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Development of enzyme-based bar code-style lateral-flow assay for hydrogen peroxide determination

机译:用于双氧水测定的基于酶的条形码式侧流测定法的开发

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A unique approach of developing a bar code version of lateral-flow enzymatic-based assay for the semi-quantification of hydrogen peroxide is described.The proposed assay system is mainly composed of a goat anti-mouse IgG-horseradish peroxidase conjugate(Gt anti-M IgG-HRP)-coated nitrocellulose(NC)membrane and a peroxidase substrate pad.Unlike the bar code immunochromatographic assay which depends on the stepwise capture of analyte,the principle of enzyme-based bar code lateral-flow assay is based on the different reaction time on successive lines due to the delay in 3,3',5,5'-tetramethylbenzidine(TMB)release.Hydrogen peroxide(H2O2)acts as a limiting factor which controls the rate of the enzymatic conversion of TMB to blue color complex.The system expresses the concentration of H2O2 in micromole range as three distinct ladder bars in 9 min therefore without the need of any reading device.The major advantages of this assay are its easily readable result,and also its simplicity and low-cost in production offers a cheaper alternative for testing those expensive biosensors might not be available to the third world countries.By incorporating with H2O2-generating oxidoreductases,the assay can be further extended to detect a variety of analytes with clinical and environmental importance.Glucose was chosen to be the model analyte where the proposed system gave signal response at between 5 mu M and 100 mu M.
机译:本文介绍了一种开发条形码形式的基于侧向酶的半定量过氧化氢检测方法的独特方法,该检测系统主要由山羊抗小鼠IgG-辣根过氧化物酶偶联物(Gt抗M IgG-HRP)包裹的硝酸纤维素(NC)膜和过氧化物酶底物垫。与条形码免疫色谱法不同,该方法依赖于逐步捕获分析物,而基于酶的条形码侧流法的原理是基于不同的由于3,3',5,5'-四甲基联苯胺(TMB)的释放延迟而导致连续生产线上的反应时间过氧化氢(H2O2)是一个限制因素,控制着TMB酶促转化为蓝色络合物的速率该系统可在9分钟内将微摩尔范围内的H2O2浓度表示为三个不同的梯形条,因此无需任何读取设备。该测定法的主要优点是其易于读取的结果,简单易行,低干扰生产中的st提供了一种更便宜的替代品来测试那些昂贵的生物传感器,而第三世界国家可能无法获得。通过与生成H2O2的氧化还原酶结合使用,该检测方法可以进一步扩展,以检测具有临床和环境重要性的各种分析物。被选为模型分析物,其中拟议系统在5μM和100μM之间产生信号响应。

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