Literature DB >> 34255302

Amphiphilic tricationic Zn(II)phthalocyanine provides effective photodynamic action to eradicate broad-spectrum microorganisms.

Estefanía Baigorria1, Javier E Durantini2, María A Di Palma1, Natalia S Gsponer1, María E Milanesio1, Edgardo N Durantini3.   

Abstract

A novel tricationic Zn(II)phthalocyanine derivative, (NCH3)3ZnPc3+, was synthesized by ring expansion reaction of boron(III) [2,9(10),16(17)-trinitrosubphthalocyaninato]chloride. First, the reaction of this subphthalocyanine with 2,3-naphthalenedicarbonitrile and Zn(CH3COO)2 catalyzed by 8-diazabicyclo[5.4.0]undec-7-ene was used to obtain the A3B-type nitrophthalocyanine. After reduction of nitro groups with Na2S and exhaustive methylation of amino groups, (NCH3)3ZnPc3+ was formed in good yields. In addition, the tetracationic analog (NCH3)4ZnPc4+ was synthesized to compare their properties. The absorption and fluorescence spectra showed the Q-bands and the red emission, respectively, which are characteristic of the Zn(II)phthalocyanine derivatives in N,N-dimethylformamide. Furthermore, photodynamic activity sensitized by these compounds was studied in the presence of different molecular probes to sense the formation of reactive oxygen species. (NCH3)3ZnPc3+ efficiently produced singlet molecular oxygen and also it sensitized the formation of superoxide anion radical in the presence of NADH, while the photodynamic activity of (NCH3)4ZnPc4+ was very poor, possibly due to the partial formation of aggregates. Furthermore, the decomposition of L-tryptophan induced by (NCH3)3ZnPc3+ was mainly mediated by a type II mechanism. Antimicrobial photodynamic inactivation sensitized by these phthalocyanines was evaluated in Staphylococcus aureus, Escherichia coli, and Candida albicans, as representative microbial cells. In cell suspensions, (NCH3)3ZnPc3+ was rapidly bound to microbial cells, showing bioimages with red fluorescence emission. After 5 min of irradiation with visible light, (NCH3)3ZnPc3+ was able to completely eliminate S. aureus, E. coli and C. albicans, using 1.0, 2.5 and 5.0 μM phthalocyanine, respectively. In contrast, a low photoinactivation activity was found with (NCH3)4ZnPc4+ as a photosensitizer. Therefore, the amphiphilic tricationic phthalocyanine (NCH3)3ZnPc3+ is a promising photosensitizing structure for application as a broad-spectrum antimicrobial phototherapeutic agent.
© 2021. The Author(s), under exclusive licence to European Photochemistry Association, European Society for Photobiology.

Entities:  

Keywords:  Microorganism; Photodynamic inactivation; Photoinactivation; Phthalocyanine; Reactive oxygen species

Year:  2021        PMID: 34255302     DOI: 10.1007/s43630-021-00074-2

Source DB:  PubMed          Journal:  Photochem Photobiol Sci        ISSN: 1474-905X            Impact factor:   3.982


  20 in total

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Review 6.  BODIPYs to the rescue: Potential applications in photodynamic inactivation.

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Journal:  Eur J Med Chem       Date:  2017-12-19       Impact factor: 6.514

Review 7.  Singlet Molecular Oxygen Reactions with Nucleic Acids, Lipids, and Proteins.

Authors:  Paolo Di Mascio; Glaucia R Martinez; Sayuri Miyamoto; Graziella E Ronsein; Marisa H G Medeiros; Jean Cadet
Journal:  Chem Rev       Date:  2019-02-05       Impact factor: 60.622

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Review 9.  Can microbial cells develop resistance to oxidative stress in antimicrobial photodynamic inactivation?

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10.  Porphyrins containing basic aliphatic amino groups as potential broad-spectrum antimicrobial agents.

Authors:  Ana C Scanone; Natalia S Gsponer; M Gabriela Alvarez; Edgardo N Durantini
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