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Issue 4, 2002
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Colorimetric detection of thiol-containing amino acids using gold nanoparticles

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This paper reports findings of an investigation of the unusual colorimetric change of gold nanoparticles in the presence of thiol-containing amino acids such as homocysteine, cysteine and glutathione. The colorimetric change for homocysteine exhibits a rate that is about two orders of magnitude higher than that for cysteine, and at least five orders of magnitude higher than that for glutathione. The reactivity is effectively reduced or suppressed by the co-existence of either cysteine or glutathione. It is believed that the reactivity involves encapsulation of the particles by the thiol-containing amino acids which is followed by crosslinking at the encapsulating shells. In comparison with cysteine and glutathione, homocysteine has a slower encapsulating rate but a faster crosslinking rate. Implications of the findings of the interfacial encapsulation and crosslinking reactivities of gold nanoparticles to potential nanoparticle-enhanced analytical detection of thiol-containing amino acids are also briefly discussed.

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Publication details

The article was received on 03 Jan 2002, accepted on 21 Feb 2002 and first published on 11 Mar 2002

Article type: Communication
DOI: 10.1039/B200007E
Citation: Analyst, 2002,127, 462-465
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    Colorimetric detection of thiol-containing amino acids using gold nanoparticles

    F. X. Zhang, L. Han, L. B. Israel, J. G. Daras, M. M. Maye, N. K. Ly and C. Zhong, Analyst, 2002, 127, 462
    DOI: 10.1039/B200007E

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