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dc.contributor.authorNieto-Chaupis, Huber
dc.date.accessioned2023-09-14T22:20:58Z
dc.date.available2023-09-14T22:20:58Z
dc.date.issued2021
dc.identifier.urihttps://hdl.handle.net/20.500.13067/2570
dc.description.abstractThe imminent advance of Nanomedicine is clearly reflected in the implementation of techniques based on drug deliv-ery towards concrete places that are contaminated by anomalous tissues and tumors. A promising as well as robust vehicle are the well- known nanoparticle. Therefore one expects a crucial role of engineered nanoparticles to accomplish exact tasks surpassing known achievements from the side of current pharmacology. However, in all those charged superficially nanoparticles one can expect a latent function that might be a disadvantage as to the main role of targeted drug delivery schemes and medical purposes. In this paper, a theory the apparition of nanocurrents produced a continue accumulation of charged nanoparticles, and that would be caused by diffusive effects is constructed and the consequences from it are identified. Thus, from the results of this paper the explicit dependence of diffusion coefficient is derived. This would acquire relevance in the advanced Oncology that requires of precision and efficiency.es_PE
dc.formatapplication/pdfes_PE
dc.language.isoenges_PE
dc.publisherIEEEes_PE
dc.rightsinfo:eu-repo/semantics/restrictedAccesses_PE
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/es_PE
dc.subjectNanoparticleses_PE
dc.subjectTargeted drug deliveryes_PE
dc.subjectOncologyes_PE
dc.subjectTrajectoryes_PE
dc.subjectSecurityes_PE
dc.subjectTask analysises_PE
dc.subjectNanomedicinees_PE
dc.titleDiffusive Nanoparticles and Generation of Repulsive Effects by Artificial Electrical Currentses_PE
dc.typeinfo:eu-repo/semantics/articlees_PE
dc.identifier.journalProceedings of the 2021 6th International Conference on Computing, Communication and Security, ICCCS 2021es_PE
dc.identifier.doihttps://doi.org/10.1109/ICCCS51487.2021.9776328
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#2.02.04es_PE


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