首页> 外文期刊>Bulletin of the Korean Chemical Society >Graphite Furnace Atomic Absorption Spectrophotometric Determination of Trace Horseradish Peroxidase Using Nanosilver
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Graphite Furnace Atomic Absorption Spectrophotometric Determination of Trace Horseradish Peroxidase Using Nanosilver

机译:纳米银-石墨炉原子吸收分光光度法测定痕量辣根过氧化物酶

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摘要

In pH 4.2 HAc-NaAc buffer solution, horseradish peroxidase (HRP) catalyzed H2O2 oxidation of nanosilver to form Ag~+. After centrifugation, Ag~+ in the supernatant can be measured by graphite furnace atomic absorption spectrophotometry (GFAAS) at the silver absorption wavelength of 328.1 nm. When HRP concentration increased, the Ag~+ concentration in the supernatant increased, and the absorption value enhanced. The HRP concentration in the range of 0.84-50 ng·mL~(-1) was linear to the enhanced absorption value (Δ4), with a regression equation of Δ4 = 0.012C+0.11, correlation coefficient of 0.9988, and detection limit of 0.41 ng·mL~(-1) HRP. The proposed GFAAS method was used to detect HRP in waste water samples, with satisfactory results.
机译:在pH 4.2 HAc-NaAc缓冲溶液中,辣根过氧化物酶(HRP)催化H2O2氧化纳米银,形成Ag〜+。离心后,可通过石墨炉原子吸收分光光度法(GFAAS)在328.1 nm的银吸收波长下测量上清液中的Ag〜+。当HRP浓度增加时,上清液中的Ag〜+浓度增加,吸收值增加。 HRP浓度在0.84-50 ng·mL〜(-1)范围内与增加的吸收值(Δ4)呈线性关系,回归方程为Δ4= 0.012C + 0.11,相关系数为0.9988,检出限为0.41 ng·mL〜(-1)HRP。所提出的GFAAS方法用于废水样品中HRP的检测,结果令人满意。

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