Azone analogues: classification, design, and transdermal penetration principles
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
22886628
DOI
10.1002/med.20227
Knihovny.cz E-resources
- MeSH
- Administration, Cutaneous MeSH
- Azepines chemistry metabolism pharmacology MeSH
- Skin Absorption drug effects MeSH
- Skin anatomy & histology drug effects MeSH
- Quantitative Structure-Activity Relationship MeSH
- Humans MeSH
- Drug Design * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Azepines MeSH
- laurocapram MeSH Browser
The development in the field of pharmaceutical dosage forms results in the discovery of additional highly sophisticated drug delivery systems that allow maintaining a constant level of the active substance in an organism. Transdermal therapeutic systems are an excellent alternative to conventional pharmaceutical dosage forms. However, the application of transdermal drug delivery faces the problem of insufficient or no penetration of active pharmaceutical substances through the skin. This review article describes the possible fundamental mechanisms of penetration through the skin barrier and refers to the classification of skin penetration enhancers. Azone-like enhancers are considered in detail and classified according to their structure on the basis of medicinal chemistry approaches. The article also provides a review of original transdermal penetration enhancers prepared in our laboratory and discusses the relationship between the chemical structure of the described Azone analogues and their penetration activity (SAR/QSAR).
References provided by Crossref.org
N-Alkylmorpholines: Potent Dermal and Transdermal Skin Permeation Enhancers
Chronic Inflammatory Diseases, Anti-Inflammatory Agents and Their Delivery Nanosystems
Investigation of Permeation of Theophylline through Skin Using Selected Piperazine-2,5-Diones
Proline-Based Carbamates as Cholinesterase Inhibitors
In vitro permeation of micronized and nanonized alaptide from semisolid formulations