EventsThe 1st International Online Conference on Photochemistry
Published
This submission belongs to the session S4. Photodynamic and Photothermal Therapy of the event The 1st International Online Conference on Photochemistry
Published date
03 Apr, 2026
Academic Editor
author-avatarRui Fausto
Citation
Aleksandra Pawska, Marcin Wysocki, Daniel Ziental, Jolanta Długaszewska, Jakub Szymczyk, Emre Güzel, Łukasz Sobotta, Marianna Szczepaniak, Amphiphilic Phthalocyanines as Dual-Mode Photo- and Sonosensitizers for Antimicrobial Applications, in Proceedings of The 1st International Online Conference on Photochemistry, 8 April–9 April 2026, MDPI: Basel, Switzerland
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Amphiphilic Phthalocyanines as Dual-Mode Photo- and Sonosensitizers for Antimicrobial Applications

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Jakub Szymczyk 1
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1. Department of Inorganic and Analytical Chemistry, Poznan University of Medical Sciences, Rokietnicka 3, 60-806 Poznan, Poland., Poland
2. Department of Genetics and Pharmaceutical Microbiology, Poznan University of Medical Sciences, Rokietnicka 3, 60-806 Poznan, Poland.
3. Department of Genetics and Pharmaceutical Microbiology, Poznan University of Medical Sciences, Rokietnicka 3, 60-806 Poznan, Poland., Poland
4. Department of Engineering Fundamental Sciences, Faculty of Technology, Sakarya University of Applied Sciences, 54050, Sakarya, Turkey., Turkey (Türkiye)
Abstract

A newly developed series of amphiphilic and cationic phthalocyanines was designed to determine how quaternization, peripheral substituents, and metal coordination govern photodynamic and sonodynamic performance. All derivatives displayed characteristic Q-band absorption between 673 and 705 nm and fluorescence quantum yields spanning Φf = 0.01–0.26. Quaternization markedly increased emission in Zn(II) complexes (Φf: 0.02 → 0.17), while reducing it in metal-free and In(III) analogues. Singlet oxygen formation was efficient across the series, with ΦΔ = 0.63 for both InPc and QInPc and a twofold increase for ZnPc upon quaternization (ΦΔ: 0.27 → 0.51). The unsubstituted ZnPc was used as a reference. Photodecomposition quantum yields (10⁻⁵–10⁻⁴) indicated that quaternization enhanced photostability for metal-free and Zn(II) derivatives, while minimally affecting the In(III) complex.

The quaternized phthalocyanines demonstrated high antimicrobial potency. In methicillin-resistant Staphylococcus aureus (MRSA) and ESBL-producing Escherichia coli, inactivation reached 4.6 logs, while Gram-negative strains showed 4.5-log reductions. Activity against fluconazole-resistant Candida albicans demonstrated the following: QH₂Pc, QInPc, and QZnPc achieved 3.2-log reductions.

Sonodynamic evaluation confirmed strong ROS formation. Non-quaternized sensitizers accelerated DPBF decay around 4.5-fold, with ZnPc showing the fastest kinetics (k = 0.152 min⁻¹; t₀.₅ = 4.55 min). Quaternized derivatives remained sonodynamically active; QZnPc has the potential to generate ROS efficiently (k = 0.130 min⁻¹) and displayed improved ultrasound stability (t₀.₅ = 59.7 min vs. 11.2 min for ZnPc).

These results establish this family of amphiphilic phthalocyanines as potent, multimodal sensitizers, capable of achieving high-log photodynamic reduction and showing potential for strong sonodynamic ROS output. Their performance, together with clear structure–property relationships, highlights their promise for next-generation antimicrobial therapy.

Keywords
phthalocyanines
MDR
PACT
SDT
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