Resumen:
lioblastoma multiforme is considered to be one of the most aggressive types of tumors of the central nervous system, with a poor prognosis and short survival periods of ~ one year. The current protocol for glioblastoma treatment includes the surgical excision of the primary tumor followed by radio and chemotherapy. Photodynamic therapy (PDT) is considered a promising strategy for the treatmentof several types of tumors. Phthalocyanines (Pcs) are good photosensitizers (PSs) for PDT becausethey induce cell death in several cellular models. ZnPc (Zn(II)phthalocyanine) is a well-known Pc, extensively tested in di erent cells and tumor models, but its evaluation on a glioblastoma modelhas been poorly studied. Herein, we compare the capacity of ZnPc and one of its derivatives, Zn(II) tetraminephthalocyanine (TAZnPc), to photoinactivate glioblastoma cells (T98G, MO59, LN229 and U87-MG) in culture. We measured the cellular uptake, the toxicity in the dark and the subcellular localization of t