材料科学
动态光散射
聚合物
纳米颗粒
磁铁矿
水溶液
磁性纳米粒子
氧化铁纳米粒子
质子
粒子(生态学)
氧化铁
粒径
光散射
核磁共振
扩散
质子磁共振
化学工程
散射
化学物理
分析化学(期刊)
纳米技术
复合材料
物理化学
光学
热力学
化学
色谱法
工程类
地质学
海洋学
量子力学
冶金
物理
作者
Matt Carroll,Phillip P Huffstetler,William C. Miles,Jonathon D Goff,Richey M. Davis,Judy S. Riffle,Michael J. House,Robert C. Woodward,Timothy G. St. Pierre
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2011-07-19
卷期号:22 (32): 325702-325702
被引量:40
标识
DOI:10.1088/0957-4484/22/32/325702
摘要
Iron oxide magnetic nanoparticles are good candidates for magnetic resonance imaging (MRI) contrast agents due to their high magnetic susceptibilities. Here we investigate 19 polyether-coated magnetite nanoparticle systems comprising three series. All systems were synthesized from the same batch of magnetite nanoparticles. A different polyether was used for each series. Each series comprised systems with systematically varied polyether loadings per particle. A highly significant (p < 0.0001) linear correlation (r = 0.956) was found between the proton relaxivity and the intensity-weighted average diameter measured by dynamic light scattering in the 19 particle systems studied. The intensity-weighted average diameter measured by dynamic light scattering is sensitive to small number fractions of larger particles/aggregates. We conclude that the primary effect leading to differences in proton relaxivity between systems arises from the small degree of aggregation within the samples, which appears to be determined by the nature of the polymer and, for one system, the degree of polymer loading of the particles. For the polyether coatings used in this study, any changes in relaxivity from differences in water exclusion or diffusion rates caused by the polymer are minor in comparison with the changes in relaxivity resulting from variations in the degree of aggregation.
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