Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.chemphyslip.2022.105181 http://hdl.handle.net/11449/223587 |
Resumo: | Cell membranes are the first barriers for drug binding and key for the action of photosensitizers (PS). Herein, we report on the incorporation of the PS hypericin into Langmuir monolayers of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and 1,2-dioleoyl-sn-glycero-3-phospho-L-serine (DOPS) to represent eukaryotic cell membranes, and 1,2-dioleoyl-sn-glycero-3-phospho(1’-rac-glycerol) (DOPG) to mimic bacterial membranes. Surface pressure (π) vs mean molecular area (Å) isotherms showed a high degree of interaction (binding, penetration and relative solubilization) of hypericin into DPPC and DOPC monolayers. On the other hand, electrostatic repulsions govern the interactions with DOPG and DOPS, favoring hypericin self-aggregation, as visualized by Brewster angle microscopy (BAM). Indeed, the larger domains in BAM were consistent with the greater expansion of DOPG monolayers with incorporated hypericin, owing to stronger electrostatic repulsions. In contrast to DPPC, light-irradiation of DOPC monolayers containing hypericin induced loss of material due to hydrocarbon chain cleavage triggered by contact-dependent reactions between triplet excited state of hypericin and chain unsaturations. The mild effects noted for both irradiated DOPS and DOPG monolayers are attributed to hypericin self-aggregation, which may have decreased the singlet oxygen quantum yield (Φ1O2) via self-quenching, despite the increased instability induced in the monolayers. |
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Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane modelsHypercin incorporationPhospholipid biomembrane modelsPhotodynamic therapyPhotooxidationCell membranes are the first barriers for drug binding and key for the action of photosensitizers (PS). Herein, we report on the incorporation of the PS hypericin into Langmuir monolayers of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and 1,2-dioleoyl-sn-glycero-3-phospho-L-serine (DOPS) to represent eukaryotic cell membranes, and 1,2-dioleoyl-sn-glycero-3-phospho(1’-rac-glycerol) (DOPG) to mimic bacterial membranes. Surface pressure (π) vs mean molecular area (Å) isotherms showed a high degree of interaction (binding, penetration and relative solubilization) of hypericin into DPPC and DOPC monolayers. On the other hand, electrostatic repulsions govern the interactions with DOPG and DOPS, favoring hypericin self-aggregation, as visualized by Brewster angle microscopy (BAM). Indeed, the larger domains in BAM were consistent with the greater expansion of DOPG monolayers with incorporated hypericin, owing to stronger electrostatic repulsions. In contrast to DPPC, light-irradiation of DOPC monolayers containing hypericin induced loss of material due to hydrocarbon chain cleavage triggered by contact-dependent reactions between triplet excited state of hypericin and chain unsaturations. The mild effects noted for both irradiated DOPS and DOPG monolayers are attributed to hypericin self-aggregation, which may have decreased the singlet oxygen quantum yield (Φ1O2) via self-quenching, despite the increased instability induced in the monolayers.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Natural Sciences and Engineering Research Council of CanadaSão Paulo State University (UNESP) School of Sciences Humanities and Languages, SPSão Carlos Institute of Physics University of São Paulo (USP) CP 369, SPDepartment of Chemistry State University of Maringá, PRDepartment of Chemistry and Biochemistry and Centre for NanoScience Research Concordia UniversitySão Paulo State University (UNESP) School of Sciences Humanities and Languages, SPFAPESP: 2018/08077–6FAPESP: 2018/14692–5FAPESP: 2018/16713–0FAPESP: 2018/22214–6CNPq: 403713/2016–1Natural Sciences and Engineering Research Council of Canada: RGPIN-2019–07043Universidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)State University of MaringáConcordia UniversityPereira, Lucas S.A. [UNESP]Camacho, Sabrina A. [UNESP]Almeida, Alexandre M. [UNESP]Gonçalves, Renato S.Caetano, WilkerDeWolf, ChristineAoki, Pedro H.B. [UNESP]2022-04-28T19:51:31Z2022-04-28T19:51:31Z2022-05-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.chemphyslip.2022.105181Chemistry and Physics of Lipids, v. 244.1873-29410009-3084http://hdl.handle.net/11449/22358710.1016/j.chemphyslip.2022.1051812-s2.0-85125992408Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengChemistry and Physics of Lipidsinfo:eu-repo/semantics/openAccess2022-04-28T19:51:31Zoai:repositorio.unesp.br:11449/223587Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:35:20.012090Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models |
title |
Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models |
spellingShingle |
Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models Pereira, Lucas S.A. [UNESP] Hypercin incorporation Phospholipid biomembrane models Photodynamic therapy Photooxidation |
title_short |
Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models |
title_full |
Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models |
title_fullStr |
Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models |
title_full_unstemmed |
Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models |
title_sort |
Mechanisms of hypericin incorporation to explain the photooxidation outcomes in phospholipid biomembrane models |
author |
Pereira, Lucas S.A. [UNESP] |
author_facet |
Pereira, Lucas S.A. [UNESP] Camacho, Sabrina A. [UNESP] Almeida, Alexandre M. [UNESP] Gonçalves, Renato S. Caetano, Wilker DeWolf, Christine Aoki, Pedro H.B. [UNESP] |
author_role |
author |
author2 |
Camacho, Sabrina A. [UNESP] Almeida, Alexandre M. [UNESP] Gonçalves, Renato S. Caetano, Wilker DeWolf, Christine Aoki, Pedro H.B. [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Universidade de São Paulo (USP) State University of Maringá Concordia University |
dc.contributor.author.fl_str_mv |
Pereira, Lucas S.A. [UNESP] Camacho, Sabrina A. [UNESP] Almeida, Alexandre M. [UNESP] Gonçalves, Renato S. Caetano, Wilker DeWolf, Christine Aoki, Pedro H.B. [UNESP] |
dc.subject.por.fl_str_mv |
Hypercin incorporation Phospholipid biomembrane models Photodynamic therapy Photooxidation |
topic |
Hypercin incorporation Phospholipid biomembrane models Photodynamic therapy Photooxidation |
description |
Cell membranes are the first barriers for drug binding and key for the action of photosensitizers (PS). Herein, we report on the incorporation of the PS hypericin into Langmuir monolayers of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) and 1,2-dioleoyl-sn-glycero-3-phospho-L-serine (DOPS) to represent eukaryotic cell membranes, and 1,2-dioleoyl-sn-glycero-3-phospho(1’-rac-glycerol) (DOPG) to mimic bacterial membranes. Surface pressure (π) vs mean molecular area (Å) isotherms showed a high degree of interaction (binding, penetration and relative solubilization) of hypericin into DPPC and DOPC monolayers. On the other hand, electrostatic repulsions govern the interactions with DOPG and DOPS, favoring hypericin self-aggregation, as visualized by Brewster angle microscopy (BAM). Indeed, the larger domains in BAM were consistent with the greater expansion of DOPG monolayers with incorporated hypericin, owing to stronger electrostatic repulsions. In contrast to DPPC, light-irradiation of DOPC monolayers containing hypericin induced loss of material due to hydrocarbon chain cleavage triggered by contact-dependent reactions between triplet excited state of hypericin and chain unsaturations. The mild effects noted for both irradiated DOPS and DOPG monolayers are attributed to hypericin self-aggregation, which may have decreased the singlet oxygen quantum yield (Φ1O2) via self-quenching, despite the increased instability induced in the monolayers. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-04-28T19:51:31Z 2022-04-28T19:51:31Z 2022-05-01 |
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/10.1016/j.chemphyslip.2022.105181 Chemistry and Physics of Lipids, v. 244. 1873-2941 0009-3084 http://hdl.handle.net/11449/223587 10.1016/j.chemphyslip.2022.105181 2-s2.0-85125992408 |
url |
http://dx.doi.org/10.1016/j.chemphyslip.2022.105181 http://hdl.handle.net/11449/223587 |
identifier_str_mv |
Chemistry and Physics of Lipids, v. 244. 1873-2941 0009-3084 10.1016/j.chemphyslip.2022.105181 2-s2.0-85125992408 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Chemistry and Physics of Lipids |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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 |
|
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1808128537357451264 |