Synthesis of magnetite-silica-carbon quantum dot nanocomposites for melatonin drug delivery

A. Faeghinia, H. Nuranian, Mojtaba Eslami
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Abstract

In targeted drug delivery, the drug is released at a specific and desired point and condition. In this research, magnetite cores (high saturation magnetization property (emu.g-159) were used to target the drug system. First, magnetite nanoparticles were synthesized by coprecipitation method from divalent and trivalent chloride salts of iron (FeCl2 and FeCl3), then mesoporous silicas (with a pore diameter of 13 nm) were formed by Stöber's method from the tetraethylorthosilicate (TEOS) silica source on magnetite cores in spheres form. After that, the carbon quantum dots were synthesized by hydrothermal method from citric acid and their surface was immobilized by dimethylamine which were placed in silica cavities by physical adsorption method. The effective drug melatonin (6.46 mg of melatonin per 100 mg of the drug system) was also loaded on this system by physical absorption method and the release of this drug was carefully determined by the release from the dialysis bag in the simulated environment of blood and cancer tissue. the quantum gain of the system was determined to be about 40%. The results showed that the loading of melatonin drug and carbon quantum dots was done well on silica nanoparticles with magnetite cores, and this system releases 30% of the drug even under temperature conditions.
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用于褪黑素药物递送的磁铁矿-硅-碳量子点纳米复合材料的合成
在靶向给药中,药物在特定的和期望的点和条件下释放。本研究采用具有高饱和磁化特性的磁铁矿(emu.g-159)作为药物体系的靶材。首先,以二价和三价氯化铁(FeCl2和FeCl3)为原料,采用共沉淀法合成了磁铁矿纳米颗粒,然后以四乙基硅酸(TEOS)硅源为原料,采用Stöber法在磁铁矿岩心上制备了孔径为13 nm的介孔二氧化硅。然后,以柠檬酸为原料,用水热法制备碳量子点,用二甲胺固定碳量子点表面,用物理吸附法将碳量子点置于硅孔中。通过物理吸收法将有效药物褪黑素(每100 mg药物系统中含有6.46 mg褪黑素)加载到该系统中,并通过透析袋在模拟血液和癌组织环境中的释放来仔细测定该药物的释放。系统的量子增益约为40%。结果表明,在具有磁铁矿核的二氧化硅纳米颗粒上很好地负载了褪黑素药物和碳量子点,即使在温度条件下,该系统也能释放30%的药物。
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