2010
DOI: 10.3109/10717540903509027
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Controlled release application of multilamellar vesicles: a novel drug delivery approach

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Cited by 20 publications
(10 citation statements)
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“…These results are compatible with other studies [60,93] that investigated that proniosomes are non-sticky provesicular powders that have higher flowability than the carriers. Improving the flowability of proniosomal powder compared to the pure carrier could be attributable to the coating of the surfactant film on the carrier surface and reducing the cohesive interactions between carrier particles [60].…”
Section: Determination Of the Micromeritic Propertiessupporting
confidence: 93%
“…These results are compatible with other studies [60,93] that investigated that proniosomes are non-sticky provesicular powders that have higher flowability than the carriers. Improving the flowability of proniosomal powder compared to the pure carrier could be attributable to the coating of the surfactant film on the carrier surface and reducing the cohesive interactions between carrier particles [60].…”
Section: Determination Of the Micromeritic Propertiessupporting
confidence: 93%
“…The phospholipid bilayer membrane was multilamellar or had several layers indicated by red arrows. This multilamellar wall serves to release antigens slowly or gradually (Agnihotri et al, 2010).…”
Section: Morphological Analysismentioning
confidence: 99%
“…[104] On the other hand, the interest in MLVs originates from the possibility of studying passive drug transport and sustained drug delivery application, due to a slower release rate in comparison to ULVs. [105] The ULVs can be, in turn, classified according to their different lateral sizes: 20-100 nmsmall unilamellar vesicles (SUVs); 100-1000 nm-large unilamellar vesicles (LUVs); and 1-200 µm-giant unilamellar liposomes/vesicles (GUVs). The MLVs are the result of direct redispersion of the lipid film in the aqueous medium from a film hydration approach.…”
Section: Wet-chemistry Preparationmentioning
confidence: 99%