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Paramagnetic Mn 8 Fe 4 - co -Polystyrene Nanobeads as a Potential T 1 -T 2 Multimodal Magnetic Resonance Imaging Contrast Agent with In Vivo Studies.

Authors :
Dahanayake V
Lyons T
Kerwin B
Rodriguez O
Albanese C
Parasido E
Lee Y
Keuren EV
Li L
Maxey E
Paunesku T
Woloschak G
Stoll SL
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2021 Aug 25; Vol. 13 (33), pp. 39042-39054. Date of Electronic Publication: 2021 Aug 10.
Publication Year :
2021

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 Mn <subscript>8</subscript> Fe <subscript>4</subscript> O <subscript>12</subscript> (O <subscript>2</subscript> CC <subscript>6</subscript> H <subscript>4</subscript> CH═CH <subscript>2</subscript> ) <subscript>16</subscript> (H <subscript>2</subscript> O) <subscript>4</subscript> , 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; r <subscript>1</subscript> increases from 3.8 to 5.2 ± 0.1 mM <superscript>-1</superscript> s <superscript>-1</superscript> , and r <subscript>2</subscript> increases from 11.9 to 50.1 ± 4.8 mM <superscript>-1</superscript> s <superscript>-1</superscript> , at 9.4 teslas, strengthening the potential for T <subscript>1</subscript> and T <subscript>2</subscript> 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.

Details

Language :
English
ISSN :
1944-8252
Volume :
13
Issue :
33
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
34375073
Full Text :
https://doi.org/10.1021/acsami.1c09232