# Self-Assembled Berberine-Sinapic Acid Nanomedicine for Synergistic Chemotherapy

**Authors:** Ying Zhao, Yubo Lu, Yushan Ma, Sijia Wang, Pin Lv, Huifang Xu, Yuanyuan Li, Weisheng Feng

PMC · DOI: 10.3390/molecules31040621 · 2026-02-10

## TL;DR

A new nanomedicine combining berberine and sinapic acid shows effective and safe breast cancer treatment in mice.

## Contribution

A novel self-assembled nanomedicine with synergistic chemotherapy and low toxicity for breast cancer treatment.

## Key findings

- BBR-SA nanomedicine effectively inhibits mouse mammary carcinoma cell proliferation.
- In vivo tests show BBR-SA has a stronger anti-tumor effect than individual drugs.
- No significant systemic toxicity was observed after 28 days of BBR-SA administration.

## Abstract

Breast cancer ranks among the most prevalent malignant tumors globally, underscoring the urgent need for efficient and low-toxicity treatment strategies. In this study, a novel nanomedicine (BBR-SA) was constructed based on the self-assembled of berberine (BBR) and sinapic acid (SA) for synergistic chemotherapy. Firstly, utilizing π-π stacking, hydrogen bonding, and electrostatic forces between BBR and SA, the BBR-SA achieved a well-defined nanostructure with high drug-loading capacity and favorable water dispersibility. Furthermore, BBR-SA nanomedicine effectively inhibited the proliferation of mouse mammary carcinoma cells (4T1), showing a significantly stronger inhibitory effect than either BBR or SA alone. Moreover, the remarkable anti-tumor effect was obtained after treatment with BBR-SA nanomedicine in vivo, further demonstrating a synergistic therapeutic effect. More importantly, no significant systemic toxicity was observed after 28 days of intravenous administration with BBR-SA nanomedicine. In summary, the BBR-SA nanomedicine represents a safe and effective therapeutic strategy for breast cancer, offering new perspectives on the application of the traditional chinese medicine in anti-tumor therapy.

## Linked entities

- **Chemicals:** berberine (PubChem CID 2353), sinapic acid (PubChem CID 10743)
- **Diseases:** breast cancer (MONDO:0004989)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Dntt (deoxynucleotidyltransferase, terminal) [NCBI Gene 21673] {aka Tdt}
- **Diseases:** Cytotoxicity (MESH:D064420), tumor metastasis (MESH:D009362), dislocation (MESH:D004204), Breast cancer (MESH:D001943), Tumor (MESH:D009369), MDR (MESH:D018088), injury to (MESH:D014947), inflammatory (MESH:D007249), bleeding (MESH:D006470)
- **Chemicals:** dUTP (MESH:C027078), 5,5',6,6'-Tetrachloro-1,1',3,3'-tetraethyl-imidacarbocyanine iodide (MESH:C068624), penicillin (MESH:D010406), hematoxylin (MESH:D006416), NaHCO3 (MESH:D017693), 1640 medium (-), H&amp;E (MESH:D006371), DMSO (MESH:D004121), DAPI (MESH:C007293), BBR (MESH:D001599), PBS (MESH:D007854), hydrogen (MESH:D006859), PFA (MESH:C003043), CO2 (MESH:D002245), streptomycin (MESH:D013307), PI (MESH:D010716), Calcein-AM (MESH:C085925), methanol (MESH:D000432), SA (MESH:C073734), phenolic acid (MESH:C017616), water (MESH:D014867), benzene (MESH:D001554)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184), 4T1 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_0125), 3T3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943594/full.md

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Source: https://tomesphere.com/paper/PMC12943594