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出 处:《青岛化工学院学报(自然科学版)》1999年第4期332-339,共8页Journal of Qingdao Institute of Chemical Technology(Natural Science Edition)
摘 要:提出了邻氨基酚(OAP)-H2O2-辣根过氧化物酶(HRP)伏安酶联免疫分析新体系并用于测定HRP及HRP标注物。HRP催化H2O2氧化OAP生成的中间产物邻苯醌亚胺在BR缓冲液中,在-0.87V(vs.SCE)处产生灵敏的极谱波。应用此极谱波测定HRP的检出限达到3.5×10-12g/mL,线性范围为6.0×10-12~4.0×10-9g/mL。对此酶催化反应产物的电极还原过程也进行了详细的探讨。A voltammetric enzyme - linked immunoassay based on a newsystem of o - aminophenol (OAP) - H2O2 - horseradish peroxidase (HRP) hasbeen used in the detection of HRP and labelled HRP. By this method, the enzyme- catalyzed reaction of OAP with H2O2 catalyzed by HRP generates anintermediate product o - benzoquinone imine, which produces a sensitivevoltarnmetric peak at - O. 87 V (vs. SCE ) in Britton - Robinson (BR) buffersolution. By using this voltammetric peak, HRP can be measured with a detectionlimit of 3. 5 X 1O- 12 g/mL and a linear range of 6. 0 x l0-12 ~ 4. 0 x 1O -9g/mL. The process of the electroreduction of the product of the enzyme - catalyzedreaction was discussed.
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