Preparation of the Myricetin-Loaded PEGylated Niosomes and Evaluation of their in vitro Anti-Cancer Potentials.
Hanieh RiaziMohammad Taghi GoodarziMasoud Homayouni TabriziMajid MozaffariAli NeamatiPublished in: Chemistry & biodiversity (2024)
Several edible plants contain flavonoids, including myricetin (Myr), which perform a wide range of biological activities. Myr has antitumor properties against various tumor cells. In this study Myr-loaded PEGylated niosomes (Myr-PN) were prepared and their anti-cancer activities were evaluated in vitro. Myr-PNs were prepared as a tool for drug delivery to the tumor site. Myr-PN was characterized in terms of size, zeta potential, and functional groups using dynamic light scattering (DLS), Fourier-transform infrared spectroscopy (FTIR), and field emission scanning electron microscopy (SEM). The Myr-PN size was 241 nm with a polydispersity index (PDI) of 0.20, and zeta potential -32.7±6.6 mV. Apoptotic properties of Myr-PN against normal and cancer cell lines were determined by flow cytometry and real-time quantitative PCR. Cancer cells showed higher cytotoxicity when treated with Myr-PN compared with normal cells, indicating that the synthesized nanoparticles pose no adverse effects. Apoptosis was induced in cells treated with 250 μg/mL of Myr-PN, in which 45.2 % of cells were arrested in subG1, suggesting that Myr-PN can induce apoptosis. In vitro, the synthesized Myr-PN demonstrated potent anticancer properties. Furthermore, more research should be conducted in vitro and in vivo to study the more details of Myr-PN anti-cancer effects.
Keyphrases
- cell cycle arrest
- drug delivery
- induced apoptosis
- cell death
- oxidative stress
- endoplasmic reticulum stress
- flow cytometry
- signaling pathway
- cancer therapy
- squamous cell carcinoma
- high resolution
- pi k akt
- photodynamic therapy
- high glucose
- young adults
- mass spectrometry
- papillary thyroid
- newly diagnosed
- drug induced
- wound healing
- lymph node metastasis