Evidence map›Paper›PMID 41980222›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

A Synergistic Hydrogel-Microalgae Platform for Dual-Targeting of Intestinal and Neuroimmune Dysfunction in Inflammatory Bowel Disease.

Jing Lu, Kangyu Jin, Bing Chen, Ruoxi Wang, Fengling Hu, Shaohua Hu, Danni Zhong, Xiaoming Li, Min Zhou

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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. Review
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.

Jing LuDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Kangyu JinInstitute of Translational Medicine, Zhejiang University, Hangzhou, China.
Bing ChenDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Ruoxi WangInstitute of Translational Medicine, Zhejiang University, Hangzhou, China.
Fengling HuDepartment of Gastroenterology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Shaohua HuDepartment of Psychiatry, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Danni ZhongInstitute of Translational Medicine, Zhejiang University, Hangzhou, China.
Xiaoming LiDepartment of Neurobiology and Department of Neurology of Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Min ZhouInstitute of Translational Medicine, Zhejiang University, Hangzhou, China.ORCID https://orcid.org/0000-0002-7319-9570

Funding

Binjiang Institute of Zhejiang University ZY202205SMKY007Key R&D Program of Zhejiang Province 2024C03150Key R&D Program of Zhejiang Province 2025C02109National Key Research and Development Program of China 2023YFC2506200National Natural Science Foundation of China 82271561
6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is frequently complicated by comorbid depression and anxiety, creating a therapeutic vicious cycle that is currently managed with fragmented, non-integrated treatments. Here, we introduce a colon-targeted, pH-responsive hydrogel microalgal system (CV@PA-gel) designed for synergistic treatment of IBD and its psychiatric comorbidities. This engineered platform co-encapsulates the natural neuroprotective agent paeoniflorin (PA) and the gut-microbiota modulator Chlorella vulgaris (CV) within a genipin-crosslinked carboxymethyl chitosan/sodium alginate matrix. The CV@PA-gel exhibits minimal drug release in the stomach but provides sustained, targeted release in the colon, significantly enhancing the oral bioavailability and intestinal retention of its cargo. In a murine model of chronic colitis, CV@PA-gel outperforms free PA by more effectively restoring gut barrier integrity, ameliorating systemic and hippocampal inflammation, and rescuing anxiety-, depressive-like, and cognitive behaviors. Mechanistically, our findings suggest that gut-derived systemic inflammation is associated with complement C3 activation and subsequent microglia-mediated polarization of neurotoxic A1 astrocytes in the hippocampus, leading to synaptic loss. PA, delivered precisely by the hydrogel, directly suppresses this cascade by inhibiting microglial release of key A1-inducing factors. Our work establishes a versatile biomaterials strategy for disrupting the gut-brain axis pathology, offering a powerful platform for the simultaneous management of intestinal and neuropsychiatric disorders.

Indexed as

GlucosidesHydrogelsInflammatory Bowel DiseasesMonoterpenesNeuroimmunomodulationAnimalsDisease Models, AnimalGlycosidesMaleMiceGlucosidesGlycosidesHydrogelsMonoterpenespeoniflorincognitiondepressioninflammatory bowel diseasemicrobiota‐gut‐brain axispaeoniflorin

Identifiers

PMID41980222
PMCPMC13317580

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.