Publicação:
Polymeric alginate nanoparticles containing the local anesthetic bupivacaine

dc.contributor.authorGrillo, Renato [UNESP]
dc.contributor.authorde Melo, Nathalie F. S. [UNESP]
dc.contributor.authorde Araujo, Daniele Ribeiro
dc.contributor.authorde Paula, Eneida
dc.contributor.authorRosa, Andre Henrique [UNESP]
dc.contributor.authorFraceto, Leonardo Fernandes [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Federal do ABC (UFABC)
dc.date.accessioned2014-05-20T13:12:13Z
dc.date.available2014-05-20T13:12:13Z
dc.date.issued2010-11-01
dc.description.abstractBupivacaine (BVC; S75-R25, NovaBupi<SU (R)</SU) is an amide-type local anesthetic. Sodium alginate is a water-soluble linear polysaccharide. The present study reports the development of alginate/bis(2-ethylhexyl) sulfosuccinate (AOT) and alginate/chitosan nanoparticle formulations containing BVC (0.5%). The amounts of BVC associated in the alginate/AOT and alginate/chitosan nanoparticles were 87 +/- 1.5 and 76 +/- 0.9%, respectively. The average diameters and zeta potentials of the nanoparticles were measured for 30 days, and the results demonstrated the good stability of these particles in solution. The in vitro release kinetics showed a different behavior for the release profile of BVC in solution, compared with BVC-loaded alginate nanoparticles. In vitro and in vivo assays showed that alginate-chitosan BVC (BVC(ALG-CHIT)) and alginate-AOT BVC (BVC(ALG-AOT)) presented low cytotoxicity in 3T3-fibroblasts, enhanced the intensity, and prolonged the duration of motor and sensory blockades in a sciatic nerve blockade model.</.en
dc.description.affiliationUnesp São Paulo State Univ, Dept Environm Engn, BR-18087180 Sorocaba, SP, Brazil
dc.description.affiliationUniv Estadual Campinas, Inst Biol, Dept Biochem, Campinas, SP, Brazil
dc.description.affiliationFed Univ ABC, Human & Nat Sci Ctr, Santo Andre, SP, Brazil
dc.description.affiliationUnespUnesp São Paulo State Univ, Dept Environm Engn, BR-18087180 Sorocaba, 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.sponsorshipFundação para o Desenvolvimento da UNESP (FUNDUNESP)
dc.description.sponsorshipIdFAPESP: 06/00121-9
dc.description.sponsorshipIdFUNDUNESP: 06/00121-9
dc.description.sponsorshipIdFUNDUNESP: 07/00127-0
dc.description.sponsorshipIdFUNDUNESP: 08/01222-9
dc.format.extent688-699
dc.identifierhttp://dx.doi.org/10.3109/10611861003649738
dc.identifier.citationJournal of Drug Targeting. London: Informa Healthcare, v. 18, n. 9, p. 688-699, 2010.
dc.identifier.doi10.3109/10611861003649738
dc.identifier.issn1061-186X
dc.identifier.lattes2188736885721242
dc.identifier.orcid0000-0002-2042-018X
dc.identifier.orcid0000-0002-0284-5782
dc.identifier.urihttp://hdl.handle.net/11449/202
dc.identifier.wosWOS:000282516600005
dc.language.isoeng
dc.publisherInforma Healthcare
dc.relation.ispartofJournal of Drug Targeting
dc.relation.ispartofjcr3.408
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectBupivacaineen
dc.subjectpolymeric nanoparticlesen
dc.subjectalginateen
dc.subjectin vivoen
dc.subjectin vitroen
dc.titlePolymeric alginate nanoparticles containing the local anesthetic bupivacaineen
dc.typeArtigo
dcterms.licensehttp://informahealthcare.com/page/resources/authors
dcterms.rightsHolderInforma Healthcare
dspace.entity.typePublication
unesp.author.lattes5228846314663888[5]
unesp.author.lattes2188736885721242[1]
unesp.author.orcid0000-0002-2042-018X[5]
unesp.author.orcid0000-0002-0284-5782[1]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, Sorocabapt
unesp.departmentEngenharia Ambiental - ICTSpt

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