1. A c-MWCNTs/AuNPs-based electrochemical cytosensor to evaluate the anticancer activity of pinoresinol from Cinnamomum camphora against HeLa cells.
- Author
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Zhou, Haixu, Huang, Rengui, Su, Tongchao, Li, Bo, Zhou, Haoyu, Ren, Jiali, and Li, Zhonghai
- Subjects
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HELA cells , *ANTINEOPLASTIC agents , *CARBON electrodes , *MULTIWALLED carbon nanotubes , *CINNAMOMUM , *TRANSMISSION electron microscopy , *CELL separation - Abstract
• Cervical carcinoma is a leading cause of mortality in women worldwide. • Lignans, as phytochemicals, have therapeutic potential for cancer cell lines. • An electrochemical cytosensor evaluated pinoresinol activity on HeLa cells. • Pinoresinol induced apoptosis in HeLa cells and hindered HeLa cell cycle. • MTS, flow cytometry, and fluorescent imaging confirmed the cytosensor results. A sensitive, simple, label-free electrochemical cytosensor was developed to evaluate the anticancer activity of pinoresinol against human cervical carcinoma (HeLa) cells. HeLa cells were immobilised on carboxylated multi-walled carbon nanotubes (c-MWCNTs)/gold nanoparticles (AuNPs) nanocomposite-modified glassy carbon electrodes. Scanning electron microscopy, transmission electron microscopy, Fourier transform-infrared spectroscopy, and X-ray diffractometry were used to characterise the morphology, crystallinity, and composition of the nanocomposites. Cyclic voltammetry was used to characterise and optimise the cytosensor. Both c-MWCNTs and AuNPs increased the electron-transfer rate between the HeLa cells and the electrode, retaining good cell compatibility. The concentration of HeLa cells immobilised on the nanocomposite electrode exhibited a good correlation with the impedance values determined by electrochemical impedance spectroscopy in the range of 102–106 cells/mL (detection limit of 102 cells/mL) with R2 = 0.975. HeLa cells were then immobilised on the nanocomposite electrode at a concentration of 104 cells/mL, and it was used as a cytosensor. The anticancer activity of pinoresinol from Cinnamomum camphora was evaluated by determining the median inhibitory concentration using the proposed cytosensor. For comparison, a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, flow cytometry, and fluorescent imaging were simultaneously performed, which confirmed the results of the cytosensor. The cytosensor is promising for future applications in anticancer drug screening. [ABSTRACT FROM AUTHOR]
- Published
- 2022
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