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机构地区:[1]山西大学化学化工学院
出 处:《分析试验室》2006年第12期35-38,共4页Chinese Journal of Analysis Laboratory
基 金:山西省自然科学基金(20041015)项目资助
摘 要:以电化学法和光度法对酸性橙Ⅱ(AOⅡ)与牛血清白蛋白(BSA)的相互作用进行了研究。在pH7.20的Tris—HCl缓冲溶液中,AOⅡ有一灵敏的还原峰,峰电位Ep约为-0.69V(vs.SCE),加入BSA后AOⅡ还原峰电位正移,峰电流下降,据此建立了一种测定BSA的电分析方法。在优化条件下,峰电流下降值与BsA的浓度在5.0×10^-8 -1.0×10^-5 mol/L(r=0.9900-0.9939)范围内呈良好的线性关系,检出限为3.0×10^- 8mol/L。测定了AOⅡ与BSA的结合比和结合常数,并对结合反应机理进行了初步的探讨。The interaction of acid orange Ⅱ with BSA was studied by electrochemical method and spectrophotometry. In pH 7.20 riffs - HCl buffer, AO Ⅱ has a sensitive reduction peak at - 0.69 V (vs. SCE). The addition of BSA to the above solution, the reduction peak current of AO Ⅱ decreases and reduction peak potential shifts positively. An electrochemical quantitive method of BSA was developed based on the interaction of AO Ⅱ with BSA. Under the optimized condition, the decrease of the reduction peak current of AO Ⅱ is proportional to the concentration of BSA in the range of 5.0 × 10^-8- 1.0 × 10^-5 mol/L. The limit of detection is 3.0 × 10^-8 mol/L. The binding ratio and binding constant of DNA with BBG were calculated. Furthermore, the binding mechanism was also preliminarily discussed.
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