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基于金属有机骨架嵌入铁卟啉的共催化纳米酶用于牛奶中沙门氏菌的灵敏检测。

A cocatalytic nanozyme based on metal-organic framework-embedded iron porphyrin for the sensitive detection of Salmonella typhimurium in milk.

机构信息

Key Laboratory of Geriatric Nutrition and Health, Ministry of Education, Beijing Technology & Business University, Beijing, 100048, PR China.

Key Laboratory of Geriatric Nutrition and Health, Ministry of Education, Beijing Technology & Business University, Beijing, 100048, PR China.

出版信息

Talanta. 2024 Dec 1;280:126765. doi: 10.1016/j.talanta.2024.126765. Epub 2024 Aug 30.

Abstract

The nanozyme, acting as the signal labeling reporter, is widely employed in colorimetric immunoassays due to its exceptional catalytic activity and reliable performance. Nonetheless, when immobilized on the nanozyme's surface, there is a decline in catalytic activity, which hinders its ability to meet the escalating demand for advanced colorimetric immunoassays. Herein, we introduce a novel MILL-88@TcP nanozyme, formed by encapsulating iron porphyrins (TcP) within metal-organic frameworks (MILL-88), where the catalytic activity of TcP is fully preserved through ethanol-induced release. Leveraging the superior encapsulation capacity and enzyme-mimicking characteristics of MILL-88, the MILL-88@TcP nanozyme demonstrates a remarkable colorimetric performance, 1430-fold higher than that of MILL-88 alone. Furthermore, we developed the MILL-88@TcP nanozyme-based Enzyme-Linked Immunosorbent Assay (N-ELISA) for enhanced sensitivity in detecting Salmonella typhimurium, achieving a detection limit of 1.68 × 10 CFU/mL, approximately 500-fold enhancement compared to the traditional HRP-based ELISA (8.35 × 10 CFU/mL). Notably, the average recoveries ranged from 91.50 % to 108.50 % with a variation of 3.53 %-10.41 %, indicating high accuracy and precision. Collectively, this study highlights that the MILL-88@TcP nanozyme, with its superior catalytic performance and anti-interference capabilities, holds promise as a colorimetric labeling reporter to enhance the detection efficacy of colorimetric immunoassays and has the potential to establish a more stable and sensitive colorimetric assay platform.

摘要

纳米酶作为信号标记物在比色免疫分析中得到了广泛应用,因为它具有出色的催化活性和可靠的性能。然而,当固定在纳米酶表面时,其催化活性会下降,从而阻碍其满足高级比色免疫分析日益增长的需求。在此,我们引入了一种新型的 MILL-88@TcP 纳米酶,它由金属有机骨架(MILL-88)内包裹铁卟啉(TcP)形成,其中 TcP 的催化活性通过乙醇诱导释放得到充分保留。利用 MILL-88 的优越封装能力和酶模拟特性,MILL-88@TcP 纳米酶表现出卓越的比色性能,比单独的 MILL-88 高 1430 倍。此外,我们开发了基于 MILL-88@TcP 纳米酶的酶联免疫吸附测定(N-ELISA),用于提高检测鼠伤寒沙门氏菌的灵敏度,检测限为 1.68×10 CFU/mL,比传统的基于 HRP 的 ELISA(8.35×10 CFU/mL)提高了约 500 倍。值得注意的是,平均回收率在 91.50%至 108.50%之间,变化范围为 3.53%-10.41%,表明具有较高的准确性和精密度。总的来说,这项研究表明,MILL-88@TcP 纳米酶具有优越的催化性能和抗干扰能力,有望作为比色标记物增强比色免疫分析的检测效果,并有可能建立更稳定和敏感的比色分析平台。

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