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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&apos;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