Magnetic UiO-66-NH 2 Core-Shell Nanohybrid as a Promising Carrier for Quercetin Targeted Delivery toward Human Breast Cancer Cells.
Mozhgan ParsaeiKamran AkhbariPublished in: ACS omega (2023)
In this study, a magnetic core-shell metal-organic framework (MOF) nanocomposite, Fe 3 O 4 -COOH@UiO-66-NH 2 , was synthesized for tumor-targeting drug delivery by incorporating carboxylate groups as functional groups onto ferrite nanoparticle surfaces, followed by fabrication of the UiO-66-NH 2 shell using a facile self-assembly approach. The anticancer drug quercetin (QU) was loaded into the magnetic core-shell nanoparticles. The synthesized magnetic nanoparticles were comprehensively evaluated through multiple techniques, including FT-IR, PXRD, FE-SEM, TEM, EDX, BET, UV-vis, ZP, and VSM. Drug release investigations were conducted to investigate the release behavior of QU from the nanocomposite at two different pH values (7.4 and 5.4). The results revealed that QU@Fe 3 O 4 -COOH@UiO-66-NH 2 exhibited a high loading capacity of 43.1% and pH-dependent release behavior, maintaining sustained release characteristics over a prolonged duration of 11 days. Furthermore, cytotoxicity assays using the human breast cancer cell line MDA-MB-231 and the normal cell line HEK-293 were performed to evaluate the cytotoxic effects of QU, UiO-66-NH 2 , Fe 3 O 4 -COOH, Fe 3 O 4 -COOH@UiO-66-NH 2 , and QU@Fe 3 O 4 -COOH@UiO-66-NH 2 . Treatment with QU@Fe 3 O 4 -COOH@UiO-66-NH 2 substantially reduced the cell viability in cancerous MDA-MB-231 cells. Cellular uptake and cell death mechanisms were further investigated, demonstrating the internalization of QU@Fe 3 O 4 -COOH@UiO-66-NH 2 by cancer cells and the induction of cancer cell death through the apoptosis pathway. These findings highlight the considerable potential of Fe 3 O 4 -COOH@UiO-66-NH 2 as a targeted nanocarrier for the delivery of anticancer drugs.
Keyphrases
- metal organic framework
- cell death
- room temperature
- drug delivery
- cell cycle arrest
- breast cancer cells
- perovskite solar cells
- cancer therapy
- endothelial cells
- squamous cell carcinoma
- oxidative stress
- induced apoptosis
- endoplasmic reticulum stress
- staphylococcus aureus
- molecularly imprinted
- magnetic nanoparticles
- escherichia coli
- quantum dots
- emergency department
- high throughput
- risk assessment
- climate change
- adverse drug
- young adults
- single molecule
- papillary thyroid