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Authordc.contributor.authorSolar, Paula 
Authordc.contributor.authorGonzález Moraga, Guillermo 
Authordc.contributor.authorVilos, Cristian 
Authordc.contributor.authorHerrera, Natalia 
Authordc.contributor.authorJuica, Natalia 
Authordc.contributor.authorMoreno, Mabel 
Authordc.contributor.authorSimón, Felipe 
Authordc.contributor.authorVelásquez, Luis 
Admission datedc.date.accessioned2015-07-30T18:59:32Z
Available datedc.date.available2015-07-30T18:59:32Z
Publication datedc.date.issued2015
Cita de ítemdc.identifier.citationJournal of Nanobiotechnology (2015) 13:14en_US
Identifierdc.identifier.otherDOI: 10.1186/s12951-015-0077-5
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/132268
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractBackground: Advances in nanostructure materials are leading to novel strategies for drug delivery and targeting, contrast media for magnetic resonance imaging (MRI), agents for hyperthermia and nanocarriers. Superparamagnetic iron oxide nanoparticles (SPIONs) are useful for all of these applications, and in drug-release systems, SPIONs allow for the localization, direction and concentration of drugs, providing a broad range of therapeutic applications. In this work, we developed and characterized polymeric nanoparticles based on poly (3-hydroxybutyric acid-co-hydroxyvaleric acid) (PHBV) functionalized with SPIONs and/or the antibiotic ceftiofur. These nanoparticles can be used in multiple biomedical applications, and the hybrid SPION-ceftiofur nanoparticles (PHBV/SPION/CEF) can serve as a multifunctional platform for the diagnosis and treatment of cancer and its associated bacterial infections. Results: Morphological examination using transmission electron microscopy (TEM) showed nanoparticles with a spherical shape and a core-shell structure. The particle size was evaluated using dynamic light scattering (DLS), which revealed a diameter of 243.0 +/- 17 nm. The efficiency of encapsulation (45.5 +/- 0.6% w/v) of these polymeric nanoparticles was high, and their components were evaluated using spectroscopy. UV-VIS, FTIR and DSC showed that all of the nanoparticles contained the desired components, and these compounds interacted to form a nanocomposite. Using the agar diffusion method and live/dead bacterial viability assays, we demonstrated that these nanoparticles have antimicrobial properties against Escherichia coli, and they retain their magnetic properties as measured using a vibrating sample magnetometer (VSM). Cytotoxicity was assessed in HepG2 cells using live/dead viability assays and MTS, and these assays showed low cytotoxicity with IC50 > 10 mg/mL nanoparticles. Conclusions: Our results indicate that hybrid and multifunctional PHBV/SPION/CEF nanoparticles are suitable as a superparamagnetic drug delivery system that can guide, concentrate and site-specifically release drugs with antibacterial activity.en_US
Patrocinadordc.description.sponsorshipCenter for the Development of Nanoscience and Nanotechnology (CEDENNA), CONICYT—PCHA/ Doctorado nacional/ 2013-21130869, Grant Number: Anillo ACT 1107. CV acknowledges the support of the Grant TPI06 and the Postdoctoral Program of Becas-Chile/CONICYT, FONDECYT 1120712 and Convenio de Desempeño de Apoyo a la Educación Superior MINEDUC-UNAB, PMI UAB1301.en_US
Lenguagedc.language.isoen_USen_US
Publisherdc.publisherBIOMED CENTRALen_US
Type of licensedc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Keywordsdc.subjectPHBVen_US
Keywordsdc.subjectSPIONen_US
Keywordsdc.subjectCeftiofuren_US
Keywordsdc.subjectPolymeric nanoparticlesen_US
Keywordsdc.subjectDrug deliveryen_US
Keywordsdc.subjectSuperparamagnetic nanoparticlesen_US
Títulodc.titleMultifunctional polymeric nanoparticles doubly loaded with SPION and ceftiofur retain their physical and biological propertiesen_US
Document typedc.typeArtículo de revista


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Atribución-NoComercial-SinDerivadas 3.0 Chile
Except where otherwise noted, this item's license is described as Atribución-NoComercial-SinDerivadas 3.0 Chile