# A Novel Green Synthesis Method of Copper Nanoparticles and Their Biological Effects on Cancer and Normal Cells

**Authors:** Maria-Alexandra Pricop, Adina Negrea, Ioan Bogdan Pascu, Mihaela Ciopec, Petru Negrea, Iustina-Mirabela Cristea, Călin Adrian Tatu, Alexandra Ivan

PMC · DOI: 10.3390/ijms27062559 · 2026-03-11

## TL;DR

This paper introduces a new green method to synthesize copper nanoparticles and explores their selective toxicity toward cancer cells.

## Contribution

A novel green synthesis method for copper nanoparticles and evidence of their selective cytotoxicity against cancer cells.

## Key findings

- Copper nanoparticles were successfully synthesized using trisodium citrate and starch.
- SKBR3 cancer cells showed higher apoptosis and lower resilience compared to normal MSC cells when exposed to CuNPs.
- CuNPs induce oxidative stress and disrupt antioxidant defenses in cancer cells.

## Abstract

Copper-based nanoparticles (Cu-based NPs) represent a major focus in nanomedicine due to their unique physicochemical properties and excellent biocompatibility. In this paper, we present an interdisciplinary study bridging engineering and biomedical sciences by employing a novel synthesis approach to produce highly stable and uniformly dispersed spherical copper nanoparticles (CuNPs), which were subsequently tested for their cytotoxic effects on SKBR3 and MSC human cells. The synthesis of CuNPs was performed in the presence of the complexing agent trisodium citrate (TSC), while starch was used for the chemical reduction step. Characterization of the Cu-based NPs via UV–Vis, FT-IR, Mie theory, DLS and SEM confirmed their nanoscale structure. The obtained CuNPs were subsequently assessed for their biological effects and cytotoxic responses induced in normal and SKBR3 cancer cell lines. The SKBR3 cell line showed a dose-dependent decrease in the cell index and a higher proportion of apoptotic cells compared to normal MSCs, with apoptosis representing the dominant mode of cell death. Although SKBR3 cells appeared to mount an antioxidant response against CuNP oxidative stress, the response was insufficient to counteract the apoptotic progression. In comparison, MSCs showed a greater resilience to CuNP-induced cellular stress. By promoting oxidative stress and disrupting the antioxidant defense system of cancer cells, CuNPs exhibit promising anti-cancer properties.

## Linked entities

- **Chemicals:** trisodium citrate (PubChem CID 6224)
- **Diseases:** cancer (MONDO:0004992)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** Cancer (MESH:D009369), cytotoxic (MESH:D064420)
- **Chemicals:** Copper (MESH:D003300), TSC (MESH:C514290), starch (MESH:D013213), CuNP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13027345/full.md

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Source: https://tomesphere.com/paper/PMC13027345