4.6 Article

Unlabeled multi tumor marker detection system based on bioinitiated light addressable potentiometric sensor

Journal

ANALYST
Volume 137, Issue 16, Pages 3806-3813

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2an35188a

Keywords

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Funding

  1. National Natural Science Foundation of China [81071260, 60602002]
  2. Tianjin Science Technology Research Foundation of China [10JCZDJC17000, 12JCZDJC22400]

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Multi biomarkers' assays are of great significance in clinical diagnosis. A label-free multi tumor markers' parallel detection system was proposed based on a light addressable potentiometric sensor (LAPS). Arrayed LAPS chips with basic structure of Si3N4-SiO2-Si were prepared on silicon wafers, and the label-free parallel detection system for this component was developed with user friendly controlling interfaces. Then the L-3,4-dihydroxyphenyl-alanine (L-Dopa) hydrochloric solution was used to initiate the surface of LAPS. The L-Dopa immobilization state was investigated by the theoretical calculation. L-Dopa initiated LAPS' chip was biofunctionalized respectively by the antigens and antibodies of four tumor markers, alpha-fetoprotein (AFP), carcinoembryonic antigen (CEA), cancer antigen 19-9 (CA19-9) and Ferritin. Then unlabeled antibodies and antigens of these four biomarkers were detected by the proposed detection systems. Furthermore physical and measuring principles in this system were described, and qualitative understanding for experimental data were given. The measured response ranges were compared with their clinical cutoff values, and sensitivities were calculated by OriginLab. The results indicate that this bioinitiated LAPS based label-free detection system may offer a new choice for the realization of unlabeled multi tumor markers' clinical assay.

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