dc.creatorFraceto L.F.
dc.creatorGrillo R.
dc.creatorSobarzo-Sanchez E.
dc.date2014
dc.date2015-06-25T17:53:27Z
dc.date2015-11-26T14:23:54Z
dc.date2015-06-25T17:53:27Z
dc.date2015-11-26T14:23:54Z
dc.date.accessioned2018-03-28T21:25:58Z
dc.date.available2018-03-28T21:25:58Z
dc.identifier
dc.identifierCurrent Topics In Medicinal Chemistry. , v. 14, n. 4, p. 518 - 525, 2014.
dc.identifier15680266
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84894077319&partnerID=40&md5=69e970d7f3217fb9edece5d80faa7bab
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/86455
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/86455
dc.identifier2-s2.0-84894077319
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1245253
dc.descriptionThis mini-review paper does not consider classical work concerning the formation of inclusion complexes between pharmaceuticals and cyclodextrins. Instead, it highlights recent reports concerning the association of these host:guest systems with other carrier systems such as liposomes and nanoparticles showing the state of art of this subject with examples of developed systems and the advantages of these strategy in order to be potential systems as drug carriers. © 2014 Bentham Science Publishers.
dc.description14
dc.description4
dc.description518
dc.description525
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dc.languageen
dc.publisher
dc.relationCurrent Topics in Medicinal Chemistry
dc.rightsfechado
dc.sourceScopus
dc.titleCyclodextrin Inclusion Complexes Loaded In Particles As Drug Carrier Systems
dc.typeArtículos de revistas


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