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Publicação:
Encapsulation of Local Anesthetic Bupivacaine in Biodegradable Poly(DL-lactide-co-glycolide) Nanospheres: Factorial Design, Characterization and Cytotoxicity Studies

dc.contributor.authorMoraes, Carolina Morales
dc.contributor.authorde Lima, Renata
dc.contributor.authorRosa, Andre Henrique [UNESP]
dc.contributor.authorde Paula, Eneida
dc.contributor.authorFraceto, Leonardo Fernandes [UNESP]
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniv Sorocaba
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:12:12Z
dc.date.available2014-05-20T13:12:12Z
dc.date.issued2009-01-01
dc.description.abstractLocal anesthetic agents cause temporary blockade of nerve impulses productiong insensitivity to painful stimuli in the area supplied by that nerve. Bupivacaine (BVC) is an amide-type local anesthetic widely used in surgery and obstetrics for sustained peripheral and central nerve blockade. in this study, we prepared and characterized nanosphere formulations containing BVC. To achieve these goals, BVC loaded poly(DL-lactide-co-glycolide) (PLGA) nanospheres (NS) were prepared by nanopreciptation and characterized with regard to size distribution, drug loading and cytotoxicity assays. The 2(3-1) factorial experimental design was used to study the influence of three different independent variables on nanoparticle drug loading. BVC was assayed by HPLC, the particle size and zeta potential were determined by dynamic light scattering. BVC was determined using a combined ultrafiltration-centrifugation technique. The results of optimized formulations showed a narrow size distribution with a polydispersivity of 0.05%, an average diameter of 236.7 +/- 2.6 nm and the zeta potential -2.93 +/- 1,10 mV. In toxicity studies with fibroblast 3T3 cells, BVC loaded-PLGA-NS increased cell viability, in comparison with the effect produced by free BVC. In this way, BVC-loaded PLGA-NS decreased BVC toxicity. The development of BVC formulations in carriers such as nanospheres could offer the possibility of controlling drug delivery in biological systems, prolonging the anesthetic effect and reducing toxicity.en
dc.description.affiliationUniv Estadual Campinas, Dept Biochem, Inst Biol, Campinas, SP, Brazil
dc.description.affiliationUniv Sorocaba, Dept Biotechnol, Sorocaba, SP, Brazil
dc.description.affiliationJulio de Mesquita Filho State Univ São Paulo, Dept Environm Engn, Sorocaba, SP, Brazil
dc.description.affiliationUnespJulio de Mesquita Filho State Univ São Paulo, Dept Environm Engn, Sorocaba, SP, Brazil
dc.format.extent106-112
dc.identifierhttp://dx.doi.org/10.1002/masy.200950714
dc.identifier.citationMacromolecular Symposia. Weinheim: Wiley-v C H Verlag Gmbh, v. 281, p. 106-112, 2009.
dc.identifier.doi10.1002/masy.200950714
dc.identifier.issn1022-1360
dc.identifier.orcid0000-0002-2042-018X
dc.identifier.urihttp://hdl.handle.net/11449/185
dc.identifier.wosWOS:000268989100015
dc.language.isoeng
dc.publisherWiley-v C H Verlag Gmbh
dc.relation.ispartofMacromolecular Symposia
dc.relation.ispartofsjr0,235
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectbupivacaineen
dc.subjectlocal anestheticen
dc.subjectpolymeric nanoparticleen
dc.subjectpoly(DL-lactide-co-glycolide) nanospheresen
dc.titleEncapsulation of Local Anesthetic Bupivacaine in Biodegradable Poly(DL-lactide-co-glycolide) Nanospheres: Factorial Design, Characterization and Cytotoxicity Studiesen
dc.typeTrabalho apresentado em evento
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-v C H Verlag Gmbh
dspace.entity.typePublication
unesp.author.lattes5228846314663888[3]
unesp.author.orcid0000-0002-2042-018X[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, Sorocabapt
unesp.departmentEngenharia Ambiental - ICTSpt

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