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Design of Engineered Cyclodextrin Derivatives for Spontaneous Coating of Highly Porous Metal-Organic Framework Nanoparticles in Aqueous Media

机译:工程性环糊精衍生物在水性介质中自发性包覆高多孔金属有机骨架纳米粒子的设计

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摘要

Nanosized metal-organic frameworks (nanoMOFs) MIL-100(Fe) are highly porous and biodegradable materials that have emerged as promising drug nanocarriers. A challenging issue concerns their surface functionalization in order to evade the immune system and to provide molecular recognition ability, so that they can be used for specific targeting. A convenient method for their coating with tetraethylene glycol, polyethylene glycol, and mannose residues is reported herein. The method consists of the organic solvent-free self-assembly on the nanoMOFs of building blocks based on β-cyclodextrin facially derivatized with the referred functional moieties, and multiple phosphate groups to anchor to the nanoparticles’ surface. The coating of nanoMOFs with cyclodextrin phosphate without further functional groups led to a significant decrease of macrophage uptake, slightly improved by polyethylene glycol or mannose-containing cyclodextrin phosphate coating. More notably, nanoMOFs modified with tetraethylene glycol-containing cyclodextrin phosphate displayed the most efficient “stealth” effect. Mannose-coated nanoMOFs displayed a remarkably enhanced binding affinity towards a specific mannose receptor, such as Concanavalin A, due to the multivalent display of the monosaccharide, as well as reduced macrophage internalization. Coating with tetraethylente glycol of nanoMOFs after loading with doxorubicin is also described. Therefore, phosphorylated cyclodextrins offer a versatile platform to coat nanoMOFs in an organic solvent-free, one step manner, providing them with new biorecognition and/or “stealth” properties.
机译:纳米级金属有机框架(nanoMOF)MIL-100(Fe)是高度多孔且可生物降解的材料,已成为有前途的药物纳米载体。一个具有挑战性的问题涉及它们的表面功能化,以逃避免疫系统并提供分子识别能力,因此它们可用于特异性靶向。本文报道了用四甘醇,聚乙二醇和甘露糖残基涂覆它们的方便方法。该方法包括基于β-环糊精的,以所述功能部分进行表面衍生的,基于构建基的nanoMOF上无有机溶剂的自组装,以及多个磷酸根基团固定在纳米颗粒的表面。纳米MOFs的磷酸环糊精涂层没有其他官能团,导致巨噬细胞摄取显着下降,而聚乙二醇或含甘露糖的磷酸环糊精涂层则稍有改善。更值得注意的是,用含四甘醇的环糊精磷酸酯修饰的nanoMOF表现出最有效的“隐身”效果。由于单糖的多价展示以及减少的巨噬细胞内化作用,被甘露糖包覆的nanoMOFs对特定甘露糖受体(例如伴刀豆球蛋白A)的结合亲和力显着提高。还描述了在装载阿霉素后用nanoMOF的四乙撑二醇包衣。因此,磷酸化的环糊精提供了一种多功能平台,以一种无有机溶剂的一步法涂覆nanoMOF,为它们提供了新的生物识别和/或“隐身”特性。

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