Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation

Bibliographic Details
Main Author: Melo, Nícolas J.
Publication Date: 2024
Other Authors: Soares, Jennifer M., Dovigo, Lívia N. [UNESP], Carmona-Vargas, Christian, Aguiar, Antônio S. N., dos Passos, Adriana C., de Oliveira, Kleber T., Bagnato, Vanderlei S., Dias, Lucas D., Inada, Natalia
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.3390/chemistry6040035
https://hdl.handle.net/11449/297774
Summary: Natural curcumin is composed of three curcuminoids, namely curcumin (CUR), deme-thoxycurcumin (DMC) and bis-demethoxycurcumin (BDMC). These compounds are utilized in various biophotonics applications, including photodynamic therapy (PDT). This work aimed to evaluate the photodynamic action (alternative to antibiotics) of synthetic curcuminoids against Staphylococcus aureus. Herein, we evaluated an optimal proportion of the three curcuminoids mixed in solution to improve photoinactivation effects. Therefore, a set of computational calculations was carried out to understand the photodynamic action (stability and mechanism) of curcuminoids. Regarding computational analysis, the curcuminoid molecules were optimized using DFT with the hybrid exchange–correlation functional M06-2X, which includes long-range correction, and the 6-311++G(d,p) basis set. DMC and BDMC were more effective as photosensitizers than curcumin at a very low concentration of 0.75 µM, inactivating more than five orders of magnitude of S. aureus. Theoretical UV-vis absorption spectra showed that at maximum absorption wavelengths, electronic transitions of the π→π* type originated from H→L excitations. The BDMC was more stable than the other two curcuminoids after photobleaching, and the fluorescence emission was also higher, which could lead to its usage as a fluorescence dye to track bacteria. In fact, the results of electronic structure calculations proved that the stability order of curcuminoids is CUR < DMC < BDMC. The mixture of synthetic curcuminoids was more effective in the inactivation of S. aureus compared to curcumin by itself; for all proposed mixtures, an equal or superior reduction was achieved.
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spelling Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluationbis-demethoxycurcumincurcumincurcuminoidsdemethoxycurcuminmolecular modelingphotodynamic inactivationStaphylococcus aureusNatural curcumin is composed of three curcuminoids, namely curcumin (CUR), deme-thoxycurcumin (DMC) and bis-demethoxycurcumin (BDMC). These compounds are utilized in various biophotonics applications, including photodynamic therapy (PDT). This work aimed to evaluate the photodynamic action (alternative to antibiotics) of synthetic curcuminoids against Staphylococcus aureus. Herein, we evaluated an optimal proportion of the three curcuminoids mixed in solution to improve photoinactivation effects. Therefore, a set of computational calculations was carried out to understand the photodynamic action (stability and mechanism) of curcuminoids. Regarding computational analysis, the curcuminoid molecules were optimized using DFT with the hybrid exchange–correlation functional M06-2X, which includes long-range correction, and the 6-311++G(d,p) basis set. DMC and BDMC were more effective as photosensitizers than curcumin at a very low concentration of 0.75 µM, inactivating more than five orders of magnitude of S. aureus. Theoretical UV-vis absorption spectra showed that at maximum absorption wavelengths, electronic transitions of the π→π* type originated from H→L excitations. The BDMC was more stable than the other two curcuminoids after photobleaching, and the fluorescence emission was also higher, which could lead to its usage as a fluorescence dye to track bacteria. In fact, the results of electronic structure calculations proved that the stability order of curcuminoids is CUR < DMC < BDMC. The mixture of synthetic curcuminoids was more effective in the inactivation of S. aureus compared to curcumin by itself; for all proposed mixtures, an equal or superior reduction was achieved.Group of Optics São Carlos Institute of Physics University of São Paulo, Av. Trabalhador São-Carlense, 400, SPDepartment of Social Dentistry Araraquara Dental School São Paulo State University, SPDepartment of Chemistry Federal University of São Carlos, São Carlos, SPLaboratório de Novos Materiais Universidade Evangélica de Goiás, GODepartment of Biomedical Engineering Texas A&M UniversityDepartment of Social Dentistry Araraquara Dental School São Paulo State University, SPUniversidade de São Paulo (USP)Universidade Estadual Paulista (UNESP)Universidade Federal de São Carlos (UFSCar)Universidade Evangélica de GoiásTexas A&M UniversityMelo, Nícolas J.Soares, Jennifer M.Dovigo, Lívia N. [UNESP]Carmona-Vargas, ChristianAguiar, Antônio S. N.dos Passos, Adriana C.de Oliveira, Kleber T.Bagnato, Vanderlei S.Dias, Lucas D.Inada, Natalia2025-04-29T18:07:42Z2024-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article581-600http://dx.doi.org/10.3390/chemistry6040035Chemistry (Switzerland), v. 6, n. 4, p. 581-600, 2024.2624-8549https://hdl.handle.net/11449/29777410.3390/chemistry60400352-s2.0-85202614497Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengChemistry (Switzerland)info:eu-repo/semantics/openAccess2025-05-01T05:58:56Zoai:repositorio.unesp.br:11449/297774Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-01T05:58:56Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation
title Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation
spellingShingle Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation
Melo, Nícolas J.
bis-demethoxycurcumin
curcumin
curcuminoids
demethoxycurcumin
molecular modeling
photodynamic inactivation
Staphylococcus aureus
title_short Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation
title_full Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation
title_fullStr Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation
title_full_unstemmed Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation
title_sort Photodynamic Action of Synthetic Curcuminoids against Staphylococcus aureus: Experimental and Computational Evaluation
author Melo, Nícolas J.
author_facet Melo, Nícolas J.
Soares, Jennifer M.
Dovigo, Lívia N. [UNESP]
Carmona-Vargas, Christian
Aguiar, Antônio S. N.
dos Passos, Adriana C.
de Oliveira, Kleber T.
Bagnato, Vanderlei S.
Dias, Lucas D.
Inada, Natalia
author_role author
author2 Soares, Jennifer M.
Dovigo, Lívia N. [UNESP]
Carmona-Vargas, Christian
Aguiar, Antônio S. N.
dos Passos, Adriana C.
de Oliveira, Kleber T.
Bagnato, Vanderlei S.
Dias, Lucas D.
Inada, Natalia
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (UNESP)
Universidade Federal de São Carlos (UFSCar)
Universidade Evangélica de Goiás
Texas A&M University
dc.contributor.author.fl_str_mv Melo, Nícolas J.
Soares, Jennifer M.
Dovigo, Lívia N. [UNESP]
Carmona-Vargas, Christian
Aguiar, Antônio S. N.
dos Passos, Adriana C.
de Oliveira, Kleber T.
Bagnato, Vanderlei S.
Dias, Lucas D.
Inada, Natalia
dc.subject.por.fl_str_mv bis-demethoxycurcumin
curcumin
curcuminoids
demethoxycurcumin
molecular modeling
photodynamic inactivation
Staphylococcus aureus
topic bis-demethoxycurcumin
curcumin
curcuminoids
demethoxycurcumin
molecular modeling
photodynamic inactivation
Staphylococcus aureus
description Natural curcumin is composed of three curcuminoids, namely curcumin (CUR), deme-thoxycurcumin (DMC) and bis-demethoxycurcumin (BDMC). These compounds are utilized in various biophotonics applications, including photodynamic therapy (PDT). This work aimed to evaluate the photodynamic action (alternative to antibiotics) of synthetic curcuminoids against Staphylococcus aureus. Herein, we evaluated an optimal proportion of the three curcuminoids mixed in solution to improve photoinactivation effects. Therefore, a set of computational calculations was carried out to understand the photodynamic action (stability and mechanism) of curcuminoids. Regarding computational analysis, the curcuminoid molecules were optimized using DFT with the hybrid exchange–correlation functional M06-2X, which includes long-range correction, and the 6-311++G(d,p) basis set. DMC and BDMC were more effective as photosensitizers than curcumin at a very low concentration of 0.75 µM, inactivating more than five orders of magnitude of S. aureus. Theoretical UV-vis absorption spectra showed that at maximum absorption wavelengths, electronic transitions of the π→π* type originated from H→L excitations. The BDMC was more stable than the other two curcuminoids after photobleaching, and the fluorescence emission was also higher, which could lead to its usage as a fluorescence dye to track bacteria. In fact, the results of electronic structure calculations proved that the stability order of curcuminoids is CUR < DMC < BDMC. The mixture of synthetic curcuminoids was more effective in the inactivation of S. aureus compared to curcumin by itself; for all proposed mixtures, an equal or superior reduction was achieved.
publishDate 2024
dc.date.none.fl_str_mv 2024-08-01
2025-04-29T18:07:42Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.3390/chemistry6040035
Chemistry (Switzerland), v. 6, n. 4, p. 581-600, 2024.
2624-8549
https://hdl.handle.net/11449/297774
10.3390/chemistry6040035
2-s2.0-85202614497
url http://dx.doi.org/10.3390/chemistry6040035
https://hdl.handle.net/11449/297774
identifier_str_mv Chemistry (Switzerland), v. 6, n. 4, p. 581-600, 2024.
2624-8549
10.3390/chemistry6040035
2-s2.0-85202614497
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Chemistry (Switzerland)
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 581-600
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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