生物传感器
共价键
纳米技术
化学
离子键合
表面改性
离子液体
固定化酶
组合化学
尿素酶
材料科学
聚合物
尿素
水解
膜
聚对苯二甲酸乙二醇酯
酶
离子强度
检出限
人工酶
作者
Angel L. Huamani,Gregorio Laucirica,María Eugenia Toimil‐Molares,Michael F. Wagner,Matías Rafti,Waldemar A. Marmisollé,Omar Azzaroni
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2025-01-01
卷期号:17 (47): 27538-27549
摘要
We present the development of an innovative nanofluidic biosensor that integrates solid-state nanochannels modified with a metal-organic framework (MOF) for the detection of urea through enzymatic activity. The Zr-based MOF chosen was UiO-66-NH2, synthesized within bullet-shaped nanochannels in track-etched polyethylene terephthalate (PET) membranes. Post-synthetic modification was employed to attach divinyl sulfone (DVS) to the amino moieties present, thus facilitating the covalent immobilization of the urease enzyme. Enzymatic hydrolysis of urea generates local pH changes within the nanochannels, which can be translated into measurable modulations of ionic transport due to the pH-sensitive surface charge of the MOF. The biosensor exhibited a detection limit of 10 μM for urea, excellent stability, reversibility, and specificity. This work represents the first report, to the best of our knowledge, of a nanofluidic sensor that utilizes a MOF covalently bonded with an enzyme for urea detection through ionic transport changes. The incorporation of post-synthetic modification techniques highlights the versatility of MOF-functionalized nanochannels in creating robust and sensitive biosensors, opening new avenues for advanced nanofluidic sensing applications.
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