TY - JOUR
T1 - Disulfide-based poly(amido amine)s for siRNA delivery
T2 - Effects of structure on siRNA complexation, cellular uptake, gene silencing and toxicity
AU - Vader, Pieter
AU - Van Der Aa, Leonardus J.
AU - Engbersen, Johan F J
AU - Storm, Gert
AU - Schiffelers, Raymond M.
PY - 2011/5
Y1 - 2011/5
N2 - Purpose: RNA interference (RNAi) is a process by which small interfering RNAs (siRNA) induce sequence-specific gene silencing. Therefore, siRNA is an emerging promise as a novel therapeutic. In order to realize the high expectations for therapeutic applications, efficient delivery systems for siRNA are necessary. Methods: In this study, a new series of biodegradable poly(amido amine)s with disulfide linkages in the backbone was synthesized out of N,N′-cystaminebisacrylamide (CBA), 4-amino-1-butanol (ABOL) and ethylene diamine (EDA). Effects of different percentages of butanolic side chains and protonatable fragments in the main chain on siRNA complexation, cellular uptake, gene silencing and toxicity were investigated. Results: Incorporation of EDA in the polymer resulted in increased siRNA condensation. Efficient siRNA condensation was shown to be necessary for cellular uptake; however, excess of polymer decreased siRNA uptake for polymers with high amounts of EDA. Silencing efficiency did not correlate with uptake, since silencing increased with increasing w/w ratio for all polymers. More than 80% knockdown was found for polyplexes formed with polymers containing 25% or 50% EDA, which was combined with low cytotoxicity. Conclusions: Poly(amido amine)s with minor fractions of protonatable fragments in the main chain are promising carriers for delivery of siRNA.
AB - Purpose: RNA interference (RNAi) is a process by which small interfering RNAs (siRNA) induce sequence-specific gene silencing. Therefore, siRNA is an emerging promise as a novel therapeutic. In order to realize the high expectations for therapeutic applications, efficient delivery systems for siRNA are necessary. Methods: In this study, a new series of biodegradable poly(amido amine)s with disulfide linkages in the backbone was synthesized out of N,N′-cystaminebisacrylamide (CBA), 4-amino-1-butanol (ABOL) and ethylene diamine (EDA). Effects of different percentages of butanolic side chains and protonatable fragments in the main chain on siRNA complexation, cellular uptake, gene silencing and toxicity were investigated. Results: Incorporation of EDA in the polymer resulted in increased siRNA condensation. Efficient siRNA condensation was shown to be necessary for cellular uptake; however, excess of polymer decreased siRNA uptake for polymers with high amounts of EDA. Silencing efficiency did not correlate with uptake, since silencing increased with increasing w/w ratio for all polymers. More than 80% knockdown was found for polyplexes formed with polymers containing 25% or 50% EDA, which was combined with low cytotoxicity. Conclusions: Poly(amido amine)s with minor fractions of protonatable fragments in the main chain are promising carriers for delivery of siRNA.
KW - delivery
KW - disulfide bonds
KW - poly(amido amine)s
KW - quantitative uptake
KW - siRNA
UR - http://www.scopus.com/inward/record.url?scp=79955620206&partnerID=8YFLogxK
U2 - 10.1007/s11095-010-0344-y
DO - 10.1007/s11095-010-0344-y
M3 - Article
C2 - 21181546
AN - SCOPUS:79955620206
SN - 0724-8741
VL - 28
SP - 1013
EP - 1022
JO - Pharmaceutical Research
JF - Pharmaceutical Research
IS - 5
ER -