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
. 2002 Aug;19(8):1144-9.
doi: 10.1023/a:1019894008885.

Sphingosine-based liposome as DNA vector for intramuscular gene delivery

Affiliations

Sphingosine-based liposome as DNA vector for intramuscular gene delivery

Karin Baraldo et al. Pharm Res. 2002 Aug.

Abstract

Purpose: The aim of this study was to develop a labile sphingosine-based liposome for intramuscular gene delivery.

Methods: Sphingosine-based liposomes were formulated in a range of solutions with phosphatidylcholine, then were associated to DNA. The physico-chemical characteristics of the sphingosine/EPC liposomes and sphingosine/EPC/DNA lipoplexes were determined. DNA stability within sphingosine-based liposomes was evaluated in the presence of a nuclease and mouse serum. In vivo gene transfer was studied by intramuscular injection with and without the electrotransfer technique.

Results: By increasing the charge ratios, colloidally stable sphingosine/DNA particles with a 170 nm average diameter and a positive zeta potential were obtained. Ethidium bromide was still able to insert into plasmid DNA within the lipoplexes, even though plasmid DNA was demonstrated to be complexed to the lipid by gel electrophoresis. Additionally, DNA was shown to be accessible to DNase I, but significantly resistant to serum enzymatic digestion. Upon intramuscular injection, lipoplexes induced an inhibition of gene expression as compared with naked DNA.

Conclusions: The cationic sphingosine/EPC/DNA complexes form weakly compacted structure, potentially labile in vivo, which might be useful for in vivo gene transfer.

PubMed Disclaimer

References

    1. Gene Ther. 1995 Dec;2(10):710-22 - PubMed
    1. Proc Natl Acad Sci U S A. 1999 Apr 13;96(8):4262-7 - PubMed
    1. J Biol Chem. 1990 May 5;265(13):7345-50 - PubMed
    1. J Pharm Biomed Anal. 2000 Jun;22(5):849-59 - PubMed
    1. Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14412-7 - PubMed

Publication types

LinkOut - more resources