# Collective Magnetic Mesoporous Silica Nanorobots for Targeted Oral Capsaicin Delivery in Colitis Intervention

**Authors:** Hongyue Zhang, Yuzhu Di, Lubo Jin, Shuai Yang, Zesheng Li, Bo Qu

PMC · DOI: 10.3390/mi17020272 · Micromachines · 2026-02-22

## TL;DR

Researchers developed magnetic nanorobots that deliver capsaicin to the colon to treat inflammatory bowel disease more effectively.

## Contribution

A novel magnetic nanorobot system for targeted oral capsaicin delivery in colitis treatment is introduced.

## Key findings

- Capsaicin-loaded nanorobots achieved collective locomotion up to 180.7 μm/s under magnetic guidance.
- The system enables targeted drug enrichment and sustained release at colonic lesion sites.
- The nanorobots overcome millimeter-scale obstacles during movement in the gut.

## Abstract

Magnetic nanoparticles, with their excellent biocompatibility and biodegradability, serve as ideal materials for constructing targeted drug delivery systems. Iron oxide (Fe3O4) nanoparticles, controllably prepared via methods such as solvothermal synthesis, can be combined with mesoporous silica to construct magnetically steerable nanorobots. Such robots enable efficient drug loading and precise delivery. To address challenges in the treatment of Inflammatory Bowel Disease (IBD), including the significant side effects of systemic drugs and the low oral bioavailability and poor colonic targeting of novel food-derived drugs (e.g., capsaicin with anti-inflammatory activity), this study designed capsaicin-loaded iron oxide-mesoporous silica composite nanorobots (Cap-M@mSbots). Driven by a rotating gradient magnetic field of up to 80 mT, Cap-M@mSbots achieve large-scale emergent collective locomotion, with a maximum collective locomotion velocity reaching 180.7 μm/s, and are capable of long-distance movement overcoming millimeter-scale obstacles. This system can be actively propelled to colonic lesion sites under magnetic guidance, achieving targeted drug enrichment and sustained release, thereby offering a novel strategy for the targeted therapy of IBD.

## Linked entities

- **Chemicals:** capsaicin (PubChem CID 1548943)
- **Diseases:** Inflammatory Bowel Disease (MONDO:0005265), colitis (MONDO:0005292)

## Full-text entities

- **Genes:** Rela (Rela proto-oncogene, NFKB subunit) [NCBI Gene 19697] {aka p65, p65 NF-kappa B, p65 NFkB}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 14433] {aka Gapd}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il18 (interleukin 18) [NCBI Gene 16173] {aka Igif, Il-18}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Nfkbia (nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor, alpha) [NCBI Gene 18035] {aka Nfkbi}, Tjp1 (tight junction protein 1) [NCBI Gene 21872] {aka ZO1}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, 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}
- **Diseases:** colonic lesion (MESH:D003108), gastric irritation (MESH:D013272), IBD (MESH:D015212), weight loss (MESH:D015431), toxicity (MESH:D064420), infection (MESH:D007239), gastrointestinal diseases (MESH:D005767), Colitis (MESH:D003092), hemolysis (MESH:D006461), bleeding (MESH:D006470), mucosal irritation (MESH:D001523), malignancy (MESH:D009369), injury to (MESH:D014947), colonic inflammation (MESH:D007249)
- **Chemicals:** Eosin (MESH:D004801), sodium acetate (MESH:D019346), PBS (MESH:D007854), PVDF (MESH:C024865), agarose (MESH:D012685), DSS (MESH:D016264), Cap (MESH:D002211), CO2 (MESH:D002245), balsam (MESH:D001453), CTAB (MESH:D000077286), Silica (MESH:D012822), penicillin (MESH:D010406), Hematoxylin (MESH:D006416), Si (MESH:D012825), FITC (-), dextran (MESH:D003911), H&amp;E (MESH:D006371), Ethanol (MESH:D000431), FITC-Dextran (MESH:C015219), Fe3O4 (MESH:C000499), biotin (MESH:D001710), SDS (MESH:D012967), copper (MESH:D003300), HCl (MESH:D006851), Fe (MESH:D007501), NaF (MESH:D012969), water (MESH:D014867), ferric chloride hexahydrate (MESH:C024555), (3-aminopropyl)triethoxysilane (MESH:C477625), streptomycin (MESH:D013307), carbon (MESH:D002244), xylene (MESH:D014992), TMB (MESH:C021758), EG (MESH:D019855), magnetite (MESH:D052203), ammonia (MESH:D000641), paraffin (MESH:D010232), TEOS (MESH:C040733)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** F200X
- **Cell lines:** NCM460 — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0460)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943128/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943128/full.md

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Source: https://tomesphere.com/paper/PMC12943128