Experimental findings utilising a new iron chelating ALA prodrug to enhance protoporphyrin IX-induced photodynamic therapy

摘要

Administration of a separate iron chelating agent during protoporphyrin IX (PpIX)-PDT has previously beendemonstrated to increase the temporary accumulation of PpIX (by reducing its iron dependent bioconversion to haem byferrochelatase), resulting in increased efficacy on irradiation. A novel ester between aminolaevulinic acid (ALA) and thehydroxypyridinone iron chelating agent CP94 was therefore synthesised (AP2-18) and experimentally evaluated todetermine if PpIX-induced PDT effectiveness could be improved by this new combinational agent. A variety of culturedhuman primary cells were investigated with both PpIX fluorescence and cell viability being assessed in comparison tothe PpIX prodrugs normally utilised in clinical practice (aminolaevulinic acid (ALA) or its methyl ester (MAL)) eitheradministered alone or concurrently with the comparator iron chelator, CP94. Iron chelation achieved via CP94 or AP2-18 administration consistently increased PpIX accumulation but the benefits of enhancement on PpIX-PDT cell kill weremost pronounced when lower doses of ALA or MAL were utilised (i.e. where PpIX accumulation was observed to bemost limited without this intervention). Importantly, AP2-18 was observed to be as least as effective as CP94 +ALA/MAL co-administration throughout and produced no significant dark toxicity in initial experimentation undertakenin lung fibroblasts. Additionally, statistically significant enhanced effects in terms of both PpIX accumulation and PDTcytotoxicity were observed experimentally with AP2-18 in both skin cancer and glioma cells. Newly synthesised AP2-18 is therefore concluded to be an efficacious combined PpIX prodrug and iron chelating agent for the enhancement ofPpIX-induced PDT that warrants further investigation.