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Updated: May 31, 2026

Rapid Nanoprobe Signal Enhancement by In Situ Gold Nanoparticle Synthesis
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Rapid Nanoprobe Signal Enhancement by In Situ Gold Nanoparticle Synthesis

Published on: March 7, 2018

A gold-nanoparticle-enhanced immune sensor based on fiber optic interferometry.

Yuan-Tai Tseng1, Yun-Ju Chuang, Yi-Chien Wu

  • 1Institute of NanoEngineering and MicroSystems (NEMS), National Tsing Hua University, Hsinchu 300, Taiwan. Center for Nanomedicine Research, National Health Research Institutes, Zhunan 307, Taiwan.

Nanotechnology
|July 7, 2011
PubMed
Summary

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Gold nanoparticles enhance fiber optic interferometry for sensitive immune-sensing. This gold nanoparticle fiber optic interferometry (GNPFOI) method achieves low detection limits for specific antibodies and antigens.

Area of Science:

  • Nanotechnology
  • Biomedical Engineering
  • Optical Sensing

Background:

  • Fiber optic interferometry offers sensitive detection but requires signal enhancement for certain applications.
  • Gold nanoparticles (GNPs) possess unique optical properties that can be leveraged to improve biosensing capabilities.

Purpose of the Study:

  • To develop and demonstrate a novel method using gold nanoparticles to enhance fiber optic interferometry (GNPFOI) for highly sensitive immune-sensing.
  • To investigate the relationship between GNP characteristics and signal enhancement in the GNPFOI system.

Main Methods:

  • Conjugating recognition proteins with gold nanoparticles (GNPs) and immobilizing them on a fiber optic interferometer.
  • Utilizing the enlarged index mismatch and elongated optical path caused by GNPs for signal amplification.

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Last Updated: May 31, 2026

Rapid Nanoprobe Signal Enhancement by In Situ Gold Nanoparticle Synthesis
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Published on: March 7, 2018

A Silicon-tipped Fiber-optic Sensing Platform with High Resolution and Fast Response
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Published on: January 7, 2019

Implementation of a Reference Interferometer for Nanodetection
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  • Performing theoretical and experimental analysis of interference fringe shift in response to GNP binding.
  • Main Results:

    • Interference fringe shift demonstrated a linear correlation with the amount and size of bound GNPs.
    • A detection limit of 18 pM (10^10 particles/ml) was achieved for 30 nm GNPs.
    • Successful immune-sensing of rabbit IgG with a detection limit of 0.17 nM (25.5 ng/ml) for 13 nm GNPs was achieved, with sensor regeneration and repeatability confirmed.

    Conclusions:

    • GNP-enhanced fiber optic interferometry provides a highly sensitive platform for immune-sensing.
    • The GNPFOI method shows promise for miniaturization into needle-type micro-devices for in-situ monitoring of immune recognition.