Binding interaction of a fluoranthene-thiol on gold nanoparticles with β-cyclodextrin and DNA

In this paper, we report the preparation of a fluoranthene-thiol derivative, the assembly of the compound onto gold nanoparticles, and their binding to β-cyclodextrin and DNA. The synthesised fluoranthene-thiol is characterised using infra-red (IR), nuclear magnetic resonance (NMR), and mass spectro...

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Veröffentlicht in:Journal of experimental nanoscience 2017-01, Vol.12 (1), p.62-71
Hauptverfasser: Thangaraj, S. Eugene, Antony, Eva Janet, Yousuf, Sameena, Selvakumar, P. Mosae, Dhanaraj, Premnath, Enoch, Israel V. M. V.
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Sprache:eng
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Zusammenfassung:In this paper, we report the preparation of a fluoranthene-thiol derivative, the assembly of the compound onto gold nanoparticles, and their binding to β-cyclodextrin and DNA. The synthesised fluoranthene-thiol is characterised using infra-red (IR), nuclear magnetic resonance (NMR), and mass spectrometric techniques. The gold nanoparticles are characterised using transmission electron microscopy and energy dispersive X-ray spectroscopy microanalysis. The size of the nanoparticles is 5 ± 1 nm. The thiol-gold nanoparticles bind to β-cyclodextrin, and DNA and the fluorescence spectra show enhancement of fluorescence on the binding. The thiol-gold nanoparticles form a host-guest complex with β-cyclodextrin and the binding constant of the complex is 1330 mol −1 dm 3 . This reveals the openness of the thiol on the surface of the gold nanoparticles.
ISSN:1745-8080
1745-8099
DOI:10.1080/17458080.2016.1258496