Marco Cereda

Dr. Marco Cereda

orcid

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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1 May 2018 in JACC
Verified
Journal Article
Closed access
FNFrancesca Maria Notarangelo
Francesca Maria Notarangelo
Giuseppe MagliettaGiuseppe Maglietta
Giuseppe Maglietta
PBPaola Bevilacqua
Paola Bevilacqua
MCMarco Cereda
Marco Cereda
PMPiera Angelica Merlini
Piera Angelica Merlini
DADiego Ardissino
Diego Ardissino

24 October 2018 in Sensors
Verified
Journal Article
Open access
PDF file
EPElisabetta Primiceri
Elisabetta Primiceri
MCMaria Serena Chiriacò
Maria Serena Chiriacò
FNFrancesca M. Notarangelo
Francesca M. Notarangelo
ACAntonio Crocamo
Antonio Crocamo
DADiego Ardissino
Diego Ardissino
Giuseppe MaruccioGiuseppe Maruccio
Giuseppe Maruccio
A major trend in biomedical engineering is the development of reliable, self-contained point-of-care (POC) devices for diagnostics and in-field assays. The new generation of such platforms increasingly addresses the clinical and environmental needs. Moreover, they are becoming more and more integrated with everyday objects, such as smartphones, and their spread among unskilled common people, has the power to improve the quality of life, both in the developed world and in low-resource settings. The future success of these tools will depend on the integration of the relevant key enabling technologies on an industrial scale (microfluidics with microelectronics, highly sensitive detection methods and low-cost materials for easy-to-use tools). Here, recent advances and perspectives will be reviewed across the large spectrum of their applications.

7 August 2018 in Sensors
Verified
Journal Article
Open access
PDF file
MCMarco Cereda
Marco Cereda
ACAlessandro Cocci
Alessandro Cocci
DCDavide Cucchi
Davide Cucchi
LRLillo Raia
Lillo Raia
DPDanilo Pirola
Danilo Pirola
MBMarco A. Bianchessi
Marco A. Bianchessi
An accurate and easy-to-use Q3 system for on-chip quantitative real-time Polymerase Chain Reaction (qPCR) is hereby demonstrated, and described in detail. The qPCR reactions take place inside a single-use Lab-on-a-Chip with multiple wells, each with 5 to 15 µL capacity. The same chip hosts a printed metal heater coupled with a calibrated sensor, for rapid and accurate temperature control inside the reaction mixture. The rest of the system is non-disposable and encased in a 7 × 14 × 8.5 (height) cm plastic shell weighing 300 g. Included in the non-disposable part is a fluorescence read-out system featuring up to four channels and a self-contained control and data storage system, interfacing with an external user-friendly software suite. Hereby, we illustrate the engineering details of the Q3 system and benchmark it with seamlessly ported testing protocols, showing that Q3 equals the performance of standard commercial systems. Overall, to the best of our knowledge, this is one of the most mature general-purpose systems for on-chip qPCR currently available.

1 September 2019 in The Journal of Molecular Diagnostics
Verified
Journal Article
Closed access
RRRita C.P. Rampazzo
Rita C.P. Rampazzo
AGAna Cláudia Graziani
Ana Cláudia Graziani
KLKeren K. Leite
Keren K. Leite
JSJhully Anni Surdi
Jhully Anni Surdi
CBCheysa A. Biondo
Cheysa A. Biondo
ACAlexandre Dias Tavares Costa
Alexandre Dias Tavares Costa

1 December 2015 in Clinica Chimica Acta
Verified
Journal Article
Closed access
NMNicola Marziliano
Nicola Marziliano
MNMaria Francesca Notarangelo
Maria Francesca Notarangelo
MCMarco Cereda
Marco Cereda
VCVittoria Caporale
Vittoria Caporale
LCLucia Coppini
Lucia Coppini
PMPiera Angelica Merlini
Piera Angelica Merlini

12 May 2023 in Heliyon
Verified
Journal Article
Open access
VGValeria Garzarelli
Valeria Garzarelli
MCMaria Serena Chiriacò
Maria Serena Chiriacò
MCMarco Cereda
Marco Cereda
GGGiuseppe Gigli
Giuseppe Gigli
Francesco FerraraFrancesco Ferrara
Francesco Ferrara
Contamination of cell cultures can result in a significant loss of precious biological material, particularly in long-term processes including amplification of chimeric antigen receptors (CAR)-T cells and differentiation of patient-derived stem cells, for therapeutic purposes. Bacterial contamination can also lead to more complex conditions such as sepsis which can cause morbidity and mortality, despite strict controls and good laboratory/manufacturing practices in the manipulation of complex biological samples such as blood used in autologous and allogeneic stem cells transplantation.