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Glucose oxidase entrapment in an electropolymerized poly(tyramine) film with sulfobutylether-\u3b2-cyclodextrin on platinum nanoparticle modified boron-doped diamond electrode

机译:磺化丁基醚-u3b2-环糊精在铂纳米粒子修饰的掺硼金刚石电极上电聚合的聚酪胺膜中的葡萄糖氧化酶截留

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摘要

Glucose oxidase (GO) was entrapped in an electrodeposited poly(tyramine) film together with a negatively charged sulfobutylether-\u3b2-cyclodextrin (SBCD) on the active area of a platinum (Pt) nanoparticle modified boron-doped diamond (BDD) electrode. Electrodeposition of tyramine and simultaneous entrapment of GO/SBCD were performed in 50 mM phosphate buffer, pH 7 containing 0.1 M tyramine, 1750 units GO, and 10 mM SBCD. Atomic force microscopy (AFM) imaging revealed the presence of semicircular nanofibers with a height of 40 nm and an averaged length of 795 nm throughout the electropolymerized film surface. The combined film of poly(tyramine) and SBCD served as an excellent matrix polymer for the GO immobilization with high stability, selectivity, and reproducibility. Sensitive and selective detection of H\u2082O\u2082 was realized at +0.4 V vs 3 M Ag/AgCl, since the poly(tyramine)/SBCD film was capable of preventing the passage of electroactive uric and ascorbic acids to the electrode. The glucose biosensor exhibited a remarkably selective response to glucose with a detection limit of 10 \u3bcM, linearity up to 110 mM, and a response time of 2 s. Glutaraldehyde cross-linking of the film with entrapped GO completely eliminated electroactive interference caused by uric and ascorbic acids.
机译:在铂(Pt)纳米粒子修饰的掺硼金刚石(BDD)电极的活性区域上,将葡萄糖氧化酶(GO)与带负电的磺丁基醚-u3b2-环糊精(SBCD)一起捕获在电沉积的聚(酪胺)膜中。在含0.1 M酪胺,1750单位GO和10 mM SBCD的50 mM磷酸盐缓冲液,pH 7中进行酪胺的电沉积和GO / SBCD的同时捕获。原子力显微镜(AFM)成像显示存在半圆形纳米纤维,整个电聚合膜表面的高度为40 nm,平均长度为795 nm。聚(酪胺)和SBCD的组合薄膜具有出色的稳定性,选择性和重现性,是用于GO固定化的优秀基质聚合物。由于聚(酪胺)/ SBCD膜能够防止电活性尿酸和抗坏血酸通过电极,因此在+0.4 V对3 M Ag / AgCl的情况下实现了H \ u2082O \ u2082的灵敏和选择性检测。葡萄糖生物传感器表现出对葡萄糖的显着选择性响应,检测极限为10μm,线性最高可达110 mM,响应时间为2 s。膜与截留的GO的戊二醛交联完全消除了尿酸和抗坏血酸引起的电活性干扰。

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