4.8 Article

Fabrication of Aptamer-Modified Paper Electrochemical Devices for On-Site Biosensing

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 6, 页码 2993-3000

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202008231

关键词

aptamers; biosensors; nanomaterials; paper electrochemical devices; small molecules

资金

  1. National Institutes of Health-National Institute on Drug Abuse [R21DA045334-01A1]
  2. National Science Foundation [1905143]
  3. University Graduate School of Florida International University
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [1905143] Funding Source: National Science Foundation

向作者/读者索取更多资源

Electrochemical aptamer-based sensors are powerful tools for analyte detection, and paper-based sensors offer a portable, low-cost, and rapid detection method for a broad range of targets. By using ambient vacuum filtration, we have developed a simple, economic, and environmentally friendly strategy for fabricating aptamer-modified paper electrochemical devices (PEDs) with customizable three-electrode systems, enabling sensitive and specific detection of small molecules in minimally processed biosamples. The sensitivity and stability of these aptamer-modified PEDs are comparable to commercial gold electrode-based E-AB sensors, suggesting the potential for high performance on-site detection of various analytes.
Electrochemical aptamer-based (E-AB) sensors offer a powerful and general means for analyte detection in complex samples for various applications. Paper-based E-AB sensors could enable portable, low-cost, and rapid detection of a broad range of targets, but it has proven challenging to fabricate suitable three-electrode systems on paper. Here, we demonstrate a simple, economic, and environmentally friendly strategy for fabricating aptamer-modified paper electrochemical devices (PEDs) via ambient vacuum filtration. The material, shape, size, and thickness of the three-electrode PED system can be fully customized. We developed aptamer-modified PEDs that enable sensitive and specific detection of small molecules in minimally processed biosamples. The sensitivity and stability of the PEDs are comparable to E-AB sensors based on commercial gold electrodes. We believe our strategy can lead to the development of high performance PEDs for the on-site detection of a variety of analytes.

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