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Genuine DNA/polyethylenimine (PEI) Complexes Improve Transfection Properties and Cell Survival

Authors :
Christian Plank
Jean-Luc Coll
Jean-Serge Remy
Emmanuel Brion
Patrick Erbacher
Thierry Bettinger
Jean-Paul Behr
Conception et application de molécules bioactives (CAMB)
Université de Strasbourg (UNISTRA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
INSERM U823, équipe 5 (cibles diagnostiques ou thérapeutiques et vectorisation de drogues dans le cancer du poumon)
Institut d'oncologie/développement Albert Bonniot de Grenoble (INSERM U823)
Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM)
Source :
Journal of Drug Targeting, Journal of Drug Targeting, Informa Healthcare, 2004, 12 (4), pp.223-236. ⟨10.1080/10611860410001723487⟩
Publication Year :
2004
Publisher :
HAL CCSD, 2004.

Abstract

Polyethylenimine (PEI) has been described as one of the most efficient cationic polymers for in vitro gene delivery. Systemic delivery of PEI/DNA polyplexes leads to a lung-expression tropism. Selective in vivo gene transfer would require targeting and stealth particles. Here, we describe two strategies for chemically coupling polyethylene glycol (PEG) to PEI, to form protected ligand-bearing particles. Pre-grafted PEG-PEI polymers lost their DNA condensing property, hence their poor performances. Coupling PEG to pre-formed PEI/DNA particles led to the expected physical properties. However, low transfection efficacies raised the question of the fate of excess free polymer in solution. We have developed a straightforward a purification assay, which uses centrifugation-based ultrafiltration. Crude polyplexes were purified, with up to 60% of the initial PEI dose being removed. The resulting purified and unshielded PEI/DNA polyplexes are more efficient for transfection and less toxic to cells in culture than the crude ones. Moreover, the in vivo toxicity of the polyplexes was greatly reduced, without affecting their efficacy.

Details

Language :
English
ISSN :
1061186X
Database :
OpenAIRE
Journal :
Journal of Drug Targeting, Journal of Drug Targeting, Informa Healthcare, 2004, 12 (4), pp.223-236. ⟨10.1080/10611860410001723487⟩
Accession number :
edsair.doi.dedup.....85e7c583702b0707061bdb8507aafa9f
Full Text :
https://doi.org/10.1080/10611860410001723487⟩