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Common Causes of Glucose Oxidase Instability in In Vivo Biosensing: A Brief Review

机译:体内生物传感中葡萄糖氧化酶不稳定的常见原因:简要综述

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摘要

Clinical management of diabetes must overcome the challenge of in vivo glucose sensors exhibiting lifetimes of only a few days. Limited sensor life originates from compromised enzyme stability of the sensing enzyme. Sensing enzymes degrade in the presence of low molecular weight materials (LMWM) and hydrogen peroxide in vivo. Sensing enzymes could be made to withstand these degradative effects by (1) stabilizing the microenvironment surrounding the sensing enzyme or (2) improving the structural stability of the sensing enzyme genetically. We review the degradative effect of LMWM and hydrogen peroxide on the sensing enzyme glucose oxidase (GOx). In addition, we examine advances in stabilizing GOx against degradation using hybrid silica gels and genetic engineering of GOx. We conclude molecularly engineered GOx combined with silica-based encapsulation provides an avenue for designing long-term in vivo sensor systems.
机译:糖尿病的临床管理必须克服仅显示几天生命的体内葡萄糖传感器的挑战。传感器寿命有限的原因是传感酶的酶稳定性受到损害。在体内存在低分子量物质(LMWM)和过氧化氢的情况下,传感酶会降解。通过(1)稳定传感酶周围的微环境或(2)从遗传上改善传感酶的结构稳定性,可以使传感酶承受这些降解作用。我们审查了LMWM和过氧化氢对传感酶葡萄糖氧化酶(GOx)的降解作用。此外,我们研究了使用混合硅胶和GOx基因工程技术稳定GOx防止降解的进展。我们得出结论,分子工程GOx与基于二氧化硅的封装相结合,为设计长期体内传感器系统提供了一条途径。

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