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Superparamagnetic Iron Oxide Nanoparticles with Variable Size and an Iron Oxidation State as Prospective Imaging Agents

机译:超顺磁性氧化铁纳米粒子具有可变尺寸和铁氧化态前瞻性显像剂

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摘要

Magnetite nanoparticles in the size range of 3.2-7.5 nm were synthesized in high yields under variable reaction conditions using high-temperature hydrolysis of the precursor iron(II) and iron(III) alkoxides in diethylene glycol solution. The average sizes of the particles were adjusted by changing the reaction temperature and time and by using a sequential growth technique. To obtain γ-iron(III) oxide particles in the same range of sizes, magnetite particles were oxidized with dry oxygen in diethylene glycol at room temperature. The products were characterized by DLS, TEM, X-ray powder diffractometry, TGA, chemical analysis, and magnetic measurements. NMR r1 and r2 relaxivity measurements in water and diethylene glycol (for OH and CH2 protons) have shown a decrease in the r2/r1 ratio with the particle size reduction, which correlates with the results of magnetic measurements on magnetite nanoparticles. Saturation magnetization of the oxidized particles was found to be 20% lower than that for Fe3O4 with the same particle size, but their r1 relaxivities are similar. Because the oxidation of magnetite is spontaneous under ambient conditions, it was important to learn that the oxidation product has no disadvantages as compared to its precursor and therefore may be a better prospective imaging agent because of its chemical stability.
机译:使用前驱体铁(II)和铁(III)醇盐在二甘醇溶液中的高温水解,在可变的反应条件下,以高收率合成了尺寸范围为3.2-7.5 nm的磁铁矿纳米颗粒。通过改变反应温度和时间并使用顺序生长技术来调节颗粒的平均尺寸。为了获得相同尺寸范围的γ-铁(III)氧化物颗粒,在室温下用二甘醇中的干燥氧气将磁铁矿颗粒氧化。通过DLS,TEM,X射线粉末衍射,TGA,化学分析和磁测量对产品进行了表征。 NMR在水和二甘醇(对于OH和CH2质子)中的r1和r2弛豫性测量结果表明,随着粒径的减小,r2 / r1比率降低,这与磁铁矿纳米粒子的磁测量结果相关。发现氧化后的颗粒的饱和磁化强度比相同粒径的Fe3O4的饱和磁化强度低20%,但它们的r1弛豫率相似。因为磁铁矿的氧化在环境条件下是自发的,所以重要的是要了解到,氧化产物与其前体相比没有任何缺点,因此由于其化学稳定性可能是更好的预期成象剂。

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