Abstract Background Gold nanoparticles (AuNPs) have shown great promise as scaffolds for gene therapy vectors due to their attractive physiochemical properties which include biocompatibility, ease of functionalization via the nearly covalent gold-sulfur dative bond, and surface plasmon optical properties. Previously, we synthesized stable AuNP-polyamidoamine (AuPAMAM) conjugates and showed their success in vitro as non-viral gene delivery vectors. Results In this study, we systematically perturbed each component of the AuPAMAM conjugates and analyzed the resulting effect on transfection efficiency. Due to the modular, bottom-u...
Cationic polyethylenimine conjugated gold nanoparticles (AuNP-PEI) are a widely studied vector for d...
The next generation of anticancer agents will emerge from rationally designed nanostructured materia...
Ph. D. University of KwaZulu-Natal, Durban 2014.Cancer is a disease characterized by accelerated cel...
Gene therapy is a promising treatment that has enormous potential for the management of numerous dis...
The development of efficient and biocompatible non-viral vectors for gene therapy remains a great ch...
The use of nanotechnology in medicine and more specifically drug delivery, is set to spread rapidly....
Gene therapy, which involves the transfer of nucleic acid into target cells in patients, has become ...
Over the past few decades, tremendous efforts have been made to develop nanomaterials for biotechnol...
The potential of RNA interference (RNAi)-based therapeutics for cancer has received much attention; ...
As gene therapies continue to be developed, the role played by siRNA technologies in anti-cancer reg...
ABSTRACT: Plasmonic nanoparticles have been increasingly investigated for numerous applications in m...
Gene therapy presents an ideal strategy for the treatment of genetic as well as acquired diseases, s...
We present a general strategy to create polypeptide–gold nanoconjugates by a one-pot synthesis appro...
Development of highly efficient nonviral gene delivery vectors still remains a great challenge. In t...
Development of nano-sized gene delivery vehicles for small interfering RNA (siRNA) delivery is of gr...
Cationic polyethylenimine conjugated gold nanoparticles (AuNP-PEI) are a widely studied vector for d...
The next generation of anticancer agents will emerge from rationally designed nanostructured materia...
Ph. D. University of KwaZulu-Natal, Durban 2014.Cancer is a disease characterized by accelerated cel...
Gene therapy is a promising treatment that has enormous potential for the management of numerous dis...
The development of efficient and biocompatible non-viral vectors for gene therapy remains a great ch...
The use of nanotechnology in medicine and more specifically drug delivery, is set to spread rapidly....
Gene therapy, which involves the transfer of nucleic acid into target cells in patients, has become ...
Over the past few decades, tremendous efforts have been made to develop nanomaterials for biotechnol...
The potential of RNA interference (RNAi)-based therapeutics for cancer has received much attention; ...
As gene therapies continue to be developed, the role played by siRNA technologies in anti-cancer reg...
ABSTRACT: Plasmonic nanoparticles have been increasingly investigated for numerous applications in m...
Gene therapy presents an ideal strategy for the treatment of genetic as well as acquired diseases, s...
We present a general strategy to create polypeptide–gold nanoconjugates by a one-pot synthesis appro...
Development of highly efficient nonviral gene delivery vectors still remains a great challenge. In t...
Development of nano-sized gene delivery vehicles for small interfering RNA (siRNA) delivery is of gr...
Cationic polyethylenimine conjugated gold nanoparticles (AuNP-PEI) are a widely studied vector for d...
The next generation of anticancer agents will emerge from rationally designed nanostructured materia...
Ph. D. University of KwaZulu-Natal, Durban 2014.Cancer is a disease characterized by accelerated cel...