Skin drug delivery using lipid vesicles: A starting guideline for their development

被引:51
|
作者
Guillot, Antonio Jose [1 ]
Martinez-Navarrete, Miquel [1 ]
Garrigues, Teresa M. [1 ]
Melero, Ana [1 ]
机构
[1] Univ Valencia, Dept Pharm & Pharmaceut Technol & Parasitol, Avda Vicente A Estelles SN, Valencia, Spain
关键词
Transdermal drug delivery; Lipid vesicles; Liposomes; Transferosomes; Ethosomes; ATOMIC-FORCE MICROSCOPY; LIPOSOME-ENCAPSULATED HEMOGLOBIN; STERICALLY STABILIZED LIPOSOMES; SIZE-EXCLUSION CHROMATOGRAPHY; ENHANCED TRANSDERMAL DELIVERY; SMALL UNILAMELLAR VESICLES; WATER-SOLUBLE DRUGS; HET-CAM TEST; IN-VITRO; LIGHT-SCATTERING;
D O I
10.1016/j.jconrel.2023.02.006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lipid vesicles can provide a cost-effective enhancement of skin drug absorption when vesicle production process is optimised. It is an important challenge to design the ideal vesicle, since their properties and features are related, as changes in one affect the others. Here, we review the main components, preparation and characterization methods commonly used, and the key properties that lead to highly efficient vesicles for transdermal drug delivery purposes. We stand by size, deformability degree and drug loading, as the most important vesicle features that determine the further transdermal drug absorption. The interest in this technology is increasing, as demonstrated by the exponential growth of publications on the topic. Although long-term preservation and scalability issues have limited the commercialization of lipid vesicle products, freeze-drying and modern escalation methods overcome these difficulties, thus predicting a higher use of these technologies in the market and clinical practice.
引用
收藏
页码:624 / 654
页数:31
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