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用于磁共振成像的锰基纳米级金属有机框架

Manganese-based nanoscale metal-organic frameworks for magnetic resonance imaging.

作者信息

Taylor Kathryn M L, Rieter William J, Lin Wenbin

机构信息

Department of Chemistry, CB#3290, University of North Carolina, Chapel Hill, North Carolina 27599, USA.

出版信息

J Am Chem Soc. 2008 Nov 5;130(44):14358-9. doi: 10.1021/ja803777x. Epub 2008 Oct 10.

Abstract

Manganese-containing nanoscale metal-organic frameworks (NMOFs) with controllable morphologies were synthesized using reverse-phase microemulsion techniques at room temperature and a surfactant-assisted procedure at 120 degrees C with microwave heating. The nanoparticles were characterized using a variety of methods including SEM, TEM, TGA, PXRD, and ICP-MS. Although the nanoparticles gave a modest longitudinal relaxivity (r1) on a per Mn basis, they provided an efficient vehicle for the delivery of large doses of Mn2+ ions which exhibited very high in vitro and in vivo r1 values and afforded excellent MR contrast enhancement. The particle surface was also modified with a silica shell to allow covalent attachment of a cyclic RGD peptide and an organic fluorophore. The cell-targeting molecules on the Mn NMOFs enhanced their delivery to cancer cells to allow for target-specific MR imaging in vitro. The MR contrast enhancement was also demonstrated in vivo using a mouse model. Such core-shell hybrid nanostructures provide an ideal platform for targeted delivery of other imaging and therapeutic agents to diseased tissues.

摘要

采用反相微乳液技术在室温下合成了具有可控形态的含锰纳米级金属有机框架(NMOF),并在120℃下通过微波加热采用表面活性剂辅助程序进行合成。使用包括SEM、TEM、TGA、PXRD和ICP-MS在内的多种方法对纳米颗粒进行了表征。尽管纳米颗粒基于每个锰原子给出了适度的纵向弛豫率(r1),但它们为大量Mn2+离子的递送提供了一种有效的载体,这些离子在体外和体内均表现出非常高的r1值,并提供了出色的磁共振对比增强效果。颗粒表面还用二氧化硅壳进行了修饰,以允许环状RGD肽和有机荧光团的共价连接。Mn NMOF上的细胞靶向分子增强了它们向癌细胞的递送,从而允许在体外进行靶向特异性磁共振成像。还使用小鼠模型在体内证明了磁共振对比增强。这种核壳杂化纳米结构为将其他成像和治疗剂靶向递送至患病组织提供了理想的平台。

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