A flow-through microfluidic system for the detection of circulating melanoma cells

We report the fabrication of polyaniline nanofiber (PANI)-modified screen-printed electrode (PANI/SPE) incorporated in a poly-dimethylsiloxane (PDMS) microfluidic channel for the detection of circulating tumor cells. We employed this device to detect melanoma skin cancer cells through specific immun...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biosensors & bioelectronics 2019-10, Vol.142, p.111522-111522, Article 111522
Hauptverfasser: Anu Prathap, Mylamparambil Udayan, Castro-Pérez, Edgardo, Jiménez-Torres, José A., Setaluri, Vijaysaradhi, Gunasekaran, Sundaram
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:We report the fabrication of polyaniline nanofiber (PANI)-modified screen-printed electrode (PANI/SPE) incorporated in a poly-dimethylsiloxane (PDMS) microfluidic channel for the detection of circulating tumor cells. We employed this device to detect melanoma skin cancer cells through specific immunogenic binding of cell surface biomarker melanocortin 1 receptor (MC1R) to anti-MC1R antibody. The antibody-functionalized PANI/SPE was used in batch-continuous flow-through fashion. An aqueous cell suspension of ferri/ferrocyanide at a flow rate of 1.5 mL/min was passed over the immunosensor, which allowed for continuous electrochemical measurements. The sensor performed exceptionally well affording an ultralow limit of quantification of 1 melanoma cell/mL, both in buffer and when mixed with peripheral blood mononuclear cells, and the response was log-linear over the range of 10–9000 melanoma cells/10 mL. •A microfluidics-based immunoelectrochemical sensor was developed.•An ultralow limit of quantification of 1 cell/mL was achieved.•The sensor performance was verified via cell culture experiments.•The sensor response is stable, repeatable, and linear over a wide range.•This system is potentially useful for rapid detection of circulating tumor cells.
ISSN:0956-5663
1873-4235
DOI:10.1016/j.bios.2019.111522