ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
A Synergistic Hydrogel-Microalgae Platform for Dual-Targeting of Intestinal and Neuroimmune Dysfunction in Inflammatory Bowel Disease.
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.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Oral hydrogel systems in lower gastrointestinal disorders: From disease-based therapy to microbiota-guided design.Materials today. Bio · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
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.
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Registered trials
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.