TY - JOUR
T1 - Paramagnetic Mn8Fe4- co-Polystyrene Nanobeads as a Potential T1-T2Multimodal Magnetic Resonance Imaging Contrast Agent with in Vivo Studies
AU - Dahanayake, Vidumin
AU - Lyons, Trevor
AU - Kerwin, Brendan
AU - Rodriguez, Olga
AU - Albanese, Christopher
AU - Parasido, Erika
AU - Lee, Yichien
AU - Keuren, Edward Van
AU - Li, Luxi
AU - Maxey, Evan
AU - Paunesku, Tatjana
AU - Woloschak, Gayle
AU - Stoll, Sarah L.
N1 - Funding Information:
This work was supported by the National Institutes of Health grants R15 EB025538-01A1 and P30 CA 051008-25 and by the Sonneborn Chair (S.L.S., C.A., and E.V.K.). Work at the Advanced Photon Source at the Argonne National Laboratory was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences contract DE-AC02-06CH11357. The authors would like to acknowledge the use of the Georgetown Lombardi Microscopy and Imaging, Flow Cytometry, the Preclinical Imaging Research Laboratory, and the Tissue Culture and Biobanking Shared Resources.
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/8/25
Y1 - 2021/8/25
N2 - 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 nanocarrier), under miniemulsion conditions is described. By including a branched hydrophobe, iso-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; r1 increases from 3.8 to 5.2 ± 0.1 mM-1 s-1, and r2 increases from 11.9 to 50.1 ± 4.8 mM-1 s-1, at 9.4 teslas, strengthening the potential for T1 and T2 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.
AB - 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 nanocarrier), under miniemulsion conditions is described. By including a branched hydrophobe, iso-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; r1 increases from 3.8 to 5.2 ± 0.1 mM-1 s-1, and r2 increases from 11.9 to 50.1 ± 4.8 mM-1 s-1, at 9.4 teslas, strengthening the potential for T1 and T2 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.
KW - MRI contrast agent
KW - XRF microscopy
KW - biocompatible
KW - cluster-nanocarrier
KW - miniemulsion
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U2 - 10.1021/acsami.1c09232
DO - 10.1021/acsami.1c09232
M3 - Article
C2 - 34375073
AN - SCOPUS:85114020037
SN - 1944-8244
VL - 13
SP - 39042
EP - 39054
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 33
ER -