Effects of Cu^sup 2+^ on aggregation behavior of poly (l-Glutamic Acid)-functionalized gold nanoparticles

The effect of Cu^sup 2+^ ions on aggregation behaviors of poly (l-glutamic acid) (PLGA)-functionalized Au nanoparticles was investigated. It was found that the concentration of Cu^sup 2+^ ions had a significant influence on the folding and the formation of intermolecular hydrogen bonding of PLGA and...

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Veröffentlicht in:Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2013-01, Vol.15 (1), p.1
Hauptverfasser: He, Ke, Li, Jun, Ni, Yuyang, Fu, Rao, Huang, Zhenzhen, Yang, Wensheng
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Sprache:eng
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Zusammenfassung:The effect of Cu^sup 2+^ ions on aggregation behaviors of poly (l-glutamic acid) (PLGA)-functionalized Au nanoparticles was investigated. It was found that the concentration of Cu^sup 2+^ ions had a significant influence on the folding and the formation of intermolecular hydrogen bonding of PLGA and thus the aggregation of the Au nanoparticles. In the absence of Cu^sup 2+^ ions, the Au nanoparticles underwent reversible pH-dependent aggregation attributed to the folding/unfolding of PLGA and the formation/breakage of intermolecular hydrogen bonds between PLGA molecules. In the presence of low concentration of Cu^sup 2+^ ions (i.e., 10 μM), folding of PLGA and aggregation of the Au nanoparticles were facilitated due to the charge screening effect of Cu^sup 2+^ ions, while the reversibility was partly maintained. In the presence of high concentration of Cu^sup 2+^ ions (i.e., 50 μM), aggregation of the Au nanoparticles was dominated by the coordination interaction between PLGA and Cu^sup 2+^ ions and the aggregation became irreversible due to the blocking of the formation of intermolecular hydrogen bonds by Cu^sup 2+^. These results suggested that Au nanoparticles may be used as a colorimetric probe to monitor the interactions between metal ions and peptides, which are essential for exploring the physiological effect of metals ions.[PUBLICATION ABSTRACT]
ISSN:1388-0764
1572-896X
DOI:10.1007/s11051-012-1403-6