Zhong Yingying, Yang Junsong, Liang Qian, Yu Xiao, Lai Hongyu, Lin Yu, Mo Qijie, Wang Qing, Chen Zijian, Wang Hongwu
School of Food & Pharmaceutical Engineering, Zhaoqing University Zhaoqing 526061 People's Republic of China
Laboratory of Quality & Safety Risk Assessment for Agro-products (Zhaoqing), Ministry of Agriculture and Rural Affairs Zhaoqing 526061 People's Republic of China.
RSC Adv. 2025 Aug 26;15(37):30446-30455. doi: 10.1039/d5ra05417f. eCollection 2025 Aug 22.
Catechin, a phenolic-active substance extracted from natural plants, exhibits a wide range of biological activities. However, exceeding safe levels can harm human health, making accurate quantification essential. Current assay methods, however, do not provide efficient or precise catechin measurements. In this study, an Os-Ru nanozyme with outstanding peroxidase-mimicking activity was first developed, showing values of 0.36 mM for 3,3',5,5'-tetramethylbenzidine (TMB) and 2.67 mM for HO. Additionally, catechin was found to effectively scavenge hydroxyl radicals (HO˙) generated from HO decomposition by the Os-Ru nanozyme. Based on this, a rapid dual-readout colorimetric method for catechin detection was established, featuring an absorbance measurement in solution and grayscale (G) analysis on a paper platform, both based on the Os-Ru nanozyme. This dual-readout colorimetric method achieved highly sensitive catechin detection across a broad linear concentration range (0 to 450 μmol L), with detection limits of 2.84 μmol L for absorbance measurement and 9.68 μmol L for the value analysis. Moreover, the method demonstrated excellent reliability and accuracy in practical applications, yielding spiked recoveries between 91.78 and 103.01% and relative standard deviations (RSD) ranging from 1.62 to 6.74% in the analysis of green tea beverages. Overall, this Os-Ru nanozyme-based dual-readout colorimetric method has considerable potential for practical catechin detection and could provide additional inspiration and ideas for the rational design and development of colorimetric sensing methods for rapid detection of nanozyme-based antioxidants.
儿茶素是一种从天然植物中提取的酚类活性物质,具有广泛的生物活性。然而,超过安全水平会损害人体健康,因此准确量化至关重要。然而,目前的检测方法无法高效、精确地测定儿茶素。在本研究中,首次开发了一种具有出色过氧化物酶模拟活性的Os-Ru纳米酶,其对3,3',5,5'-四甲基联苯胺(TMB)的Km值为0.36 mM,对H2O2的Km值为2.67 mM。此外,发现儿茶素能有效清除Os-Ru纳米酶分解H2O2产生的羟基自由基(·OH)。基于此,建立了一种快速双读数比色法检测儿茶素,该方法基于Os-Ru纳米酶,在溶液中进行吸光度测量,并在纸平台上进行灰度(G)分析。这种双读数比色法在宽线性浓度范围(0至450 μmol/L)内实现了高灵敏度的儿茶素检测,吸光度测量的检测限为2.84 μmol/L,G值分析的检测限为9.68 μmol/L。此外,该方法在实际应用中表现出出色的可靠性和准确性,在绿茶饮料分析中的加标回收率为91.78%至103.01%,相对标准偏差(RSD)为1.62%至6.74%。总体而言,这种基于Os-Ru纳米酶的双读数比色法在实际儿茶素检测中具有很大潜力,可为基于纳米酶的抗氧化剂快速检测比色传感方法的合理设计和开发提供额外的灵感和思路。