http://www.cnr.it/ontology/cnr/individuo/prodotto/ID290763
Host-guest interactions in Fe(III)-trimesate MOF nanoparticles loaded with doxorubicin (Articolo in rivista)
- Type
- Label
- Host-guest interactions in Fe(III)-trimesate MOF nanoparticles loaded with doxorubicin (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/jp503809w (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Anand R.; Borghi F.; Manoli F.; Manet I.; Agostoni V.; Reschiglian P.; Gref R.; Monti S. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://www.scopus.com/inward/record.url?eid=2-s2.0-84905028698&partnerID=q2rCbXpz (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Note
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto per la Sintesi Organica e la Fotoreattività, ISOF-CNR, Via Piero Gobetti 101, Bologna I-40129, Italy; Université Paris-Sud, UMR CNRS 8612, 5 rue JB Clément, Châtenay Malabry 92290, France; Dipartimento di Chimica G. Ciamician, Università di Bologna, Via Selmi 2, Bologna I-40126, Italy; ByFlow Srl, Via Piero Gobetti 52/3, Bologna I-40129, Italy (literal)
- Titolo
- Host-guest interactions in Fe(III)-trimesate MOF nanoparticles loaded with doxorubicin (literal)
- Abstract
- Doxorubicin (DOX) entrapment in porous Fe(III)-trimesate metal
organic frameworks (MIL-100(Fe)) nanoparticles was investigated in neutral Tris
buffer via UV-vis absorption, circular dichroism (CD), and fluorescence. The binding
constants and the absolute spectra of the DOX-MIL-100(Fe) complexes were
determined via absorption and fluorescence titrations. A binding model where DOX
associates as monomer to the dehydrated Fe3O (OH)(H2O)2 [(C6H3)(CO2)3]2
structural unit in 1:1 stoichiometry, with apparent association constant of (1.1 to
1.8) × 104 M-1, was found to reasonably fit the experimental data. Spectroscopic data
indicate that DOX binding occurs via the formation of highly stable coordination bonds
between one or both deprotonated hydroxyl groups of the aglycone moiety and
coordinatively unsaturated Fe(III) centers. Complete quenching of the DOX
fluorescence and remarkable thermal and photochemical stability were observed for
DOX incorporated in the MIL-100(Fe) framework. (literal)
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- Autore CNR
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