Literature DB >> 25536113

Polyene-based cationic lipids as visually traceable siRNA transfer reagents.

Emile Jubeli1, Liji Raju2, Nada Abdul Khalique2, Natalia Bilchuk3, Cory Zegel3, Agape Chen3, Howard H Lou3, Christer L Øpstad4, Muhammad Zeeshan4, Hans-Richard Sliwka4, Vassilia Partali4, Philip L Leopold3, Michael D Pungente5.   

Abstract

Cationic lipids are promising non-viral vectors for the cellular delivery of nucleic acids. Important considerations for the development of new delivery vectors are enhanced uptake efficiency, low toxicity and traceability. Traceable gene transfer systems however typically require the inclusion of a labeled excipient, and highly sensitive imaging instrumentation to detect the presence of the label. Recently, we reported the synthesis and characterization of colored, polyene cationic phospholipidoids composed of a rigid, polyenoic acid of predetermined dimension (C20:5 and C30:9) paired with flexible saturated alkyl chains of varying lengths (12:0, 14:0, 16:0, 18:0, 20:0 carbons). Herein, the potential of these cationic phospholipids as siRNA carriers was evaluated through standard liposomal formulations in combination with a neutral helper lipid DOPE. The polyene-based lipids were compared with a standard cationic lipid for siRNA-delivery into luciferase expressing HR5-CL11 cells. Within the series of lipids screened, knockdown results indicated that polyene cationic phospholipids paired with longer saturated alkyl chains are more effective as gene transfer agents, and perform comparably with the commercial lipid EPC. Furthermore, the chromophore associated with the polyene chain allowed tracking of the siRNA delivery using direct observation. The polyene lipoplexes were tracked on both a macroscopic and microscopic level either as a single-component or as a multi-component lipoplex formulation. When combined with a reference EPC, effective knockdown and tracking abilities were combined in a single preparation.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Carotenoids; Cationic liposomes; Gene delivery; Knockdown; Polyene-based lipids; Traceable; siRNA

Mesh:

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Year:  2014        PMID: 25536113     DOI: 10.1016/j.ejpb.2014.12.011

Source DB:  PubMed          Journal:  Eur J Pharm Biopharm        ISSN: 0939-6411            Impact factor:   5.571


  2 in total

Review 1.  In vitro 3D model and miRNA drug delivery to target calcific aortic valve disease.

Authors:  Casper F T van der Ven; Pin-Jou Wu; Mark W Tibbitt; Alain van Mil; Joost P G Sluijter; Robert Langer; Elena Aikawa
Journal:  Clin Sci (Lond)       Date:  2017-02-01       Impact factor: 6.124

2.  Low-Molecular-Weight Polyethyleneimine Grafted Polythiophene for Efficient siRNA Delivery.

Authors:  Pan He; Kyoji Hagiwara; Hui Chong; Hsiao-hua Yu; Yoshihiro Ito
Journal:  Biomed Res Int       Date:  2015-10-11       Impact factor: 3.411

  2 in total

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