首页> 外文期刊>Journal of biological inorganic chemistry: JBIC: a publication of the Society of Biological Inorganic Chemistry >Immobilization of tyrosinase on Fe(3)o(4)@Au core-shell nanoparticles as bio-probe for detection of dopamine, phenol and catechol
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Immobilization of tyrosinase on Fe(3)o(4)@Au core-shell nanoparticles as bio-probe for detection of dopamine, phenol and catechol

机译:Fe(3)o(4)o(4)@ u(4)o(4)@ u(4)粒子 - 壳纳米粒子的固定化,作为检测多巴胺,苯酚和儿茶酚的生物探针

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摘要

An optical bio-probe based on the immobilized tyrosinase on the surface of Fe3O4@Au was described for the detection of dopamine, phenol and catechol. The prepared bio-probe (Fe3O4@Au@tyrosinase) was characterized by means such as TEM, SEM, VSM, DLS and TGA. In the presence of the bio-probe, the phenol, catechol and dopamine were converted to benzoquinone, o-quinone and dopaquinone, and the fluorescence spectra appeared at 308 nm, 329 nm and 336 nm with ex = 270 nm, respectively. However, by increasing the concentration of phenolic compounds in the bio-probe, the amount of products (benzoquinone, o-quinone and dopaquinone) was increased which was the reason for the increase in fluorescence intensity. Using this mechanism, a bio-probe was designed such that the intensity of the fluorescence spectra increased proportionally with the increase of the substrate concentrations after different time periods. The 0.003 mg/mL of tyrosinase was loaded on 1.65 mg/mL of the Fe3O4@Au. The highest performance for a bio-probe was demonstrated at room temperature and pH 6.8. By investigating the characteristics of the response of the bio-probe to different phenolic compounds, it was found that the bio-probe had a linear response in the concentration range 5.0-75.0 mu M, 10.0-100.0 mu M for phenol and dopamine and 50.0-500.0 M for catechol. The Michaelis-Menten constant (K-m) of the bio-probe was calculated as 0.6 mu M. Finally, the bio-probe seems to be stable and efficient even after about 2 months. Graphic abstract A novel and easy method for the detection of dopamine, phenol and catechol by florescence that uses oxide capability to identify the phenolic compounds was introduced.
机译:描述了基于Fe3O4 @ Au表面上的固定酪氨酸酶的光学生物探针用于检测多巴胺,苯酚和儿茶酚。通过TEM,SEM,VSM,DLS和TGA,表征制备的生物探针(Fe3O4 @ Au @酪氨酸酶)的特征在于。在生物探针存在下,将苯酚,儿茶酚和多巴胺转化为苯醌,醌和多醌,荧光光谱分别以308nm,329nm和336nm出现在ex = 270nm处。然而,通过增加生物探针中酚类化合物的浓度,增加产物(苯并醌,O-醌和多醌),这是荧光强度增加的原因。使用该机制,设计了一种生物探针,使得荧光光谱的强度随着在不同时间段之后的基材浓度的增加而比例增加。将0.003mg / ml酪氨酸酶加载到1.65mg / ml的Fe 3 O 4 @ Au上。在室温和pH 6.8时对生物探针的最高性能进行说明。通过研究生物探针对不同酚类化合物的响应的特征,发现生物探针在浓度范围内具有线性响应5.0-75.0μm,10.0-100.0μm的苯酚和多巴胺和50.0 -500.0 m用于儿茶酚。将生物探针的迈克莱斯 - 麦片常数(K-M)计算为0.6μm。最后,即使在大约2个月后,生物探针似乎也稳定和有效。图形摘要引入了一种用氟化荧光检测多巴胺,苯酚和儿茶酚的一种新颖简便的方法,用于鉴定鉴定酚类化合物的荧光性。

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