Phospholipid based colloidal poloxamer–nanocubic vesicles for brain targeting via the nasal route

[Display omitted] ► New phospholipid based nanocubic vesicular systems were developed. ► The polymeric non-ionic surfactant, poloxamer was incorporated in its lipid bilayer. ► The effect of surfactant concentration on the physicochemical properties of the nanocubic vesicles was investigated. ► The b...

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Veröffentlicht in:Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2012-12, Vol.100, p.146-154
Hauptverfasser: Salama, Hamed A., Mahmoud, Azza A., Kamel, Amany O., Abdel Hady, Mayssa, Awad, Gehanne A.S.
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Sprache:eng
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Zusammenfassung:[Display omitted] ► New phospholipid based nanocubic vesicular systems were developed. ► The polymeric non-ionic surfactant, poloxamer was incorporated in its lipid bilayer. ► The effect of surfactant concentration on the physicochemical properties of the nanocubic vesicles was investigated. ► The brain targeting efficiency of these vesicles were evaluated after intranasal administration to rats. In this study, new phospholipid based colloidal nanocubic vesicles encapsulating olanzapine for its brain targeting via the nasal route were developed. The nanocubic vesicles were prepared by incorporating non-ionic copolymers, poloxamer 188 or 407, in the lipid bilayer. The effect of phospholipid:poloxamer molar ratio on the physicochemical properties of the nanocubic vesicles was investigated. The in vivo behavior and brain targeting of these vesicles were evaluated in rats. TEM photographs showed that the vesicles looked spherical before adding poloxamer. However, after poloxamer incorporation, the vesicles showed a predominant cubic shape, except those containing phospholipid:poloxamer in the molar ratio 5:1 which were spherical. DSC study confirmed perturbation of the packing characteristics as well as fluidization of the lipid bilayer by the polymer with consequent formation of the nanocubic structure. The mean diameter of the vesicles was in the range of 363–645nm. All vesicles were elastic and the elasticity was found to depend on both poloxamer type and concentration. The intranasal nanocubic vesicles were significantly more efficient in targeting olanzapine to the brain compared to the liposomal vesicles with drug targeting efficiency values of 100% and 80%, respectively, and absolute bioavailability of 37.9% and 14.9%, respectively.
ISSN:0927-7765
1873-4367
DOI:10.1016/j.colsurfb.2012.05.010