Abstract
The
currently used photodynamic therapy (PDT) photosensitizers (PSs) are generally associated
with a poor cancer cell selectivity, which is responsible for some undesirable side
effects. To overcome these problems, the use of selective drug delivery
systems is currently envisioned. In this article, the encapsulation of a
promising Ru(II) polypyridine complex-based PDT PS in a polymer with terminal
folate groups to form nanoparticles is presented. While showing a high
selectivity for cancerous cells over non-cancerous cells, the nanoparticles were
found to be highly phototoxic in 2D monolayer cells as well as 3D multicellular
tumor spheroids upon 480 nm or 595 nm irradiation. Promisingly, the nanoparticles
were also active in drug resistant cancer cells lines, indicating
that they are able to overcome drug resistances.