Abstract
Novel platinum(IV) complexes were synthesised to examine the facile modulation of the lipophilicity of the complex by incorporating axial ligands of increasing length, ranging from 2–6 carbons. RP-HPLC was used to establish the lipophilicity of each complex. The in vitro cytotoxicities of all complexes were determined against a panel of malignant cell lines and a non-cancerous cell line. While there was no clear correlation between lipophilicity and cytotoxicity, all complexes demonstrated nanomolar activity against all cell lines. The most potent complexes exhibited 850-fold greater activity than cisplatin against HT29 colon carcinoma with GI50 values of 13 nM.
Original language | English |
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Pages (from-to) | 17217-17227 |
Number of pages | 11 |
Journal | Dalton Transactions |
Volume | 48 |
Issue number | 46 |
DOIs | |
Publication status | Published - 2019 |
Keywords
- drug lipophilicity
- platinum compounds
- therapeutic use