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. 2014 Jul;31(7):1665-75.
doi: 10.1007/s11095-013-1271-5. Epub 2014 Jan 22.

A novel formulation based on 2,3-di(tetradecyloxy)propan-1-amine cationic lipid combined with polysorbate 80 for efficient gene delivery to the retina

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A novel formulation based on 2,3-di(tetradecyloxy)propan-1-amine cationic lipid combined with polysorbate 80 for efficient gene delivery to the retina

Gustavo Puras Ochoa et al. Pharm Res. 2014 Jul.

Abstract

Purpose: The aim of the present study was to evaluate the potential application of a novel formulation based on a synthesized cationic lipid 2,3-di(tetradecyloxy)propan-1-amine, combined with polysorbate 80 to deliver the pCMS-EGFP plasmid into the rat retina.

Methods: We elaborated lipoplexes by mixing the formulation containing the cationic lipid and the polysorbate 80 with the plasmid at different cationic lipid/DNA ratios (w/w). Resulted lipoplexes were characterized in terms of size, charge, and capacity to condense, protect and release the DNA. In vitro transfection studies were performed in HEK-293 and ARPE-19 cells. Formulations were also tested in vivo by monitoring the expression of the EGFP after intravitreal and subretinal injections in rat eyes.

Results: At 2/1 cationic lipid/DNA mass ratio, the resulted lipoplexes had 200 nm of hydrodynamic diameter; were positive charged, spherical, protected DNA against enzymatic digestion and transfected efficiently HEK-293 and ARPE-19 cultured cells exhibiting lower cytotoxicity than LipofectamineTM 2000. Subretinal administrations transfected mainly photoreceptors and retinal pigment epithelial cells; whereas intravitreal injections produced a more uniform distribution of transfection through the inner part of the retina.

Conclusions: These results hold great expectations for other gene delivery formulations based on this cationic lipid for retinal gene therapy purposes.

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References

    1. Prog Retin Eye Res. 2013 Jan;32:22-47 - PubMed
    1. Bioconjug Chem. 2010 Apr 21;21(4):563-77 - PubMed
    1. Pharm Res. 1996 Nov;13(11):1642-6 - PubMed
    1. Gene Ther. 2004 Oct;11 Suppl 1:S10-7 - PubMed
    1. Nat Rev Genet. 2003 May;4(5):346-58 - PubMed

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