Title of article
High aspect ratio gold nanorods displayed augmented cellular internalization and surface chemistry mediated cytotoxicity
Author/Authors
DeBrosse، نويسنده , , Madeleine C. and Comfort، نويسنده , , Kristen K. and Untener، نويسنده , , Emily A. and Comfort، نويسنده , , Donald A. and Hussain، نويسنده , , Saber M.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2013
Pages
7
From page
4094
To page
4100
Abstract
Due to their unique properties, gold nanorods (GNRs) have shown tremendous potential for advancing bio-imaging and sensing applications. As these nanoparticles display size-dependent optical properties, high aspect ratio GNRs are of particular interest for these applications because of their increased scattering contrast. While studies are emerging that demonstrate successful synthesis of high aspect ratio GNRs, their behavior and fate in a physiological environment has yet to be investigated. The goal of this study was to evaluate the rate of cellular internalization and cytotoxicity of long GNRs (aspect ratio 32) in a human keratinocyte cell line. Additionally, the critical role of surface chemistry in extent of cellular interactions and cytotoxicity was evaluated. Through comparison with aspect ratio 3 GNRs, it was identified that high aspect ratio GNRs displayed enhanced cellular internalization. Furthermore, surface functionalization dictated the quantity of GNRs internalized, with tannic acid having a significant increase over polyethylene glycol. However, the augmented intracellular concentration identified with long, tannic acid GNRs resulted in a considerable degree of cytotoxicity, which was not associated with other GNR conditions. Therefore, while the inclusion of high aspect ratio GNRs may increase the capabilities for nano-based applications, there exist some unintentional toxicological consequences that must also be considered.
Keywords
High Aspect ratio , cytotoxicity , Cellular internalization , Tannic acid , gold nanorods
Journal title
Materials Science and Engineering C
Serial Year
2013
Journal title
Materials Science and Engineering C
Record number
2103502
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