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硼掺杂石墨相氮化碳负载铜纳米酶用于比色-荧光-智能手机检测α-葡萄糖苷酶

Boron-doped g-CN supporting Cu nanozyme for colorimetric-fluorescent-smartphone detection of α-glucosidase.

作者信息

Fu Qingjie, Liang Shuang, Zhang Siqi, Zhou Chenyu, Lv Yuntai, Su Xingguang

机构信息

Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, PR China.

Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, PR China.

出版信息

Anal Chim Acta. 2024 Jul 4;1311:342715. doi: 10.1016/j.aca.2024.342715. Epub 2024 May 10.

Abstract

BACKGROUND

Due to that the higher activity of nanozymes would bring outstanding performance for the nanozyme-based biosensing strategies, great efforts have been made by researchers to improve the catalytic activity of nanozymes, and novel nanozymes with high catalytic activity are desired. Considering the crucial role in controlling blood glucose level, strategies like colorimetric and chemiluminescence to monitor α-glucosidase are developed. However, multi-mode detection with higher sensitivity was insufficient. Therefore, developing triple-mode detection method for α-glucosidase based on great performance nanozyme is of great importance.

RESULTS

In this work, a novel nanozyme Cu-BCN was synthesized by loading Cu on boron doped carbon substrate g-CN and applied to the colorimetric-fluorescent-smartphone triple-mode detection of α-glucosidase. In the presence of HO, Cu-BCN catalyzed the generation of O from HO, O subsequently oxidized TMB to blue colored oxTMB. In the presence of hydroquinone (HQ), the ROS produced from HO was consumed, inhibiting the oxidation of TMB, which endows the possibility of colorimetric and visual on-site detection of HQ. Further, due to that the fluorescence of Mg-CQDs at 444 nm could be quenched by oxTMB, HQ could also be quantified through fluorescent mode. Since α-glucosidase could efficiently hydrolyze α-arbutin into HQ, the sensitive detection of α-glucosidase was realized. Further, colorimetric paper-based device (c-PAD) was fabricated for on-site α-glucosidase detection. The LODs for α-glucosidase via three modes were 2.20, 1.62 and 2.83 U/L respectively, high sensitivities were realized.

SIGNIFICANCE

The nanozyme Cu-BCN possesses higher peroxidase-like activity by doping boron to the substrate than non-doped Cu-CN. The proposed triple-mode detection of α-glucosidase is more sensitive than most previous reports, and is reliable when applied to practical sample. Further, the smartphone-based colorimetric paper-based analytical device (c-PAD) made of simple materials could also detect α-glucosidase sensitively. The smartphone-based on-site detection provided a convenient, instrument-free and sensitive sensing method for α-glucosidase.

摘要

背景

由于纳米酶的较高活性会为基于纳米酶的生物传感策略带来出色性能,研究人员已做出巨大努力来提高纳米酶的催化活性,并且需要具有高催化活性的新型纳米酶。考虑到在控制血糖水平中的关键作用,已开发出比色法和化学发光法等用于监测α-葡萄糖苷酶的策略。然而,具有更高灵敏度的多模式检测还不够。因此,基于高性能纳米酶开发α-葡萄糖苷酶的三模式检测方法具有重要意义。

结果

在这项工作中,通过将铜负载在硼掺杂的碳基底g-CN上合成了一种新型纳米酶Cu-BCN,并将其应用于α-葡萄糖苷酶的比色-荧光-智能手机三模式检测。在过氧化氢(HO)存在下,Cu-BCN催化HO生成氧(O),O随后将3,3',5,5'-四甲基联苯胺(TMB)氧化为蓝色的氧化型TMB(oxTMB)。在对苯二酚(HQ)存在下,HO产生的活性氧(ROS)被消耗,抑制了TMB的氧化,这赋予了比色法和现场目视检测HQ的可能性。此外,由于oxTMB可以淬灭444nm处的Mg-碳量子点(Mg-CQDs)的荧光,HQ也可以通过荧光模式进行定量。由于α-葡萄糖苷酶可以有效地将α-熊果苷水解为HQ,因此实现了对α-葡萄糖苷酶的灵敏检测。此外,制备了基于比色纸的装置(c-PAD)用于现场检测α-葡萄糖苷酶。通过三种模式对α-葡萄糖苷酶的检测限分别为2.20、1.62和2.83U/L,实现了高灵敏度。

意义

通过向基底中掺杂硼,纳米酶Cu-BCN具有比未掺杂的Cu-CN更高的过氧化物酶样活性。所提出的α-葡萄糖苷酶三模式检测比大多数先前的报道更灵敏,并且应用于实际样品时是可靠的。此外,由简单材料制成的基于智能手机的比色纸分析装置(c-PAD)也可以灵敏地检测α-葡萄糖苷酶。基于智能手机的现场检测为α-葡萄糖苷酶提供了一种方便、无需仪器且灵敏的传感方法。

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