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

被引:70
作者
Mishra, NN
Retterer, S
Zieziulewicz, TJ
Isaacson, M
Szarowski, D
Mousseau, DE
Lawrence, DA
Turner, JN
机构
[1] New York State Dept Hlth, Wadsworth Ctr, ESP, Albany, NY 12201 USA
[2] SUNY SPH, Dept Environm Hlth & Toxicol, Albany, NY USA
[3] Univ Albany, Sch Publ Hlth, Albany, NY USA
[4] Cornell Univ, Ithaca, NY USA
基金
美国国家科学基金会;
关键词
micro-electrode; CD4 cell biosensor; impedance; micro-fabrication; human blood;
D O I
10.1016/j.bios.2005.01.011
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The current study was undertaken to fabricate a small micro-electrode on-chip to rapidly detect and quantify human CD4(+) 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(+) cells present in human blood. The binding of these biomolecules to the micro-electrodes was verified by impedance and cyclic voltarnmetry 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(+) 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(+) 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(+) cells. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:696 / 704
页数:9
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