TY - JOUR
T1 - Structure-Function Correlation of Aminated Poly(α)glutamate as siRNA Nanocarriers
AU - Krivitsky, Adva
AU - Polyak, Dina
AU - Scomparin, Anna
AU - Eliyahu, Shay
AU - Ori, Asaf
AU - Avkin-Nachum, Sharon
AU - Krivitsky, Vadim
AU - Satchi-Fainaro, Ronit
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/9/12
Y1 - 2016/9/12
N2 - It has been two decades since cationic polymers were introduced to the world of oligonucleotides delivery. However, the optimal physicochemical properties to make them a successful delivery vehicle are yet unknown. An ideal system became particularly interesting and necessary with the introduction of RNA interference as a promising therapeutic approach. Such nanocarrier should overcome challenges such as low plasma stability, poor cellular internalization and endosomal escape to induce gene silencing. To that end, we synthesized a library of biodegradable aminated poly(α)glutamate varied by amine moieties. In an attempt to elucidate the structure-function relationship, our polyplexes were physicochemically characterized and their silencing activity and cytotoxicity were evaluated. We found several structures that demonstrated improved cellular internalization. These candidates silenced gene expression to less than 50% of their initial levels, while being safe to cells and mice. Based on our research, an improved and promising tailor-designed siRNA delivery platform can be developed.
AB - It has been two decades since cationic polymers were introduced to the world of oligonucleotides delivery. However, the optimal physicochemical properties to make them a successful delivery vehicle are yet unknown. An ideal system became particularly interesting and necessary with the introduction of RNA interference as a promising therapeutic approach. Such nanocarrier should overcome challenges such as low plasma stability, poor cellular internalization and endosomal escape to induce gene silencing. To that end, we synthesized a library of biodegradable aminated poly(α)glutamate varied by amine moieties. In an attempt to elucidate the structure-function relationship, our polyplexes were physicochemically characterized and their silencing activity and cytotoxicity were evaluated. We found several structures that demonstrated improved cellular internalization. These candidates silenced gene expression to less than 50% of their initial levels, while being safe to cells and mice. Based on our research, an improved and promising tailor-designed siRNA delivery platform can be developed.
UR - http://www.scopus.com/inward/record.url?scp=84986879732&partnerID=8YFLogxK
U2 - 10.1021/acs.biomac.6b00555
DO - 10.1021/acs.biomac.6b00555
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C2 - 27377188
AN - SCOPUS:84986879732
SN - 1525-7797
VL - 17
SP - 2787
EP - 2800
JO - Biomacromolecules
JF - Biomacromolecules
IS - 9
ER -