Journal of Oleo Science · 2018 · 12 citations · 23 references
PharmacyBiochemistryPharmaceuticsDrug DeliveryLipid BiochemistryOral Drug DeliveryLipid-based Drug Delivery SystemsLiposomal FormulationsNanoparticle CharacterizationNanoparticle Delivery SystemsNanoparticle FormulationsParticle Size ControlLiposome CharacterizationLiposome Delivery SystemsLiposome Drug DeliveryLiposome Size ControlLiposomesMultilamellar VesiclesParticle Size ReductionStability Of Liposomal Formulations
The effect of β-sitosteryl sulfate (PSO4) on the liposomal size, stability, fluidity, and dispersibility of DPPC liposomes prepared by vortex mixing, bath-sonication, and probe-sonication has been studied. PSO4 significantly decreases the particle size of the multilamellar liposomes (MLVs). The sizes of the vortexmixed and the bath-sonicated liposomes vary as a function of PSO4 concentration. On the other hand, PSO4 has only little effect on the particle sizes of probe sonicated liposomes. In some cases, the liposomal stability at higher PSO4 concentrations depends on the preparation method. PSO4 improves the dispersibility of the DPPC liposomes and enhances their hydration. It also increases the fluidity of the liposomes prepared by each method. Our results suggest that liposomes consisting of DPPC and PSO4 can be suitable as a cosmetic or pharmaceutical ingredient for the effective delivery of the active components into the body.
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Liposome: classification, preparation, and applications
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