期刊
NANOMATERIALS
卷 13, 期 12, 页码 -出版社
MDPI
DOI: 10.3390/nano13121811
关键词
iron oxide nanoparticles; dextran; 5-Fluorouracil; Caco-2 cells; toxicity; drug-delivery system; anti-proliferative effect
This study aimed to design and test dextran-coated iron oxide nanoparticles (IONPs) loaded with 5-Fluorouracil (5-FU) at different nanoparticle:drug ratios on colorectal cancer cells. The stable suspension of IONPs was synthesized using co-precipitation method and mixed with dextran and 5-FU solubilized in saline solution. The optimized ratios of IONP:5-FU in the final suspensions were 0.5:1, 1:1, and 1.5:1. The efficacy of the drug-delivery system was evaluated by analyzing nanoparticle uptake, antitumor activity, and cellular response. The nanoformulation with the ratio IONP:5-FU 1.5:1 showed the highest anti-tumor efficiency.
This study aims to design and test different formulations composed of dextran-coated iron oxide nanoparticles (IONPs) loaded with 5-Fluorouracil (5-FU) with varying nanoparticle:drug ratios on colorectal cancer cells. The stable suspension of IONPs s was synthesized by the adapted co-precipitation method. The stable suspension of IONPs was mixed with a solution of dextran and 5-FU solubilized in a saline solution. The final suspensions with optimized ratios of IONP:5-FU in the final suspension were 0.5:1, 1:1, and 1.5:1. The information on the morphology and size distribution of the IONPs suspension and IONP loads with 5-FU was obtained using scanning electron microscopy (SEM). The presence of 5-FU and dextran on the surface of the IONPs was highlighted by energy-dispersive X-ray spectroscopy (EDS) studies. The determination of the surface charge of the nanoparticles in the final suspensions of IONP:5-FU was achieved by measuring the zeta potential (& zeta;). The hydrodynamic diameter of the resulting suspensions of IONP:5-FU was determined by dynamic light scattering (DLS). A cytocompatibility analysis was performed using Caco-2 (human epithelial colorectal adenocarcinoma) cells. In this research, our goal was to find a relationship between the formulation ratio of nanoparticles and drug, and the cellular response after exposure, as a strategy to increase the efficacy of this drug-delivery system. The nanoparticle uptake and antitumor activity, including modulation of oxidative stress, apoptosis, and proliferation biomarkers, were analyzed. The present study showed that the nanoformulation with the ratio IONP:5-FU 1.5:1 had the highest anti-tumor efficiency. Moreover, decreased MCM-2 expression in Caco-2 cells exposed to dextran-coated iron oxide nanoparticles loaded with 5-FU was demonstrated for the first time.
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