Giancarlo Canavese

Dr. Giancarlo Canavese

Department of Applied Science & Technology, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino 10129, Italy

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

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14 March 2014 in Sensors
Verified
Journal Article
Open access
PDF file
Stefano StassiStefano Stassi
Stefano Stassi
VCValentina Cauda
Valentina Cauda
GCGiancarlo Canavese
Giancarlo Canavese
Candido PirriCandido Pirri
Candido Pirri
The large expansion of the robotic field in the last decades has created a growing interest in the research and development of tactile sensing solutions for robot hand and body integration. Piezoresistive composites are one of the most widely employed materials for this purpose, combining simple and low cost preparation with high flexibility and conformability to surfaces, low power consumption, and the use of simple read-out electronics. This work provides a review on the different type of composite materials, classified according to the conduction mechanism and analyzing the physics behind it. In particular piezoresistors, strain gauges, percolative and quantum tunnelling devices are reviewed here, with a perspective overview on the most used filler types and polymeric matrices. A description of the state-of-the-art of the tactile sensor solutions from the point of view of the architecture, the design and the performance is also reviewed, with a perspective outlook on the main promising applications.

18 June 2013 in ACS Applied Materials & Interfaces
Verified
Journal Article
Closed access
VCValentina Cauda
Valentina Cauda
Stefano StassiStefano Stassi
Stefano Stassi
Katarzyna BejtkaKatarzyna Bejtka
Katarzyna Bejtka
GCGiancarlo Canavese
Giancarlo Canavese

1 February 2014 in Sensors and Actuators A: Physical
Verified
Journal Article
Closed access
GCGiancarlo Canavese
Giancarlo Canavese
Stefano StassiStefano Stassi
Stefano Stassi
CFCarmelo Fallauto
Carmelo Fallauto
SCSimone Corbellini
Simone Corbellini
VCValentina Cauda
Valentina Cauda
Candido PirriCandido Pirri
Candido Pirri

1 April 2015 in Nano Energy
Verified
Journal Article
Closed access
Stefano StassiStefano Stassi
Stefano Stassi
VCValentina Cauda
Valentina Cauda
Carminna OttoneCarminna Ottone
Carminna Ottone
Angelica ChiodoniAngelica Chiodoni
Angelica Chiodoni
Candido PirriCandido Pirri
Candido Pirri
GCGiancarlo Canavese
Giancarlo Canavese

1 November 2017 in Journal of Materials Chemistry B
Verified
Journal Article
Open access
PDF file
BDB. Dumontel
B. Dumontel
MCM. Canta
M. Canta
HEHanna Engelke
Hanna Engelke
Angelica ChiodoniAngelica Chiodoni
Angelica Chiodoni
LRL. Racca
L. Racca
VCValentina Cauda
Valentina Cauda
The widespread use of ZnO nanomaterials for biomedical applications, including therapeutic drug delivery or stimuli-responsive activation, as well as imaging, imposes a careful control over the colloidal stability and long-term behaviour of ZnO in biological media. Moreover, the effect of ZnO nanostructures on living cells, in particular cancer cells, is still under debate. This paper discusses the role of surface chemistry and charge of zinc oxide nanocrystals, of around 15 nm in size, which influence their behaviour in biological fluids and effect on cancer cells. In particular, we address this problem by modifying the surface of pristine ZnO nanocrystals (NCs), rich of hydroxyl groups, with positively charged amino-propyl chains or, more innovatively, by self-assembling a double-lipidic membrane, shielding the ZnO NCs. Our findings show that the prolonged immersion in simulated human plasma and in the cell culture medium leads to highly colloidally dispersed ZnO NCs only when coated by the lipidic bilayer. In contrast, the pristine and amine-functionalized NCs form huge aggregates after already one hour of immersion. Partial dissolution of these two samples into potentially cytotoxic Zn2+ cations takes place, together with the precipitation of phosphate and carbonate salts on the NCs’ surface. When exposed to living HeLa cancer cells, higher amounts of lipid-shielded ZnO NCs are internalized with respect to the other samples, thus showing a reduced cytotoxicity, based on the same amount of internalized NCs. These results pave the way for the development of novel theranostic platforms based on ZnO NCs. The new formulation of ZnO shielded with a lipid-bilayer will prevent strong aggregation and premature degradation into toxic by-products, and promote a highly efficient cell uptake for further therapeutic or diagnostic functions.

7 May 2012 in Journal of Polymer Science Part B: Polymer Physics
Verified
Journal Article
Closed access
PDF file
Stefano StassiStefano Stassi
Stefano Stassi
GCGiancarlo Canavese
Giancarlo Canavese