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Stream/Area:
-
Subject:
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Paper ID:
IJSREM68461
Volume:
10 |
10 |
Oct 2026
Pages:
1-14
Publication Frequency:
Monthly (12 issues per year)
License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.
Assistant Professor Department of Biotechnology
Ramaiah Institute of Technology
Department of Biotechnology
Ramaiah Institute of Technology
Department of Biotechnology
Ramaiah Institute of Technology
Department of Biotechnology
Ramaiah Institute of Technology
Department of Biotechnology
Ramaiah Institute of Technology
Department of Biotechnology
Ramaiah Institute of Technology
Sulfur quantum dots (SQDs) are metal-free fluorescent nanomaterials with low toxicity and tunable optical properties. In this study, SQDs were synthesized from sulfur powder and NaOH with PEG by a microwave-assisted method and characterized by UV–Visible spectroscopy, powder X-ray diffraction, fluorescence spectroscopy and transmission electron microscopy, which showed crystalline, quasi-spherical particles of approximately 5–10 nm. The SQDs were applied as a fluorescent nanosensor for the antibiotic ciprofloxacin: fluorescence intensity increased with ciprofloxacin concentration over 0.01–5 µM, with a linear range of 0.01–0.5 µM (R2 = 0.9851) and limits of detection and quantification of approximately 116.9 nM and 354.2 nM, respectively. The anticancer activity of the SQDs was evaluated against human colon cancer (Caco-2) cells. The MTT assay showed dose-dependent cytotoxicity after 24 h, with an IC50 of 72.51 ± 2.15 µg/mL, and confocal laser scanning microscopy confirmed cellular uptake of the SQDs. These results indicate that SQDs are a promising multifunctional platform for antibiotic sensing and anticancer studies.
KEYWORDS
In the present study, sulfur quantum dots (SQDs) were successfully synthesized by a microwave-assisted method using PEG6000 as the precursor material. The synthesized SQDs were characterized using UV–Visible spectroscopy, fluorescence spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), and Raman spectroscopy, which confirmed the formation of stable, fluorescent, quasi-spherical nanoparticles with nanoscale dimensions. The optical studies demonstrated strong fluorescence emission and effective “switch-on” fluorescence behavior, indicating the suitability of SQDs for bioimaging applications. The biological activity of the synthesized SQDs was evaluated against Caco-2 cancer cell lines through MTT assay,reactive oxygen species (ROS) analysis, cellular uptake studies, confocal laser scanning microscopy (CLSM), apoptosis assay, and cell cycle analysis. The results revealed that SQDs exhibited significant concentration-dependent cytotoxicity and effectively reduced the viability of Caco-2 cells. Enhanced intracellular uptake and fluorescence imaging confirmed efficient penetration of SQDs into cancer cells. Further studies demonstrated that SQDs induced oxidative stress-mediated apoptosis and cell cycle arrest, thereby contributing to their anticancer activity. Overall, the synthesized SQDs showed excellent optical properties along with promising in vitro anticancer potential against Caco-2 cancer cells, suggesting their possible application as fluorescent nanomaterials for cancer diagnosis, bioimaging, and therapeutic purposes.
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Publication Date
10/29/2026
Peer Review Type
Double-Blind Peer Review
Review Rounds: 2
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