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顺磁性 MnFe--聚苯乙烯纳米微球作为一种潜在的 T1-T2 多模态磁共振成像对比剂的研究。

Paramagnetic MnFe--Polystyrene Nanobeads as a Potential T-T Multimodal Magnetic Resonance Imaging Contrast Agent with Studies.

机构信息

Department of Chemistry, Georgetown University, 37th and O Streets NW, Washington, D.C. 20057, United States.

Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, D.C. 20057, United States.

出版信息

ACS Appl Mater Interfaces. 2021 Aug 25;13(33):39042-39054. doi: 10.1021/acsami.1c09232. Epub 2021 Aug 10.

Abstract

In developing a cluster-nanocarrier design, as a magnetic resonance imaging contrast agent, we have investigated the enhanced relaxivity of a manganese and iron-oxo cluster grafted within a porous polystyrene nanobead with increased relaxivity due to a higher surface area. The synthesis of the cluster-nanocarrier for the cluster MnFeO(OCCHCH═CH)(HO), cross-linked with polystyrene (the nanocarrier), under miniemulsion conditions is described. By including a branched hydrophobe, -octane, the resulting nanobeads are porous and ∼70 nm in diameter. The increased surface area of the nanobeads compared to nonporous nanobeads leads to an enhancement in relaxivity; increases from 3.8 to 5.2 ± 0.1 mM s, and increases from 11.9 to 50.1 ± 4.8 mM s, at 9.4 teslas, strengthening the potential for T and T imaging. Several metrics were used to assess stability, and the porosity produced no reduction in metal stability. Synchrotron X-ray fluorescence microscopy was used to demonstrate that the nanobeads remain intact . In depth, physicochemical characteristics were determined, including extensive pharmacokinetics, imaging, and systemic biodistribution analysis.

摘要

在开发一种簇纳米载体设计时,我们将作为磁共振成像造影剂,研究了在具有更高表面积的多孔聚苯乙烯纳米珠内接枝的锰和铁氧簇的增强弛豫率。描述了在 miniemulsion 条件下合成簇纳米载体(纳米载体)的簇 MnFeO(OCCHCH═CH)(HO)。通过包含支化疏水性物质-辛烷,得到的纳米珠是多孔的,直径约为 70nm。与非多孔纳米珠相比,纳米珠的表面积增加导致弛豫率增强;在 9.4 特斯拉下,从 3.8 增加到 5.2±0.1mM·s-1,从 11.9 增加到 50.1±4.8mM·s-1,增强了 T1 和 T2 成像的潜力。使用了几种指标来评估稳定性,并且孔隙率并没有降低金属的稳定性。同步加速器 X 射线荧光显微镜被用来证明纳米珠保持完整。深入研究了理化特性,包括广泛的药代动力学、成像和系统生物分布分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/453e/10506655/33453104095d/nihms-1926368-f0001.jpg

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