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Published on: November 13, 2017
Multiplex measurement of seven tumor markers using an electrochemical protein chip
1EIC Laboratories, Inc., 111 Downey Street, Norwood, Massachusetts 02062, USA. mwilson@eiclabs.com
Insights
A novel electrochemical immunosensor enables simultaneous detection of multiple tumor markers. This chip-based biosensor offers precise and accurate results, paving the way for economical lab-on-a-chip devices.
Area of Science:
- Biomedical Engineering
- Analytical Chemistry
- Biosensor Technology
Background:
- Current tumor marker detection often involves single-analyte assays.
- There is a need for efficient, cost-effective, and high-throughput diagnostic tools.
Purpose of the Study:
- To develop and evaluate an electrochemical immunosensor for simultaneous multianalyte detection of tumor markers.
- To assess the performance of the sensor compared to traditional methods.
Main Methods:
- Fabrication of an array of immunosensing electrodes on a glass substrate.
- Immobilization of specific antigens on each electrode for competitive immunoassay.
- Electrochemical detection of seven key tumor markers: AFP, ferritin, CEA, hCG-beta, CA 15-3, CA 125, and CA 19-9.
Main Results:
- The immunosensor demonstrated excellent precision and accuracy for multianalyte measurements.
- Performance was comparable to single-analyte ELISAs, with low interassay coefficients of variation (1.9-8.1%).
- Achieved detection limits below 2 ng/mL (or units/mL) for most analytes.
Conclusions:
- Multianalyte assays using this chip-based sensor offer significant advantages in cost, labor, and throughput.
- The developed sensor is suitable for mass production of miniaturized, economical lab-on-a-chip devices.
- Potential applications span clinical diagnostics, environmental monitoring, and biodefense.
Abstract:
An electrochemical immunosensor for performing multianalyte measurements of tumor markers is described. The sensor consisted of an array of immunosensing electrodes fabricated on a glass substrate. Each electrode contained a different immobilized antigen and was capable of measuring a specific tumor marker using electrochemical enzyme-based competitive immunoassay. Using this arrangement, multiple analytes could be measured simultaneously by performing the technical operations for a single assay. The biosensor was used to measure the concentrations of seven important tumor markers: AFP, ferritin, CEA, hCG-beta, CA 15-3, CA 125, and CA 19-9. The sensor had excellent precision and accuracy and was comparable in performance to single-analyte ELISAs (1.9-8.1% interassay CV; <2 ng/mL (or units/mL) detection limit for most analytes). Multianalyte assays provide significant advantages over single-analyte tests in terms of cost per test, labor, test throughput, and convenience. We anticipate that chip-based sensors, as described herein, will be suitable for the mass production of economical, miniaturized lab-on-a-chip devices that will have applications in a wide range of clinical, environmental, and biodefense applications.
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