Doxorubicin-loaded nanostructured lipid carriers functionalized with folic acid against MCF-7 breast cancer cell line
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , |
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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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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1808128469484175360 |