http://www.cnr.it/ontology/cnr/individuo/prodotto/ID304277
beta-Cyclodextrin-grafted on multiwalled carbon nanotubes as versatile nanoplatform for entrapment of guanine-based drugs (Articolo in rivista)
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- Label
- beta-Cyclodextrin-grafted on multiwalled carbon nanotubes as versatile nanoplatform for entrapment of guanine-based drugs (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Alternative label
Iannazzo, Daniela; Mazzaglia, Antonino; Scala, Angela; Pistone, Alessandro; Galvagno, Signorino; Lanza, Maurizio; Riccucci, Cristina; Ingo, Gabriel Maria; Colao, Ivana; Sciortino, Maria Teresa; Valle, Francesco; Piperno, Anna; Grassi, Giovanni (2014)
beta-Cyclodextrin-grafted on multiwalled carbon nanotubes as versatile nanoplatform for entrapment of guanine-based drugs
in Colloids and surfaces. B, Biointerfaces (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Iannazzo, Daniela; Mazzaglia, Antonino; Scala, Angela; Pistone, Alessandro; Galvagno, Signorino; Lanza, Maurizio; Riccucci, Cristina; Ingo, Gabriel Maria; Colao, Ivana; Sciortino, Maria Teresa; Valle, Francesco; Piperno, Anna; Grassi, Giovanni (literal)
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- ISI Web of Science (WOS) (literal)
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- Univ Messina; Univ Messina; Consiglio Nazl Ric CNR IPCF; Consiglio Nazl Ric CNR ISMN; Univ Messina; Consiglio Nazl Ric CNR ISMN; Univ Messina (literal)
- Titolo
- beta-Cyclodextrin-grafted on multiwalled carbon nanotubes as versatile nanoplatform for entrapment of guanine-based drugs (literal)
- Abstract
- The design of beta-cyclodextrin/multiwalled carbon nanotubes hybrid (beta-CD-MWCNT) as nanoplatform for the entrapment and delivery of guanine based drugs is described here. The functionalized carbon nanomaterials have been characterized by XPS spectroscopy, electron microscopy (FEG-SEM and TEM), AFM, TGA, and FT-IR to achieve insights on structure, morphology and chemical composition. The drug binding abilities of nanocarrier towards the guanine (G) and Acyclovir (Acy) were proved by UV-vis and DSC experiments. Host-guest equilibrium association constants and drug loading have been evaluated for G/beta-CD-MWCNT and Acy/beta-CD-MWCNT complexes. The release studies showed a sustained delivery of Acy without initial burst effect confirming a strong interaction of drug with the nanoplatform sites. The preliminary antiviral data indicated that the Acyclovir loaded into the beta-CD-MWCNT platform interferes with HSV-1 replication and the antireplicative effect was higher than the free drug. (C) 2014 Elsevier B.V. All rights reserved. (literal)
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