4.6 Article

Rapid and Sensitive Detection of miRNA Based on AC Electrokinetic Capacitive Sensing for Point-of-Care Applications

期刊

SENSORS
卷 21, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/s21123985

关键词

capacitive sensing; alternating current electrokinetic effects; miRNA sensing; point-of-care diagnostics

资金

  1. University of Tennessee (UT) Organized Research Unit-Initiative for PON/POC Nanobiosensing
  2. UT Research Foundation Maturation Fund
  3. USDA National Institute of Food and Agriculture [2017-67007-26150]
  4. Fundamental Research Funds for the Central Universities [2019CDYGZD006]
  5. National Key R&D Program of China [2020YFC1522900]
  6. Venture & Innovation Support Program for Chongqing Overseas Returnees [cx2018017]

向作者/读者索取更多资源

There is a strong demand for a sensitive and efficient method for microRNAs (miRNAs) detection in clinical settings, and new methodologies are needed to overcome the limitations of current detection methods. The integration of capacitive sensing and alternating current electrokinetic effects in this study shows significant improvements in sensitivity, response time, and cost over existing miRNA detection methods, with potential applications at point-of-care.
A sensitive and efficient method for microRNAs (miRNAs) detection is strongly desired by clinicians and, in recent years, the search for such a method has drawn much attention. There has been significant interest in using miRNA as biomarkers for multiple diseases and conditions in clinical diagnostics. Presently, most miRNA detection methods suffer from drawbacks, e.g., low sensitivity, long assay time, expensive equipment, trained personnel, or unsuitability for point-of-care. New methodologies are needed to overcome these limitations to allow rapid, sensitive, low-cost, easy-to-use, and portable methods for miRNA detection at the point of care. In this work, to overcome these shortcomings, we integrated capacitive sensing and alternating current electrokinetic effects to detect specific miRNA-16b molecules, as a model, with the limit of detection reaching 1.0 femto molar (fM) levels. The specificity of the sensor was verified by testing miRNA-25, which has the same length as miRNA-16b. The sensor we developed demonstrated significant improvements in sensitivity, response time and cost over other miRNA detection methods, and has application potential at point-of-care.

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