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dc.contributor.authorGounko, Iouri
dc.date.accessioned2021-03-18T17:10:09Z
dc.date.available2021-03-18T17:10:09Z
dc.date.issued2018
dc.date.submitted2018en
dc.identifier.citationMartínez-Carmona, M., Gun'ko, Y.K., Vallet-Regí, M., Mesoporous Silica Materials as Drug Delivery: "The Nightmare" of Bacterial Infection, Pharmaceutics, 2018 Dec 15;10(4):279en
dc.identifier.otherY
dc.identifier.urihttp://hdl.handle.net/2262/95770
dc.description.abstractMesoporous silica materials (MSM) have a great surface area and a high pore volume, meaning that they consequently have a large loading capacity, and have been demonstrated to be unique candidates for the treatment of different pathologies, including bacterial infection. In this text, we review the multiple ways of action in which MSM can be used to fight bacterial infection, including early detection, drug release, targeting bacteria or biofilm, antifouling surfaces, and adjuvant capacity. This review focus mainly on those that act as a drug delivery system, and therefore that have an essential characteristic, which is their great loading capacity. Since MSM have advantages in all stages of combatting bacterial infection; its prevention, detection and finally in its treatment, we can venture to talk about them as the “nightmare of bacteria”.en
dc.language.isoenen
dc.relation.ispartofseriesPharmaceutics;
dc.relation.ispartofseries10;
dc.relation.ispartofseries4;
dc.rightsYen
dc.subjectMesoporous silicaen
dc.subjectMultifunctional nanoparticlesen
dc.subjectDrug deliveryen
dc.subjectBacterial infectionen
dc.subjectBacterial biofilmen
dc.subjectBiofilmen
dc.subjectAntibioticresistanceen
dc.subjectTargeting bacteriaen
dc.subjectTargeting biofilmen
dc.titleMesoporous Silica Materials as Drug Delivery: "The Nightmare" of Bacterial Infectionen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/igounko
dc.identifier.rssinternalid226130
dc.identifier.doihttp://dx.doi.org/10.3390/pharmaceutics10040279
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0002-4772-778X


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