Ultra-small manganese dioxide nanoparticles with high T 1 relaxivity for magnetic resonance angiography
Gadolinium (Gd)-based contrast agents (CAs) for clinical magnetic resonance imaging are facing the problems of low longitudinal relaxivity ( ) and toxicity caused by gadolinium deposition. Manganese-based small molecule complexes and manganese oxide nanoparticles (MONs) are considered as potential a...
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Veröffentlicht in: | Biomaterials science 2023-06, Vol.11 (12), p.4359-4369 |
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Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Gadolinium (Gd)-based contrast agents (CAs) for clinical magnetic resonance imaging are facing the problems of low longitudinal relaxivity (
) and toxicity caused by gadolinium deposition. Manganese-based small molecule complexes and manganese oxide nanoparticles (MONs) are considered as potential alternatives to Gd-based CAs due to their better biocompatibility, but their relatively low
values and complicated synthesis routes slow down their clinical translation. Herein, we presented a facile one-step co-precipitation method to prepare MONs using poly(acrylic acid) (PAA) as a coating agent (MnO
/PAA NPs), which exhibited good biocompatibility and high
values. A series of MnO
/PAA NPs with different particle sizes were prepared and the relationship between the particle size and
was studied, revealing that the MnO
/PAA NPs with a particle size of 4.9 nm exhibited higher
. The finally obtained MnO
/PAA NPs had a high
value (29.0 Mn mM
s
) and a low
/
ratio (1.8) at 1.5 T, resulting in a strong
contrast enhancement.
magnetic resonance angiography with Sprague-Dawley (SD) rats further proved that the MnO
/PAA NPs showed better angiographic performance at low-dosage administration than commercial Gadovist® (Gd-DO3A-Butrol). Moreover, the MnO
/PAA NPs could be rapidly cleared out after imaging, which effectively minimized the toxic side effects. The MnO
/PAA NPs are promising candidates for MR imaging of vascular diseases. |
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ISSN: | 2047-4830 2047-4849 |
DOI: | 10.1039/d3bm00443k |