ArticleNanoscale advances2025
Chemically synthesized CdSe quantum dots induce apoptosis in AGS gastric cancer cells
Article in Nanoscale advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
2 citing papers in PubMed.
- Plant-Derived Diterpenoids as Potential Chemotherapeutics for Gastric Cancer.Current oncology reports · 2026Review
- Microwave-assisted synthesis of silica quantum dots: a novel approach for targeting PI3K/AKT signaling in breast cancer therapy.RSC advances · 2025Article
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Authors and funding
7 authors.
Funding
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Abstract
CdSe quantum dots (QDs) with size in the range of 3.5-5.8 nm and a zinc blende (ZB) crystal structure were synthesized by the wet chemical method. The morphology of the synthesized QDs was assessed by transmission electron microscopy (TEM). The structural and optical properties were characterized by X-ray diffraction (XRD), absorption spectroscopy (Abs) and photoluminescence (PL) spectroscopy. The anti-cancer activity of CdSe QDs was investigated on AGS gastric cancer cells through cell viability screening (MTT assay), cell cycle and apoptosis analysis using flow cytometry. The generation of reactive oxygen species (ROS) was analyzed using the cell fluorescence staining method with H2DCFDA. Three QD series of CdSe1 (3.5 nm), CdSe2 (4.7 nm) and CdSe3 (5.8 nm) have been selected to study their effects on the extermination of stomach cancer cells. The CdSe QDs all exhibited the potential to induce toxicity to cells at concentrations ranging from 5 to 20 μg mL
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Registered trials
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