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A.C. Amperometric Method for Lipase Activity Quantification

机译:A.C.脂肪酶活性定量的余量法

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The working electrode modification applying some specific modifiers results in capacitors formationnot related to the charges exchange occurring and double layer formation at the electrode – solutioninterface. Chemical or biochemical processes involving the modification layer cause its thicknessvariations leading to capacitance changes resulting in AC amperometric response. An ACamperometric method for lipase activity quantification based on this approach was developed andcharacterized. A thin layer of nanocomposite (SiO2 nanoparticles charged olive oil) deposited on theworking electrode served as both: sensitive layer toward the lipase and dielectric layer of anelectrolytic capacitor formed on the electrode – solution interface. The nanocomposite enzymaticdegradation by the lipase causes its thickness decrease proportional to the lipase activity and acorresponding rise of the AC current is registered as analytical response by AC amperometry at fixedsmall AC amplitude (100 mV p.p.) and frequency of 240 Hz. The developed method was characterizedin terms of: LOD, sensitivity, linear quantification range, precision, response time and reproducibility,as well as was validated by spiked samples determination using the standardized titrimetric method asreference..
机译:施加一些特定改性剂的工作电极改性导致电容器形成有关电荷交换的电容器和电极在电极的双层形成。涉及修改层的化学或生化过程导致其厚度变化导致电容变化导致AC电流响应。基于该方法的脂肪酶活性定量的脂肪酶活性定量的杂种素法。薄层的纳米复合材料(SiO2纳米颗粒带电橄榄油)沉积在工业电极上,其两者兼作:敏感层朝向在电极溶液界面上形成的电氢电容器的脂肪酶和介电层。通过脂肪酶的纳米复合酶致癌成比例与脂肪酶活性成比例的厚度降低,并且AC电流的ACrorm对应的升高被AC Amperometry在固定式AC幅度(100mV P.P.)处注册为分析响应,并且240Hz的频率。开发方法的特征在于:LOD,灵敏度,线性量化范围,精度,响应时间和再现性,以及使用标准化滴定法缺点的尖刺样品确定的验证。

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