# Engineering Biocompatible Glutathione-Capped Cu2ZnSnS4 Quantum Dots Toward Integrated Photothermal and Photodynamic Effects

**Authors:** Ning Lu, Yufeng Zang, Lingshuai Kong

PMC · DOI: 10.3390/ma19040763 · 2026-02-15

## TL;DR

Researchers developed tiny quantum dots that can both heat up and produce reactive oxygen under infrared light, offering a new way to treat cancer.

## Contribution

The study introduces glutathione-capped Cu2ZnSnS4 quantum dots with dual photothermal and photodynamic capabilities for cancer therapy.

## Key findings

- CZTS@GSH QDs showed effective photothermal conversion under 808 nm laser irradiation.
- The QDs generated singlet oxygen, confirming their photodynamic therapy capability.
- The QDs have a band gap of 1.47 eV and an average hydrodynamic diameter of ~6.2 nm.

## Abstract

Ultrasmall near-infrared (NIR)-responsive quantum dots (QDs) are highly promising for deep-tissue phototherapy but often face challenges with biocompatibility and clearance. In this study, Cu2ZnSnS4 quantum dots (CZTS QDs) were synthesized via a non-injection method and surface-functionalized with glutathione (GSH) to create water-dispersible and biocompatible CZTS@GSH QDs. Comprehensive characterization using XRD, TEM, DLS, XPS, and UV-Vis spectroscopy confirmed a sphalerite-type ZnS crystal structure, an average hydrodynamic diameter of ~6.2 nm, and a band gap of 1.47 eV (843.5 nm). The CZTS@GSH QDs demonstrated effective photothermal conversion under 808 nm laser irradiation, achieving a temperature increase sufficient for photothermal therapy (PTT). Furthermore, using a DPBF assay, the QDs were shown to generate singlet oxygen, confirming their photodynamic therapy (PDT) capability. Owing to their ultrasmall size, strong NIR absorption, and demonstrated dual PTT/PDT functions, the CZTS@GSH QDs are established as a nanoplatform with potential for combined cancer treatment.

## Linked entities

- **Chemicals:** glutathione (PubChem CID 124886), DPBF (PubChem CID 21649)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Diseases:** Cytotoxicity (MESH:D064420), carcinogenicity (MESH:D011230), breast cancer (MESH:D001943), cancer (MESH:D009369), injury to (MESH:D014947), inflammatory (MESH:D007249), hyperthermia (MESH:D005334)
- **Chemicals:** ZnCl2 (MESH:C016837), MTT (MESH:C070243), Cu2-xSe (-), S (MESH:D013455), Mg (MESH:D008274), ROS (MESH:D017382), CO2 (MESH:D002245), GSH (MESH:D005978), N, N-dimethylformamide (MESH:D004126), 1,3-diphenylisobenzofuran (MESH:C011238), 3-mercaptopropionic acid (MESH:D015097), N2 (MESH:D009584), Cu2ZnSnS4 (MESH:C571853), oleylamine (MESH:C008703), Singlet oxygen (MESH:D026082), RB (MESH:D012413), Au (MESH:D006046), Zn (MESH:D015032), sulfide (MESH:D013440), thiourea (MESH:D013890), Rose Bengal (MESH:D012395), Sn (MESH:D014001), Copper (MESH:D003300), ethanol (MESH:D000431), SnS2 (MESH:C078041), water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** 4T1 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_0125)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941955/full.md

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Source: https://tomesphere.com/paper/PMC12941955