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Rapid Nanoprobe Signal Enhancement by In Situ Gold Nanoparticle Synthesis
Published on: March 7, 2018
Enhanced lateral flow immunoassay using gold nanoparticles loaded with enzymes
Claudio Parolo1, Alfredo de la Escosura-Muñiz, Arben Merkoçi
1Nanobioelectronics & Biosensors Group, CIN2 (ICN-CSIC), Catalan Institute of Nanotechnology, Campus UAB, Bellaterra (Barcelona), Spain.
Biosensors & Bioelectronics
|July 17, 2012
Summary
This study enhances optical lateral flow immunoassays (LFIA) by combining gold nanoparticles (AuNPs) with horseradish peroxidase (HRP) enzyme activity. This novel
Area of Science:
- Biotechnology
- Nanotechnology
- Analytical Chemistry
Background:
- Lateral flow immunoassays (LFIA) are widely used for rapid diagnostics.
- Enhancing the sensitivity of LFIA without compromising its simplicity is a key challenge.
Purpose of the Study:
- To develop an improved optical lateral flow immunoassay (LFIA) using gold nanoparticles (AuNPs) and horseradish peroxidase (HRP).
- To investigate strategies for enhancing signal intensity and sensitivity in LFIA.
Main Methods:
- Functionalizing AuNPs with a detection antibody modified with HRP to create an 'enhanced' label.
- Evaluating two detection strategies: direct AuNP color visualization and HRP substrate-mediated color enhancement.
- Assessing the performance with three different HRP substrates.
Main Results:
- The combined AuNP-HRP label significantly enhances LFIA sensitivity, achieving up to a 10-fold increase.
- HRP substrate-based detection provides a darker color, amplifying the signal from the AuNPs.
- The enhanced LFIA maintains the format's inherent simplicity.
Conclusions:
- Combining AuNPs and HRP offers a simple yet effective method to boost LFIA sensitivity.
- This approach allows for on-demand performance tuning of LFIA for various analytical needs.
- The enhanced LFIA opens new possibilities for sensitive and rapid diagnostic applications.
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Enzyme-Linked Immunosorbent Assay
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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 quantified.
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 quantified.
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