alexa Biocompatible Gold Nanorod Conjugates for Preclinical Biomedical Research | OMICS International | Abstract
ISSN: 2157-7439

Journal of Nanomedicine & Nanotechnology
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Research Article

Biocompatible Gold Nanorod Conjugates for Preclinical Biomedical Research

Anton Liopo1*, André Conjusteau1, Dmitri Tsyboulski1, Boris Ermolinsky2, Alexander Kazansky2 and Alexander Oraevsky1

1TomoWave Laboratories, Houston, TX 77081, USA

2Department of Biomedicine, University of Texas at Brownsville, TX 78520, USA

*Corresponding Author:
Anton Liopo
TomoWave Laboratories, 6550 Mapleridge St
Suite 124, Houston TX 77081-4629, USA
Tel: 1 713 270 5393
Fax: 1 713 270 5392
E-mail: [email protected]

Received July 19, 2012; Accepted August 03, 2012; Published Date: August 03, 2012

Citation: Liopo A, Conjusteau A, Tsyboulski D, Ermolinsky B, Kazansky A, et al. (2012) Biocompatible Gold Nanorod Conjugates for Preclinical Biomedical Research. J Nanomedic Nanotechnol 6:274. doi:10.4172/2157-7439.1000274

Copyright: © 2012 Liopo A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


Gold nanorods with a peak absorption wavelength of 760 nm were prepared using a seed-mediated method. A novel protocol has been developed to replace hexadecyltrimethylammonium bromide on the surface of the nanorods with 16-mercaptohexadecanoic acid and metoxy-poly(ethylene glycol)-thiol, and the monoclonal antibody HER2. The physical chemistry properties of the conjugates were monitored through optical and zeta-potential measurements to confirm surface chemistry changes. The efficiency of the modifications was quantified through measurement of the average number of antibodies per gold nanorod. The conjugates were investigated for different cells lines: BT-474, MCF7, MCF10, MDCK, and fibroblast. The results show successful cell accumulation of the gold nanorod HER2 conjugates in cells with HER2 overexpression. Incubation of the complexes in heparinized mouse blood demonstrated the low aggregation of the metallic particles through stability of the spectral properties, as verified by UV/VIS spectrometry. Cytotoxicity analysis with LDH release and MTT assay confirms strong targeting and retention of functional activity of the antibody after their conjugation with gold nanorods. Silver staining confirms efficient specific binding to BT-474 cells even in cases where the nanorod complexes were incubated in heparinized mouse blood. This is confirmed through in vivo studies where, following intravenous injection of gold nanorod complexes, silver staining reveals noticeably higher rates of specific binding in mouse tumors than in healthy liver.

The conjugates are reproducible, have strong molecular targeting capabilities, have long term stability in vivo and can be used in pre-clinical applications. The conjugates can also be used for molecular and optoacoustic imaging, quantitative sensing of biological substrates, and photothermal therapy


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