2008
DOI: 10.1186/1743-8977-5-14
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Optimized dispersion of nanoparticles for biological in vitro and in vivo studies

Abstract: Background: The aim of this study was to establish and validate a practical method to disperse nanoparticles in physiological solutions for biological in vitro and in vivo studies.

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Cited by 414 publications
(314 citation statements)
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“…The ZnO-hydro particles without lecithin in the stock suspension also remained stable, eliminating the need for lecithin as a stabilizing agent in protein-containing media. The findings confirmed the results of our own studies [25][26][27][28] and those of other groups [23,39,43] that proteins, especially BSA, stabilize different kinds of nanoparticles under physiological conditions. Furthermore, Tantra et al [44] were able to demonstrate a stabilizing effect of BSA for ZnO particles, but these investigations were carried out in deionized water and not in physiological media.…”
Section: Discussionsupporting
confidence: 81%
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“…The ZnO-hydro particles without lecithin in the stock suspension also remained stable, eliminating the need for lecithin as a stabilizing agent in protein-containing media. The findings confirmed the results of our own studies [25][26][27][28] and those of other groups [23,39,43] that proteins, especially BSA, stabilize different kinds of nanoparticles under physiological conditions. Furthermore, Tantra et al [44] were able to demonstrate a stabilizing effect of BSA for ZnO particles, but these investigations were carried out in deionized water and not in physiological media.…”
Section: Discussionsupporting
confidence: 81%
“…This conformity suggests that serum proteins adsorbed onto the particle surface, with the result that protein-coated ZnO particles appeared electrostatically to be like the free serum proteins. Such zeta potential values of protein-covered particles in physiological media are often found and seem to be particleindependent [23,45,46].…”
Section: Discussionmentioning
confidence: 99%
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“…Therefore some groups have focussed on the development of methods to create a stable and uniform dispersion via surface modification, addition of surfactants etc. [118][119][120] . But opposing opinions exist on whether NP agglomerates must be redispersed before addition to the cells or not since results from a study by Oberdörster et al in which surfactant stabilised dispersions were used, has been put to question as the observed toxicity might have been caused by surfactant residuals 121 .…”
Section: Issues With Routine In Vitro Methodsmentioning
confidence: 99%
“…When MNPs get inside of the human body, they come into contact with different biomolecules, especially protein (Bihari et al 2008;Lynch and Dawson 2008), which lead to altered properties of MNPs, thereby affect their biodistribution and interactions with biostructures and cells. The binding of protein with MNPs can trigger conformational changes in protein folding, altering its biological function, and affecting the signaling pathways activated by MNPs (Bihari et al 2008;Lynch and Dawson 2008).…”
Section: Mnps' Health Effect By Life Cyclementioning
confidence: 99%