Synthesis and Anticancer Activity of Oral Pt(IV) Prodrugs Containing α-furancarboxylate as an Axial Ligand

Abstract

Background:: The clinical applications of platinum-based anticancer drugs are largely compromised by side effects and drug resistance. Therefore, novel platinum-based anticancer drugs with improved injected or oral therapeutic index and low resistance need to be developed. background: The clinical applications of platinum-based anticancer drugs are largely compromised by side effects anddrug resistance. Therefore, novel platinum-based anticancer drugs with improved injected or oral therapeutic index and low resistance need to be developed. Objective:: This study aimed at the synthesis and anticancer activity testing of Pt(IV) prodrugs containing α-furancarboxylate as an axial ligand. This would pave the way for obtaining novel Pt(IV) prodrugs with better anticancer activity by comparing the anticancer activity with their parent platinum( II) complexes. objective: This study aimed at the synthesis, anticancer activity testing of Pt(IV) prodrugs containing α-furancarboxylate as an axial ligand. This would pave way for obtaining novel Pt(IV) prodrugs with better anticancer activity by comparing the anticancer activity with their parent platinum(II) complexes. Methods:: In this study, synthesis, in vitro cytoxicity assay, and in vivo anticancer activity evaluation of three Pt(IV) complexes, cis,trans,cis-[Pt(NH3)2(OH)(α-furancarboxylato)Cl2] (FPt-1), cis,trans,cis- [Pt(NH3)2(OH)(α-furancarboxylato)(1,1'-cylobutanedicarboxylato)] (FPt-2), and cis,trans,cis- [Pt(1R,2R-diaminocyclohexane)(OH)(α-furancarboxylato)(C2O4)] (FPt-3), were carried out. Results:: Three Pt(IV) complexes exhibited considerable cytoxicity against the tested human cancer cells (MCF-7, A549 and HCT116), which was found to be slightly lower than the corresponding Pt(II) drugs. However, FPt-1 and FPt-3 displayed comparable antitumor efficacy to cisplatin and oxaliplatin in the murine S180 sarcoma model after intraperitoneal administration. More importantly, the intragastric administration test indicated the antitumor efficacy of FPt-3 to be much greater than oxaliplatin. result: Three Pt(IV) complexes exhibit considerable cytoxicity against the tested human cancer cells (MCF-7, A549 and HCT116), lower than the corresponding Pt(II) drugs. However, FPt-1 and FPt-3 display comparable antitumor efficacy to cisplatin and oxaliplatin in murine S180 sarcoma model after intraperitoneal administration. More importantly, intragastric administration test indicates that the antitumor efficacy of FPt-3 is much greater than oxaliplatin. Conclusion:: FPt-3 has shown excellent oral antitumor activity and it could be administrated in an oral dosage form. other: No.