首页> 外文期刊>International Journal of Pharmaceutics >Long-term investigation on the phase stability, magnetic behavior, toxicity, and MRI characteristics of superparamagnetic Fe/Fe-oxide core/shell nanoparticles
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Long-term investigation on the phase stability, magnetic behavior, toxicity, and MRI characteristics of superparamagnetic Fe/Fe-oxide core/shell nanoparticles

机译:长期研究超顺磁性Fe / Fe-氧化物核/壳纳米粒子的相稳定性,磁行为,毒性和MRI特性

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To efficiently enhance the contrast obtaining from magnetic resonance imaging (MRI), pharmaceutical grade colloidal dispersions of PEG coated iron-based nanoparticles were prepared and compared to conventional pure iron oxide contrast agent. In this study, we synthesized ~14 nm iron nanoparticles via NaBH4 reduction of iron(III) chloride in an aqueous medium. The resulting nanoparticles were further oxidized by two different methods via (CH3)3NO oxygen transferring agent and exposure to oxygen flow. XRD and electron microscopy analyses confirmed the formation of a second layer on the surface of α-Fe core. As magnetic measurements and M?ssbauer spectra of 4-months post prepared nanoparticles showed, 2.3 ± 0.5 nm amorphous oxide shell produced in oxygen flow could not protect the inner metallic iron from oxidation and resulting sample suffered from drastic change in its characteristics. However, (CH3) 3NO yielded nanoparticles with 3.6 ± 0.4 and 4.5 ± 0.7 nm crystalline oxide shells that retained their key properties even in long-term examinations. In addition, no significant difference was detected in cytotoxicity results of MTT assay test up to 4-months for core/shell nanoparticles, in comparison with pure iron oxide sample, and all fall below 50% viability in the iron concentration of 400 μg. In vitro MR signal reduction and corresponding relaxometry parameters, especially r2/r1 2, assure that all nanoparticles can be administrated for negative contrast enhancement. Accumulation of core/shell nanoparticles in axillary and brachial lymph nodes of examined rats and minimum contrast enhancement of 20% regarding to pure iron oxide implies the efficiency of these materials as potential contrast agent.
机译:为了有效增强从磁共振成像(MRI)获得的对比度,制备了PEG包被的铁基纳米颗粒的药物级胶体分散体,并将其与常规的纯氧化铁造影剂进行了比较。在这项研究中,我们通过在水性介质中用NaBH4还原氯化铁(III)合成了〜14 nm的铁纳米颗粒。通过两种不同的方法,通过(CH 3)3 NO氧转移剂和暴露于氧气流,进一步氧化所得的纳米颗粒。 XRD和电子显微镜分析证实了在α-Fe核的表面上形成了第二层。如制备的纳米粒子经过4个月的磁性测量和Msssbauer光谱显示,氧气流中产生的2.3±0.5 nm无定形氧化物壳无法保护内部金属铁免于氧化,从而导致样品的特性发生剧烈变化。但是,(CH3)3NO生成的纳米粒子具有3.6±0.4和4.5±0.7 nm的结晶氧化物壳,即使在长期检查中也能保持其关键性能。此外,与纯氧化铁样品相比,对于核/壳纳米颗粒,长达4个月的MTT分析测试的细胞毒性结果未发现显着差异,并且在400μg铁浓度下均低于50%的活力。体外MR信号降低和相应的弛豫参数,尤其是r2 / r1> 2,确保可以对所有纳米颗粒进行负对比度增强。被检查大鼠腋窝和臂部淋巴结中核/壳纳米颗粒的积累以及相对于纯氧化铁的最低20%的对比度增强意味着这些材料作为潜在的造影剂的效率。

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