Anionic hexadeca-carboxylate tetrapyrazinoporphyrazine: synthesis and in vitro photodynamic studies of a water-soluble, non-aggregating photosensitizer

0455793 - ÚFCH JH 2017 RIV GB eng J - Článek v odborném periodiku
Macháček, M. - Kollár, J. - Miletin, M. - Kučera, R. - Kubát, Pavel - Šimůnek, T. - Nováková, V. - Zimčík, P.
Anionic hexadeca-carboxylate tetrapyrazinoporphyrazine: synthesis and in vitro photodynamic studies of a water-soluble, non-aggregating photosensitizer.
RSC Advances. Roč. 6, JAN 2016 (2016), s. 10064-10077. E-ISSN 2046-2069
Institucionální podpora: RVO:61388955
Klíčová slova: synthesis * in vitro photodynamic studies * phthalocyanines
Kód oboru RIV: CF - Fyzikální chemie a teoretická chemie
Impakt faktor: 3.108, rok: 2016

A sodium salt of zinc tetrapyrazinoporphyrazine bearing eight 3,5-dicarboxylatophenyl substituents (1) was synthesized. The presence of sixteen negative charges in a rigid arrangement on the periphery of the macrocycle inhibited its aggregation in water or buffers at pH > 5.8. Strong aggregation was, however, observed in buffers at pH < 4.8 due to the protonation of carboxylate functions. Fluorescence microscopy revealed that the compound localized to lysosomes and endosomes in cells. The compound's photodynamic activity on HeLa cancer cells (IC50 = 5.7 ± 1.1 μM) was found to be influenced by both pH and interactions with serum proteins. This was demonstrated with a detailed in vitro study based on the inhibition of vacuolar H+-ATPase using bafilomycin A1, which increased the intracellular fluorescence of 1. Compound 1 also formed interactions with serum proteins that partially quenched its excited states; however, they also protected the compound from self-aggregation at low pH.

Trvalý link: http://hdl.handle.net/11104/0256429