# Nano-in-Micro GelMA depots assist electro-thermal-immuno orchestral treatment for solid triple negative breast tumor

**Authors:** Jiachen Li, Yaping Zhuang, Huijie Han, Yuewen Zhu, Chao Lin, Rui Wang, Ana Catarina Rodrigues da Silva, Marc C.A. Stuart, Guimei Jiang, Siyu Fan, Romana Schirhagl, Mohammad-Ali Shahbazi, Lígia Raquel Marona Rodrigues, Wenguo Cui, Hélder A. Santos

PMC · DOI: 10.1016/j.mtbio.2026.102848 · Materials Today Bio · 2026-01-30

## TL;DR

A new injectable microsphere depot is developed to enhance local treatment of triple-negative breast cancer by combining electrical, thermal, and immune therapies.

## Contribution

The nano-in-micro depot integrates conductivity, photothermal conversion, oxygen generation, and immune activation for multimodal tumor treatment.

## Key findings

- The depot enabled staged therapy that significantly suppressed tumor regrowth in a mouse model.
- Co-delivery of immune agonists and nanoparticles increased interferon-β secretion and pro-inflammatory cytokines.
- Treatment maintained body weight while inhibiting tumor growth in vivo.

## Abstract

Triple-negative breast cancer (TNBC) exhibits high local-recurrence risk despite modern systemic therapy assisted with surgery or irradiation therapy. Here, we report an injectable nano-in-micro microsphere depot (cPAG) that integrates conductivity enhancement, photothermal conversion, O2 and reactive oxygen species (ROS) generation, and innate immune agonist co-delivery to support staged, local multimodal therapy. Monodispersed Au@GelMA microspheres prepared via microfluidics and photocrosslinking reduced high electrostatic resistance of GelMA hydrogels and provided stable 808 nm laser-responsive heating. The porous surface possessed abundant electrostatic adsorption sites for loading MnOx nanoflowers and anionic stimulator of interferon genes (STING) agonist. MnOx nanoflowers catalyzed H2O2 to generate O2, produced free radical signals and increased pro-inflammatory cytokines secretion in vitro. Co-delivery of agonist and MnOx nanoparticles further increased interferon-β secretion, consistent with induction of type I interferon response. In a 4T1 residual-tumor model established by partial tumor resection, a staged regimen consisting of cPAG-assisted irreversible electroporation followed by cPAG-mediated photothermal therapy showed the strongest suppression of local tumor regrowth among tested groups, with maintained body weight during the study window. Overall, cPAG provides a modular nano-in-micro depot strategy to integrate multiple local treatments for postoperative control of TNBC tumor.

Image 1

•A nano-in-micro c-di-AMP@PM@Au@GelMA microsphere depot was developed for triple negative breast cancer local comprehensive intervention.•Depots integrate electrical conductivity tuning, photothermal effect, oxygen generation, ROS amplification, and immune activation.•Microsphere depot-based multimodal local regimen inhibited tumor regrowth and prolonged survival while stabilizing body weight in vivo.

A nano-in-micro c-di-AMP@PM@Au@GelMA microsphere depot was developed for triple negative breast cancer local comprehensive intervention.

Depots integrate electrical conductivity tuning, photothermal effect, oxygen generation, ROS amplification, and immune activation.

Microsphere depot-based multimodal local regimen inhibited tumor regrowth and prolonged survival while stabilizing body weight in vivo.

## Linked entities

- **Chemicals:** c-di-AMP (PubChem CID 11158091), H2O2 (PubChem CID 784)
- **Diseases:** triple-negative breast cancer (MONDO:0005494)

## Full-text entities

- **Genes:** STING1 (stimulator of interferon response cGAMP interactor 1) [NCBI Gene 340061] {aka ERIS, MITA, MPYS, NET23, SAVI, STING}, IFNB1 (interferon beta 1) [NCBI Gene 3456] {aka IFB, IFF, IFN-beta, IFNB}
- **Diseases:** inflammatory (MESH:D007249), breast tumor (MESH:D001943), TNBC (MESH:D064726), triple (MESH:C536008), tumor (MESH:D009369)
- **Chemicals:** H2O2 (MESH:D006861), ROS (MESH:D017382), Au@GelMA (-)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12890829/full.md

## References

82 references — full list in the complete paper: https://tomesphere.com/paper/PMC12890829/full.md

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Source: https://tomesphere.com/paper/PMC12890829