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Enzymatic Synthesis of Magnetic Nanoparticles

机译:酶法合成磁性纳米粒子

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We report the first in vitro enzymatic synthesis of paramagnetic and antiferromagnetic nanoparticles toward magnetic ELISA reporting. With our procedure, alkaline phosphatase catalyzes the dephosphorylation of l-ascorbic-2-phosphate, which then serves as a reducing agent for salts of iron, gadolinium, and holmium, forming magnetic precipitates of Fe45±14Gd5±2O50±15 and Fe42±4Ho6±4O52±5. The nanoparticles were found to be paramagnetic at 300 K and antiferromagnetic under 25 K. Although weakly magnetic at 300 K, the room-temperature magnetization of the nanoparticles found here is considerably greater than that of analogous chemically-synthesized LnxFeyOz (Ln = Gd, Ho) samples reported previously. At 5 K, the nanoparticles showed a significantly higher saturation magnetization of 45 and 30 emu/g for Fe45±14Gd5±2O50±15 and Fe42±4Ho6±4O52±5, respectively. Our approach of enzymatically synthesizing magnetic labels reduces the cost and avoids diffusional mass-transfer limitations associated with pre-synthesized magnetic reporter particles, while retaining the advantages of magnetic sensing.
机译:我们报告了顺磁性和反铁磁性纳米粒子的首次体外酶法合成,向磁性ELISA报告。按照我们的程序,碱性磷酸酶催化l-抗坏血酸2-磷酸的脱磷酸作用,然后将其用作铁盐,g盐和盐的还原剂,形成Fe 45±14 的磁性沉淀Gd 5±2 O 50±15 和Fe 42±4 Ho 6±4 O 52 ±5 。发现该纳米粒子在300 K下为顺磁性,在25 K下为反铁磁性。尽管在300 K下为弱磁性,但此处发现的纳米粒子的室温磁化强度远大于化学合成的Ln x Fe y O z (Ln = Gd,Ho)样品。在5 K下,Fe 45±14 Gd 5±2 O 50±15 < / sub>和Fe 42±4 Ho 6±4 O 52±5 。我们通过酶法合成磁性标记的方法降低了成本,并避免了与预合成的磁性报告分子相关的扩散传质限制,同时保留了磁传感的优势。

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