Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2006 Aug;23(8):1868-76.
doi: 10.1007/s11095-006-9009-2.

Biophysical and structural characterization of polyethylenimine-mediated siRNA delivery in vitro

Affiliations

Biophysical and structural characterization of polyethylenimine-mediated siRNA delivery in vitro

Amy C Richards Grayson et al. Pharm Res. 2006 Aug.

Abstract

Purpose: The goals of this study were as follows: 1) to evaluate the efficacy of different polyethylenimine (PEI) structures for siRNA delivery in a model system, and 2) to determine the biophysical and structural characteristics of PEI that relate to siRNA delivery.

Materials and methods: Biophysical characterization (effective diameter and zeta potential), cytotoxicities, relative binding affinities and in vitro transfection efficiencies were determined using nano-complexes formed from PEI's of 800, 25,000, (both branched) and 22,000 (linear) molecular weights at varying N:P ratios and siRNA concentrations. The HR5-CL11 cell line stably expressing luciferase was used as a model system in vitro.

Results: Successful siRNA delivery was observed within a very narrow window of conditions, and only with the 25,000 branched PEI at an N:P ratio of 6:1 and 8:1 and with 200 nM siRNA. While the zeta potential and size of PEI:siRNA complexes correlated to transfection efficacy in some cases, complex stability may also affect transfection efficacy.

Conclusions: The ability of PEI to transfer functionally active siRNA to cells in culture is surprisingly dependent on its biophysical and structural characteristics when compared to its relative success and ease of use for DNA delivery.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Rev Med Virol. 1997 Dec;7(4):199-209 - PubMed
    1. Int J Pharm. 2000 Dec 4;210(1-2):97-107 - PubMed
    1. J Gene Med. 2005 Feb;7(2):198-207 - PubMed
    1. Biomacromolecules. 2002 Nov-Dec;3(6):1197-207 - PubMed
    1. Biomacromolecules. 2003 May-Jun;4(3):683-90 - PubMed

Publication types

LinkOut - more resources