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Design of Magnetic Gelatine/Silica Nanocomposites by Nanoemulsification: Encapsulation versus in Situ Growth of Iron Oxide Colloids

机译:通过纳米乳化法设计磁性明胶/二氧化硅纳米复合材料:氧化铁胶体的封装与原位生长

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摘要

The design of magnetic nanoparticles by incorporation of iron oxide colloids within gelatine/silica hybrid nanoparticles has been performed for the first time through a nanoemulsion route using the encapsulation of pre-formed magnetite nanocrystals and the in situ precipitation of ferrous/ferric ions. The first method leads to bi-continuous hybrid nanocomposites containing a limited amount of well-dispersed magnetite colloids. In contrast, the second approach allows the formation of gelatine-silica core-shell nanostructures incorporating larger amounts of agglomerated iron oxide colloids. Both magnetic nanocomposites exhibit similar superparamagnetic behaviors. Whereas nanocomposites obtained via an in situ approach show a strong tendency to aggregate in solution, the encapsulation route allows further surface modification of the magnetic nanocomposites, leading to quaternary gold/iron oxide/silica/gelatine nanoparticles. Hence, such a first-time rational combination of nano-emulsion, nanocrystallization and sol-gel chemistry allows the elaboration of multi-component functional nanomaterials. This constitutes a step forward in the design of more complex bio-nanoplatforms.
机译:通过将氧化铁胶体掺入明胶/二氧化硅杂化纳米颗粒中来设计磁性纳米颗粒,是通过使用预先形成的磁铁矿纳米晶体的包封和铁/铁离子的原位沉淀,通过纳米乳化途径首次进行的。第一种方法导致包含有限数量的良好分散的磁铁矿胶体的双连续杂化纳米复合材料。相反,第二种方法允许形成明胶-二氧化硅核-壳纳米结构,其中掺入了大量的聚集的氧化铁胶体。两种磁性纳米复合材料均表现出相似的超顺磁性行为。尽管通过原位方法获得的纳米复合材料显示出很强的在溶液中聚集的趋势,但封装路径允许磁性纳米复合材料进行进一步的表面修饰,从而形成季金/氧化铁/二氧化硅/明胶纳米粒子。因此,纳米乳液,纳米晶化和溶胶-凝胶化学的这种首次合理组合允许精细加工多组分功能纳米材料。这构成了设计更复杂的生物纳米平台的一步。

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