The effect of entrapped \u3b2-cyclodextrin (\u3b2-CD) on the stability of multilamellar vesicles (MLVs) of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), prepared by the dehydration-rehydration method, was studied by monitoring the release of 5(6)-carboxyfluorescein encapsulated into the liposomes. Different hydrophobic guests, such as Fullerene C60, have been incorporated into the POPC bilayer in order to modify the membrane composition. The kinetic results as well as ESI-MS measurements evidenced that the destabilizing activity of \u3b2-CD is due to the formation of \u3b2-CD inclusion complexes and the consequent removal of selected bilayer constituents from the liposomal membrane. Hence, when \u3b2-CD was added to the liposomes...
Penetration and partition of C-60 to the lipid bilayer core are both relevant to C60 toxicity, and u...
The lipophilicity of many therapeutic agents has compromised their use in parenteral delivery. Tradi...
In this article, we describe the introduction of amphiphilic β-cyclodextrins into liposomes to act a...
International audienceLiposomes loaded with drug–cyclodextrin complexes are widely used as drug deli...
The cationic large unilamellar mixed liposomes from 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPC) ...
International audienceCyclodextrins (CDs) are cyclic oligosaccharides able to improve drug water sol...
International audienceAmphiphilic cyclodextrins (CDs) are good candidates to functionalize natural m...
Nanoparticle (NP) interactions that may destabilize cell membranes and cause toxicity can also be us...
The incorporation of hydrophobic guest molecules into lipid membranes by the exchange of the guest m...
<p>In this article, we describe the introduction of amphiphilic beta-cyclodextrins into liposomes to...
The interaction of β-cyclodextrin (β-CD) with different lipids has been studied, using Langmuir mono...
AbstractCyclodextrins are hydrophilic molecular cages with a hydrophobic interior allowing the inclu...
It is well known that cyclodextrins are able to extract lipids constituting membranes, increasing th...
Penetration and partition of C60 to the lipid bilayer core are both relevant to C60 toxicity, and us...
In this study we evaluate the use of dipalmitoylphosphatidylcholine (DPPC) as a biomolecular dispers...
Penetration and partition of C-60 to the lipid bilayer core are both relevant to C60 toxicity, and u...
The lipophilicity of many therapeutic agents has compromised their use in parenteral delivery. Tradi...
In this article, we describe the introduction of amphiphilic β-cyclodextrins into liposomes to act a...
International audienceLiposomes loaded with drug–cyclodextrin complexes are widely used as drug deli...
The cationic large unilamellar mixed liposomes from 1-palmitoyl-2-oleoyl-phosphatidylcholine (POPC) ...
International audienceCyclodextrins (CDs) are cyclic oligosaccharides able to improve drug water sol...
International audienceAmphiphilic cyclodextrins (CDs) are good candidates to functionalize natural m...
Nanoparticle (NP) interactions that may destabilize cell membranes and cause toxicity can also be us...
The incorporation of hydrophobic guest molecules into lipid membranes by the exchange of the guest m...
<p>In this article, we describe the introduction of amphiphilic beta-cyclodextrins into liposomes to...
The interaction of β-cyclodextrin (β-CD) with different lipids has been studied, using Langmuir mono...
AbstractCyclodextrins are hydrophilic molecular cages with a hydrophobic interior allowing the inclu...
It is well known that cyclodextrins are able to extract lipids constituting membranes, increasing th...
Penetration and partition of C60 to the lipid bilayer core are both relevant to C60 toxicity, and us...
In this study we evaluate the use of dipalmitoylphosphatidylcholine (DPPC) as a biomolecular dispers...
Penetration and partition of C-60 to the lipid bilayer core are both relevant to C60 toxicity, and u...
The lipophilicity of many therapeutic agents has compromised their use in parenteral delivery. Tradi...
In this article, we describe the introduction of amphiphilic β-cyclodextrins into liposomes to act a...