Institut Charles Gerhardt Montpellier, UMR 5253 CNRS-UM2, Chimie Moléculaire et Organisation du Solide, Université Montpellier II, Place E. Bataillon, 34095 Montpellier Cedex 5, France.
J Am Chem Soc. 2011 Jul 13;133(27):10459-72. doi: 10.1021/ja111448t. Epub 2011 Jun 16.
Synthesis of functionalized magnetic nanoparticles (NPs) for biomedical applications represents a current challenge. In this paper we present the synthesis and characterization of water-dispersible sugar-coated iron oxide NPs specifically designed as magnetic fluid hyperthermia heat mediators and negative contrast agents for magnetic resonance imaging. In particular, the influence of the inorganic core size was investigated. To this end, iron oxide NPs with average size in the range of 4-35 nm were prepared by thermal decomposition of molecular precursors and then coated with organic ligands bearing a phosphonate group on one side and rhamnose, mannose, or ribose moieties on the other side. In this way a strong anchorage of the organic ligand on the inorganic surface was simply realized by ligand exchange, due to covalent bonding between the Fe(3+) atom and the phosphonate group. These synthesized nanoobjects can be fully dispersed in water forming colloids that are stable over very long periods. Mannose, ribose, and rhamnose were chosen to test the versatility of the method and also because these carbohydrates, in particular rhamnose, which is a substrate of skin lectin, confer targeting properties to the nanosystems. The magnetic, hyperthermal, and relaxometric properties of all the synthesized samples were investigated. Iron oxide NPs of ca. 16-18 nm were found to represent an efficient bifunctional targeting system for theranostic applications, as they have very good transverse relaxivity (three times larger than the best currently available commercial products) and large heat release upon application of radio frequency (RF) electromagnetic radiation with amplitude and frequency close to the human tolerance limit. The results have been rationalized on the basis of the magnetic properties of the investigated samples.
用于生物医学应用的功能化磁性纳米粒子(NPs)的合成是当前的一个挑战。本文介绍了水散性糖涂层氧化铁 NPs 的合成与表征,这些 NPs 专门设计用作磁流体热疗的热介质和磁共振成像的负对比剂。特别是,研究了无机核尺寸的影响。为此,通过热分解分子前体制备了平均尺寸在 4-35nm 范围内的氧化铁 NPs,然后用有机配体进行涂层处理,该有机配体一侧带有膦酸基团,另一侧带有鼠李糖、甘露糖或核糖部分。通过配体交换,铁(III)原子与膦酸基团之间的共价键可简单地实现有机配体在无机表面上的强锚固。这些合成的纳米物体可以完全分散在水中形成胶体,在很长一段时间内都保持稳定。选择甘露糖、核糖和鼠李糖来测试该方法的多功能性,也是因为这些碳水化合物,特别是作为皮肤凝集素的底物的鼠李糖,赋予纳米系统靶向特性。对所有合成样品的磁性、热疗和弛豫性能进行了研究。发现约 16-18nm 的氧化铁 NPs 是用于治疗诊断应用的高效双功能靶向系统,因为它们具有非常好的横向弛豫率(比目前最好的商业产品大三倍),并且在应用接近人体耐受极限的幅度和频率的射频(RF)电磁辐射时会释放大量热量。根据所研究样品的磁性对结果进行了合理化。
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