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High-resolution colorimetric detection of lipase activity based on enzyme-controlled reshaping of gold nanorods

机译:基于酶控制的金纳米棒重塑的高分辨率比色法检测脂肪酶活性

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We developed a novel enzyme-controlling colorimetric assay to measure lipase activity. The method relied on enzymatic reaction-assisted gold deposition on gold nanorods (AuNRs) to generate a significant color change, which was strongly dependent on lipase activity. The H2O2 produced by autoxidation of the ethylene oxide subunits in Tween 80 reduced AuCl4? ions to Au atoms, which were coated onto of the surface of the AuNRs. In addition, lipase catalyzed the hydrolysis of the carboxyl ester bond in Tween 80, which controlled the rate of reshaping of AuNRs and tailored the localized surface plasmon resonance of the AuNRs. A linear response ranging from 0 to 4.5 mg mL?1 and a detection limit of 0.017 mg mL?1 for lipase were obtained. The methodology provided a sensitive, convenient, and rapid assay to monitor enzyme activities by judging different colors using both naked-eye detection and colorimetric instruments.
机译:我们开发了一种新型的酶控制比色测定法来测量脂肪酶的活性。该方法依赖于酶反应辅助金在金纳米棒(AuNRs)上的沉积,以产生显着的颜色变化,这强烈依赖于脂肪酶的活性。由吐温80中的环氧乙烷亚基自氧化产生的过氧化氢还原了AuCl4?离子形成Au原子,然后将其涂覆到AuNRs的表面上。此外,脂肪酶催化吐温80中羧基酯键的水解,从而控制了AuNRs的重整速率并调整了AuNRs的局部表面等离子体共振。获得的脂酶线性响应范围为0至4.5 mg mL?1,检出限为0.017 mg mL?1。该方法通过肉眼检测和比色仪器来判断不同的颜色,从而提供了一种灵敏,方便,快速的检测方法来监测酶的活性。

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