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Effects of imidazolium ionic liquids on skin barrier lipids - Perspectives for drug delivery

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11160%2F24%3A10480106" target="_blank" >RIV/00216208:11160/24:10480106 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=3vSS9-MkLN" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=3vSS9-MkLN</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jcis.2023.12.139" target="_blank" >10.1016/j.jcis.2023.12.139</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Effects of imidazolium ionic liquids on skin barrier lipids - Perspectives for drug delivery

  • Original language description

    Ionic liquids (ILs) have great potential to facilitate transdermal and topical drug delivery. Here, we investigated the mechanism of action of amphiphilic ILs 1-methyl-3-octylimidazolium bromide (C(8)MIM) and 3-dodecyl-1-methylimidazolium bromide (C(12)MIM) in skin barrier lipid models in comparison to their complex effects in human skin. C(8)MIM incorporated in a skin lipid model was a better permeation enhancer than C(12)MIM for water and model drugs, theophylline and diclofenac. Solid state 2H NMR and X-ray diffraction indicated that both ILs prefer the cholesterol-rich regions in skin lipids without significantly perturbing their lamellar arrangement and that C(8)MIM induces the formation of an isotropic lipid phase to a greater extent compared to C(12)MIM. C(12)MIM applied topically to the lipid model or human skin as a pretreatment was more potent than C(8)MIM. When co-applied with the drugs to human skin, aqueous C(12)MIM was more potent than C(8)MIM in enhancing theophylline permeation, but neither IL affected (even decreased) diclofenac permeation. Thus, the IL&apos;s ability to permeabilize skin lipid barrier is strongly modulated by its ability to reach the site of action and its interactions with drug and solvent. Such an interplay is far from trivial and requires detailed investigation to realize the full potential of ILs.

  • 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

    30104 - Pharmacology and pharmacy

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

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Colloid and Interface Science

  • ISSN

    0021-9797

  • e-ISSN

    1095-7103

  • Volume of the periodical

    659

  • Issue of the periodical within the volume

    April

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    14

  • Pages from-to

    449-462

  • UT code for WoS article

    001154614100001

  • EID of the result in the Scopus database

    2-s2.0-85182890369