# Research on Polysaccharide–Protein Composite Hydrogels for Gastrointestinal Targeted Delivery: A Review

**Authors:** Jingjing Guo, Yuxin Cai, Ran Zou, Chen Ai, Qun Fu

PMC · DOI: 10.3390/gels12020168 · Gels · 2026-02-14

## TL;DR

This review explores how polysaccharide-protein hydrogels can be used to deliver drugs specifically to the gastrointestinal tract, highlighting their smart release properties and future potential.

## Contribution

The paper systematically reviews the mechanisms, applications, and future directions of polysaccharide–protein composite hydrogels for gastrointestinal drug delivery.

## Key findings

- Polysaccharide–protein hydrogels show smart release behaviors triggered by pH, enzymes, and magnetic fields.
- These hydrogels effectively protect bioactive ingredients like curcumin and probiotics during delivery.
- Challenges include material stability, targeting precision, and large-scale production.

## Abstract

Polysaccharide–protein composite hydrogels have demonstrated remarkable potential in targeted gastrointestinal delivery owing to their excellent biocompatibility, adjustable physicochemical characteristics, and intelligent responsiveness. This review provides a comprehensive overview of the underlying mechanisms and diverse applications of these composite hydrogels in gastrointestinal targeted delivery, with a particular emphasis on their stimuli-responsive release behaviors triggered by internal and external factors such as pH, enzymes, magnetic fields. Special attention is also given to their advantages in protecting sensitive bioactive ingredients, including curcumin, EGCG, probiotics. Furthermore, this review highlights their capabilities in achieving high encapsulation efficiency, smart controlled release and targeted delivery, while also presenting current challenges associated with material stability, targeting precision, large-scale production, and clinical translation. Finally, future perspectives are discussed, focusing on the development of multi-response system design, innovative biomaterials, advanced manufacturing technology applications, and AI-assisted optimization. These directions aim to provide theoretical foundations and technical strategies for advanced research and practical applications of polysaccharide–protein composite hydrogels in a targeted gastrointestinal delivery system. Overall, this review underscores the significant promise of polysaccharide–protein composite hydrogels as intelligent gastrointestinal delivery platforms and provides a systematic reference for their rational design and future translational development.

## Linked entities

- **Chemicals:** curcumin (PubChem CID 969516), EGCG (PubChem CID 65064)

## Full-text entities

- **Genes:** F13B (coagulation factor XIII B chain) [NCBI Gene 2165] {aka FXIIIB}, Mucin [NCBI Gene 100508689], HSPA4 (heat shock protein family A (Hsp70) member 4) [NCBI Gene 3308] {aka APG-2, HEL-S-5a, HS24/P52, HSPH2, RY, hsp70}
- **Diseases:** constipation (MESH:D003248), allergies (MESH:D004342), diarrhea (MESH:D003967), gastric rupture (MESH:D013275), irritable bowel syndrome (MESH:D043183), obesity (MESH:D009765), ulcerative colitis (MESH:D003093), inflammation (MESH:D007249), injury to (MESH:D014947), ulcer (MESH:D014456), Infection (MESH:D007239), tumor (MESH:D009369), colitis (MESH:D003092), gastrointestinal and systemic disorders (MESH:D005767)
- **Chemicals:** iron (MESH:D007501), sulfonic acid (MESH:D013451), lactone (MESH:D007783), cysteine (MESH:D003545), lipids (MESH:D008055), meropenem (MESH:D000077731), water (MESH:D014867), GG (MESH:C007894), AP (MESH:D000667), cobalt (MESH:D003035), kaempferol (MESH:C006552), sodium carboxymethyl cellulose (MESH:D002266), diclofenac (MESH:D004008), flavonoids (MESH:D005419), formaldehyde (MESH:D005557), Olsa (MESH:C032587), glucose (MESH:D005947), hyaluronic acid (MESH:D006820), EDC (MESH:C024565), 1,4-butanediol diglycidyl ether (MESH:C014376), glycine (MESH:D005998), iron oxide (MESH:C000499), hydrogen (MESH:D006859), MXene (MESH:C000723374), carboxymethyl chitosan (MESH:C514968), Inulin (MESH:D007444), salts (MESH:D012492), Chitosan (MESH:D048271), oligosaccharide (MESH:D009844), disulfide (MESH:D004220), NH3 (MESH:D000641), ALG (MESH:D000464), kappa-carrageenan (MESH:D002351), EGCG (MESH:C045651), graphene (MESH:D006108), Fe3+ (-), citrus pectin (MESH:C586814), bile salts (MESH:D001647), COO (MESH:C041069), saline (MESH:D012965), TA@n- (MESH:D014216), proline (MESH:D011392), Curcumin (MESH:D003474), hydroxyapatite (MESH:D017886), starch (MESH:D013213), chitin (MESH:D002686), DPPH (MESH:C004931), GDL (MESH:C010730), sialic acid (MESH:D019158), polymer (MESH:D011108), carbohydrates (MESH:D002241), polyacrylamide (MESH:C016679), konjac glucomannan (MESH:C022901), DCb (MESH:D015101), FeO4 (MESH:C020748), sulfhydryl (MESH:D013438), pectin (MESH:D010368), Polysaccharide (MESH:D011134), beta-CD (MESH:C031215), CKGM (MESH:C538690)
- **Species:** Curcuma longa (turmeric, species) [taxon 136217], Bacillus sp. SA (species) [taxon 1168094], Kangiella shandongensis (species) [taxon 2763258], Lactiplantibacillus plantarum (species) [taxon 1590], Escherichia coli (E. coli, species) [taxon 562], Rodentia (rodent, order) [taxon 9989], Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280], Rattus norvegicus (brown rat, species) [taxon 10116], Helicobacter pylori (species) [taxon 210], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Bacteroides (genus) [taxon 816]

## Full text

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## Figures

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## References

106 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941238/full.md

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Source: https://tomesphere.com/paper/PMC12941238