Evidence map›Paper›PMID 40883575›Full record

ArticleDrug delivery and translational research2026

Oral colon-targeted paeonol emulsion for ameliorating ulcerative colitis based on charge adsorption.

Lan Zhang, Xi Xiong, Weiwen Lu, Jiazheng Li, Ruotong Zhang, Zhipeng Cai, Huixia Lv, Zhenhai Zhang, Jianming Ju, Ye Yang

Abstract read
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In one paragraph

Article in Drug delivery and translational research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Lan ZhangSchool of Medicine, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
Xi XiongAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China.
Weiwen LuAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China.
Jiazheng LiAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China.
Ruotong ZhangAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China.
Zhipeng CaiAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China.
Huixia LvDepartment of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing, 211198, China.
Zhenhai ZhangAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China. david23932@163.com.
Jianming JuAffiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, 210028, China. jjm405@sina.com.ORCID 0000-0002-8101-162X
Ye YangSchool of Medicine, Nanjing University of Chinese Medicine, Nanjing, 210023, China. yangye876@sina.com.

Funding

Postgraduate Research & Practice Innovation Program of Jiangsu Province KYCX24_2268Post Subsidy Project for High-Quality Research Results of Jiangsu Academy of Traditional Chinese Medicine HBZ202404Post Subsidy Project for High-Quality Research Results of Jiangsu Academy of Traditional Chinese Medicine HBZ202411Post Subsidy Project for High-Quality Research Results of Jiangsu Academy of Traditional Chinese Medicine HBZ202412
6 · The paper itself

Abstract

Ulcerative colitis (UC), an inflammatory bowel disease, poses a severe threat to human health. Paeonol has demonstrated potential for the treatment of UC, particularly because of its remarkable anti-inflammatory properties. However, the high volatility and low oral bioavailability of paeonol hinder its application in the treatment of UC. To address this challenge, a paeonol emulsion (PEM)-based oral delivery system was developed for the treatment of UC. In this study, we investigated the colonic-targeting efficacy of PEM and the mechanisms underlying its ability to alleviate colitis. The results revealed that the negatively charged PEM specifically adhered to the positively charged inflamed colonic tissues via electrostatic interactions, enabling effective targeted delivery. Additionally, the PEM maintained the balance between M1 and M2 macrophages, exhibiting excellent efficacy in alleviating UC. Mechanistic studies have shown that PEM significantly inhibits the expression of inflammatory cytokines and repairs the intestinal barrier. Furthermore, PEM modulates the composition of the gut microbiota by inhibiting the growth of harmful bacteria and promoting the growth of beneficial bacteria. In conclusion, the negatively charged emulsion delivery system constructed provides new insights into the development of an oral colon-targeted drug delivery system.

Indexed as

AcetophenonesAnti-Inflammatory AgentsColitis, UlcerativeColonAdministration, OralAdsorptionAnimalsDrug Delivery SystemsEmulsionsGastrointestinal MicrobiomeHumansMacrophagesMaleMiceMice, Inbred C57BLRAW 264.7 CellsAcetophenonesAnti-Inflammatory AgentsEmulsionspaeonolBiodistributionColitisColon-targetedEmulsionPaeonolTherapeutic mechanisms

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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.