{"title":"合理设计掺银 MnFe2O4/HNTs 的过氧化物酶模拟活性和人血清中尿酸的比色传感。","authors":"Han Lu, Zhenbo Xiang, Hailong Pang, Qiang Ren","doi":"10.1016/j.talanta.2024.126913","DOIUrl":null,"url":null,"abstract":"<p><p>Mimicking enzyme have significantly advanced sensing assays by replicating native enzyme functions, yet achieving both high catalytic activity and easy recyclability remains a challenge. In this study, Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/halloysite nanotubes (HNTs) were rationally designed as a novel nanozyme by depositing in-situ Ag and MnFe<sub>2</sub>O<sub>4</sub> nanoparticles onto HNTs. The resulting nanocomposite exhibited excellent peroxidase-like activity along with magnetic properties. Leveraging these features, a highly efficient and sensitive colorimetric system for detecting uric acid (UA) was developed. The Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/HNTs catalyzed the oxidation of 3,3',5,5'-tetramethylbenzidine in the presence of H<sub>2</sub>O<sub>2</sub>, causing a color change from colorless to blue. The system showed a linear absorbance response to UA concentrations ranging from 1 to 20 μM, with a detection limit of 59 nM. Mechanistic studies revealed that reactive oxygen species intermediates (<sup>1</sup>O<sub>2</sub>) were generated through the decomposition of H<sub>2</sub>O<sub>2</sub>, leading to peroxidase-like activity in the Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/HNTs. The assay was successfully applied to detect UA in human serum with recoveries over 99.68 %. This study indicates the successful application of Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/HNTs for colorimetric UA detection in human serum. This research introduces a novel approach for designing recyclable, high-performance mimicking enzyme and establishes an effective colorimetric sensing platform for UA detection in human serum.</p>","PeriodicalId":435,"journal":{"name":"Talanta","volume":"281 ","pages":"126913"},"PeriodicalIF":5.6000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rational design of Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/HNTs for peroxidase-mimicking activity and colorimetric sensing of uric acid in human serum.\",\"authors\":\"Han Lu, Zhenbo Xiang, Hailong Pang, Qiang Ren\",\"doi\":\"10.1016/j.talanta.2024.126913\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Mimicking enzyme have significantly advanced sensing assays by replicating native enzyme functions, yet achieving both high catalytic activity and easy recyclability remains a challenge. In this study, Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/halloysite nanotubes (HNTs) were rationally designed as a novel nanozyme by depositing in-situ Ag and MnFe<sub>2</sub>O<sub>4</sub> nanoparticles onto HNTs. The resulting nanocomposite exhibited excellent peroxidase-like activity along with magnetic properties. Leveraging these features, a highly efficient and sensitive colorimetric system for detecting uric acid (UA) was developed. The Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/HNTs catalyzed the oxidation of 3,3',5,5'-tetramethylbenzidine in the presence of H<sub>2</sub>O<sub>2</sub>, causing a color change from colorless to blue. The system showed a linear absorbance response to UA concentrations ranging from 1 to 20 μM, with a detection limit of 59 nM. Mechanistic studies revealed that reactive oxygen species intermediates (<sup>1</sup>O<sub>2</sub>) were generated through the decomposition of H<sub>2</sub>O<sub>2</sub>, leading to peroxidase-like activity in the Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/HNTs. The assay was successfully applied to detect UA in human serum with recoveries over 99.68 %. This study indicates the successful application of Ag-doped MnFe<sub>2</sub>O<sub>4</sub>/HNTs for colorimetric UA detection in human serum. 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引用次数: 0
摘要
模拟酶通过复制原生酶的功能大大推进了传感检测的发展,然而要同时实现高催化活性和易回收性仍然是一项挑战。在这项研究中,通过在 HNTs 上原位沉积 Ag 和 MnFe2O4 纳米颗粒,合理设计了 Ag 掺杂 MnFe2O4/halloysite 纳米管(HNTs)作为新型纳米酶。由此产生的纳米复合材料具有出色的过氧化物酶样活性和磁性。利用这些特性,我们开发出了一种用于检测尿酸(UA)的高效、灵敏的比色系统。掺银的 MnFe2O4/HNTs 在 H2O2 的存在下催化了 3,3',5,5'-四甲基联苯胺的氧化,导致颜色从无色变为蓝色。该系统对 1 至 20 μM 的 UA 浓度呈线性吸光度响应,检测限为 59 nM。机理研究表明,活性氧中间产物(1O2)是通过 H2O2 的分解产生的,从而导致掺银 MnFe2O4/HNTs 具有类似过氧化物酶的活性。该检测方法成功地用于检测人血清中的 UA,回收率超过 99.68%。这项研究表明,掺银 MnFe2O4/HNTs 可成功用于人血清中 UA 的比色检测。这项研究为设计可回收的高性能模拟酶引入了一种新方法,并为检测人血清中的尿素氮建立了一个有效的比色传感平台。
Rational design of Ag-doped MnFe2O4/HNTs for peroxidase-mimicking activity and colorimetric sensing of uric acid in human serum.
Mimicking enzyme have significantly advanced sensing assays by replicating native enzyme functions, yet achieving both high catalytic activity and easy recyclability remains a challenge. In this study, Ag-doped MnFe2O4/halloysite nanotubes (HNTs) were rationally designed as a novel nanozyme by depositing in-situ Ag and MnFe2O4 nanoparticles onto HNTs. The resulting nanocomposite exhibited excellent peroxidase-like activity along with magnetic properties. Leveraging these features, a highly efficient and sensitive colorimetric system for detecting uric acid (UA) was developed. The Ag-doped MnFe2O4/HNTs catalyzed the oxidation of 3,3',5,5'-tetramethylbenzidine in the presence of H2O2, causing a color change from colorless to blue. The system showed a linear absorbance response to UA concentrations ranging from 1 to 20 μM, with a detection limit of 59 nM. Mechanistic studies revealed that reactive oxygen species intermediates (1O2) were generated through the decomposition of H2O2, leading to peroxidase-like activity in the Ag-doped MnFe2O4/HNTs. The assay was successfully applied to detect UA in human serum with recoveries over 99.68 %. This study indicates the successful application of Ag-doped MnFe2O4/HNTs for colorimetric UA detection in human serum. This research introduces a novel approach for designing recyclable, high-performance mimicking enzyme and establishes an effective colorimetric sensing platform for UA detection in human serum.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.