| Autor: |
Dominique Duchêne, Amélie Bochot, Laury Trichard, P. Chaminade, J. L. Grossiord, M. Hamoudi, G. Le Bas, Elias Fattal |
| Rok vydání: |
2009 |
| Předmět: |
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| Zdroj: |
Annales Pharmaceutiques Françaises. 67:391-398 |
| ISSN: |
0003-4509 |
| DOI: |
10.1016/j.pharma.2009.08.003 |
| Popis: |
Natural cyclodextrins are cyclic oligosaccharides which can be modified to obtain more water soluble or insoluble derivatives. The main interest of cyclodextrins results from their ability to form an inclusion complex with hydrophobic molecules. Inclusion constitutes a true molecular encapsulation. This property is employed in pharmaceutical industry to facilitate the formulation of poorly water soluble and/or fragile drugs. A more recent application of cyclodextrins consists in their use in the preparation of dispersed systems such as micro- and nanoparticles or even liposomes. When incorporated in dispersed systems, cyclodextrin can enhance drug solubility, drug stability and drug loading. Interestingly, cyclodextrins themselves can also be employed to form or stabilise dispersed systems (material or emulsifying agent). For example, the interactions between cyclodextrins with components of the vegetable oils (more especially with triglycerides) allow to stabilise simple or multiple emulsions but also to form particles called "beads". Very rich in oil, this novel lipid carrier presents an important potential for the encapsulation of highly lipophilic compounds and their delivery by topical and oral routes. These two applications are more particularly developed in the present paper. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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