ArticleAdvanced healthcare materials2025
Ionic Liquid-Mediated Delivery of Ruxolitinib to Skin Using an Adhesive Topical Hydrogel System.
Article in Advanced healthcare materials, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Solubility, Release Behavior and Membrane Permeability of a Ibuprofen Hydrogel Co-Assembled with N-Methyl-D-Glucosamine.Gels (Basel, Switzerland) · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Delivery of many drug types to the skin is prohibited by the stratum corneum, and drugs that can penetrate the epidermal barrier (e.g., small, nonpolar molecules) often have limited permeation in the dermis. Ionic liquids (ILs) are well-known penetration enhancers, yet, achieving sustained, controlled drug release from ILs alone remains a significant challenge. Herein, ILs are incorporated into a removable, phenolic-functionalized tissue-adhesive hydrogel system for the treatment of atopic dermatitis. The hydrogel, enriched with galloyl groups from plant polyphenols, provides robust skin adhesion, effectively securing IL and ruxolitinib (Janus kinase (JAK) 1/2 inhibitor)-loaded nanoparticles at the target site and enabling sustained delivery of the IL-carried ruxolitinib into the dermis. The IL choline trans-2-butenoic acid (CA2BE) 1:1 can be embedded within the adhesive hydrogel without compromising its mechanical properties or inflaming macrophages. Importantly, the IL-mediated transport of drug into the skin causes a significant increase in ruxolitinib accumulation within the dermis, surpassing that of a clinical ointment analog. By combining efficient skin permeation, controlled release, and strong adhesion, this multifunctional platform offers significant potential for topical drug delivery across a range of skin disorders, extending beyond atopic dermatitis.
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Registered trials
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