1. Synthesis, characterization, and cytotoxicity of dinuclear platinum-bisphosphonate complexes to be used as prodrugs in the local treatment of bone tumours
- Author
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Giovanni Natile, Nicola Margiotta, Valentina Gandin, Cristina Marzano, Sara Piccinonna, and Rosa Ostuni
- Subjects
Magnetic Resonance Spectroscopy ,Stereochemistry ,medicine.medical_treatment ,chemistry.chemical_element ,Antineoplastic Agents ,Bone Neoplasms ,Context (language use) ,Inorganic Chemistry ,Coordination Complexes ,Cell Line, Tumor ,medicine ,Humans ,Prodrugs ,Cytotoxicity ,Platinum ,Cisplatin ,Diphosphonates ,Bridging ligand ,Prodrug ,Bisphosphonate ,chemistry ,Drug Resistance, Neoplasm ,Drug Screening Assays, Antitumor ,medicine.drug - Abstract
For over 30 years cisplatin has been one of the most active antitumour agents in clinical use, nevertheless research for overcoming cisplatin toxicity and resistance or for improving its efficacy has never ceased. In this context we have recently proposed dinuclear Pt complexes with bridging geminal bisphosphonates as novel Pt-prodrugs with potential activity at the bone surface after embedment in inorganic matrices and implantation at the tumour site. In the present paper we report the synthesis and full characterization of four new platinum complexes having a dinuclear structure with a bisphosphonate (2-ammonium-1-hydroxyethane-1,1-diyl-bisphosphonate or 3-ammonium-1-hydroxypropane-1,1-diyl-bisphosphonate, AHBP-H and PAM-H, respectively) acting as a bridging ligand between two platinum moieties (cis-[Pt(NH(3))(2)](2+), directly related to cisplatin, and [Pt(cis-1,4-DACH)](2+), known to be able to overcome the cisplatin resistance). Moreover, as a preliminary investigation, the in vitro cytotoxicity of the new complexes has been evaluated on a panel of 13 human tumour cell lines including cisplatin- and multidrug-resistant sublines.
- Published
- 2009
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