Evidence map›Paper›PMID 41983181›Full record

ArticleRSC advances2026

Azelaic acid-integrated therapeutic deep eutectic systems: overcoming solubility and permeability barriers for enhanced transdermal drug delivery.

Liyong Du, Shixian Wang, Haihui Chen, Chunhui Liu, Shuyan Yang, Yue Wang, Beilei Cai, Jingguo Yang, Yuqiang Ding

Abstract read
In one paragraph

Article in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Liyong DuKey Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University Wuxi 214122 China dlyong@jiangnan.edu.cn.ORCID https://orcid.org/0009-0004-6566-8180
Shixian WangKey Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University Wuxi 214122 China dlyong@jiangnan.edu.cn.
Haihui ChenKey Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University Wuxi 214122 China dlyong@jiangnan.edu.cn.
Chunhui LiuKey Laboratory of Micro-Nano Materials for Energy Storage and Conversion of Henan Province, Institute of Surface Micro and Nano Materials, College of Chemical and Materials Engineering, Xuchang University Xuchang Henan 461000 China.
Shuyan YangWuxi Zhiyan Biotechnology Co., Ltd Xuxi 214194 China.
Yue WangWuxi Zhiyan Biotechnology Co., Ltd Xuxi 214194 China.
Beilei CaiWuxi Zhiyan Biotechnology Co., Ltd Xuxi 214194 China.
Jingguo YangKey Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University Wuxi 214122 China dlyong@jiangnan.edu.cn.
Yuqiang DingKey Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University Wuxi 214122 China dlyong@jiangnan.edu.cn.ORCID https://orcid.org/0000-0003-3849-4942

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Azelaic acid (AzA) is a saturated dicarboxylic acid used to treat skin disorders like acne, rosacea, and melasma. However, its transdermal application is limited by its poor water solubility and permeability. In this study, therapeutic deep eutectic systems (THEDES) are synthesized by combining azelaic acid (AzA) and D-panthenol (DP) in various molar ratios (3 : 1, 2 : 1, 1 : 1, 1 : 2, 1 : 3). The optimal molar ratio of the THEDES (AzA : DP = 1 : 2) is analyzed with molecular simulation calculations, polarized optical microscopy (POM), Fourier Infrared Spectroscopy (FTIR), Nuclear Magnetic Resonance (1H NMR), Thermogravimetric Analysis (TGA), and water solubility and stability tests. In addition, the THEDES system is evaluated for toxicity, antibacterial and anti-inflammatory efficacy, and transdermal properties. The results show that it outperforms AzA raw material by demonstrating good water solubility and permeability, lower transdermal toxicity and skin irritation, and improved bioactivity compared to AzA raw material. Furthermore, its antimicrobial, anti-inflammatory, and transdermal properties are also superior to those of the AzA raw material. Using molecular docking analysis and molecular dynamics simulation, its mechanisms of action in the treatment of acne and skin permeation are investigated. In conclusion, AzA-DP THEDES effectively resolves AzA's solubility and permeability issues while enhancing its efficacy in Transdermal Drug Delivery Systems (TDDS).

Identifiers

PMID41983181
PMCPMC13071801

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.