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. 2008 Jan 25;8(1):582-593.
doi: 10.3390/s8010582.

Using Monoclonal Antibody to Determine Lead Ions with a Localized Surface Plasmon Resonance Fiber-optic Biosensor

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Using Monoclonal Antibody to Determine Lead Ions with a Localized Surface Plasmon Resonance Fiber-optic Biosensor

Tsao-Jen Lin et al. Sensors (Basel). .

Abstract

A novel reflection-based localized surface plasmon resonance (LSPR) fiber-optic probe has been developed to determine the heavy metal lead ion concentration. Monoclonal antibody as the detecting probe containing massive amino groups to capture Pb(II)-chelate complexes was immobilized onto gold nanoparticle-modified optical fiber (NMAuOF). The optimal immobilizing conditions of monoclonal antibody on to the NMAuOF are 189 μg/mL in pH7.4 PBS for 2 h at 25°C. The absorbability of the functionalized NMAuOF sensor increases to 12.2 % upon changing the Pb(II)-EDTA level from 10 to 100 ppb with a detection limit of 0.27 ppb. The sensor retains 92.7 % of its original activity and gives reproducible results after storage in 5% D-( )-Trehalose dehydrate solution at 4°C for 35 days. In conclusion, the monoclonal antibody-functionalized NMAuOF sensor shows a promising result for determining the concentration of Pb(II) with high sensitivity.

Keywords: biosensor; gold nanoparticle; lead-chelate complex; lead-chelate complex. antibody; localized surface plasmon resonance; monoclonal antibody.

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Figures

Figure 1.
Figure 1.
(a) Images of 2-D and 3-D AFM surfaces on the prepared MPTMS; (b) Electron micrograph and particle size distribution of pure Au nanoparticles.
Figure 2.
Figure 2.
The chemical reactions scheme carried out for covalent binding of monoclonal antibody to the fiber-based LSPR sensor.
Figure 3.
Figure 3.
The schematic representation of the LSPR biosensor system.
Figure 4.
Figure 4.
An example of serial Pb(II)-EDTA complex response signal in the range of 10∼100 ppb by two sensors with/without monoclonal antibody coating.
Figure 5.
Figure 5.
Effects of (a) the incubating monoclonal antibody concentration, (b) incubating time, and (c) pH on the response for detecting 10∼100 ppb Pb(II)-EDTA complex in pH 7.4 PBS buffer solution at 25°C.
Figure 6.
Figure 6.
Effect of the detection temperature on the response for detecting 10∼100 ppb Pb(II)-EDTA complex in pH 7.4 PBS buffer solution at 25°C.
Figure 7.
Figure 7.
Comparison of the responses between different metal-chelate complexes (i.e., Mg(II)-, Cu(II)-, and Ni(II)-EDTA) through the monoclonal antibody-functionalized LSPR biosensor.

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