Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2505575 | International Journal of Pharmaceutics | 2008 | 6 Pages |
The enzymatically degradable poly(amino acid)–lipid conjugate poly(hydroxyethyl l-glutamine)–N-succinyl-dioctadecylamine (PHEG–DODASuc) has been shown to effectively prolong liposome circulation times. In this paper, we investigated whether PHEG–DODASuc can stabilize liposomes composed of the fusogenic, non-bilayer-forming lipid dioleoyl phosphatidylethanolamine (DOPE). Moreover, we evaluated the release of an entrapped compound after enzyme-induced shedding of the PHEG-coating, interbilayer contact and membrane destabilizing phase changes. Contents release was monitored using the fluorescent model compound calcein. Liposome destabilization and lipid mixing was studied by dynamic light scattering (DLS), fluorescence resonance energy transfer (FRET) and cryogenic-temperature transmission electron microscopy (cryo-TEM). It was shown that PHEG–DODASuc is able to stabilize DOPE-based liposomes and that contents release can be triggered by shedding of the PHEG-coating.