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A Hybrid Silica Nanoreactor Framework for Encapsulation of Hollow Manganese Oxide Nanoparticles of Superior T-1 Magnetic Resonance Relaxivity

机译:混合二氧化硅纳米反应器框架,用于封装具有优异T-1磁共振弛豫性的空心氧化锰纳米粒子

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摘要

A new hybrid nanoreactor framework with poly(ethylene oxide)-perforated silica walls is designed to encapsulate hollow manganese oxide nanoparticles (MONs) of high distinctness and homogeneity. Achieved by an interfacial templating scheme, the nanoreactor ensures that acidic etching of MONs by an acetate buffer solution is highly controlled for precise control of the hollow interior. As such, hollow MONs with different nanostructures are developed successfully through a facile acetate buffer solution etching. The resultant hollow MONs are integrated within the hybrid nanoreactor and demonstrate superior r(1) relativity of up to 2.58 mm(-1) s(-1) for T-1 magnetic resonance imaging (MRI). By modifying the nanoreactor architecture, it is also demonstrated that the efficacy of MONs as T-1 MRI contrast agents can be significantly improved if an optimal cluster of hollow MONs is encapsulated into the hybrid silica framework. The evolution of core morphology with time is studied to elucidate the etching mechanism. It is revealed that the hollow formation arises due to the surface stabilization of MONs by acetate ions and the subsequent acidic etching of the interior core in a sporadic manner. This is different from the commonly reported nanoscale Kirkendall effect or the selective etching of the core-shell MnO/Mn3O4 structure.
机译:设计了一种新的具有聚(环氧乙烷)穿孔二氧化硅壁的混合纳米反应器框架,用于封装具有高清晰性和均质性的中空氧化锰纳米颗粒(MONs)。通过界面模板方案,纳米反应器可确保通过醋酸盐缓冲溶液对MONs进行酸性蚀刻,从而实现对中空内部的精确控制。这样,通过简便的醋酸盐缓冲溶液蚀刻成功开发了具有不同纳米结构的空心MON。所得的空心MONs集成在杂化纳米反应器中,并且对于T-1磁共振成像(MRI)展示了高达2.58 mm(-1)s(-1)的优异r(1)相关性。通过修改纳米反应器的结构,还表明,如果将空心MONs的最佳簇封装到杂化二氧化硅骨架中,则可以显着提高MONs作为T-1 MRI造影剂的功效。研究了核心形态随时间的演变,以阐明蚀刻机理。揭示出中空的形成是由于乙酸根离子对MONs的表面稳定作用和随后对内芯的酸蚀性的散发性。这不同于通常报道的纳米级柯肯德尔效应或核-壳MnO / Mn3O4结构的选择性蚀刻。

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