Nanomaterials (Oct 2022)

Synthesis, Characterization, and Antimicrobial and Antiproliferative Effects of CuO-TiO<sub>2</sub>-Chitosan-Escin Nanocomposites on Human Leukemic MOLT4 Cells

  • Abozer Y. Elderdery,
  • Abdulaziz H. Alhamidi,
  • Ahmed M. E. Elkhalifa,
  • Maryam M. Althobiti,
  • Nawal Eltayeb Omer,
  • Mahdi H. Alsugoor,
  • Naif Alsuhaymi,
  • Entesar M. Atebien,
  • Siddiqa M. A. Hamza,
  • Badr Alzahrani,
  • Fehaid Alanazi,
  • Suresh S. Kumar,
  • Pooi Ling Mok

DOI
https://doi.org/10.3390/nano12213753
Journal volume & issue
Vol. 12, no. 21
p. 3753

Abstract

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Nanocomposites comprised of CuO-TiO2-chitosan-escin, which has adjustable physicochemical properties, provide a solution for therapeutic selectivity in cancer treatment. By controlling the intrinsic signaling primarily through the mitochondrial signaling pathway, we desired nanocomposites with enhanced anticancer activity by containing CuO-TiO2-chitosan-escin. The metal oxides CuO and TiO2, the natural polymer chitosan, and a phytochemical compound escin were combined to form CuO-TiO2-chitosan-escin nanocomposites. The synthesized nanocomposites were confirmed and characterized using FTIR spectroscopy, TEM, and UV-Vis absorption spectroscopy. A human leukemia cell line (MOLT-4) was used to assess the efficacy and selectivity of nanocomposites. Based on a cytotoxicity study, CuO-TiO2-chitosan-escin nanocomposites had inhibition concentrations (IC50) of 13.68, 8.9, and 7.14 µg/mL against human T lymphoblast cells after 24, 48, and 72 h of incubation, respectively. Compared with untreated MOLT-4 cells, CuO-TiO2-chitosan-escin nanocomposite-treated cells significantly increased (p p 2-chitosan-escin nanocomposite-mediated control of cell cycles were mainly achieved through the activation of caspase-3, -8, and -9.

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