The biophysical analysis of single-cells by microfluidic impedance cytometry is emerging as a label-free and high-throughput means to stratify the heterogeneity of cellular systems based on their electrophysiology. Emerging applications range from fundamental life-science and drug assessment research to point-of-care diagnostics and precision medicine. Recently, novel chip designs and data analytic strategies are laying the foundation for multiparametric cell characterization and subpopulation distinction, which are essential to understand biological function, follow disease progression and monitor cell behaviour in microsystems. In this tutorial review, we present a comparative survey of the approaches to elucidate cellular and subcellular features from impedance cytometry data, covering the related subjects of device design, data analytics (i.e., signal processing, dielectric modelling, population clustering), and phenotyping applications. We give special emphasis to the exciting recent developments of the technique (timeframe 2017-2020) and provide our perspective on future challenges and directions. Its synergistic application with microfluidic separation, sensor science and machine learning can form an essential tool-kit for label-free quantification and isolation of subpopulations to stratify heterogeneous biosystems.

Honrado, C., Bisegna, P., Swami, N.s., Caselli, F. (2020). Single-cell microfluidic impedance cytometry: From raw signals to cell phenotypes using data analytics. LAB ON A CHIP, 21(1), 22-54 [10.1039/d0lc00840k].

Single-cell microfluidic impedance cytometry: From raw signals to cell phenotypes using data analytics

Bisegna P.;Caselli F.
2020-01-01

Abstract

The biophysical analysis of single-cells by microfluidic impedance cytometry is emerging as a label-free and high-throughput means to stratify the heterogeneity of cellular systems based on their electrophysiology. Emerging applications range from fundamental life-science and drug assessment research to point-of-care diagnostics and precision medicine. Recently, novel chip designs and data analytic strategies are laying the foundation for multiparametric cell characterization and subpopulation distinction, which are essential to understand biological function, follow disease progression and monitor cell behaviour in microsystems. In this tutorial review, we present a comparative survey of the approaches to elucidate cellular and subcellular features from impedance cytometry data, covering the related subjects of device design, data analytics (i.e., signal processing, dielectric modelling, population clustering), and phenotyping applications. We give special emphasis to the exciting recent developments of the technique (timeframe 2017-2020) and provide our perspective on future challenges and directions. Its synergistic application with microfluidic separation, sensor science and machine learning can form an essential tool-kit for label-free quantification and isolation of subpopulations to stratify heterogeneous biosystems.
2020
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore ING-IND/34 - BIOINGEGNERIA INDUSTRIALE
Settore IBIO-01/A - Bioingegneria
English
Data Science
Electric Impedance
Flow Cytometry
Phenotype
Microfluidic Analytical Techniques
Microfluidics
Honrado, C., Bisegna, P., Swami, N.s., Caselli, F. (2020). Single-cell microfluidic impedance cytometry: From raw signals to cell phenotypes using data analytics. LAB ON A CHIP, 21(1), 22-54 [10.1039/d0lc00840k].
Honrado, C; Bisegna, P; Swami, Ns; Caselli, F
Articolo su rivista
File in questo prodotto:
File Dimensione Formato  
Honrado_Caselli_LOC_2020_iris.pdf

accesso aperto

Tipologia: Documento in Post-print
Licenza: Non specificato
Dimensione 3.16 MB
Formato Adobe PDF
3.16 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/292172
Citazioni
  • ???jsp.display-item.citation.pmc??? 28
  • Scopus 140
  • ???jsp.display-item.citation.isi??? 125
social impact