利用酶促反应和化学发光法测定动物血清中葡萄糖的多换流系统。

Cherrine K Pires, Patrícia B Martelli, Boaventura F Reis, José L F C Lima, Maria Lúcia M F S Saraiva
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引用次数: 8

摘要

描述了一种基于多交换的自动流动程序,用于使用葡萄糖氧化酶与化学发光检测测定动物血清中的葡萄糖。流量歧管由一组三通电磁阀组合而成,实现多换向。一台配有电子接口和用Quick BASIC 4.5编写的软件的微机控制流形并进行数据采集。葡萄糖氧化酶固定在多孔硅珠(玻璃氨丙基)上,装在一个小柱(15 x 5 mm)中。该过程基于葡萄糖的酶降解,产生过氧化氢,过氧化氢在六氰高铁酸盐(III)存在下氧化发光氨,引起化学发光。通过分析一组未经事先处理的血清动物样本对该系统进行了测试。结果与常规方法(LABTEST Kit)的结果在95%的置信水平上一致。检出限和变异系数分别为12.0 mg l(-1)(99.7%置信水平)和3.5% (n = 20)。采样率约为60次h(-1),样品浓度为50 ~ 600 mg l(-1)葡萄糖。血清样品、六氰高铁酸盐(III)和鲁米诺的消耗量分别为46 μ l、10.0 mg和0.2 mg/次。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multicommuted flow system for the determination of glucose in animal blood serum exploiting enzymatic reaction and chemiluminescence detection.

An automatic flow procedure based on multicommutation dedicated for the determination of glucose in animal blood serum using glucose oxidase with chemiluminescence detection is described. The flow manifold consisted of a set of three-way solenoid valves assembled to implement multicommutation. A microcomputer furnished with an electronic interface and software written in Quick BASIC 4.5 controlled the manifold and performed data acquisition. Glucose oxidase was immobilized on porous silica beads (glass aminopropyl) and packed in a minicolumn (15 x 5 mm). The procedure was based on the enzymatic degradation of glucose, producing hydrogen peroxide, which oxidized luminol in the presence of hexacyanoferrate(III), causing the chemiluminescence. The system was tested by analysing a set of serum animal samples without previous treatment. Results were in agreement with those obtained with the conventional method (LABTEST Kit) at the 95% confidence level. The detection limit and variation coefficient were estimated as 12.0 mg l(-1) (99.7% confidence level) and 3.5% (n = 20), respectively. The sampling rate was about 60 determinations h(-1) with sample concentrations ranging from 50 to 600 mg l(-1) glucose. The consumptions of serum sample, hexacyanoferrate(III) and luminol were 46 microl, 10.0 mg and 0.2 mg/determination, respectively.

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