2007
DOI: 10.1021/jp0731710
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Small Angle Scattering and Zeta Potential of Liposomes Loaded with Octa(carboranyl)porphyrazine

Abstract: In this work, the physicochemical characterization of liposomes loaded with a newly synthesized carboranyl porphyrazine (H2HECASPz) is described. This molecule represents a potential drug for different anticancer therapies, such as boron neutron capture therapy and for photodynamic therapy or photothermal therapy. Different loading methods and different lipid mixtures were tested. The corresponding loaded vectors were studied by small angle scattering, light scattering, and zeta potential. The combined analysi… Show more

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Cited by 36 publications
(30 citation statements)
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“…It is, however, unlikely that these effects are responsible for the lack of exchange in the closed state. The thickness of the bilayers varies only by 1-2 Å among POPE, DOTAP, and DPhPC according to small angle neutron scattering measurements (28,30). Against a physical separation by phase or domain borders between vesicle and bulk lipids also argues that the bulk lipids can come into close vicinity of the channels, as evidenced by the modulation of the GVs by DOTAP and POPG in the bulk bilayer (Figs.…”
Section: Discussionmentioning
confidence: 96%
“…It is, however, unlikely that these effects are responsible for the lack of exchange in the closed state. The thickness of the bilayers varies only by 1-2 Å among POPE, DOTAP, and DPhPC according to small angle neutron scattering measurements (28,30). Against a physical separation by phase or domain borders between vesicle and bulk lipids also argues that the bulk lipids can come into close vicinity of the channels, as evidenced by the modulation of the GVs by DOTAP and POPG in the bulk bilayer (Figs.…”
Section: Discussionmentioning
confidence: 96%
“…36 The study employed lipid/particle assemblies composed of positively charged PLGA nanoparticles (150 nm in diameter), covered by a bilayer of DPPC (200 nm for LNPs). In this context, DMAB consists of a bromide headgroup with two hydrophobic tails connecting them together; that is, one hydrophobic chain of DMAB is adsorbed onto the surface of PLGA nanoparticles; and the other acts as electrostatic glue that enhances the stability of the self-assembled particles by molecular electronegativity interaction with the oppositely charged phosphocholine headgroups.…”
Section: Discussionmentioning
confidence: 99%
“…They can simply encapsulate the hydrophobic molecules, during the bilayer formation, into the lipophilic space due to their hydrophobic ends (Decker et al 2012). Consequently, loaded liposomes can easily transport the hydrophobic drug in aqueous medium to the target tissue and the similarity between their structures and the cell membrane, allows an easy diffusion and the drug unload into the cytoplasm (Salvati et al 2007). Additionally, their nanometric size (classically 60-120 nm) confer them a high loading capacity of the therapeutic agent.…”
Section: Liposomesmentioning
confidence: 99%