ReviewCurrent pharmaceutical design2026
Microbiota-Sensitive Nanocarriers for the Targeted Delivery of Therapeutic Agents into the Gut: Advanced Treatment Strategy for Inflammatory Bowel Disease.
Review in Current pharmaceutical design, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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Who cites it
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Inflammatory bowel disease (IBD) is a gastrointestinal condition that impacts millions of individuals across the globe, causing recurring inflammation and serious consequences. Traditional treatments, like corticosteroids and immunosuppressants, can cause systemic adverse effects owing to their lack of targeted delivery. Nanotechnology-based techniques, especially microbiota-sensitive nanocarriers, provide a potential route to more effective and targeted treatment. This study aims to explore the potential of microbiota-sensitive nanocarriers to enhance targeted drug delivery for inflammation associated with IBD. Microbiota-sensitive nanocarriers have been established to specifically deliver therapeutic agents in response to changes in pH, redox status, and enzyme activity that occur in the gut. The regulated release of drugs at the target location is ensured by these nanocarriers, as their size and surface features enable them to penetrate the mucus barrier and remain in the inflammatory areas. These minimise negative effects by reducing systemic drug absorption and increasing therapeutic effectiveness via interactions with the gut bacteria. Moreover, such nanocarriers enhance the total bioavailability of the drug and protect it against degradation in the gastrointestinal tract. In conclusion, microbiota-sensitive nanocarriers have tremendous potential for improving IBD treatment outcomes by delivering targeted, localized drug delivery and minimizing adverse effects associated with traditional therapies.
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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 OpenQuestion graph.