2017
DOI: 10.1016/j.ijpharm.2016.11.011
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Lipid vesicular nanocarrier: Quick encapsulation efficiency determination and transcutaneous application

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Cited by 35 publications
(13 citation statements)
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“…However, in vivo immunization studies were not performed. Zhang et al compared OVA-and saponin-loaded ethosomes, liposomes, and transfersomes as regards their immunization potency in mice (65). In vivo immunization experiments revealed the highest anti-OVA IgG titers for immunization with ethosomes compared with liposomal or transfersomal TCI.…”
Section: Passive Delivery Methodsmentioning
confidence: 99%
“…However, in vivo immunization studies were not performed. Zhang et al compared OVA-and saponin-loaded ethosomes, liposomes, and transfersomes as regards their immunization potency in mice (65). In vivo immunization experiments revealed the highest anti-OVA IgG titers for immunization with ethosomes compared with liposomal or transfersomal TCI.…”
Section: Passive Delivery Methodsmentioning
confidence: 99%
“…Taking advantage of the deformable property of transfersomes and ethosomes, modification of lipid vesicles with the cationic lipids stearylamine or octadecylamine can promote potent immune responses in TCI. Skin treatment such as microneedle puncture can further facilitate the penetration of cationic vesicles‐vaccine complexes into the epidermis …”
Section: Advanced Technologies For Transcutaneous Gene Deliverymentioning
confidence: 99%
“…The second group malleable liposomes generally called ethosomes are made from phospholipids with ethanol. Some recent findings proved that ethosomes are more effective transdermal carriers than deformable liposomes [6]. Ethosomes were first described by Touitou in 1996 as a skin permeation enhancing system, which is formed from phospholipids in the presence of water and ethanol.…”
Section: Introductionmentioning
confidence: 99%