4.7 Article

Copper oxide nanoparticles synthesized from an endophytic fungus Aspergillus terreus: Bioactivity and anti-cancer evaluations

Journal

ENVIRONMENTAL RESEARCH
Volume 201, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2021.111502

Keywords

Angiogenesis; Antioxidant; Copper oxide nanoparticles; DPPH; Endophytic fungi

Funding

  1. Taif University, Taif, Saudi Arabia [TURSP-2020/40]

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The study focused on synthesizing Copper Oxide Nanoparticles (CuONPs) using an endophytic fungus isolated from a medicinal tree in India, and evaluated their antibacterial, antifungal, antioxidant, and anti-cancer activities. The CuONPs exhibited significant anti-cancer effects on colon cancer cell lines and angiogenesis inhibition in tumor cells in a concentration-dependent manner, highlighting their potential in cancer therapeutics.
The mycofabricated metal nanoparticles (NPs) plays a significant role in cancer therapeutics and imparts a strategy in medicine. The current investigation focused to synthesize the Copper Oxide Nanoparticles (CuONPs) using an endophytic fungus isolated from Aegle marmelosa medicinal tree located in Western Ghats, India. The endophytic fungus FCBY1 explored the highest antagonistic and antioxidant activities among the 16 pigmented endophytic fungal strains which were isolated from the collected samples. The fungus FCBY1 was identified for its morphological and molecular characteristics where the (Internal Transcribed Spacer) ITS 1, 5.8 ribosomal gene and ITS 2 were sequenced; and the organism FCBY1 is Aspergillus terreus. The endophyte was put through for the synthesis of CuONPs and the size and structure of the synthesized particles were characterized by Scanning Electron Microscope (SEM). The confirmation of the CuONPs was characterized by FT-IR, EDAX and XRD ana -lyses. The CuONPs exhibited the maximized antibacterial and antifungal activities against the human clinical pathogens; moreover the particles also explicated the free radicals/ROS scavenging at minimum concentration, which was assessed through DPPH, nitric oxide radical scavenging assays, and reductive power ability. The anti-cancer activity of CuONPs on colon cancer cell lines (HT-29) was evaluated by MTT (IC50: 22 mu g/mL) and FACS analyses (32.11% cells gated in S phase of cell cycle). Angiogenesis inhibition in tumor cells was estimated through in vivo HET-CAM assessment and the highest concentration 60 mu L tested inhibited the blood vessels at the percentage of 31.36% and 81.81%. The CuONPs explicated the anti-cancer activities in a concentration - dependent manner and the results of this investigation manifest the significant role of the CuONPs in cancer therapeutics.

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