Pt(II)-BODIPY complexes combine the chemotherapeutic activity of Pt(II) with the photocytotoxicity of BODIPYs. Additional conjugation with targeting ligands can boost the uptake by cancer cells that overexpress the corresponding receptors. We describe two Pt(II) triangles, and , built with pyridyl BODIPYs functionalized with glucose () or triethylene glycol methyl ether (), respectively. Both and showed higher singlet oxygen quantum yields than and , due to the enhanced singlet-to-triplet intersystem crossing. To evaluate the targeting effect of the glycosylated derivative, in vitro experiments were performed using glucose transporter 1 (GLUT1)-positive HT29 and A549 cancer cells, and noncancerous HEK293 cells as control. Both and showed higher cellular uptake than and . Specifically, was selective and highly cytotoxic toward HT29 and A549 cells. The synergistic chemo- and photodynamic behavior of the metallacycles was also confirmed. Notably, exhibited superior efficacy toward the cisplatin-resistant R-HepG2 cells.
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| http://dx.doi.org/10.1021/acs.jmedchem.2c01940 | DOI Listing |
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