dc.creatorGonzález, Belén
dc.creatorBrugnoni, Lorena Inés
dc.creatorSaidman, Silvana Beatriz
dc.date.accessioned2020-05-05T20:49:40Z
dc.date.accessioned2022-10-14T22:45:46Z
dc.date.available2020-05-05T20:49:40Z
dc.date.available2022-10-14T22:45:46Z
dc.date.created2020-05-05T20:49:40Z
dc.date.issued2019-03
dc.identifierGonzález, Belén; Brugnoni, Lorena Inés; Saidman, Silvana Beatriz; Salicylate release from a polypyrrole matrix; Elsevier; Materials Today Communications; 18; 3-2019; 119-123
dc.identifier2352-4928
dc.identifierhttp://hdl.handle.net/11336/104301
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4315589
dc.description.abstractSalicylate release from a microstructured polypyrrole coating with a large surface area was investigated. Thedrug was incorporated as a dopant in the polymer matrix via electropolymerization of pyrrole in a simple one-step process. The influence of several parameters such as applied potential and hydrodynamic conditions on thereleasing behavior was studied. Once the drug has been delivered from the polymeric matrix, the electrode canbe reloaded with salicylate for later release. The amount of eluted salicylate was effective in inhibiting albumindenaturation which is associated with antiinflammatory effects.
dc.languageeng
dc.publisherElsevier
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/j.mtcomm.2018.11.012
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S235249281830271X
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectANTIINFLAMMATORY AGENT
dc.subjectDRUG DELIVERY
dc.subjectELECTROPOLYMERIZATION
dc.subjectPOLYPYRROLE
dc.subjectSALICYLATE
dc.titleSalicylate release from a polypyrrole matrix
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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