Polyethylenimine PEI F25-LMW allows the long-term storage of frozen complexes as fully active reagents in siRNA-mediated gene targeting and DNA delivery
- PMID: 18499413
- DOI: 10.1016/j.ejpb.2008.03.014
Polyethylenimine PEI F25-LMW allows the long-term storage of frozen complexes as fully active reagents in siRNA-mediated gene targeting and DNA delivery
Abstract
Background: Polyethylenimines (PEIs) are synthetic, charged polymers which function as transfection reagents based on their ability to compact DNA into complexes. Recently, PEI-mediated delivery of nucleic acids has been extended towards small interfering RNAs (siRNAs) which are instrumental in the induction of RNA interference (RNAi). Since RNAi represents a powerful method for specific gene silencing, the PEI-based delivery of siRNAs is a promising tool for novel putative therapeutic strategies.
Aim: For therapeutic use, major requirements are the development of formulations which (i) are sufficiently stable in the presence of serum, and which can be (ii) easily and reproducibly manufactured and (iii) stored for a prolonged time with full retention of their integrity and bioactivity. In this paper, we explore the potential of PEI F25-LMW, a low-molecular weight PEI with superior transfection efficacy and low toxicity, towards these goals.
Results: We have systematically analyzed and determined optimal DNA and siRNA complexation conditions with regard to various parameters including buffer concentration, ionic strength, pH and incubation time. As opposed to 22kDa linear PEI (L-PEI), the low-molecular weight (4-10kDa) PEI F25-LMW performs DNA transfection and siRNA gene targeting with identical efficacies in the presence of serum, thus emphasizing its usefulness in vivo. Furthermore, in contrast to other polyethylenimines, PEI F25-LMW-based DNA or siRNA complexes allow freeze/thawing and frozen storage for several months. Their activity is fully retained without requiring specific buffer conditions or the addition of any lyoprotectant. Physicochemical analysis and atomic force microscopy reveal a distinct size pattern with the presence of two complex subgroups and show that frozen PEI F25-LMW complexes remain stable with little increase in complex size, no changes regarding their zeta potential and cytotoxicity, and full retention of nucleic acid protection.
Conclusions: Frozen PEI F25-LMW-based complexes represent efficient and stable ready-to-use formulations of DNA- or siRNA-based gene therapy products.
Similar articles
-
A low molecular weight fraction of polyethylenimine (PEI) displays increased transfection efficiency of DNA and siRNA in fresh or lyophilized complexes.J Control Release. 2006 May 15;112(2):257-70. doi: 10.1016/j.jconrel.2006.02.009. Epub 2006 Mar 6. J Control Release. 2006. PMID: 16574264
-
Liposome-polyethylenimine complexes for enhanced DNA and siRNA delivery.Biomaterials. 2010 Sep;31(26):6892-900. doi: 10.1016/j.biomaterials.2010.05.043. Epub 2010 Jun 18. Biomaterials. 2010. PMID: 20561681
-
Polyethylenimine/small interfering RNA-mediated knockdown of vascular endothelial growth factor in vivo exerts anti-tumor effects synergistically with Bevacizumab.J Gene Med. 2010 Mar;12(3):287-300. doi: 10.1002/jgm.1431. J Gene Med. 2010. PMID: 20052738
-
Polyethylenimines for RNAi-mediated gene targeting in vivo and siRNA delivery to the lung.Eur J Pharm Biopharm. 2011 Apr;77(3):438-49. doi: 10.1016/j.ejpb.2010.11.007. Epub 2010 Nov 18. Eur J Pharm Biopharm. 2011. PMID: 21093588 Review.
-
Gene silencing through RNA interference (RNAi) in vivo: strategies based on the direct application of siRNAs.J Biotechnol. 2006 Jun 25;124(1):12-25. doi: 10.1016/j.jbiotec.2005.12.003. Epub 2006 Jan 18. J Biotechnol. 2006. PMID: 16413079 Review.
Cited by
-
Anti-tumor effects of fibroblast growth factor-binding protein (FGF-BP) knockdown in colon carcinoma.Mol Cancer. 2011 Nov 23;10:144. doi: 10.1186/1476-4598-10-144. Mol Cancer. 2011. PMID: 22111880 Free PMC article.
-
Exploring the MIR143-UPAR Axis for the Inhibition of Human Prostate Cancer Cells In Vitro and In Vivo.Mol Ther Nucleic Acids. 2019 Jun 7;16:272-283. doi: 10.1016/j.omtn.2019.02.020. Epub 2019 Feb 27. Mol Ther Nucleic Acids. 2019. PMID: 30933831 Free PMC article.
-
Targeted CRM197-PEG-PEI/siRNA Complexes for Therapeutic RNAi in Glioblastoma.Pharmaceuticals (Basel). 2011 Dec 16;4(12):1591-1606. doi: 10.3390/ph4121591. Pharmaceuticals (Basel). 2011. PMID: 27721338 Free PMC article.
-
Polyethyleneimine coating enhances the cellular uptake of mesoporous silica nanoparticles and allows safe delivery of siRNA and DNA constructs.ACS Nano. 2009 Oct 27;3(10):3273-86. doi: 10.1021/nn900918w. ACS Nano. 2009. PMID: 19739605 Free PMC article.
-
Polyethylenimine functionalized magnetic nanoparticles as a potential non-viral vector for gene delivery.J Mater Sci Mater Med. 2012 Nov;23(11):2697-708. doi: 10.1007/s10856-012-4720-5. Epub 2012 Jul 24. J Mater Sci Mater Med. 2012. PMID: 22826003
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials