The development of controlled-release nanoparticle (NP) technologies has great potential to further improve the therapeutic efficacy of RNA interference (RNAi), by prolonging the release of small interfering RNA (siRNA) for sustained, long-term gene silencing. Herein, we present a NP platform with sustained siRNA-release properties, which can be self-assembled using biodegradable and biocompatible polymers and lipids. The hybrid lipid-polymer NPs showed excellent silencing efficacy, and the temporal release of siRNA from the NPs continued for over one month. When tested on luciferase-expressed HeLa cells and A549 lung carcinoma cells after short-term transfection, the siRNA NPs showed greater sustained silencing activity than lipofectamine ...
\u3cp\u3eGenetic drugs based on RNA or DNA have remarkable therapeutic potential as virtually any di...
Mantle cell lymphoma (MCL) is an extremely difficult to treat subtype of non-Hodgkin lymphoma (NHL) ...
Genetic drugs based on RNA or DNA have remarkable therapeutic potential as virtually any disease can...
Gene silencing using small interfering RNA (siRNA) has shown significant potential in the treatment ...
The clinical success of therapeutics of small interfering RNA (siRNA) is still hindered by its deliv...
RNA interference is an evolutionarily conserved gene-silencing phenomenon that shows great promise f...
The present work proposes a unique de-PEGylation strategy for controllable delivery of small interfe...
RNA interference (RNAi) is an emerging technology in which the introduction of double-stranded RNA (...
Nanoparticles represent particularly attractive delivery systems for small interfering RNA (siRNA) a...
Copyright: © 2012 Fatih Uckun, et al. This is an OpenAccess article distributed under the terms of ...
RNA interference (RNAi) is an emerging technology in which the introduction of double-stranded RNA (...
Nanoparticles represent particularly attractive delivery systems for small interfering RNA (siRNA) a...
Successfully employing therapeutic nucleic acids, such as small interfering RNA (siRNA), requires ch...
Degradation of mRNA by RNA interference is one of the most powerful and specific mechanisms for gene...
Technological advances in both siRNA (small interfering RNA) and whole genome sequencing have demons...
\u3cp\u3eGenetic drugs based on RNA or DNA have remarkable therapeutic potential as virtually any di...
Mantle cell lymphoma (MCL) is an extremely difficult to treat subtype of non-Hodgkin lymphoma (NHL) ...
Genetic drugs based on RNA or DNA have remarkable therapeutic potential as virtually any disease can...
Gene silencing using small interfering RNA (siRNA) has shown significant potential in the treatment ...
The clinical success of therapeutics of small interfering RNA (siRNA) is still hindered by its deliv...
RNA interference is an evolutionarily conserved gene-silencing phenomenon that shows great promise f...
The present work proposes a unique de-PEGylation strategy for controllable delivery of small interfe...
RNA interference (RNAi) is an emerging technology in which the introduction of double-stranded RNA (...
Nanoparticles represent particularly attractive delivery systems for small interfering RNA (siRNA) a...
Copyright: © 2012 Fatih Uckun, et al. This is an OpenAccess article distributed under the terms of ...
RNA interference (RNAi) is an emerging technology in which the introduction of double-stranded RNA (...
Nanoparticles represent particularly attractive delivery systems for small interfering RNA (siRNA) a...
Successfully employing therapeutic nucleic acids, such as small interfering RNA (siRNA), requires ch...
Degradation of mRNA by RNA interference is one of the most powerful and specific mechanisms for gene...
Technological advances in both siRNA (small interfering RNA) and whole genome sequencing have demons...
\u3cp\u3eGenetic drugs based on RNA or DNA have remarkable therapeutic potential as virtually any di...
Mantle cell lymphoma (MCL) is an extremely difficult to treat subtype of non-Hodgkin lymphoma (NHL) ...
Genetic drugs based on RNA or DNA have remarkable therapeutic potential as virtually any disease can...