Abstract
Liposomes are used as carriers to deliver the entrapped drugs into the skin, beneath the skin or into the systemic circulation, but the major limitation of using liposomes topically onto the skin is the liquid nature of the preparation, as they may leak from the application site upon their administration. However, this disadvantage of using liposome dispersion can be overcome by their incorporation in an adequate vehicle, where original structure of vesicles is preserved and their rheological and/or mucoadhesive properties are adjusted. This can be achieved by adding gelling agents into liposomal dispersions or by incorporating liposome dispersions into hydrogels, when liposomal gels are formed.
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Abbreviations
- Chol:
-
Cholesterol
- DSPC-Chol:
-
Distearoyl-glycero-PC and cholesterol
- EPC:
-
Egg phosphatidylcholine
- EPC-Na:
-
Egg phosphatidylglycerol sodium
- HEC:
-
Hydroxyethyl cellulose
- HPC:
-
Hydrogenated PC
- HPMC:
-
Hydroxypropyl methylcellulose
- PC:
-
Phosphatidylcholine
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Tavano, L. (2015). Liposomal Gels in Enhancing Skin Delivery of Drugs. In: Dragicevic, N., Maibach, H. (eds) Percutaneous Penetration Enhancers Chemical Methods in Penetration Enhancement. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-45013-0_23
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