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Transgene delivery using poly(amino ether)‐gold nanorod assemblies
Author(s) -
Ramos James,
Rege Kaushal
Publication year - 2012
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.24408
Subject(s) - nanorod , gene delivery , photothermal therapy , nanotechnology , polymer , ethylene glycol , chemistry , transgene , biophysics , zeta potential , materials science , combinatorial chemistry , transfection , biochemistry , nanoparticle , organic chemistry , biology , gene
Gold nanorods (GNRs) have emerged as promising nanomaterials for biosensing, imaging, photothermal treatment, and therapeutic delivery for several diseases, including cancer. We have generated poly(amino ether)‐functionalized gold nanorods (PAE‐GNRs) using a layer‐by‐layer deposition approach; polymers from a poly(amino ether) library recently synthesized in our laboratory were employed to generate the PAE‐GNR assemblies. PAE‐GNR assemblies demonstrate long‐term colloidal stability as well as the capacity to bind plasmid DNA by means of electrostatic interactions. Sub‐toxic concentrations of PAE‐GNRs were employed to deliver plasmid DNA to prostate cancer cells in vitro. PAE‐GNRs generated using 1,4C‐1,4Bis, a cationic polymer from our laboratory demonstrated significantly higher transgene expression and exhibited lower cytotoxicities when compared to similar assemblies generated using 25 kDa poly(ethylene imine) (PEI25k‐GNRs), a current standard for polymer‐mediated gene delivery. The roles of polyelectrolyte chemistry and zeta‐potential in determining transgene expression efficacies of PAE‐GNR assemblies were investigated. Our results indicate that stable and effective PAE‐GNR assemblies are a promising engineered platform for transgene delivery. PAE‐GNRs also have the potential to be used simultaneously for photothermal ablation, photothermally enhanced drug and gene delivery, and biological imaging, thus making them a powerful theranostic platform. Biotechnol. Bioeng. 2012; 109:1336–1346. © 2011 Wiley Periodicals, Inc.