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Figure 2.12 When the capture/target/probe sandwich is positioned in the gap between two<br />

electrodes, catalytic reduction of silver onto the sandwich system results in a signal that can be<br />

detected electrically.<br />

Source: Science http://www.aaas.org<br />

Gold nanoparticles have been investigated for use in sensors for both chemical and<br />

biological warfare agents. One example, ‘chemiresistors’, makes use of thin films of gold<br />

nanoparticles encapsulated in monomolecular layers of functionalized alkanethiols that<br />

have been deposited on interdigitated microelectrodes. These reversibly absorb vapours<br />

leading to monolayer swelling or dielectric alteration in the thin film and production of a<br />

small current. The system appears to have minimal water sensitivity, and can detect<br />

harmful vapours down to the parts per billion level or lower. Selectivity of the sensors<br />

can be tailored by changing the structure and functionality of the alkanethiol. This sensor<br />

has been developed by STREM chemicals.<br />

• Colorimetric<br />

Nanoparticles have shown exceptional colorimetric properties that can easily replace<br />

traditional fluorescent detection systems. For example, a single 80 nm gold particle has a<br />

light-scattering power equivalent to the signal generated from about 10 6 fluorescein<br />

molecules, and unlike molecular fluorophores, the light-scattering signal from metal<br />

nanoparticles is quench resistant. (N.L. Rosi and C.A. Mirkin, 2005).<br />

Researchers from Georgia Institute of Technology have used 2.5 nm gold nanoparticles<br />

as quenchers in a molecular fluorophore nucleic acid probe, to detect the presence of<br />

target DNA (S. Nie et al., 2002, see Figure 2.13).<br />

Figure 2.13 Gold nanoparticles are modified with oligonucleotides functionalized on one end<br />

with a thiol and the other end with a molecular fluorophore. The thiol binds to the surface of the<br />

gold particle, and the fluorophore can interact non-specifically with the gold, resulting in a “loop”<br />

structure in which the gold nanoparticle quenches the emission from the fluorophore. In the<br />

presence of target DNA the “loop” is broken, separating the fluorophore from the nanoparticle<br />

quencher, and resulting in measurable fluorescence.<br />

Source: http://pubs.acs.org/spotlight/november2002/ja025814p.pdf?sessid=7922<br />

12

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