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Anti-EGFR liquid crystalline nanodispersions for docetaxel delivery: Formulation, characterization and cytotoxicity in cancer cells

dc.contributor.authorTrevizan, Lucas Noboru Fatori [UNESP]
dc.contributor.authorEloy, Josimar O.
dc.contributor.authorLuiz, Marcela Tavares
dc.contributor.authorPetrilli, Raquel
dc.contributor.authorJunior, Sergio Luiz Ramos
dc.contributor.authorBorges, Julio César
dc.contributor.authorMarchetti, Juliana Maldonado
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionDentistry and Nursing
dc.contributor.institutionInstitute of Health Sciences
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2021-06-25T10:49:19Z
dc.date.available2021-06-25T10:49:19Z
dc.date.issued2021-03-20
dc.description.abstractProstate cancer is one of the most frequent neoplasms, associated with high mortality. Some factors may intensify its aggressiveness, for example, the overexpression of the epidermal growth factor receptor (EGFR) in some subtypes of prostate tumors. In this context, the inhibition of EGFR helps to fight neoplasia, with the use of the chimeric anti-EGFR monoclonal antibody, cetuximab (CTX). For cancer treatment in the metastatic stage, chemotherapy using docetaxel (DTX) is widely employed, however the drug is very liposoluble, hampering its bioavailability. In this sense, liquid crystalline systems have great potential for the delivery of DTX. Particularly, liquid crystalline nanodispersions can be used in parenteral routes, with many advantages, including the possibility of prolonged drug release, improved pharmacokinetics, allowing passive tumor accumulation by the EPR effect. Thus, the objective of this work was to develop a liquid crystalline nanodispersion (LCN) based on ethoxylated cetyl alcohol 20 and propoxylated 5 as surfactant (Procetyl®), oleic acid, DSPE-PEG-MAL (anchor for CTX binding) and soy phosphatidylcholine as oily phase and 1.5 % poloxamer dispersion in PBS buffer as an aqueous phase. The formulation was loaded with DTX and covalently functionalized with CTX to evaluate its cytotoxic potential against prostate cancer cells. The results suggested that the obtained system has a predominantly hexagonal crystalline phase, was able to be nanodispersed with low polydispersity, and presented negative zeta potential. CTX did not have its structure compromised after thiolation and was successfully covalently linked to LCN. In a prostate cancer cells, PC3, LCNs functionalized with CTX underwent greater cell uptake, resulting in greater cytotoxicity, compared to free DTX and non-functionalized DTX-loaded LCNs. Therefore, the present study reports for the first time an EGFR-targeted liquid crystal nanodispersion for selective to deliver DTX to prostate cellsen
dc.description.affiliationSchool of Pharmaceutical Sciences of Araraquara São Paulo State University UNESP Department of Drugs and Medicines
dc.description.affiliationFederal University of Ceará College of Pharmacy Dentistry and Nursing Department of Pharmacy
dc.description.affiliationUniversity of International Integration of the Afro-Brazilian Lusophony Institute of Health Sciences
dc.description.affiliationSão Carlos Institute of Chemistry University of São Paulo, São Carlos
dc.description.affiliationSchool of Pharmaceutical Sciences of Ribeirão Preto University of São Paulo Ribeirão Preto
dc.description.affiliationUnespSchool of Pharmaceutical Sciences of Araraquara São Paulo State University UNESP Department of Drugs and Medicines
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdCNPq: # 465687/2014-8
dc.description.sponsorshipIdFAPESP: #2014/50928-2
dc.identifierhttp://dx.doi.org/10.1016/j.colsurfa.2020.126058
dc.identifier.citationColloids and Surfaces A: Physicochemical and Engineering Aspects, v. 613.
dc.identifier.doi10.1016/j.colsurfa.2020.126058
dc.identifier.issn1873-4359
dc.identifier.issn0927-7757
dc.identifier.scopus2-s2.0-85099263069
dc.identifier.urihttp://hdl.handle.net/11449/207124
dc.language.isoeng
dc.relation.ispartofColloids and Surfaces A: Physicochemical and Engineering Aspects
dc.sourceScopus
dc.subjectCetuximab
dc.subjectDocetaxel
dc.subjectHexosome
dc.subjectLiquid crystal
dc.subjectNanodispersion
dc.titleAnti-EGFR liquid crystalline nanodispersions for docetaxel delivery: Formulation, characterization and cytotoxicity in cancer cellsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.author.orcid0000-0003-4856-748X[6]
unesp.departmentFármacos e Medicamentos - FCFpt

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