Evidence map›Paper›PMID 39727555›Full record

ArticleGels (Basel, Switzerland)2024

Preparation of Patchouli Oil Microemulsion Gel and Its Topical Application to Ameliorate Atopic Dermatitis in Mice.

Tingting Chen, Changjin Xu, Min Wang, Yan Cui, Riqing Cheng, Wenyao Zhang, Xin Gao, Laibing Wang, Herima Qi, Shuyan Yu and 3 more

Abstract read
In one paragraph

Article in Gels (Basel, Switzerland), 2024. 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
–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

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

13 authors.

Tingting ChenSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Changjin XuSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Min WangSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Yan CuiCollege of Humanities Education, Inner Mongolia Medical University, Hohhot 010100, China.
Riqing ChengSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Wenyao ZhangSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Xin GaoSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Laibing WangSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Herima QiSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Shuyan YuSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Jianping ChenSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Lan MaSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.
Huiqing GuoSchool of Pharmacy, Inner Mongolia Medical University, Hohhot 010100, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patchouli oil (PO) is a natural substance famous for its immune-enhancing and anti-inflammatory effects. Atopic dermatitis (AD) is characterized by epidermal gene mutations, skin barrier dysfunction, and immune dysregulation, making patchouli volatile oil a potential candidate for AD treatment. Initially, PO was mixed with ethyl oleate (EO), castor oil ethoxylated ether-40 (EL-40), anhydrous ethanol, and water to form a patchouli oil microemulsion (PO-ME) system. The formulation ratios were optimized using the Box-Behnken design-effect surface method, and their products were characterized for type, particle size, polydispersity index (PDI), and appearance. Additionally, patchouli oil microemulsion gel (PO-MEG) was developed with a specified concentration of 1.5% carbomer-940 as the matrix, and its pH, stability, viscosity, and permeability were evaluated. We assessed the irritation tests of PO-MEG using a rat self-control model and the Cell Counting Kit-8 (CCK-8) assay. The results demonstrated that should be attributed to non-irritating. This study also assessed the efficacy of optimized PO-MEG on AD-like symptoms using a 2,4-dinitrochlorobenzene (DNCB)-induced BALB/c mouse model. Compared with the model group, the in vivo efficacy studies have shown the PO-MEG group significantly reduces dermatitis scores, mast cell counts, epidermal thickness, and levels of pro-inflammatory cytokines and immune factors in skin homogenates. This suggests that PO-MEG would become a safer topical formulation for treating atopic dermatitis.

Indexed as

atopic dermatitismicroemulsionmicroemulsion gelpatchouli oilpreparation processquality evaluation

Identifiers

PMID39727555
PMCPMC11675264

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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.