Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line

Detalhes bibliográficos
Autor(a) principal: Costa, Kammila Martins Nicolau
Data de Publicação: 2023
Outros Autores: Barros, Rafaella Moreno, Jorge, Emmily Oliveira, Sato, Mariana Rillo [UNESP], Chorilli, Marlus [UNESP], de Lima Damasceno, Bolívar Ponciano Goulart, Nicholas, Dean, Callan, John F., Oshiro Junior, João Augusto
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s11051-023-05704-7
http://hdl.handle.net/11449/248569
Resumo: Doxorubicin (DOX) is used in chemotherapy for the treatment of breast cancer (BC), however with several side effects. Nanostructured lipid carriers (NLCs) were developed from a mixture of surfactants, thermoresponsive and cationic quaternary ammonium, such as pluronic F-127 (PF-127-FA) and cetrimonium bromide (CTAB), respectively, and functionalized with folic acid as a strategy to target BC cells. This research aimed to develop NLC functionalized with folic acid containing DOX, directing its activity against BC cells (MCF-7). The NLCs obtained by the fusion-emulsification technique with (NLC +) and without (NLC-) cetrimonium bromide were developed and characterized to verify the guarantee of cationic or anionic charge. The results of dynamic light scattering sizes and scanning electron microscopy varied between 124 and 180 nm and, spherical morphology. Polydispersity < 0.3, indicating low polydispersity. Zeta potential revealed values between 22 and 13.2 for NLC + and -12.2 and -17 for NLC-. The encapsulation efficiency was 79% and 102% for NLC + and NLC-, respectively. The release profile was 100% after 10 h for DOX-NLC, while commercial DOX ≤ 30 min. Cell viability demonstrates that NLC- has higher cytotoxicity (87%) compared to commercial DOX (54%) (46 µM). NLC + with or without DOX increases greater toxicity (~ 90%). It is possible to conclude that NLCs have characteristics that point them as a potential alternative for preclinical studies in vivo, to elucidate their toxicity and antitumor activities. Graphical Abstract: As an alternative for the treatment of breast cancer, nanostructured lipid carriers containing doxorubicin functionalized with folic acid showed promising characteristics, such as high encapsulation index, high cytotoxicity to the target tissue and improved release when compared to commercial DOX.[Figure not available: see fulltext.]
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spelling Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell lineCancer therapyDrug delivery systemsNanoparticlesNanotechnologyDoxorubicin (DOX) is used in chemotherapy for the treatment of breast cancer (BC), however with several side effects. Nanostructured lipid carriers (NLCs) were developed from a mixture of surfactants, thermoresponsive and cationic quaternary ammonium, such as pluronic F-127 (PF-127-FA) and cetrimonium bromide (CTAB), respectively, and functionalized with folic acid as a strategy to target BC cells. This research aimed to develop NLC functionalized with folic acid containing DOX, directing its activity against BC cells (MCF-7). The NLCs obtained by the fusion-emulsification technique with (NLC +) and without (NLC-) cetrimonium bromide were developed and characterized to verify the guarantee of cationic or anionic charge. The results of dynamic light scattering sizes and scanning electron microscopy varied between 124 and 180 nm and, spherical morphology. Polydispersity < 0.3, indicating low polydispersity. Zeta potential revealed values between 22 and 13.2 for NLC + and -12.2 and -17 for NLC-. The encapsulation efficiency was 79% and 102% for NLC + and NLC-, respectively. The release profile was 100% after 10 h for DOX-NLC, while commercial DOX ≤ 30 min. Cell viability demonstrates that NLC- has higher cytotoxicity (87%) compared to commercial DOX (54%) (46 µM). NLC + with or without DOX increases greater toxicity (~ 90%). It is possible to conclude that NLCs have characteristics that point them as a potential alternative for preclinical studies in vivo, to elucidate their toxicity and antitumor activities. Graphical Abstract: As an alternative for the treatment of breast cancer, nanostructured lipid carriers containing doxorubicin functionalized with folic acid showed promising characteristics, such as high encapsulation index, high cytotoxicity to the target tissue and improved release when compared to commercial DOX.[Figure not available: see fulltext.]Graduate Program in Pharmaceutical Sciences Biological and Health Sciences Center State University of Paraíba (UEPB), ParaíbaUNIFACISA Centro Universitário, PBDepartment of Drugs and Medicines Faculdade de Ciências Farmacêuticas UNESP - Univ. Estadual Paulista, Campus Araraquara, SPBiomedical Sciences Research Institute University of UlsterDepartment of Drugs and Medicines Faculdade de Ciências Farmacêuticas UNESP - Univ. Estadual Paulista, Campus Araraquara, SPState University of Paraíba (UEPB)Centro UniversitárioUniversidade Estadual Paulista (UNESP)University of UlsterCosta, Kammila Martins NicolauBarros, Rafaella MorenoJorge, Emmily OliveiraSato, Mariana Rillo [UNESP]Chorilli, Marlus [UNESP]de Lima Damasceno, Bolívar Ponciano GoulartNicholas, DeanCallan, John F.Oshiro Junior, João Augusto2023-07-29T13:47:37Z2023-07-29T13:47:37Z2023-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s11051-023-05704-7Journal of Nanoparticle Research, v. 25, n. 4, 2023.1572-896X1388-0764http://hdl.handle.net/11449/24856910.1007/s11051-023-05704-72-s2.0-85150905710Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Nanoparticle Researchinfo:eu-repo/semantics/openAccess2024-06-24T13:45:18Zoai:repositorio.unesp.br:11449/248569Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:09:24.345875Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
title Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
spellingShingle Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
Costa, Kammila Martins Nicolau
Cancer therapy
Drug delivery systems
Nanoparticles
Nanotechnology
title_short Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
title_full Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
title_fullStr Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
title_full_unstemmed Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
title_sort Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
author Costa, Kammila Martins Nicolau
author_facet Costa, Kammila Martins Nicolau
Barros, Rafaella Moreno
Jorge, Emmily Oliveira
Sato, Mariana Rillo [UNESP]
Chorilli, Marlus [UNESP]
de Lima Damasceno, Bolívar Ponciano Goulart
Nicholas, Dean
Callan, John F.
Oshiro Junior, João Augusto
author_role author
author2 Barros, Rafaella Moreno
Jorge, Emmily Oliveira
Sato, Mariana Rillo [UNESP]
Chorilli, Marlus [UNESP]
de Lima Damasceno, Bolívar Ponciano Goulart
Nicholas, Dean
Callan, John F.
Oshiro Junior, João Augusto
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv State University of Paraíba (UEPB)
Centro Universitário
Universidade Estadual Paulista (UNESP)
University of Ulster
dc.contributor.author.fl_str_mv Costa, Kammila Martins Nicolau
Barros, Rafaella Moreno
Jorge, Emmily Oliveira
Sato, Mariana Rillo [UNESP]
Chorilli, Marlus [UNESP]
de Lima Damasceno, Bolívar Ponciano Goulart
Nicholas, Dean
Callan, John F.
Oshiro Junior, João Augusto
dc.subject.por.fl_str_mv Cancer therapy
Drug delivery systems
Nanoparticles
Nanotechnology
topic Cancer therapy
Drug delivery systems
Nanoparticles
Nanotechnology
description Doxorubicin (DOX) is used in chemotherapy for the treatment of breast cancer (BC), however with several side effects. Nanostructured lipid carriers (NLCs) were developed from a mixture of surfactants, thermoresponsive and cationic quaternary ammonium, such as pluronic F-127 (PF-127-FA) and cetrimonium bromide (CTAB), respectively, and functionalized with folic acid as a strategy to target BC cells. This research aimed to develop NLC functionalized with folic acid containing DOX, directing its activity against BC cells (MCF-7). The NLCs obtained by the fusion-emulsification technique with (NLC +) and without (NLC-) cetrimonium bromide were developed and characterized to verify the guarantee of cationic or anionic charge. The results of dynamic light scattering sizes and scanning electron microscopy varied between 124 and 180 nm and, spherical morphology. Polydispersity < 0.3, indicating low polydispersity. Zeta potential revealed values between 22 and 13.2 for NLC + and -12.2 and -17 for NLC-. The encapsulation efficiency was 79% and 102% for NLC + and NLC-, respectively. The release profile was 100% after 10 h for DOX-NLC, while commercial DOX ≤ 30 min. Cell viability demonstrates that NLC- has higher cytotoxicity (87%) compared to commercial DOX (54%) (46 µM). NLC + with or without DOX increases greater toxicity (~ 90%). It is possible to conclude that NLCs have characteristics that point them as a potential alternative for preclinical studies in vivo, to elucidate their toxicity and antitumor activities. Graphical Abstract: As an alternative for the treatment of breast cancer, nanostructured lipid carriers containing doxorubicin functionalized with folic acid showed promising characteristics, such as high encapsulation index, high cytotoxicity to the target tissue and improved release when compared to commercial DOX.[Figure not available: see fulltext.]
publishDate 2023
dc.date.none.fl_str_mv 2023-07-29T13:47:37Z
2023-07-29T13:47:37Z
2023-04-01
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/10.1007/s11051-023-05704-7
Journal of Nanoparticle Research, v. 25, n. 4, 2023.
1572-896X
1388-0764
http://hdl.handle.net/11449/248569
10.1007/s11051-023-05704-7
2-s2.0-85150905710
url http://dx.doi.org/10.1007/s11051-023-05704-7
http://hdl.handle.net/11449/248569
identifier_str_mv Journal of Nanoparticle Research, v. 25, n. 4, 2023.
1572-896X
1388-0764
10.1007/s11051-023-05704-7
2-s2.0-85150905710
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Nanoparticle Research
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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