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A Simple and Cost-effective Microfluidic Paper-Based Biosensor Analytical Device and its Application for Hypoxanthine Detection in Meat Samples

机译:一种简单且经济高效的微流体纸体生物传感器分析装置及其在肉类样品中缺氧检测的应用

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摘要

In this paper, we combined lab-on-paper technology with biosensor techniques to fabricate a new analytical tool for hypoxanthine detection. The combination of these two technologies produces a quick, selective, and cost-effective analytical metrology for detection of hypoxanthine in meat samples. The paper-based colorimetric biosensor was developed based on dienzyme catalytic reactions. In presence of hypoxanthine, xanthine oxidase (XOD) catalyzes to form hydrogen peroxide (H2O2). Then H2O2 couples with o-dianisidine in the presence of horseradish peroxidase (HRP), resulting in a brown color. The color intensity of the detection zone on the paper was imaged using a scanner. For quantitative analysis of hypoxanthine, the images of the colorimetric results were analyzed with ImageJ software using a blue histogram. Under optimum conditions, the developed paper-based biosensor was found to detect hypoxanthine with a detection limit of 1.8 mg L-1 and a quantitative limit of 6.1 mg L-1. The proposed assay exhibited a linear dynamic in the range of 5-40 mg L-1. The analysis time was 5 min for triplicate measurement. This method was further evaluated by measuring the recovery of hypoxanthine added to meat samples. Finally, this method was applied to detect hypoxanthine in fresh and processed meat samples, and the results were validated against spectrophotometric detection, showing good accuracy. This simple method is cost-effective and requires no advanced instruments, offering an alternative to conventional methods.
机译:在本文中,我们将实验室技术与生物传感器技术合并制造新的次黄嘌呤检测的新分析工具。这两种技术的组合产生了一种快速,选择性和具有成本效益的分析计量,用于检测肉类样品中的次黄嘌呤。基于纸的比色生物传感器是基于Dizyme催化反应开发的。在次黄嘌呤存在下,黄嘌呤氧化酶(XOD)催化形成过氧化氢(H 2 O 2)。然后在辣根过氧化物酶(HRP)存在下与O-Dianisidine进行H2O2夫妇,导致棕色。使用扫描仪对纸张上的检测区域的颜色强度进行成像。对于缺氧素的定量分析,使用蓝色直方图与ImageJ软件分析了比色结果的图像。在最佳条件下,发现初发纸的生物传感器检测缺氧,检测限为1.8mg L-1的定量限制为6.1mg L-1。所提出的测定在5-40mg L-1的范围内显示出线性动态。分析时间为三次测量时间为5分钟。通过测量添加到肉样品中的次黄嘌呤的回收来进一步评估该方法。最后,将该方法应用于新鲜和加工肉类样品中的次黄嘌呤,并验证了分光光度检测,结果效果良好。这种简单的方法具有成本效益,不需要先进的仪器,提供传统方法的替代方法。

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