Department of Chemical and Materials Engineering, Chang Gung University, Tao-Yuan 33302, Taiwan, ROC.
Anal Chim Acta. 2013 Aug 20;792:101-9. doi: 10.1016/j.aca.2013.07.006. Epub 2013 Jul 9.
A colloidal suspension of nanostructured poly(N-butyl benzimidazole)-graphene sheets (PBBIns-Gs) was used to modify a gold electrode to form a three-dimensional PBBIns-Gs/Au electrode that was sensitive to hydrogen peroxide (H2O2) in the presence of acetic acid (AcOH). The positively charged nanostructured poly(N-butyl benzimidazole) (PBBIns) separated the graphene sheets (Gs) and kept them suspended in an aqueous solution. Additionally, graphene sheets (Gs) formed "diaphragms" that intercalated Gs, which separated PBBIns to prevent tight packing and enhanced the surface area. The PBBIns-Gs/Au electrode exhibited superior sensitivity toward H2O2 relative to the PBBIns-modified Au (PBBIns/Au) electrode. Furthermore, a high yield of glucose oxidase (GOD) on the PBBIns-Gs of 52.3mg GOD per 1mg PBBIns-Gs was obtained from the electrostatic attraction between the positively charged PBBIns-Gs and negatively charged GOD. The non-destructive immobilization of GOD on the surface of the PBBIns-Gs (GOD-PBBIns-Gs) retained 91.5% and 39.2% of bioactivity, respectively, relative to free GOD for the colloidal suspension of the GOD-PBBIns-Gs and its modified Au (GOD-PBBIns-Gs/Au) electrode. Based on advantages including a negative working potential, high sensitivity toward H2O2, and non-destructive immobilization, the proposed glucose biosensor based on an GOD-PBBIns-Gs/Au electrode exhibited a fast response time (5.6s), broad detection range (10μM to 10mM), high sensitivity (143.5μAmM(-1)cm(-2)) and selectivity, and excellent stability. Finally, a choline biosensor was developed by dipping a PBBIns-Gs/Au electrode into a choline oxidase (ChOx) solution for enzyme loading. The choline biosensor had a linear range of 0.1μM to 0.83mM, sensitivity of 494.9μAmM(-1)cm(-2), and detection limit of 0.02μM. The results of glucose and choline measurement indicate that the PBBIns-Gs/Au electrode provides a useful platform for the development of oxidase-based biosensors.
一种纳米结构聚(正丁基苯并咪唑)-石墨烯片(PBBIns-Gs)的胶体悬浮液被用于修饰金电极,形成对在乙酸(AcOH)存在下的过氧化氢(H2O2)敏感的三维 PBBIns-Gs/Au 电极。带正电荷的纳米结构聚(正丁基苯并咪唑)(PBBIns)将石墨烯片(Gs)分离并保持它们悬浮在水溶液中。此外,石墨烯片(Gs)形成了“隔板”,将 Gs 插入其中,从而将 PBBIns 隔开以防止紧密堆积并增加表面积。与 PBBIns 修饰的 Au(PBBIns/Au)电极相比,PBBIns-Gs/Au 电极对 H2O2 表现出更高的灵敏度。此外,通过带正电荷的 PBBIns-Gs 与带负电荷的 GOD 之间的静电吸引,在 PBBIns-Gs 上获得了 52.3mg GOD 每 1mg PBBIns-Gs 的高葡萄糖氧化酶(GOD)产量。GOD 在 PBBIns-Gs 上的非破坏性固定化(GOD-PBBIns-Gs)分别保留了 91.5%和 39.2%的生物活性,相对于 GOD 的胶体悬浮液及其修饰的 Au(GOD-PBBIns-Gs/Au)电极中的游离 GOD。基于包括负工作电位、对 H2O2 的高灵敏度和非破坏性固定化在内的优势,基于 GOD-PBBIns-Gs/Au 电极的葡萄糖生物传感器具有快速的响应时间(5.6s)、宽检测范围(10μM 至 10mM)、高灵敏度(143.5μAmM(-1)cm(-2))和选择性以及出色的稳定性。最后,通过将 PBBIns-Gs/Au 电极浸入胆碱氧化酶(ChOx)溶液中进行酶负载,制备了胆碱生物传感器。胆碱生物传感器的线性范围为 0.1μM 至 0.83mM,灵敏度为 494.9μAmM(-1)cm(-2),检测限为 0.02μM。葡萄糖和胆碱测量结果表明,PBBIns-Gs/Au 电极为基于氧化酶的生物传感器的开发提供了一个有用的平台。