4.5 Article

Synthesis and Characterization of Zinc Oxide Nanoparticles of Solanum nigrum and Its Anticancer Activity via the Induction of Apoptosis in Cervical Cancer

Journal

BIOLOGICAL TRACE ELEMENT RESEARCH
Volume 200, Issue 6, Pages 2684-2697

Publisher

SPRINGERNATURE
DOI: 10.1007/s12011-021-02898-6

Keywords

Cervical cancer; Apoptosis; Zinc oxide nanoparticles; Solanum nigrum; Transmission electron microscopy; X-ray diffraction

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This study conducted green synthesis of ZnO nanoparticles using the plant Solanum nigrum and demonstrated their significant anticancer activity against HeLa cell lines through various experiments. The results indicate a dose-dependent cytotoxic effect of ZnO nanoparticles against HeLa cell lines by inhibiting beta-catenin and increasing the levels of p53, caspase-3, and caspase-9.
Effective cancer therapy can be achieved by using nano-drug delivery systems which provide a targeted drug delivery strategy by overcoming the drawbacks of conventional treatments like chemotherapy and radiation. ZnO nanoparticles are a potent anticancer agent that causes tumor cell destruction with the targeted drug delivery. In this present study, green synthesis of ZnO nanoparticles has been done using the plant Solanum nigrum. The synthesized ZnO nanoparticles were studied by the characterization techniques like UV-visible spectroscopy, SEM, TEM, DLS, zeta potential, FTIR, and XRD. The synthesized ZnO nanoparticles of Solanum nigrum exhibited a significant anticancer activity against HeLa cell lines through the apoptotic pathway. The cytotoxicity of ZnO nanoparticles was assessed using MTT assay, wound healing assay, DAPI staining, and acridine orange and ethidium bromide double staining. The expression patterns of beta-catenin, p53, caspase-3, and caspase-9 were analyzed using reverse transcriptase-PCR. The results obtained from the study indicate that the ZnO nanoparticles of Solanum nigrum possess a dose-dependent cytotoxic effect against HeLa cell lines through the inhibition of beta-catenin and increasing the levels of p53, caspase-3, and caspase-9.

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