4.8 Article

Continuous Nanoflow-Scanning Electrochemical Microscopy: Voltammetric Characterization and Application for Accurate and Reproducible Imaging of Enzyme-Labeled Protein Microarrays

期刊

ANALYTICAL CHEMISTRY
卷 87, 期 8, 页码 4523-4529

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.5b00625

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资金

  1. National Science Foundation [NSF 1112105]
  2. National Key Basic Research Program of China [2014CB744502]
  3. NSF-CREST Program at California State University, Los Angeles [NSF HRD-0931421]
  4. Direct For Education and Human Resources
  5. Division Of Human Resource Development [0932421] Funding Source: National Science Foundation
  6. Division Of Chemistry
  7. Direct For Mathematical & Physical Scien [1112105] Funding Source: National Science Foundation

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The coupling of scanning electrochemical microscopy (SECM) to a continuous nanoflow (CNF) system is accomplished with the use of a microconcentric ring electrode/injector probe. The gold microring electrode encapsulated by a glass sheath is robust and can be beveled and polished. The CNF system, comprising a precision gas displacement pump and a rotary valve, is capable of delivering solution to the center of the SECM probe in the range of 1-150 nL/min. Major advantages of the CNF-SECM imaging mode over the conventional SECM generation/collection (G/C) mode include higher imaging resolution, immunity from interferences by species in the bulk solution or at other sites of the substrate, elimination of the feedback current that could interfere with the G/C data interpretation, and versatility of initiating surface reactions/processes via introducing different reactants into the flowing stream. Parameters such as flow rates, probe/substrate separations, and collection efficiencies are examined and optimized. Higher resolution, reproducibility, and accuracy are demonstrated through the application of CNF-SECM to horseradish peroxidase (HRP)-amplified imaging of protein microarrays. By flowing H2O2 and ferrocenemethanol through the injector and detecting the surface-generated ferriceniummethanol, human IgG spots covered with HPR-labeled antihuman IgG can be detected in the range of 13 nM-1.333 mu M with a detection limit of 3.0 nM. In addition, consistent images of microarray spots for selective and high-density detection of analytes can be attained.

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