ReviewInternational journal of pharmaceutics: X2025
Biomimetic nanocarriers for the therapy and management of intestinal inflammations.
Review in International journal of pharmaceutics: X, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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
2 citing papers in PubMed.
- Hesperidin-loaded Eudragit S100 nanoparticles alleviate ulcerative colitis by repairing intestinal barrier and modulating gut microbiota.International journal of pharmaceutics: X · 2026Article
- Navigating a thorny path: oral nanomedicines for the precision management of radiation-induced intestinal injury.Journal of nanobiotechnology · 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
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Intestinal inflammation particularly inflammatory bowel disease poses significant clinical challenges due to its chronic nature, limited treatment efficacy and adverse effects of conventional therapies like corticosteroids and biologics. Biomimetic nanocarriers have emerged as a transformative strategy to overcome these limitations by leveraging natural cell membranes for targeted drug delivery. This review critically examines the application of biomimetic nanocarriers as precision therapeutics for intestinal inflammation. We discuss key fabrication techniques including extrusion, sonication and microfluidics used to coat synthetic nanocarriers with membranes derived from several biological sources such as macrophages, neutrophils, platelets, stem cells and bacteria. These biomimetic coatings exploit inherent biological functions such as immune evasion, receptor-mediated binding to inflamed endothelium and responsiveness to inflammatory stimuli. Preclinical studies demonstrate that biomimetic nanocarriers effectively suppress pro-inflammatory pathways like NF-κB, NLRP3, sequester cytokines, promote mucosal healing and restore gut microbiota balance while minimizing systemic toxicity. Despite promising outcomes in animal models, clinical translation faces hurdles in membrane isolation standardization, long-term biosafety, and regulatory alignment. Future advancements require interdisciplinary efforts to optimize pharmacokinetics, enhance tissue-specific targeting, and integrate personalized designs. Biomimetic nanocarriers represent a paradigm shift toward disease-modifying therapies, offering potential for sustained remission in intestinal inflammation management.
Indexed as
Identifiers
What Socratic holds
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.