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Investigation of Drug Delivery of Rattle-Structured Gold Nanorod-Mesoporous Silica Nanoparticles Core–Shell as Curcumin Carrier and Their Effect on MCF7 and 4T1 Cell Lines

介孔二氧化硅 姜黄素 动态光散射 纳米颗粒 药物输送 胶体金 材料科学 介孔材料 纳米技术 分散性 核化学 化学 有机化学 高分子化学 生物化学 催化作用
作者
Hossein Danafar,Hamid Reza Kheiri Manjili,Elaheh Attari,Ali Sharafi
出处
期刊:Journal of Advances in Medical and Biomedical Research 卷期号:25 (113): 122-134 被引量:1
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摘要

Background and Objective: Curcumin is a polyphenolic anti-cancer and anti-inflammatory agent and can be used both orally and by injection. In this study, nanoparticles of silica mesopore- gold nano were synthesized as a new drug delivery system. For this aim, gold nanoparticles as a promising system for effective drug delivery of curcumin was used and nano gold were delivered to breast cancer cells . Materials and Methods: The synthetic nanoparticles characteristics were determined with different techniques such as transmission electron microscopy (TEM), nitrogen gas desorption, absorption analysis and dynamic light scattering techniques (DLS). The anti-cancer effects of this system were evaluated in cell culture, using MTT cytotoxicity test. The efficiency of this system was tested on human breast cancer (MCF-7) and 4T1 cell lines. Results: The mean size of nano system was less than 30 nm, similar to the data obtained from Dynamic light scattering technique. The amount of curcumin loading in nano- system was about 80 percent. Isotherm - nitrogen adsorption AuNR@msio2 and CUR @ AuNR @ msio2 show that specific area of nano-Au @ msio2 was about -1834 m2g but by creating medication this particular area decrease to 234 m2g-1. IC50 for curcumin loaded mesoporous silica nanoparticles for MCF-7 at the time of 48 hours and 4T1 were 19.5 and 14.6 micro molar respectively. The survival rate of the cells after treatment with different concentrations did not change considerably in the nano structures which demonstrate the lack of toxicity of nanoparticles. Conclusion: The nanoparticle caused apoptosis in breast cancer cells more than free drug.

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