-based resistance and provides strong cancer cell selectivity. Enzyme inhibition assays on human GST P1 and human COX-2 and cross-experiments with complex 1, analogous to 2-4 but lacking bio-groups, revealed a clear synergy between the Pt-II frame and the bioactive organic components.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 12
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