Salvatore Petralia

Prof. Salvatore Petralia

Department of Drug Science, University of Catania, via S. Sofia 64, 95123 Catania, Italy
orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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18 July 2017 in ACS Sensors
Verified
Journal Article
Closed access
SPSalvatore Petralia
Salvatore Petralia
SCSabrina Conoci
Sabrina Conoci

21 April 2021 in Cancers
Verified
Journal Article
Open access
PDF file
GNGiuseppe Nocito
Giuseppe Nocito
GCGiovanna Calabrese
Giovanna Calabrese
Stefano ForteStefano Forte
Stefano Forte
SPSalvatore Petralia
Salvatore Petralia
CPCaterina Puglisi
Caterina Puglisi
SCSabrina Conoci
Sabrina Conoci
Carbon Dots (CDs) are the latest members of carbon-based nanomaterials, which since their discovery have attracted notable attention due to their chemical and mechanical properties, brilliant fluorescence, high photostability, and good biocompatibility. Together with the ease and affordable preparation costs, these intrinsic features make CDs the most promising nanomaterials for multiple applications in the biological field, such as bioimaging, biotherapy, and gene/drug delivery. This review will illustrate the most recent applications of CDs in the biomedical field, focusing on their biocompatibility, fluorescence, low cytotoxicity, cellular uptake, and theranostic properties to highlight above all their usefulness as a promising tool for cancer diagnosis and therapy.

31 December 2021 in Cancers
Verified
Journal Article
Open access
PDF file
Giorgio Ivan RussoGiorgio Ivan Russo
Giorgio Ivan Russo
Nicolò MussoNicolò Musso
Nicolò Musso
ARAlessandra Romano
Alessandra Romano
Giuseppe CarusoGiuseppe Caruso
Giuseppe Caruso
SPSalvatore Petralia
Salvatore Petralia
Massimo CamardaMassimo Camarda
Massimo Camarda
Liquid biopsy is emerging as a potential diagnostic tool for prostate cancer (PC) prognosis and diagnosis. Unfortunately, most circulating tumor cells (CTC) technologies, such as AdnaTest or Cellsearch®, critically rely on the epithelial cell adhesion molecule (EpCAM) marker, limiting the possibility of detecting cancer stem-like cells (CSCs) and mesenchymal-like cells (EMT-CTCs) that are present during PC progression. In this context, dielectrophoresis (DEP) is an epCAM independent, label-free enrichment system that separates rare cells simply on the basis of their specific electrical properties. As compared to other technologies, DEP may represent a superior technique in terms of running costs, cell yield and specificity. However, because of its higher complexity, it still requires further technical as well as clinical development. DEP can be improved by the use of microfluid, nanostructured materials and fluoro-imaging to increase its potential applications. In the context of cancer, the usefulness of DEP lies in its capacity to detect CTCs in the bloodstream in their epithelial, mesenchymal, or epithelial–mesenchymal phenotype forms, which should be taken into account when choosing CTC enrichment and analysis methods for PC prognosis and diagnosis.

7 December 2020 in Biotechnology and Bioengineering
Verified
Journal Article
Closed access
PDF file
ESEmanuele Luigi Sciuto
Emanuele Luigi Sciuto
SPSalvatore Petralia
Salvatore Petralia
JMJan Roelof van der Meer
Jan Roelof van der Meer
SCSabrina Conoci
Sabrina Conoci

1 October 2013 in Sensors and Actuators B: Chemical
Verified
Journal Article
Closed access
SPSalvatore Petralia
Salvatore Petralia
RVRoberto Verardo
Roberto Verardo
EKEnio Klaric
Enio Klaric
Sebastiano CavallaroSebastiano Cavallaro
Sebastiano Cavallaro
EAEnrico Alessi
Enrico Alessi
CSClaudio Schneider
Claudio Schneider

21 November 2016 in The Analyst
Verified
Journal Article
Closed access
PDF file
SPSalvatore Petralia
Salvatore Petralia
ESEmanuele Luigi Sciuto
Emanuele Luigi Sciuto
SCSabrina Conoci
Sabrina Conoci
New miniaturised microfluidic biofilter (BF) devices based on silicon micropillars have been developed and tested regarding their ability to extract HBV (Hepatitis B Virus) bacterial DNA from biological sample solutions.