Effects of branched or linear architecture of bioreducible poly(amido amine)s on their in vitro gene delivery properties


Martello, F. and Piest, M. and Engbersen, J.F.J. and Ferruti, P. (2012) Effects of branched or linear architecture of bioreducible poly(amido amine)s on their in vitro gene delivery properties. Journal of controlled release, 164 (3). 372 - 379. ISSN 0168-3659

open access
Abstract:In this study, the gene delivery properties of new hyperbranched poly(amido amine)s (PAAs) with disulfide linkages in the main chain were investigated in comparison with their linear analogs. Eight different bioreducible PAAs were prepared by Michael addition of N,N′-bisacryloylpiperazine (BP) with cystamine (CYST) or N,N′-dimethylcystamine (DMC) and of N,N′-cystaminebisacrylamide (CBA) with N,N′-ethylenediamine (EDA) or N,N′-dimethylethylenediamine (DMEDA). In order to study the effect of terminal groups on the transfection efficiency, each polymer was terminated with 4-aminobutanol (ABOL) or with 2-aminoethanol (ETA). The hyperbranched and the linear PAAs generally formed polyplexes with plasmid DNA with sizes around 200 nm and positive zeta potentials ranging from + 10 to + 22 mV at polymer/DNA weight ratios equal or higher than 3/1. Remarkably low or no cytotoxicity was observed for both hyperbranched and linear PAAs. Hyperbranched CBA-containing PAAs showed higher gene expression in DNA transfection tests with COS-7 cells than their linear analogs and up to two times higher than linear PEI that was used as the reference polymer. Transfection efficiencies of the branched PAAs were generally enhanced by the presence of serum, which is a promising property for future in vivo studies with these hyperbranched PAAs.

In this study the ease of synthetic modification of both linear and hyperbranched poly(amido amide)s and the versatility of hyperbranched PAAs in regulating DNA transfection and cytotoxicity are demonstrated. The results show the large possibilities for this class of polymers to provide polymeric vectors with controllable properties for gene therapy applications.
Item Type:Article
Copyright:© 2012 Elsevier
Science and Technology (TNW)
Research Group:
Link to this item:http://purl.utwente.nl/publications/81835
Official URL:https://doi.org/10.1016/j.jconrel.2012.07.029
Export this item as:BibTeX
HTML Citation
Reference Manager


Repository Staff Only: item control page

Metis ID: 288456