N-(2-hydroxy)-propyl-3-trimethylammonium, O-palmitoyl chitosan: Synthesis, physicochemical and biological properties

dc.contributor.authorSilva, Daniella Souza [UNESP]
dc.contributor.authorFacchinatto, William Marcondes
dc.contributor.authorSantos, Danilo Martins dos
dc.contributor.authorBoni, Fernanda Isadora [UNESP]
dc.contributor.authorValdes, Talita Alvarenga
dc.contributor.authorLeitao, Andrei
dc.contributor.authorGremiao, Maria Palmira Daflon [UNESP]
dc.contributor.authorColnago, Luiz Alberto
dc.contributor.authorCampana-Filho, Sergio Paulo
dc.contributor.authorRibeiro, Sidney Jose Lima [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)
dc.date.accessioned2021-06-26T06:17:21Z
dc.date.available2021-06-26T06:17:21Z
dc.date.issued2021-05-01
dc.description.abstractTwo samples of N-(2-hydroxy)-propyl-3-trimethylammonium, O-palmitoyl chitosan (DPCat) with different av-erage degrees of quaternization named as DPCat35 (DQ = 35%) and DPCat80 (DQ = 80%), were successfully syn-thesized by reacting glycidyltrimethylammonium chloride (GTMAC) with O-palmitoyl chitosan (DPCh) derivative (DS = 12%). Such amphiphilic derivatives of chitosan were fully water-soluble at 1.0 < pH < 12.0 and showed significant electrostatic stability enhancement of a self-assembly micellar nanostructure (100 & ndash;320 nm) due to its positively-charged out-layer. In vitro mucoadhesive and cytotoxicity essays toward healthy fibroblast cells (Balb/C 3T3 clone A31 cell), human prostate cancer (DU145) and liver cancer (HepG2/ C3A) cell lines revealed that the biological properties of DPCat derivatives were strongly dependent on DQ. Ad-ditionally, DPCat35 had better interactions with the biological tissue and with mucin glycoproteins at pH 7.4 as well as exhibited potential to be used on the development of drug delivery systems for prostate and liver cancer treatment. (c) 2021 Elsevier B.V. All rights reserved.en
dc.description.affiliationSao Paulo State Univ, Inst Chem, Av Prof Francisco Degni 55,237, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUniv Sao Paulo, Sao Carlos Inst Chem, Av Trabalhador Sao Carlense 400,780, BR-13566590 Sao Carlos, SP, Brazil
dc.description.affiliationBrazilian Corp Agr Res, Embrapa Instrumentat, Rua XV Novembro 1452, BR-13560970 Sao Carlos, SP, Brazil
dc.description.affiliationSao Paulo State Univ, Sch Pharmaceut Sci, Rod Araraquara Jau Km 01 S-N, BR-14800903 Araraquara, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Inst Chem, Av Prof Francisco Degni 55,237, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Sch Pharmaceut Sci, Rod Araraquara Jau Km 01 S-N, BR-14800903 Araraquara, SP, Brazil
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.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipAuxilio Financeiro a Projeto Educacional ou de Pesquisa
dc.description.sponsorshipIdFAPESP: FAPESP 2016/20970-2
dc.description.sponsorshipIdFAPESP: 2017/20973-4
dc.description.sponsorshipIdFAPESP: 2019/13656-8
dc.description.sponsorshipIdCNPq: CNPq 141353/2016-3
dc.description.sponsorshipIdCNPq: 150964/2017-0
dc.description.sponsorshipIdCNPq: 309568/2019-6
dc.description.sponsorshipIdCAPES: 001
dc.description.sponsorshipIdAuxilio Financeiro a Projeto Educacional ou de Pesquisa: AUXPE 139/2015
dc.format.extent558-568
dc.identifierhttp://dx.doi.org/10.1016/j.ijbiomac.2021.02.031
dc.identifier.citationInternational Journal Of Biological Macromolecules. Amsterdam: Elsevier, v. 178, p. 558-568, 2021.
dc.identifier.doi10.1016/j.ijbiomac.2021.02.031
dc.identifier.issn0141-8130
dc.identifier.urihttp://hdl.handle.net/11449/210763
dc.identifier.wosWOS:000643948500008
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofInternational Journal Of Biological Macromolecules
dc.sourceWeb of Science
dc.subjectPositively-charged amphiphilic chitosan
dc.subjectMucoadhesive
dc.subjectCytocompatible
dc.subjectCancer therapy
dc.titleN-(2-hydroxy)-propyl-3-trimethylammonium, O-palmitoyl chitosan: Synthesis, physicochemical and biological propertiesen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
unesp.author.orcid0000-0002-1846-2700[2]
unesp.author.orcid0000-0002-6601-6609[6]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentFármacos e Medicamentos - FCFpt
unesp.departmentQuímica Inorgânica - IQARpt

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