Silvia Nappini

Dr. Silvia Nappini

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Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 June 2017 in Journal of the American Chemical Society
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Journal Article
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Marco FavaroMarco Favaro
Marco Favaro
JYJinhui Yang
Jinhui Yang
SNSilvia Nappini
Silvia Nappini
EMELENA MAGNANO
ELENA MAGNANO
FTFrancesca M. Toma
Francesca M. Toma
ISIan D. Sharp
Ian D. Sharp

16 November 2009 in Soft Matter
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Journal Article
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SNSilvia Nappini
Silvia Nappini
FBFrancesca Baldelli Bombelli
Francesca Baldelli Bombelli
MBMassimo Bonini
Massimo Bonini
BNBengt Nordén
Bengt Nordén
PBPiero Baglioni
Piero Baglioni
In this work we have studied the effect of a low-frequency alternating magnetic field (LF-AMF) on the permeability of magnetoliposomes, i.e. liposomes including magnetic nanoparticles within their water pool. Large unilamellar liposomes loaded with magnetic cobalt ferrite nanoparticles (CoFe2O4) have been prepared and characterized. Structural characterization of the liposomal dispersion has been performed by dynamic light scattering (DLS). The enhancement of liposome permeability upon exposure to LF-AMF has been measured as the self-quenching decrease of a fluorescent hydrophilic molecule (carboxyfluorescein, CF) entrapped in the liposome pool. Liposome leakage has been monitored as a function of field frequency, time of exposure and concentration, charge and size of the embedded nanoparticles. The results show that CF release from magnetoliposomes is strongly promoted by LF-AMF, reasonably as a consequence of nanoparticle motions in the liposome pool at the applied frequency. CF release as a function of time in magnetoliposomes unexposed to magnetic field follows Fickian diffusion, while samples exposed to LF-AMF show zero-order kinetics, consistently with an anomalous transport, due to an alteration of the bilayer permeability. These preliminary results open up new perspectives in the use of these systems as carriers in targeted and controlled release of drugs.

3 November 2015 in The Journal of Physical Chemistry C
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SNSilvia Nappini
Silvia Nappini
EMELENA MAGNANO
ELENA MAGNANO
FBFederica Bondino
Federica Bondino
IPIgor Píš
Igor Píš
ABAlessandro Barla
Alessandro Barla
PBPiero Baglioni
Piero Baglioni

27 November 2017 in Chemical Science
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Journal Article
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ECEmilia A. Carbonio
Emilia A. Carbonio
TRTulio C. R. Rocha
Tulio C. R. Rocha
AKAlexander Yu. Klyushin
Alexander Yu. Klyushin
IPIgor Píš
Igor Píš
EMELENA MAGNANO
ELENA MAGNANO
TJTravis E. Jones
Travis E. Jones
The nature of the oxygen species active in ethylene epoxidation is a long-standing question. While the structure of the oxygen species that participates in total oxidation (nucleophilic oxygen) is known the atomic structure of the selective species (electrophilic oxygen) is still debated. Here, we use both in situ and UHV X-ray Photoelectron Spectroscopy (XPS) to study the interaction of oxygen with a silver surface. We show experimental evidence that the unreconstructed adsorbed atomic oxygen (Oads) often argued to be active in epoxidation has a binding energy (BE) ≤ 528 eV, showing a core-level shift to lower BE with respect to the O-reconstructions, as previously predicted by DFT. Thus, contrary to the frequent assignment, adsorbed atomic oxygen cannot account for the electrophilic oxygen species with an O 1s BE of 530–531 eV, thought to be the active species in ethylene epoxidation. Moreover, we show that Oads is present at very low O-coverages during in situ XPS measurements and that it can be obtained at slightly higher coverages in UHV at low temperature. DFT calculations support that only low coverages of Oads are stable. The highly reactive species is titrated by background gases even at low temperature in UHV conditions. Our findings suggest that at least two different species could participate in the partial oxidation of ethylene on silver.

26 November 2010 in Soft Matter
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SNSilvia Nappini
Silvia Nappini
MBMassimo Bonini
Massimo Bonini
FBFrancesca Baldelli Bombelli
Francesca Baldelli Bombelli
Francesco PineiderFrancesco Pineider
Francesco Pineider
CSClaudio Sangregorio
Claudio Sangregorio
BNBengt Nordén
Bengt Nordén
The paper describes the effect of a low-frequency alternating magnetic field (LF-AMF) on the permeability and release properties of large (LUVs) and giant (GUVs) unilamellar vesicles loaded with citrate coated cobalt ferrite nanoparticles (NPs). The citrate shell allows a high loading of NPs in lipid vesicles without modifying their magnetic properties. The increase of magnetic LUVs permeability upon exposure to LF-AMF has been evaluated as the fluorescence self-quenching of carboxyfluorescein (CF) entrapped inside the liposome aqueous pool. Liposome leakage has been monitored as a function of field frequency, time exposure and concentration of the citrate coated NPs. Confocal Laser Scanning Microscopy (CLSM) experiments performed on magnetic GUVs labeled with the fluorescent probe DiIC18 and loaded with Alexa 488-C5-maleimide fluorescent dye provided insights on the release mechanism induced by LF-AMF. The results show that LF-AMF strongly affects vesicles permeability, suggesting the formation of pores in the lipid bilayer due to both hyperthermic effects and nanoparticle oscillations in the vesicles pool at the applied frequency. The behaviour of these magnetic vesicles in the presence of LF-AMF makes this system a good candidate for controlled drug delivery.

29 March 2020 in Advanced Functional Materials
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SNSilvia Nappini
Silvia Nappini
Danil BoukhvalovDanil Boukhvalov
Danil Boukhvalov
GDGianluca D'OLimpio
Gianluca D'OLimpio
LZLibo Zhang
Libo Zhang
BGBarun Ghosh
Barun Ghosh
APAntonio Politano
Antonio Politano