On-chip micro-biosensor for the detection of human CD4 super(+) cells based on AC impedance and optical analysis

The current study was undertaken to fabricate a small micro-electrode on- chip to rapidly detect and quantify human CD4 super(+) cells in a minimal volume of blood through impedance measurements made with simple electronics that could be battery operated implemented in a hand held device. The micro-...

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Veröffentlicht in:Biosensors & bioelectronics 2006-01, Vol.21 (5), p.696-704
Hauptverfasser: Mishra, Nirankar N, Retterer, Scott, Zieziulewicz, Thomas J, Isaacson, Michael, Szarowski, Donald, Mousseau, Donald E, Lawrence, David A, Turner, James N
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Sprache:eng
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Zusammenfassung:The current study was undertaken to fabricate a small micro-electrode on- chip to rapidly detect and quantify human CD4 super(+) cells in a minimal volume of blood through impedance measurements made with simple electronics that could be battery operated implemented in a hand held device. The micro-electrode surface was non-covalently modified sequentially by incubation with solutions of protein G', human albumin, monoclonal mouse anti-human CD4, and mouse IgG. The anti- human CD4 antibody served as the recognition and capture molecule for CD4 super(+) cells present in human blood. The binding of these biomolecules to the micro- electrodes was verified by impedance and cyclic voltammetry measurements. An increase in impedance was detected for each layer of protein adsorbed onto the micro-electrode surface. This process was shown to be highly repeatable. Increased impedance was measured when CD4 super(+) cells were captured on the micro- electrode, and the impedance also increased as the number of captured cells increased. Fluorescence microscopy of captured cells immunolabeled with anti- human CD4, CD8, and CD19 antibodies, and the nuclear label DAPI, confirmed that only CD4 super(+) cells were captured. The results were highly dependent on the specimen preparation method used. We conclude that the on-chip capture system can efficiently quantify the number of CD4 super(+) cells.
ISSN:0956-5663
DOI:10.1016/j.bios.2005.01.011