Phospholipid-Based Microemulsions for Cutaneous Imiquimod Delivery
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F22%3A43925654" target="_blank" >RIV/60461373:22310/22:43925654 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11160/22:10450967
Result on the web
<a href="https://www.mdpi.com/1424-8247/15/5/515" target="_blank" >https://www.mdpi.com/1424-8247/15/5/515</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/ph15050515" target="_blank" >10.3390/ph15050515</a>
Alternative languages
Result language
angličtina
Original language name
Phospholipid-Based Microemulsions for Cutaneous Imiquimod Delivery
Original language description
Imiquimod (IMQ) is a potent immune response modifier with antiviral and antitumor properties. IMQ's low aqueous solubility and unsatisfactory cutaneous permeability limit its formulation into effective dosage forms. This work aimed to develop IMQ-loaded microemulsions (MEs) based on phospholipids and oleic acid to improve IMQ penetration into the epidermis. A pseudo-ternary phase diagram was constructed, and the microstructure of the formulations was examined by measuring the conductivity values. Selected MEs were characterized and studied for their ability to deliver IMQ into and through ex vivo human skin. ME1 with 1% IMQ (bicontinuous ME with Bingham rheology) delivered similar IMQ quantities to the human epidermis ex vivo as the commercial product while having a 5-fold lower IMQ dose. IMQ was not detected in the acceptor phase after the permeation experiment, suggesting a lower systemic absorption risk than the established product. Infrared spectroscopy of the stratum corneum revealed less ordered and less tightly packed lipids after ME1 application. The ME1-induced barrier disruption recovered within less than 5 h after the formulation removal, as detected by transepidermal water loss measurements. In conclusion, our findings demonstrate that phospholipid and oleic acid-based MEs could become a promising alternative for topical IMQ administration.
Czech name
—
Czech description
—
Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
30502 - Other medical science
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Pharmaceuticals
ISSN
1424-8247
e-ISSN
1424-8247
Volume of the periodical
15
Issue of the periodical within the volume
5
Country of publishing house
CH - SWITZERLAND
Number of pages
13
Pages from-to
nestrankovano
UT code for WoS article
000803374700001
EID of the result in the Scopus database
2-s2.0-85129752799