Controlled growth of redox polymer network on single enzyme molecule for stable and sensitive enzyme electrode

原子转移自由基聚合 纳米凝胶 电化学 电极 聚合 高分子化学 氧化还原 聚合物 化学 二茂铁 材料科学 有机化学 物理化学 药物输送
作者
Seungkeun Kim,Al‐Monsur Jiaul Haque,Kyungmin Ahn,Youngho Wee,Hyojin Hwang,Yoon Huh,Joona Bang,Jeongkwon Kim,Jeongkwon Kim,Jungbae Kim,Jungbae Kim
出处
期刊:Biosensors and Bioelectronics [Elsevier BV]
卷期号:215: 114576-114576 被引量:4
标识
DOI:10.1016/j.bios.2022.114576
摘要

The electrochemical applications of enzymes are often hampered by poor enzyme stability and low electron conductivity. In this work, a novel enzyme nanogel based on atom transfer radical polymerization (ATRP) has been developed for highly sensitive detection of glucose based on ferrocene (Fc) embedded in crosslinked polymer network nanogel. Enzyme surfaces are successively modified with Br initiator, and then in situ atom transfer radical polymerization (ATRP) was performed to build up crosslinked polyacrylamide network. The resulting single enzyme nanogel (ATRP-SEG) is uniform in size fairly. ATRP-SEG reveals bi-phasic inactivation, and the half-life of stable ATRP-SEG after 18-day incubation at 50 °C is 47 days, which is 197 times longer than that of free Gox (5.7 h). By introducing a ferrocene (Fc) containing redox polymer, poly(acrylamide-co-vinylferrocene), the half-life of Fc-ATRP-SEG after 18-day incubation at 50 °C is 49 days. Fc-ATRP-SEG is used for preparation of glucose-sensing electrode, and the sensitivity of Fc-ATRP-SEG electrode is 111 μA cm −2 mM −1 , which is 366 and 1270 times higher than those of free GOx (0.303 μA cm −2 mM −1 ) and ATRP-SEG (0.0874 μA cm −2 mM −1 ), respectively. Fc-ATRP-SEG electrode maintained 90% of initial current density under 4 °C storage condition and repetitive usages every day for 7 days. Even the electrode repeatedly used in continuous harsh condition (250 rpm, room temperature), the current density maintained 96% after 12 hours incubation at operational condition.
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