Evidence map›Paper›PMID 42650806›Full record

ArticleBiomolecules2026

Chitosan-Unconjugated Bilirubin Microspheres Alleviate Dysbiosis, Immune Dysregulation, and Intestinal Barrier Damage in Ulcerative Colitis.

Xinyu Lyu, Xiaotong Xu, Mengqi Shi, Rui Wang, Xiaoqing Yu, Yan Liu, Xiangyu Xue, Fengmin Zhang, Xiuhong Wang

Abstract read
In one paragraph

Article in Biomolecules, 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
–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

9 authors.

Xinyu LyuDepartment of Microbiology, School of Basic Medical Sciences, WU Lien-Teh Institute, Harbin Medical University, Harbin 150081, China.ORCID 0000-0003-4651-806X
Xiaotong XuDepartment of Microbiology, School of Basic Medical Sciences, WU Lien-Teh Institute, Harbin Medical University, Harbin 150081, China.
Mengqi ShiDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin 150081, China.
Rui WangDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin 150081, China.
Xiaoqing YuDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin 150081, China.
Yan LiuDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin 150081, China.
Xiangyu XueDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin 150081, China.
Fengmin ZhangDepartment of Microbiology, School of Basic Medical Sciences, WU Lien-Teh Institute, Harbin Medical University, Harbin 150081, China.ORCID 0000-0002-5177-1927
Xiuhong WangDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Harbin Medical University, Harbin 150081, China.ORCID 0009-0004-7673-0293

Funding

Heilongjiang Provincial Science and Technology Department No. 304004001
6 · The paper itself

Abstract

Ulcerative colitis (UC) is a chronic inflammatory bowel disease marked by immune dysregulation, microbiota imbalance, and intestinal barrier damage. Unconjugated bilirubin (UCB) shows promise in treating UC due to its anti-inflammatory properties but is limited by poor solubility and potential toxicity. This study developed a chitosan-based controlled-release microsphere (CBMS) treatment to overcome these issues. CBMS utilizes the mucoadhesive properties of chitosan to achieve targeted, controlled UCB release in the colon, enhancing its stability and bioavailability. In a DSS-induced UC mouse model, CBMS alleviated clinical symptoms, reduced colon shortening, and improved histological outcomes, including reduced inflammation and enhanced mucosal repair. The mechanism involves CBMS retention in the intestinal lumen, UCB inactivation of digestive proteases, and restoration of microbiota balance, suppressing pro-inflammatory pathways. CBMS offers a promising new therapeutic strategy for UC and insights into polysaccharide-based drug delivery systems.

Indexed as

BilirubinChitosanColitis, UlcerativeDysbiosisMicrospheresAnimalsDisease Models, AnimalGastrointestinal MicrobiomeIntestinal Barrier FunctionIntestinal MucosaMiceBilirubinChitosanchitosandigestive proteasesgut microbiotamicrospheresulcerative colitisunconjugated bilirubin

Identifiers

PMID42650806
PMCPMC13511252

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.