TY - JOUR
T1 - Characterization of oligonucleotide/lipid interactions in submicron cationic emulsions
T2 - Influence of the cationic lipid structure and the presence of PEG-lipids
AU - Teixeira, H.
AU - Rosilio, V.
AU - Laigle, A.
AU - Lepault, J.
AU - Erk, I.
AU - Scherman, D.
AU - Benita, S.
AU - Couvreur, P.
AU - Dubernet, C.
PY - 2001/9/18
Y1 - 2001/9/18
N2 - We have recently described how oligonucleotide (ON) stability and release from O/W cationic emulsions are governed by the lipid composition. The aim of the present paper was to investigate the properties of the ON/lipid complexes through fluorescence resonance energy transfer (FRET), size, surface tension measurements and cryomicroscopy. Starting from a typical emulsion containing stearylamine as a cationic lipid, the influence of the lipid structure (monocationic molecules bearing mono or diacyl chains, or polycations) as well as of the presence of PEGylated lipids, were studied. The presence of a positive charge on the droplet surface clearly contributed to enhance the ON interaction with lipid monolayers and to bring the ON molecules closer to the interface. Hydrophobic interactions through the acyl chains were shown to further enhance the anchorage of the ON/lipid complexes. In contrast, the incorporation of PEGylated lipids acted as a barrier against the establishment of electrostatic bindings, the polyethyleneglycol chains acting themselves as interaction sites for the ON leading to hydrophilic complexes. Similar features were observed for the polycationic lipid, and cryomicroscopy revealed the existence of bridges of various intensities between the droplets of the emulsion containing either PEG or the polycation, probably because of the configuration of the ON at the interface.
AB - We have recently described how oligonucleotide (ON) stability and release from O/W cationic emulsions are governed by the lipid composition. The aim of the present paper was to investigate the properties of the ON/lipid complexes through fluorescence resonance energy transfer (FRET), size, surface tension measurements and cryomicroscopy. Starting from a typical emulsion containing stearylamine as a cationic lipid, the influence of the lipid structure (monocationic molecules bearing mono or diacyl chains, or polycations) as well as of the presence of PEGylated lipids, were studied. The presence of a positive charge on the droplet surface clearly contributed to enhance the ON interaction with lipid monolayers and to bring the ON molecules closer to the interface. Hydrophobic interactions through the acyl chains were shown to further enhance the anchorage of the ON/lipid complexes. In contrast, the incorporation of PEGylated lipids acted as a barrier against the establishment of electrostatic bindings, the polyethyleneglycol chains acting themselves as interaction sites for the ON leading to hydrophilic complexes. Similar features were observed for the polycationic lipid, and cryomicroscopy revealed the existence of bridges of various intensities between the droplets of the emulsion containing either PEG or the polycation, probably because of the configuration of the ON at the interface.
KW - Cationic emulsion
KW - DSPE-PEG
KW - FRET
KW - Oligonucleotide delivery
KW - Stearylamine
KW - Surface tension
UR - http://www.scopus.com/inward/record.url?scp=0035908901&partnerID=8YFLogxK
U2 - 10.1016/S0301-4622(01)00186-7
DO - 10.1016/S0301-4622(01)00186-7
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C2 - 11583834
AN - SCOPUS:0035908901
SN - 0301-4622
VL - 92
SP - 169
EP - 181
JO - Biophysical Chemistry
JF - Biophysical Chemistry
IS - 3
ER -