# Structural and temporal dynamics of nano-based therapies in ulcerative colitis: history, hotspots, and emerging trends

**Authors:** Junzu Shi, Danyang Cui, Li Yu, Yang Gong

PMC · DOI: 10.3389/fimmu.2026.1739037 · Frontiers in Immunology · 2026-02-18

## TL;DR

This paper maps the growth and trends in nano-based therapies for ulcerative colitis over 25 years, highlighting shifts toward intelligent and mechanism-driven approaches.

## Contribution

A comprehensive bibliometric analysis reveals emerging themes and core areas in UC nanotherapeutics, guiding future research directions.

## Key findings

- Nanomaterial-based therapies for UC show sustained growth and increased international collaboration.
- Five emerging themes include gut microbiota, reactive oxygen species, and drug delivery systems.
- Future research should focus on nanodesign, safety, and personalized therapies for translational innovation.

## Abstract

Nanomaterial-based therapies have emerged as a promising approach for ulcerative colitis (UC). To systematically map the field, we performed a bibliometric analysis of research over the past 25 years, aiming to reveal knowledge evolution, core themes, and emerging trends.

We searched the Web of Science Core Collection and Scopus for English-language publications (2001–2025) using the keywords “nanomaterials” and “ulcerative colitis” including original articles and reviews. After deduplication, 1,316 publications were analyzed using CiteSpace, HistCite, and R to construct collaboration networks, keyword co-occurrence maps, co-citation networks, and thematic evolution analyses.

UC-focused nanotherapeutics show sustained growth and increasing international collaboration, with China as the leading contributor. Analysis identified 57 subject categories, 537 keywords, and 899 publications with citation bursts. Five emerging themes were highlighted: gut microbiota, reactive oxygen species, NLRP3 inflammasome, drug delivery systems, and polymeric nanoparticles. Nanotechnology is increasingly integrated into UC pathogenesis studies, with a shift from passive drug delivery toward intelligent, mechanism-driven, and combination therapies. Co-citation analysis identified seven core areas, including inflammation regulation, targeted delivery, immune modulation, hydrogel carriers, and nanotherapeutics.

This study maps the evolving landscape of UC nanotherapeutics, highlighting the field’s shift toward precise, intelligent, and mechanism-guided strategies. Future research should emphasize nanodesign, safety evaluation, and personalized therapies, facilitating translational innovation.

Infographic illustrating the role of nanotechnology in ulcerative colitis includes diagrams of the digestive tract, nanoparticles targeting colon cells, and annotated sections on nanodrug mechanisms such as targeted delivery, antioxidant action, immunoregulation, and intestinal barrier repair, leading to clinical applications like personalized treatment, precise delivery, and multifunctional nano-platforms.

## Linked entities

- **Diseases:** ulcerative colitis (MONDO:0005101)

## Full-text entities

- **Genes:** Myd88 (myeloid differentiation primary response gene 88) [NCBI Gene 17874], Nfkb1 (nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105) [NCBI Gene 18033] {aka NF-KB1, NF-kappaB, NF-kappaB1, p105, p50, p50/p105}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, Il22 (interleukin 22) [NCBI Gene 50929] {aka IL-22, IL-22a, ILTIFa, If2b1, Iltif}, Ltf (lactotransferrin) [NCBI Gene 17002] {aka Csp82, Lf, MMS10R, Ms10r}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}
- **Diseases:** IBD (MESH:D015212), diarrhea (MESH:D003967), UC (MESH:D003093), colonic damage (MESH:D003108), burst (MESH:C562695), metabolic disturbances (MESH:D024821), Chronic inflammation (MESH:D007249), colorectal cancer (MESH:D015179), COLITIS (MESH:D003092), Pulmonary and Allergic Diseases (MESH:D008171), immune system abnormalities (MESH:D007154), infections (MESH:D007239), Ulcerative (MESH:D014456), toxicity (MESH:D064420), abdominal pain (MESH:D015746)
- **Chemicals:** CP (MESH:C003181), Lipid (MESH:D008055), vitamin C (MESH:D001205), PLGA (MESH:D000077182), HA (MESH:D006820), ROS (MESH:D017382), Budesonide (MESH:D019819), flavonoid (MESH:D005419), nitric oxide (MESH:D009569), NO (MESH:D009614), chondroitin sulfate (MESH:D002809), curcumin (MESH:D003474), aminosalicylates (MESH:D010131), CoFe PBA (-), cyclosporine A. (MESH:D016572), Prussian blue (MESH:C000170), quercetin (MESH:D011794), bilirubin (MESH:D001663), Magnolol (MESH:C005498), dexamethasone (MESH:D003907)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12957217/full.md

## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12957217/full.md

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Source: https://tomesphere.com/paper/PMC12957217