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Determination of Urea in Serum Based on the Combination of an Enzymatic Reaction with Immobilized Urease and Ion Chromatographic Analysis

机译:酶促反应与固定化脲酶联用和离子色谱法联用测定血清中的尿素

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A quantitative method for the determination of urea in serum was studied. An ion chromatograph (IC) with a conductivity detector was used in this method, where the chromatograph was modified by placing an immobilized urease column between the injection loop and a guard column of the cation analysis column. Immobilized urease was prepared by the adsorption of urease on cedar sawdust with triethylenetetramine. The adsorption capacity of urease was 190 mg g~(?1), and its activity was 3500 U g~(?1). The conversion efficiency of urea to ammonium ion was 100%, and the half life of immobilized urease was 60 days. It was possible to use the immobilized urease in a pH range of 3.0 to 9.0, and at temperatures up to 60°C. The determination of urea was attempted by IC attaching an immobilized urease column. The limit of detection of urea was 0.2 mg L~(?1), and the calibration curves of urea were very linear over 0.8 ? 25 mg L~(?1). The urea concentration in the human serum could be determined with a standard deviation of 0.06 ? 0.13 within 5 min after injecting the serum sample.
机译:研究了测定血清中尿素的定量方法。此方法使用带有电导检测器的离子色谱仪(IC),其中通过在注入环和阳离子分析柱的保护柱之间放置固定的脲酶柱对色谱仪进行修改。通过用三亚乙基四胺将雪松木屑上的脲酶吸附来制备脲酶。脲酶的吸附容量为190mg g·(·1),其活性为3500U g·(·1)。尿素向铵离子的转化效率为100%,固定化脲酶的半衰期为60天。可以在3.0到9.0的pH范围内以及高达60°C的温度下使用固定的脲酶。通过连接固定化脲酶色谱柱的IC尝试测定尿素。尿素的检出限为0.2 mg L〜(?1),尿素的校正曲线在0.8?L以上呈线性关系。 25 mg L〜(?1)。人血清中尿素浓度的标准偏差可以确定为0.06?注射血清样品后5分钟内0.13。

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