Schatzlein, A.G., Zinselmeyer, B.H., Elouzi, A., Dufes, C., Chim, Y.A., Roberts, C.J., Davies, M.C., Munro, A., Gray, A. and Uchegbu, I.F. (2005) Preferential liver gene expression with polypropylenimine dendrimers. Journal of Controlled Release, 101 (1-3). pp. 247-258. 10.1016/j.jconrel.2004.08.024.
Full text not available from this repository.
Previously, the lower generation (DAB 8–generation 2 and DAB 16–generation 3) polypropyleniminedendrimers have been shown to be effective gene delivery systems in vitro. In the current work, we sought to: (a) test the effect of the strength of the carrier, DNA electrostatic interaction on gene transfer and (b) to study the in vivo gene transfer activity of these low molecular weight (<1687 Da) non-amphiphilic plain and quaternary ammonium gene carriers. Towards this aim, methyl quaternary ammonium derivatives of DAB 4 (generation 1), DAB 8, DAB 16 and DAB 32 (generation 4) were synthesised to give Q4, Q8, Q16 and Q32, respectively. Quaternisation of DAB 8 proved to be critical in improving DNA binding, as evidenced by data from the ethidium bromide exclusion assay and dendrimer–DNA colloidal stability data. This improved colloidal stability had a major effect on vector tolerability, as Q8–DNA formulations were well tolerated on intravenous injection while a similar DAB 8–DNA dose was lethally toxic by the same route. Quaternisation also improved the in vitro cell biocompatibility of DAB 16–DNA and DAB 32–DNA dendrimer complexes by about 4-fold but not that of the lower generation DAB 4–DNA and DAB 8–DNA formulations. In contrast to previous reports with non-viral gene delivery systems, the intravenous administration of DAB 16–DNA and Q8–DNA formulations resulted in liver targeted geneexpression as opposed to the lung targeted geneexpression obtained with the control polymer-Exgen 500 [linear poly(ethylenimine)] and a lung avoidance hypothesis is postulated. We conclude that the polypropyleniminedendrimers are promising gene delivery systems which may be used to target the liver and avoid the lung and also that molecular modifications conferring colloidal stability on gene delivery formulations have a profound effect on their tolerability on intravenous administration.
|Uncontrolled Keywords:||Polypropyleniminedendrimers; Dendrimers; Gene delivery; Quaternary ammonium dendrimers; Liver targeting; Liver; Particles|
|Departments, units and centres:||Department of Pharmaceutical and Biological Chemistry > Department of Pharmaceutical and Biological Chemistry|
|Journal or Publication Title:||Journal of Controlled Release|
|Deposited By:||Library Staff|
|Deposited On:||20 Apr 2012 14:38|
|Last Modified:||20 Apr 2012 14:38|
Item downloaded times since 20 Apr 2012 14:38.
Repository Staff Only: Item control page
School of Pharmacy Staff Only: Edit a copy to replace this item