TY - JOUR
T1 - Nanostructured AABB Zn (II) Phthalocyanines as Photodynamic Agents for Bacterial Inactivation
AU - Paramio, Irene
AU - Salazar, Ainhoa
AU - Jordà-Redondo, Mireia
AU - Nonell, Santi
AU - Torres, Tomás
AU - de la Torre, Gema
N1 - Funding Information:
I.P., A.S., and M.J.‐R. contributed equally to this work. The authors gratefully acknowledge financial support from the Spanish AEI through grants PID2020‐116490GB‐I00, PID2020‐115801RB‐C21, and PID2020‐115801RB‐C22. The authors also thank financial support to the Comunidad de Madrid and the Spanish State through the Recovery, Transformation and Resilience Plan [“Materiales Disruptivos Bidimensionales (2D)” (MAD2D‐CM) (UAM1)‐MRR Materiales Avanzados], and the European Union through the Next Generation EU funds. IMDEA Nanociencia acknowledges support from the “Severo Ochoa” Program for Centers of Excellence in R&D (MINECO, Grant SEV2016‐0686). S.N. thanks the Departament de Recerca i Universitats de la Generalitat de Catalunya for the support given to the research group (2021 SGR 01023) and the ICREA‐Catalan Institution for Research and Advanced Studies for grant No. Ac2232308.
Publisher Copyright:
© 2023 The Authors. Advanced Therapeutics published by Wiley-VCH GmbH.
PY - 2023/11
Y1 - 2023/11
N2 - In this work, the ability of amphiphilic Phthalocyanine (Pc) photosensitizers (PS) (Zn(II)Pcs PS1, PS2, and PS3) to assemble into cationic nanoparticles in water and to photo-inactivate bacterial strains is demonstrated. All the synthesized Zn(II)Pcs exhibit an AABB functionalization pattern, having a binaphthyloxy-linked bisisoindole (AA) functionalized at the chiral binaphthol core with branched (PS1) or linear (PS2 and PS3) poly-ammonium chains, and two non-functionalized isoindole rings (BB). The aggregation behavior and the stability of the nanoparticles formed by the three PS in water is studied by UV–vis, fluorescence and circular dichroism (CD) spectroscopies, and their shape and size is determined by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The PS nanoparticles prove efficient in the photoinactivation of S. aureus and E. coli. Although PS2 and PS3 present better photophysical features in their monomeric form (i.e., improved singlet oxygen quantum yield), PS1 is more effective in killing both types of strains, especially the gram-negative E. coli. This observation may derive from the low stability found for PS1 nanoparticles, which easily disassemble after binding to the bacteria surface, recovering the photophysical properties of the non-aggregated species.
AB - In this work, the ability of amphiphilic Phthalocyanine (Pc) photosensitizers (PS) (Zn(II)Pcs PS1, PS2, and PS3) to assemble into cationic nanoparticles in water and to photo-inactivate bacterial strains is demonstrated. All the synthesized Zn(II)Pcs exhibit an AABB functionalization pattern, having a binaphthyloxy-linked bisisoindole (AA) functionalized at the chiral binaphthol core with branched (PS1) or linear (PS2 and PS3) poly-ammonium chains, and two non-functionalized isoindole rings (BB). The aggregation behavior and the stability of the nanoparticles formed by the three PS in water is studied by UV–vis, fluorescence and circular dichroism (CD) spectroscopies, and their shape and size is determined by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The PS nanoparticles prove efficient in the photoinactivation of S. aureus and E. coli. Although PS2 and PS3 present better photophysical features in their monomeric form (i.e., improved singlet oxygen quantum yield), PS1 is more effective in killing both types of strains, especially the gram-negative E. coli. This observation may derive from the low stability found for PS1 nanoparticles, which easily disassemble after binding to the bacteria surface, recovering the photophysical properties of the non-aggregated species.
KW - amphiphiles
KW - nanoparticles
KW - photodynamic inactivation
KW - phthalocyanines
KW - self-assembly
UR - http://www.scopus.com/inward/record.url?scp=85169136306&partnerID=8YFLogxK
U2 - 10.1002/adtp.202300116
DO - 10.1002/adtp.202300116
M3 - Article
AN - SCOPUS:85169136306
SN - 2366-3987
VL - 6
JO - Advanced Therapeutics
JF - Advanced Therapeutics
IS - 11
M1 - 2300116
ER -