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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Cyclovoltammetric acetylcholinesterase activity assay after inhibition and subsequent reactivation by using a glassy carbon electrode modified with palladium nanorods composited with functionalized C-60 fullerene
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Cyclovoltammetric acetylcholinesterase activity assay after inhibition and subsequent reactivation by using a glassy carbon electrode modified with palladium nanorods composited with functionalized C-60 fullerene

机译:抑制后的环伏安氏乙酰胆碱酯酶活性测定,然后通过使用钯纳米棒修饰的玻碳电极修饰碳原子,该钯纳米棒与功能化的C-60富勒烯复合

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摘要

A glassy carbon electrode (GCE) was modified with a nanocomposite consisting of tetraoctylammonium bromide (TOAB), C-60 fullerene, and palladium nanorods (PdNRs). The PdNRs were hydrothermally prepared and had a typical width of 20 +/- 2 nm. The nanocomposite forms stable films on the GCE and exhibits a reversible redox pair for the C-60/C-60 (-) system while rendering the surface to be positively charged. The modified GCE was applied to fabricate an electrochemical biosensor for detecting acetylcholinesterase (AChE) by measurement of the amount of thiocholine formed from acetylthiocholine, best at a working voltage of -0.19 V (vs. SCE). The detection scheme is based on (a) measurement of the activity of ethyl paraoxon-inhibited AChE, and (b) measurement of AChE activity after reactivation with pralidoxime (2-PAM). Compared to the conventional methods using acetylthiocholine as a substrate, the dual method presented here provides data on the AChE activity after inhibition and subsequent reactivation, thereby yielding credible data on reactivated enzyme activity. The linear analytical range for AChE activity extends from 2.5 U L-1 to 250 kU center dot L-1, and the detection limit is 0.83 U L-1.
机译:玻碳电极(GCE)用由四辛基溴化铵(TOAB),C-60富勒烯和钯纳米棒(PdNRs)组成的纳米复合材料改性。 PdNRs是水热制备的,其典型宽度为20 +/- 2 nm。纳米复合材料在GCE上形成稳定的膜,并在C-60 / C-60(-)体系中表现出可逆的氧化还原对,同时使表面带正电。修饰的GCE应用于制造电化学生物传感器,以通过测量乙酰乙酰胆碱形成的巯胆碱的量来检测乙酰胆碱酯酶(AChE),最好在-0.19 V(vs. SCE)的工作电压下进行。该检测方案基于(a)对乙基对氧磷抑制的AChE活性的测量,以及(b)对吡咯肟(2-PAM)活化后的AChE活性的测量。与使用乙酰硫胆碱作为底物的常规方法相比,此处介绍的双重方法提供了抑制和随后的再活化后有关AChE活性的数据,从而获得了有关再活化酶活性的可靠数据。 AChE活性的线性分析范围从2.5 U L-1扩展到250 kU中心点L-1,检测极限为0.83 U L-1。

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