ReviewFood chemistry: X2026
Polysaccharide-based conjugate systems for probiotic encapsulation and colon - targeted release: A review.
Review in Food chemistry: X, 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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oral probiotics face viability challenges during processing, storage, and gastrointestinal transit. This critical review provides a unified analytical framework for polysaccharide-based conjugated probiotic encapsulation, bridging synthesis chemistry, delivery mechanisms, and industrial feasibility. Covalent modification and network-forming routes, including Maillard glycation, chemical crosslinking, enzymatic crosslinking, radical-mediated grafting, and thiol-based functionalization, are compared with non-covalent assembly and energy-assisted processing in terms of network architecture, thermal resistance, and scalability. Colon-targeted release mechanisms, including pH-responsive swelling, enzymatic degradation, microbiota fermentation, and multi-stimuli architectures, are critically evaluated. Practical applicability in commercial matrices like yogurt, kefir, honey, and ice cream is discussed alongside processing and regulatory considerations. While conjugated matrices offer superior gastric protection and controllable release, critical gaps remain in release kinetics, long-term storage data, residual crosslinker safety, and strain-specific variability. Translational readiness requires integrating AI-driven predictive design, life cycle assessment, and standardized gastrointestinal simulation protocols.
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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.