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Preparation, characterization, and magnetic resonance imaging of Fe nanowires

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(2) by sol–gel method to i...

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Detalles Bibliográficos
Autores principales: Cao, Xiaoming, Hu, Shike, Zheng, Hua, Mukhtar, Aiman, Wu, KaiMing, Gu, Liyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615998/
https://www.ncbi.nlm.nih.gov/pubmed/37903989
http://dx.doi.org/10.1186/s11671-023-03916-3
Descripción
Sumario: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(2) 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(2) nanowires were evaluated. The study revealed that the SiO(2)-coated Fe nanowires functioned effectively as transverse relaxation time (T(2)) contrast agents (CAs). Notably, as the length of the Fe@SiO(2) nanowires increased, their diameter decreased, leading to a higher the transverse relaxivity (r(2)) value. Our study identified that among the Fe nanowires synthesized, the Fe3@SiO(2) nanowires, characterized by a diameter of around 30 nm and a length of approximately 500 nm, exhibited the highest r(2) value of 59.3 mM(−1) s(−1). 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(2) nanowires as T(2) CAs, with the possibility of tuning their size for optimized results.