葡萄糖氧化酶
药物输送
基质(水族馆)
材料科学
金属有机骨架
纳米技术
胰岛素释放
固定化酶
酶
化学
组合化学
化学工程
有机化学
生物传感器
工程类
吸附
内分泌学
糖尿病
地质学
海洋学
医学
1型糖尿病
作者
Yi Feng,Xun Cao,Lin Zhang,Jingyi Li,Shitong Cui,Yunxiu Bai,Kequan Chen,Jun Ge
标识
DOI:10.1016/j.cej.2022.135736
摘要
A biological system that can efficiently respond to external signals to release its cargo is promising in many areas. Here, we report a method of engineering defects in enzyme-embedded metal–organic frameworks (MOFs) which brings advantageous properties for drug delivery, showing that defects sometimes can bring out miraculous performances. The glucose oxidase (GOx) encapsulated in MOFs with defects displayed much higher apparent activity than that in normal MOFs. By the combination of Fourier transformation of extended X-ray absorption fine structures and molecular simulations, we proved that the defects generated mesopores and thus enhanced the enzyme substrate transportation. Based on this defect engineering approach, a drug delivery system was constructed by co-encapsulating GOx and insulin in defected MOFs. The insulin in defected MOFs can be efficiently released in response to a high glucose concentration while scarcely released with a low glucose concentration, providing a new possible route for intelligent insulin delivery.
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