Synthesis and Analysis of the Structure,Diffusion and Cytotoxicity of Heterocyclic Platinum(IV) Complexes |
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Authors: | Freddy J Macias Krishant M Deo Benjamin J Pages Prof Paul Wormell Dr Jack K Clegg Dr Yingjie Zhang Dr Feng Li Dr Gang Zheng Dr Jennette Sakoff Dr Jayne Gilbert Prof Janice R Aldrich‐Wright |
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Institution: | 1. Nanoscale Organisation and Dynamics Group, Western Sydney University, Campbelltown, NSW 2560 (Australia);2. School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane St. Lucia, QLD 4072 (Australia);3. Australian Nuclear Science and Technology Organisation, Kirrawee DC, NSW 2232 (Australia);4. Calvary Mater Newcastle, Waratah, NSW 2298 (Australia) |
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Abstract: | We have developed six dihydroxidoplatinum(IV) compounds with cytotoxic potential. Each derived from active platinum(II) species, these complexes consist of a heterocyclic ligand (HL) and ancillary ligand (AL) in the form Pt(HL)(AL)(OH)2]2+, where HL is a methyl‐functionalised variant of 1,10‐phenanthroline and AL is the S,S or R,R isomer of 1,2‐diaminocyclohexane. NMR characterisation and X‐ray diffraction studies clearly confirmed the coordination geometry of the octahedral platinum(IV) complexes. The self‐stacking of these complexes was determined using pulsed gradient stimulated echo nuclear magnetic resonance. The self‐association behaviour of square planar platinum(II) complexes is largely dependent on concentration, whereas platinum(IV) complexes do not aggregate under the same conditions, possibly due to the presence of axial ligands. The cytotoxicity of the most active complex, exhibited in several cell lines, has been retained in the platinum(IV) form. |
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Keywords: | antitumor agents cancer cytotoxicity platinum X‐ray diffraction |
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