Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy

Detalhes bibliográficos
Autor(a) principal: Oshiro-Junior, João A.
Data de Publicação: 2020
Outros Autores: Sato, Mariana Rillo [UNESP], Boni, Fernanda Isadora [UNESP], Santos, Karen Loraine Macena, de Oliveira, Kleber Thiago, de Freitas, Laura Marise [UNESP], Fontana, Carla Raquel [UNESP], Nicholas, Dean, McHale, Anthony, Callan, John F., Chorilli, Marlus [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.msec.2019.110462
http://hdl.handle.net/11449/199714
Resumo: Breast cancer is a serious public health problem that causes thousands of deaths annually. Chemotherapy continues to play a central role in the management of breast cancer but is associated with extreme off-target toxicity. Therefore, treatments that directly target the tumor and display reduced susceptibility to resistance could improve the outcome and quality of life for patients suffering from this disease. Photodynamic therapy is a targeted treatment based on the use of light to activate a photosensitizer (PS) that then interacts with molecular oxygen and other biochemical substrates to generate cytotoxic levels of Reactive Oxygen Species. Currently approved PS also tends to have poor aqueous solubility that can cause problems when delivered intravenously. In order to circumvent this limitation, in this manuscript, we evaluate the potential of a phthalocyanine-loaded nanostructured lipid carrier (NLC) functionalized with folic acid (FA). To prepare the FA labelled NLC, the polymer PF127 was first esterified with FA and emulsified with an oil phase containing polyoxyethylene 40 stearate, capric/caprylic acid triglycerides, ethoxylated hydrogenated castor oil 40 and the PS zinc phthalocyanine. The resulting PS loaded FA-NLC had a hydrodynamic diameter of 180 nm and were stable in suspension for >90 days. Interestingly, the amount of singlet oxygen generated upon light activation for the PS loaded FA-NLC was substantially higher than the free PS, yet at a lower PS concentration. The PS was released from the NLC in a sustained manner with 4.13 ± 0.58% and 27.7 ± 3.16% after 30 min and 7 days, respectively. Finally, cytotoxicity assays showed that NLC in the concentrations of 09.1 μM of PS present non-toxic with >80 ± 6.8% viable and after 90 s of the light-exposed the results show a statistically significant decrease in cell viability (57 ± 4%). The results obtained allow us to conclude that the functionalized NLC incorporated with PS associated with the PDT technique have characteristics that make them potential candidates for the alternative treatment of breast cancer.
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spelling Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapyBreast cancerFolic acidFunctionalizationNanostructured lipid carriersPhotodynamic therapyPhthalocyaninesBreast cancer is a serious public health problem that causes thousands of deaths annually. Chemotherapy continues to play a central role in the management of breast cancer but is associated with extreme off-target toxicity. Therefore, treatments that directly target the tumor and display reduced susceptibility to resistance could improve the outcome and quality of life for patients suffering from this disease. Photodynamic therapy is a targeted treatment based on the use of light to activate a photosensitizer (PS) that then interacts with molecular oxygen and other biochemical substrates to generate cytotoxic levels of Reactive Oxygen Species. Currently approved PS also tends to have poor aqueous solubility that can cause problems when delivered intravenously. In order to circumvent this limitation, in this manuscript, we evaluate the potential of a phthalocyanine-loaded nanostructured lipid carrier (NLC) functionalized with folic acid (FA). To prepare the FA labelled NLC, the polymer PF127 was first esterified with FA and emulsified with an oil phase containing polyoxyethylene 40 stearate, capric/caprylic acid triglycerides, ethoxylated hydrogenated castor oil 40 and the PS zinc phthalocyanine. The resulting PS loaded FA-NLC had a hydrodynamic diameter of 180 nm and were stable in suspension for >90 days. Interestingly, the amount of singlet oxygen generated upon light activation for the PS loaded FA-NLC was substantially higher than the free PS, yet at a lower PS concentration. The PS was released from the NLC in a sustained manner with 4.13 ± 0.58% and 27.7 ± 3.16% after 30 min and 7 days, respectively. Finally, cytotoxicity assays showed that NLC in the concentrations of 09.1 μM of PS present non-toxic with >80 ± 6.8% viable and after 90 s of the light-exposed the results show a statistically significant decrease in cell viability (57 ± 4%). The results obtained allow us to conclude that the functionalized NLC incorporated with PS associated with the PDT technique have characteristics that make them potential candidates for the alternative treatment of breast cancer.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Ulster UniversityConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Graduation Program in Pharmaceutical Sciences Center for Biological and Health Sciences State University of Paraíba (UEPB)São Paulo State University (UNESP) School of Pharmaceutical Sciences Araraquara Department of Drugs and Medicines, Rodovia Araraquara-Jaú, km 1Departamento de Química Universidade Federal de São CarlosSão Paulo State University (UNESP) School of Pharmaceutical Sciences Araraquara Department of Clinical Analyses, Rodovia Araraquara-Jaú, km 1Biomedical Sciences Research Institute University of UlsterSão Paulo State University (UNESP) School of Pharmaceutical Sciences Araraquara Department of Drugs and Medicines, Rodovia Araraquara-Jaú, km 1São Paulo State University (UNESP) School of Pharmaceutical Sciences Araraquara Department of Clinical Analyses, Rodovia Araraquara-Jaú, km 1FAPESP: 2014/50928-2Ulster University: 2016/11198-4Ulster University: 2018/17573-7CNPq: 465687/2014-8State University of Paraíba (UEPB)Universidade Estadual Paulista (Unesp)Universidade Federal de São Carlos (UFSCar)University of UlsterOshiro-Junior, João A.Sato, Mariana Rillo [UNESP]Boni, Fernanda Isadora [UNESP]Santos, Karen Loraine Macenade Oliveira, Kleber Thiagode Freitas, Laura Marise [UNESP]Fontana, Carla Raquel [UNESP]Nicholas, DeanMcHale, AnthonyCallan, John F.Chorilli, Marlus [UNESP]2020-12-12T01:47:21Z2020-12-12T01:47:21Z2020-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.msec.2019.110462Materials Science and Engineering C, v. 108.1873-01910928-4931http://hdl.handle.net/11449/19971410.1016/j.msec.2019.1104622-s2.0-85075568921Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMaterials Science and Engineering Cinfo:eu-repo/semantics/openAccess2024-06-24T13:45:38Zoai:repositorio.unesp.br:11449/199714Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T17:12:58.235343Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy
title Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy
spellingShingle Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy
Oshiro-Junior, João A.
Breast cancer
Folic acid
Functionalization
Nanostructured lipid carriers
Photodynamic therapy
Phthalocyanines
title_short Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy
title_full Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy
title_fullStr Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy
title_full_unstemmed Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy
title_sort Phthalocyanine-loaded nanostructured lipid carriers functionalized with folic acid for photodynamic therapy
author Oshiro-Junior, João A.
author_facet Oshiro-Junior, João A.
Sato, Mariana Rillo [UNESP]
Boni, Fernanda Isadora [UNESP]
Santos, Karen Loraine Macena
de Oliveira, Kleber Thiago
de Freitas, Laura Marise [UNESP]
Fontana, Carla Raquel [UNESP]
Nicholas, Dean
McHale, Anthony
Callan, John F.
Chorilli, Marlus [UNESP]
author_role author
author2 Sato, Mariana Rillo [UNESP]
Boni, Fernanda Isadora [UNESP]
Santos, Karen Loraine Macena
de Oliveira, Kleber Thiago
de Freitas, Laura Marise [UNESP]
Fontana, Carla Raquel [UNESP]
Nicholas, Dean
McHale, Anthony
Callan, John F.
Chorilli, Marlus [UNESP]
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv State University of Paraíba (UEPB)
Universidade Estadual Paulista (Unesp)
Universidade Federal de São Carlos (UFSCar)
University of Ulster
dc.contributor.author.fl_str_mv Oshiro-Junior, João A.
Sato, Mariana Rillo [UNESP]
Boni, Fernanda Isadora [UNESP]
Santos, Karen Loraine Macena
de Oliveira, Kleber Thiago
de Freitas, Laura Marise [UNESP]
Fontana, Carla Raquel [UNESP]
Nicholas, Dean
McHale, Anthony
Callan, John F.
Chorilli, Marlus [UNESP]
dc.subject.por.fl_str_mv Breast cancer
Folic acid
Functionalization
Nanostructured lipid carriers
Photodynamic therapy
Phthalocyanines
topic Breast cancer
Folic acid
Functionalization
Nanostructured lipid carriers
Photodynamic therapy
Phthalocyanines
description Breast cancer is a serious public health problem that causes thousands of deaths annually. Chemotherapy continues to play a central role in the management of breast cancer but is associated with extreme off-target toxicity. Therefore, treatments that directly target the tumor and display reduced susceptibility to resistance could improve the outcome and quality of life for patients suffering from this disease. Photodynamic therapy is a targeted treatment based on the use of light to activate a photosensitizer (PS) that then interacts with molecular oxygen and other biochemical substrates to generate cytotoxic levels of Reactive Oxygen Species. Currently approved PS also tends to have poor aqueous solubility that can cause problems when delivered intravenously. In order to circumvent this limitation, in this manuscript, we evaluate the potential of a phthalocyanine-loaded nanostructured lipid carrier (NLC) functionalized with folic acid (FA). To prepare the FA labelled NLC, the polymer PF127 was first esterified with FA and emulsified with an oil phase containing polyoxyethylene 40 stearate, capric/caprylic acid triglycerides, ethoxylated hydrogenated castor oil 40 and the PS zinc phthalocyanine. The resulting PS loaded FA-NLC had a hydrodynamic diameter of 180 nm and were stable in suspension for >90 days. Interestingly, the amount of singlet oxygen generated upon light activation for the PS loaded FA-NLC was substantially higher than the free PS, yet at a lower PS concentration. The PS was released from the NLC in a sustained manner with 4.13 ± 0.58% and 27.7 ± 3.16% after 30 min and 7 days, respectively. Finally, cytotoxicity assays showed that NLC in the concentrations of 09.1 μM of PS present non-toxic with >80 ± 6.8% viable and after 90 s of the light-exposed the results show a statistically significant decrease in cell viability (57 ± 4%). The results obtained allow us to conclude that the functionalized NLC incorporated with PS associated with the PDT technique have characteristics that make them potential candidates for the alternative treatment of breast cancer.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T01:47:21Z
2020-12-12T01:47:21Z
2020-03-01
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.msec.2019.110462
Materials Science and Engineering C, v. 108.
1873-0191
0928-4931
http://hdl.handle.net/11449/199714
10.1016/j.msec.2019.110462
2-s2.0-85075568921
url http://dx.doi.org/10.1016/j.msec.2019.110462
http://hdl.handle.net/11449/199714
identifier_str_mv Materials Science and Engineering C, v. 108.
1873-0191
0928-4931
10.1016/j.msec.2019.110462
2-s2.0-85075568921
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Materials Science and Engineering C
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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