Effect of fluorinated substituents of Zn phthalocyanine: nanoencapsulation and phototoxicity

Phthalocyanines are promising photosensitizers for photodynamic therapy due to their advantageous light absorption properties and low dark toxicity. Two non-peripheral substituted phthalocyanines, tetra-ethoxy-Zn-phthalocyanine (CH<sub>3</sub>Pc) and its fluorinated analogue (CF<sub>3</sub>Pc), were combined with different nanocarriers, and their photophysical properties and biological activities were studied. Carrier-encapsulation and phthalocyanines' aggregation state were probed by NMR-, UV-Vis-, and fluorescence spectroscopy. Five different carrier systems were compared: polyvinylpyrrolidone (PVP), two triblock copolymer micelles (Synperonic P84, "P84", and Pluronic F127, "F127"), self-emulsifying detergent micelles (Kolliphor RH40, "RH40"), and 1, 2-dioleoyl-sn-glycero-3-phosphocholine unilamellar vesicles (ULVs). CH<sub>3</sub>Pc inserted efficiently into P84, F127 and RH40 micelles in monomeric form, while CF<sub>3</sub>Pc was encapsulated as dimers and oligomers. ULVs were capable to efficiently monomerize and encapsulate both phthalocyanines. PVP was not suitable to solubilize neither of these phthalocyanines. The localization of CH<sub>3</sub>Pc and CF<sub>3</sub>Pc at the carrier interfaces was determined by NMR-experiments with atomic resolution. All phthalocyanine-carrier systems - except PVP - exhibited efficient singlet oxygen production, with ULVs reaching the highest quantum yields. The photodynamic potential of the different CH<sub>3</sub>Pc- and CF<sub>3</sub>Pc-formulations was studied using a human breast cancer cell line (MCF-7) by measuring the dark toxicity and phototoxicity after light irradiation at 655 nm. Encapsulation into ULVs and RH40 micelles exhibited the highest photodynamic efficiency for both phthalocyanines at low concentrations (0.05-1 µM). The fluorinated phthalocyanine showed enhanced photodynamic activity compared to its non-fluorinated analogue. While micellar carriers easily monomerized CH<sub>3</sub>Pc, ULV-encapsulated CF<sub>3</sub>Pc turned out to be the best candidate as efficient sensitizer for photodynamic therapy.

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Publication Details

Journal
International Journal of Pharmaceutics
Published
2026-03-13
DOI
https://doi.org/10.1016/j.ijpharm.2026.126771
Primary Topic
Porphyrin and Phthalocyanine Chemistry
Type
article
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article

Effect of fluorinated substituents of Zn phthalocyanine: nanoencapsulation and phototoxicity

Bernhard Spingler, Mónica Trincado, Peter Vermathen, Fabienne Dumoulin et al.
International Journal of Pharmaceutics
Porphyrin and Phthalocyanine Chemistry
article

Effect of fluorinated substituents of Zn phthalocyanine: nanoencapsulation and phototoxicity

Bernhard Spingler, Mónica Trincado, Peter Vermathen, Fabienne Dumoulin, Julien Furrer, Martina Vermathen, Joel J. Bruegger, Atefeh Emami, Ilche Gjuroski, Ümit İşçi, Christophe Nguyen, Magali Gary-Bobo
article en

Abstract

Phthalocyanines are promising photosensitizers for photodynamic therapy due to their advantageous light absorption properties and low dark toxicity. Two non-peripheral substituted phthalocyanines, tetra-ethoxy-Zn-phthalocyanine (CH<sub>3</sub>Pc) and its fluorinated analogue (CF<sub>3</sub>Pc), were combined with different nanocarriers, and their photophysical properties and biological activities were studied. Carrier-encapsulation and phthalocyanines' aggregation state were probed by NMR-, UV-Vis-, and fluorescence spectroscopy. Five different carrier systems were compared: polyvinylpyrrolidone (PVP), two triblock copolymer micelles (Synperonic P84, "P84", and Pluronic F127, "F127"), self-emulsifying detergent micelles (Kolliphor RH40, "RH40"), and 1, 2-dioleoyl-sn-glycero-3-phosphocholine unilamellar vesicles (ULVs). CH<sub>3</sub>Pc inserted efficiently into P84, F127 and RH40 micelles in monomeric form, while CF<sub>3</sub>Pc was encapsulated as dimers and oligomers. ULVs were capable to efficiently monomerize and encapsulate both phthalocyanines. PVP was not suitable to solubilize neither of these phthalocyanines. The localization of CH<sub>3</sub>Pc and CF<sub>3</sub>Pc at the carrier interfaces was determined by NMR-experiments with atomic resolution. All phthalocyanine-carrier systems - except PVP - exhibited efficient singlet oxygen production, with ULVs reaching the highest quantum yields. The photodynamic potential of the different CH<sub>3</sub>Pc- and CF<sub>3</sub>Pc-formulations was studied using a human breast cancer cell line (MCF-7) by measuring the dark toxicity and phototoxicity after light irradiation at 655 nm. Encapsulation into ULVs and RH40 micelles exhibited the highest photodynamic efficiency for both phthalocyanines at low concentrations (0.05-1 µM). The fluorinated phthalocyanine showed enhanced photodynamic activity compared to its non-fluorinated analogue. While micellar carriers easily monomerized CH<sub>3</sub>Pc, ULV-encapsulated CF<sub>3</sub>Pc turned out to be the best candidate as efficient sensitizer for photodynamic therapy.

International Journal of PharmaceuticsVol. 695
University of Bern (CH), École Nationale Supérieure de Chimie de Montpellier (FR), Centre National de la Recherche Scientifique (FR), Bern University of Applied Sciences (CH), Université de Montpellier (FR), University of Zurich (CH), Kent Hastanesi (TR), Institut des Biomolécules Max Mousseron (FR), Marmara University (TR)
Openalex Percentile: Top 26%
Porphyrin and Phthalocyanine Chemistry
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