Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT

Detalhes bibliográficos
Autor(a) principal: Nave, Micaela
Data de Publicação: 2023
Outros Autores: Costa, Francisco J. P., Alves, Cátia, Sousa, Rita Lima, Melo, Bruna L., Correia, I.J., Diogo, Duarte de Melo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.6/13290
Resumo: Near infrared (NIR) light-responsive nanomaterials hold potential to mediate combinatorial therapies targeting several cancer hallmarks. When irradiated, these nanomaterials produce reactive oxygen species (photodynamic therapy) and/or a temperature increase (photothermal therapy). These events can damage cancer cells and trigger the release of drugs from the nanomaterials’ core. However, engineering nanomaterials for cancer chemophotodynamic/photothermal therapy is a complex process. First, nanomaterials with photothermal capacity are synthesized, being then loaded with photosensitizers plus chemotherapeutics, and, finally functionalized with polymers for achieving suitable biological properties. To overcome this limitation, in this work, a novel straightforward approach to attain NIR light-responsive nanosystems for cancer chemo-photodynamic/ photothermal therapy was established. Such was accomplished by synthesizing poly(2-ethyl-2-oxazoline)- IR780 amphiphilic conjugates, which can be assembled into nanoparticles with photodynamic/photothermal capabilities that simultaneously encapsulate Doxorubicin (DOX/PEtOx-IR NPs). The DOX/PEtOx-IR NPs presented a suitable size and surface charge for cancer-related applications. When irradiated with NIR light, the DOX/PEtOx-IR NPs produced singlet oxygen as well as a smaller thermic effect that boosted the release of DOX by 1.7-times. In the in vitro studies, the combination of DOX/PEtOx-IR NPs and NIR light could completely ablate breast cancer cells (viability ≈ 4 %), demonstrating the enhanced outcome arising from the nanomaterials' chemo-photodynamic/photothermal therapy.
id RCAP_9d3c6284e11d7c8bf9c14df8ff32256b
oai_identifier_str oai:ubibliorum.ubi.pt:10400.6/13290
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTTCombinatorial triple therapyLight responsive nanoparticlesMultifunctional nanomaterialsPhotodynamic therapyPoly(2-ethyl-2-oxazoline)Polymer-IR780 conjugateNear infrared (NIR) light-responsive nanomaterials hold potential to mediate combinatorial therapies targeting several cancer hallmarks. When irradiated, these nanomaterials produce reactive oxygen species (photodynamic therapy) and/or a temperature increase (photothermal therapy). These events can damage cancer cells and trigger the release of drugs from the nanomaterials’ core. However, engineering nanomaterials for cancer chemophotodynamic/photothermal therapy is a complex process. First, nanomaterials with photothermal capacity are synthesized, being then loaded with photosensitizers plus chemotherapeutics, and, finally functionalized with polymers for achieving suitable biological properties. To overcome this limitation, in this work, a novel straightforward approach to attain NIR light-responsive nanosystems for cancer chemo-photodynamic/ photothermal therapy was established. Such was accomplished by synthesizing poly(2-ethyl-2-oxazoline)- IR780 amphiphilic conjugates, which can be assembled into nanoparticles with photodynamic/photothermal capabilities that simultaneously encapsulate Doxorubicin (DOX/PEtOx-IR NPs). The DOX/PEtOx-IR NPs presented a suitable size and surface charge for cancer-related applications. When irradiated with NIR light, the DOX/PEtOx-IR NPs produced singlet oxygen as well as a smaller thermic effect that boosted the release of DOX by 1.7-times. In the in vitro studies, the combination of DOX/PEtOx-IR NPs and NIR light could completely ablate breast cancer cells (viability ≈ 4 %), demonstrating the enhanced outcome arising from the nanomaterials' chemo-photodynamic/photothermal therapy.ElsevieruBibliorumNave, MicaelaCosta, Francisco J. P.Alves, CátiaSousa, Rita LimaMelo, Bruna L.Correia, I.J.Diogo, Duarte de Melo2023-01-142025-04-04T00:00:00Z2023-01-14T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.6/13290eng10.1016/j.ejpb.2023.01.009info:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-12-15T09:56:47Zoai:ubibliorum.ubi.pt:10400.6/13290Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:52:45.040487Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT
title Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT
spellingShingle Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT
Nave, Micaela
Combinatorial triple therapy
Light responsive nanoparticles
Multifunctional nanomaterials
Photodynamic therapy
Poly(2-ethyl-2-oxazoline)
Polymer-IR780 conjugate
title_short Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT
title_full Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT
title_fullStr Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT
title_full_unstemmed Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT
title_sort Simple preparation of POxylated nanomaterials for cancer chemo-PDT/PTT
author Nave, Micaela
author_facet Nave, Micaela
Costa, Francisco J. P.
Alves, Cátia
Sousa, Rita Lima
Melo, Bruna L.
Correia, I.J.
Diogo, Duarte de Melo
author_role author
author2 Costa, Francisco J. P.
Alves, Cátia
Sousa, Rita Lima
Melo, Bruna L.
Correia, I.J.
Diogo, Duarte de Melo
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv uBibliorum
dc.contributor.author.fl_str_mv Nave, Micaela
Costa, Francisco J. P.
Alves, Cátia
Sousa, Rita Lima
Melo, Bruna L.
Correia, I.J.
Diogo, Duarte de Melo
dc.subject.por.fl_str_mv Combinatorial triple therapy
Light responsive nanoparticles
Multifunctional nanomaterials
Photodynamic therapy
Poly(2-ethyl-2-oxazoline)
Polymer-IR780 conjugate
topic Combinatorial triple therapy
Light responsive nanoparticles
Multifunctional nanomaterials
Photodynamic therapy
Poly(2-ethyl-2-oxazoline)
Polymer-IR780 conjugate
description Near infrared (NIR) light-responsive nanomaterials hold potential to mediate combinatorial therapies targeting several cancer hallmarks. When irradiated, these nanomaterials produce reactive oxygen species (photodynamic therapy) and/or a temperature increase (photothermal therapy). These events can damage cancer cells and trigger the release of drugs from the nanomaterials’ core. However, engineering nanomaterials for cancer chemophotodynamic/photothermal therapy is a complex process. First, nanomaterials with photothermal capacity are synthesized, being then loaded with photosensitizers plus chemotherapeutics, and, finally functionalized with polymers for achieving suitable biological properties. To overcome this limitation, in this work, a novel straightforward approach to attain NIR light-responsive nanosystems for cancer chemo-photodynamic/ photothermal therapy was established. Such was accomplished by synthesizing poly(2-ethyl-2-oxazoline)- IR780 amphiphilic conjugates, which can be assembled into nanoparticles with photodynamic/photothermal capabilities that simultaneously encapsulate Doxorubicin (DOX/PEtOx-IR NPs). The DOX/PEtOx-IR NPs presented a suitable size and surface charge for cancer-related applications. When irradiated with NIR light, the DOX/PEtOx-IR NPs produced singlet oxygen as well as a smaller thermic effect that boosted the release of DOX by 1.7-times. In the in vitro studies, the combination of DOX/PEtOx-IR NPs and NIR light could completely ablate breast cancer cells (viability ≈ 4 %), demonstrating the enhanced outcome arising from the nanomaterials' chemo-photodynamic/photothermal therapy.
publishDate 2023
dc.date.none.fl_str_mv 2023-01-14
2023-01-14T00:00:00Z
2025-04-04T00:00:00Z
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://hdl.handle.net/10400.6/13290
url http://hdl.handle.net/10400.6/13290
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.ejpb.2023.01.009
dc.rights.driver.fl_str_mv info:eu-repo/semantics/embargoedAccess
eu_rights_str_mv embargoedAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799136415854886912