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Amperometric detection of Uric Acid and Hypoxantine with Xanthine oxidase immobilized and carbon based screen-printed electrode for fish freshness determination

机译:用黄嘌呤氧化酶固定化和碳基丝网印刷电极进行尿酸和低氧式的尿酸和低氧式检测,用于鱼类新鲜度测定

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A continuous system for the detemination of fish freshness with carbon-based screen-printed electrode was developed and applied to the determination of the freshness indicator K = 100 (HxR + Hx) / (IMP + HxR + Hx), where IMP, HxR and Hx are Inosine monophosphate. Inosine and Hypoxanthine, respectively. Hypoxanthine and related compounds determination was based on Uric acid (AU) detection at a potential of 450 mV vs Ag/AgCl. Xanthine oxidase (XO) was immobilized in a reactor with CPG aminopropylsilane in a FLA assembly. Higher reproducibility and lifetime was obtained and optimum conditions were found for the determination of AU, Hx, HxR and IMP. Calibration graphs are linear up to 50 muM with detection limit of 1 muM for 50 mul injection. One assay is completed within 30 seconds. The reproducibility of 20 muM of Hx was obtaned with CV 2percent.
机译:开发了用碳基丝网印刷电极进行了防范鱼类新鲜度的连续系统,并施加到新鲜指标K = 100(HXR + HX)/(Imp + HXR + HX)的测定,其中Imp,HXR和 HX是单磷酸肌苷。 分别分别为肌苷和缺氧。 缺氧素和相关化合物测定基于450mV Vs Ag / AgCl的潜在尿酸(Au)检测。 将黄嘌呤氧化酶(XO)固定在用CPG氨基丙基硅烷中的反应器中固定在FLA组件中。 获得了更高的再现性和寿命,发现了Au,Hx,HXR和Imp的测定。 校准图是线性的,最高可达50毫米,检测限为1毫米,50多米喷射。 一个测定在30秒内完成。 用CV 2percent进行20毫米HX的再现性。

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