Paramagnetic Mn8Fe4-co-Polystyrene Nanobeads as a Potential T1-T2 Multimodal Magnetic Resonance Imaging Contrast Agent with In Vivo Studies

被引:7
|
作者
Dahanayake, Vidumin [1 ]
Lyons, Trevor [1 ]
Kerwin, Brendan [1 ]
Rodriguez, Olga [2 ]
Albanese, Christopher [2 ,3 ]
Parasido, Erika [2 ]
Lee, Yichien [2 ]
Van Keuren, Edward [4 ]
Li, Luxi [5 ]
Maxey, Evan [5 ]
Paunesku, Tatjana [6 ]
Woloschak, Gayle [6 ]
Stoll, Sarah L. [1 ]
机构
[1] Georgetown Univ, Dept Chem, Washington, DC 20057 USA
[2] Georgetown Univ, Lombardi Comprehens Canc Ctr, Dept Oncol, Med Ctr, Washington, DC 20057 USA
[3] Georgetown Univ, Dept Radiol, Med Ctr, Washington, DC 20057 USA
[4] Georgetown Univ, Dept Phys, Washington, DC 20057 USA
[5] Argonne Natl Lab, Xray Sci Div, Adv Photon Source, Argonne, IL 60439 USA
[6] Northwestern Univ, Dept Radiat Oncol, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
MRI contrast agent; miniemulsion; cluster-nanocarrier; XRF microscopy; biocompatible; CELLULAR UPTAKE; POLYMERIC NANOPARTICLES; IRON-OXIDE; POLYSTYRENE NANOPARTICLES; MRI; GADOLINIUM; BIODISTRIBUTION; MANGANESE; SIZE; PHARMACOKINETICS;
D O I
10.1021/acsami.1c09232
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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 Mn8Fe4O12(O2CC6H4CH=CH2)(16)(H2O)(4), cross-linked with polystyrene (the nano-carrier), under miniemulsion conditions is described. By including a branched hydrophobe, iso-octane, the resulting nanobeads are porous and similar to 70 nm in diameter. The increased surface area of the nanobeads compared to nonporous nanobeads leads to an enhancement in relaxivity; r(1) increases from 3.8 to 5.2 +/- 0.1 mM(-1) s(-1), and r(2) increases from 11.9 to 50.1 +/- 4.8 mM(-1) s(-1), at 9.4 teslas, strengthening the potential for T-1 and T-2 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 vivo. In depth, physicochemical characteristics were determined, including extensive pharmacokinetics, in vivo imaging, and systemic biodistribution analysis.
引用
收藏
页码:39042 / 39054
页数:13
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