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Related Concept Videos

Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

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In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or...
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Related Experiment Video

Updated: Jun 19, 2025

Quantitative SERS Detection of Uric Acid via Formation of Precise Plasmonic Nanojunctions within Aggregates of Gold Nanoparticles and Cucurbit[n]uril
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A novel SERS method for detecting E. coli based on an aptamer-functionalized Au-Ag@Si triangular pyramid substrate.

Xiaochen Qu1, Guohui You1, Shufang Wang2

  • 1College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.

Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy
|July 25, 2024
PubMed
Summary

A new aptamer-based surface-enhanced Raman spectroscopy (SERS) method offers rapid and sensitive detection of Escherichia coli (E. coli). This technique provides a promising alternative for on-site E. coli detection in pharmaceutical and food samples.

Keywords:
AptamerAu-Ag@Si triangular pyramid substrateEscherichia coliSurface enhanced Raman spectroscopy

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Area of Science:

  • Analytical Chemistry
  • Biosensing
  • Nanotechnology

Background:

  • Escherichia coli (E. coli) contamination poses a significant risk in food and pharmaceuticals, necessitating stringent regulatory control.
  • Current methods for E. coli detection often lack the required speed and sensitivity for effective monitoring.
  • Developing rapid and sensitive detection techniques is crucial for ensuring public health and product safety.

Purpose of the Study:

  • To develop a novel aptamer-based surface-enhanced Raman spectroscopy (SERS) sandwich method for the rapid and sensitive detection of E. coli.
  • To utilize aptamer-functionalized gold-silver@silicon triangular pyramid (Au-Ag@Si TP) substrates for enhanced E. coli detection.
  • To validate the method's efficacy in detecting E. coli in complex matrices like pharmaceutical preparations.

Main Methods:

  • Fabrication of an aptamer-functionalized Au-Ag@Si TP substrate serving as both capture probe and SERS tag.
  • Integration of a Raman reporter (6-carboxy-X-rhodamine) for signal amplification.
  • Development of a sandwich assay format for selective E. coli capture and detection.

Main Results:

  • The aptamer-functionalized Au-Ag@Si TP substrate was fabricated rapidly (20.5 hours).
  • The developed method achieved selective and rapid E. coli detection with a limit of detection of 2.8 CFU/mL within approximately 3 hours.
  • Successful application to Xinhuang tablets demonstrated high recovery rates (90.19%–104.17%), indicating robustness.

Conclusions:

  • The aptamer-based SERS sandwich method offers a simple, rapid, and sensitive approach for E. coli detection.
  • This technique shows significant potential as an alternative for on-site E. coli monitoring in pharmaceutical and food industries.
  • The use of functionalized Au-Ag@Si TP substrates enhances detection capabilities for bacterial contaminants.