Evidence map›Paper›PMID 40380336›Full record

ArticleJournal of nanobiotechnology2025

Enhanced therapeutic effects of all-trans retinoic acid nanostructured lipid carrier composite gel drug delivery system for alopecia areata.

Lingling Zheng, Yang Du, Lulu Zhang, Fuxing Jin, Wangting Li, Xuan Zhou, Yanping Yin, Yan Weng, Dong Xu, Jingwen Wang

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Trial
  2. Article
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  4. Review
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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

10 authors.

Lingling ZhengDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China.
Yang DuDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China.
Lulu ZhangDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China.
Fuxing JinDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China.
Wangting LiDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China.
Xuan ZhouDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China.
Yanping YinDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China.
Yan WengDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China. guowawa521@163.com.
Dong XuDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China. dongxu418@163.com.
Jingwen WangDepartment of Pharmacy, Xijing Hospital, Air Force Medical University, Xi'an, 710032, China. wangjingwen8021@163.com.

Funding

Clinical Medicine and Pharmacy Research Center of Air Force Medical University LHJJ2024-YX03Talent Special Fund Project of the Hospital Pharmacy Special Committee of the Chinese Pharmaceutical Association NO. CPA-Z05-ZC-2022-003Xijing Hospital Project for Enhancing the Training of Medical Staff XJZT24CZ14
6 · The paper itself

Abstract

backgroundAlopecia areata (AA) affects approximately 2% of the global population and causes psychological distress. All-trans retinoic acid (ATRA) has the potential to promote hair regeneration; however, its clinical use is limited by skin irritation and low targeting specificity. To address these limitations, we designed an ATRA-loaded nanostructured lipid carrier gel (ATRA-NLC-Gel) drug delivery system to enhance the therapeutic effects of ATRA in AA.

resultsATRA-NLC showed a uniform nanoparticle size distribution and excellent biocompatibility. In vitro, they enhanced the uptake ability of dermal papilla cells, increased cell viability, and promoted cell proliferation by facilitating the cell cycle process. Compared to ATRA cream, ATRA-NLC-Gel significantly reduced skin irritation, prolonged residence time on the skin, and achieved a sustained and slow release of ATRA. Treatment with ATRA-NLC-Gel enhanced transdermal penetration and targeted enrichment in the hair follicle region, thereby significantly promoting hair regrowth. ATRA-NLC-Gel improved AA symptoms by upregulating CD200 and Ki-67 expression, activating the Wnt/β-catenin pathway.

conclusionsATRA-NLC-Gel enhanced the transdermal permeability and follicle-targeting efficacy of ATRA, alleviated ATRA-induced skin dryness and irritation, and effectively improved the symptoms of AA in AA model mice. ATRA-NLC-Gel offers a highly promising strategy for transdermal treatment of AA in clinical setting.

Indexed as

Alopecia AreataDrug CarriersDrug Delivery SystemsLipidsNanostructuresTretinoinAdministration, CutaneousAnimalsCell ProliferationCell SurvivalGelsHair FollicleHumansMaleMiceSkinDrug CarriersGelsLipidsTretinoinAll-trans retinoic acidAlopecia areataDrug delivery systemHair regenerationNanostructured lipid carrier

Identifiers

PMID40380336
PMCPMC12083027

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.