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Preparation, characterization, and magnetic resonance imaging of Fe nanowires.
- Source :
- Discover Nano; 10/31/2023, Vol. 18 Issue 1, p1-16, 16p
- Publication Year :
- 2023
-
Abstract
- A facile template method was employed to synthesize Fe nanowires of different sizes, dimensions. Comprehensive analyses were conducted to explore their morphology, structure, composition, and magnetic properties. The surface of as-prepared Fe nanowires was modified with SiO<subscript>2</subscript> by sol–gel method to improve the dispersion of as-prepared Fe nanowires in aqueous solution. Furthermore, the relaxation properties, biocompatibility and in vivo imaging abilities of the Fe@SiO<subscript>2</subscript> nanowires were evaluated. The study revealed that the SiO<subscript>2</subscript>-coated Fe nanowires functioned effectively as transverse relaxation time (T<subscript>2</subscript>) contrast agents (CAs). Notably, as the length of the Fe@SiO<subscript>2</subscript> nanowires increased, their diameter decreased, leading to a higher the transverse relaxivity (r<subscript>2</subscript>) value. Our study identified that among the Fe nanowires synthesized, the Fe3@SiO<subscript>2</subscript> nanowires, characterized by a diameter of around 30 nm and a length of approximately 500 nm, exhibited the highest r<subscript>2</subscript> value of 59.3 mM<superscript>−1</superscript> s<superscript>−1</superscript>. These nanowires demonstrated good biocompatibility and non-toxicity. Notably, upon conducting small animal imaging a 1.5 T with Sprague–Dawley rats, we observed a discernible negative enhancement effect in the liver. These findings indicate the promising potential of Fe@SiO<subscript>2</subscript> nanowires as T<subscript>2</subscript> CAs, with the possibility of tuning their size for optimized results. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 27319229
- Volume :
- 18
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Discover Nano
- Publication Type :
- Academic Journal
- Accession number :
- 173340301
- Full Text :
- https://doi.org/10.1186/s11671-023-03916-3