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血红素负载的 Zn-N-C 单原子纳米酶用于食品样品中没食子酸丙酯和甲醛的测定。

Hemin loaded Zn-N-C single-atom nanozymes for assay of propyl gallate and formaldehyde in food samples.

机构信息

Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China; Institute of Agro-Products Processing, Yunnan Academy of Agricultural Sciences, Kunming 650221, China.

Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China.

出版信息

Food Chem. 2022 Sep 30;389:132985. doi: 10.1016/j.foodchem.2022.132985. Epub 2022 Apr 15.

Abstract

Single-atom nanozymes (SAzymes) show distinct advantages in catalytic activity and selectivity owing to their stability and special characteristic of maximum atomic utilization. Inspired by the structure of natural horseradish peroxidase (HRP), we developed a simple method for specific determination of both propyl gallate (PG) and formaldehyde (HCHO) by utilizing the intrinsic peroxidase mimics activity of hemin (hem) loaded Zn-nitrogen-carbon single-atom nanozymes (Zn-N-C@hem SAzymes). Zn-N-C@hem was prepared via a salt-template strategy and self-assembly, where hemin exhibits enhancing peroxidase-like activity can catalyze oxidation of colorless PG to yellow product. Upon introduction of HCHO into Zn-N-C@hem/PG system, complete suppression of PG oxidation was showed, resulting in distinguished decrease in absorbance. The colorimetric sensors of PG and HCHO based on Zn-N-C@hem/PG were developed at their respective linear range of concentration 1.25-200 mg/kg and 5-250 mg/kg. The practicability of the rapid analysis of PG and HCHO in food samples has been verified with reliable results.

摘要

单原子纳米酶 (SAzymes) 由于其稳定性和最大限度原子利用率的特殊特性,在催化活性和选择性方面表现出明显的优势。受天然辣根过氧化物酶 (HRP) 结构的启发,我们开发了一种简单的方法,利用负载血红素 (hem) 的锌-氮-碳单原子纳米酶 (Zn-N-C@hem SAzymes) 的固有过氧化物酶模拟活性,特异性测定丙基没食子酸 (PG) 和甲醛 (HCHO)。通过盐模板策略和自组装制备 Zn-N-C@hem,其中血红素表现出增强的过氧化物酶样活性,可以催化无色 PG 氧化为黄色产物。当将 HCHO 引入 Zn-N-C@hem/PG 体系时,PG 氧化完全受到抑制,导致吸光度明显下降。基于 Zn-N-C@hem/PG 的 PG 和 HCHO 比色传感器在各自的浓度线性范围 1.25-200 mg/kg 和 5-250 mg/kg 内得到了验证。已经验证了该方法在食品样品中快速分析 PG 和 HCHO 的实用性,结果可靠。

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