Ultrasmall high-entropy alloy-nanolabels based immunochromatographic test strip for rapid, ultrasensitive, and catalytic detection of Staphylococcus aureus.

IF 5.3 2区 化学 Q1 CHEMISTRY, ANALYTICAL
Wei Huang, Zhen Ren, Xukui Li, Rong Chen, Dinglin Fan, Jingjing Da, Yan Zha, Yongjie Xu
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Abstract

The use of ultrasmall high-entropy alloys (HEAs, ≈5 nm) with unique catalytic properties, integrating them into lateral flow immunoassay (LFIA) for the detection of Staphylococcus aureus is proposed. Under optimal conditions, the detection limits of the HEAs-based LFIA were 1.5 × 103 CFU/mL via direct coloration and 15 CFU/mL using the DAB-enhanced catalytic signal, representing improvements of 103-fold and 105-fold, respectively. The HEAs demonstrated superior performance compared with traditional AuNPs, including enhanced sensitivity and high peroxidase activity (Km = 0.066 M, Vmax = 1.132 × 10-6 M min-1), as well as excellent specificity and repeatability, with relative standard deviation (RSD) of less than 10%. Moreover, the incubation time for HEAs functionalized with antibodies to bind Staphylococcus aureus was only 5 min, compared with 20 min for functionalized AuNPs. The method also showed high specificity, effectively discriminating Staphylococcus aureus from other foodborne pathogens. The HEAs-based LFIA was successfully applied to food sample analysis, including milk and orange juice, demonstrating its robust applicability for real-world detection scenarios. This approach not only lowered the detection limit but also reduced the total detection time, making it a highly promising candidate for on-site detection of Staphylococcus aureus and other foodborne pathogens by simply changing the recognition element.

用于快速、超灵敏和催化检测金黄色葡萄球菌的超小型高熵合金纳米标签免疫层析试纸条。
利用具有独特催化性能的超小高熵合金(HEAs,≈5 nm),将其整合到侧流免疫分析法(LFIA)中检测金黄色葡萄球菌。在最佳条件下,直接显色法的检测限为1.5 × 103 CFU/mL, dab增强催化信号法的检测限为15 CFU/mL,分别提高了103倍和105倍。与传统的AuNPs相比,HEAs具有更高的灵敏度和较高的过氧化物酶活性(Km = 0.066 M, Vmax = 1.132 × 10-6 M min-1),具有良好的特异性和重复性,相对标准偏差(RSD)小于10%。此外,抗体功能化的HEAs与金黄色葡萄球菌结合的孵育时间仅为5分钟,而功能化的AuNPs则为20分钟。该方法对金黄色葡萄球菌和其他食源性病原菌具有较高的特异性。基于heas的LFIA已成功应用于食品样品分析,包括牛奶和橙汁,证明了其对现实世界检测场景的强大适用性。该方法不仅降低了检出限,而且缩短了总检测时间,通过简单改变识别元素,使其成为金黄色葡萄球菌和其他食源性病原体现场检测的极具前景的候选方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microchimica Acta
Microchimica Acta 化学-分析化学
CiteScore
9.80
自引率
5.30%
发文量
410
审稿时长
2.7 months
期刊介绍: As a peer-reviewed journal for analytical sciences and technologies on the micro- and nanoscale, Microchimica Acta has established itself as a premier forum for truly novel approaches in chemical and biochemical analysis. Coverage includes methods and devices that provide expedient solutions to the most contemporary demands in this area. Examples are point-of-care technologies, wearable (bio)sensors, in-vivo-monitoring, micro/nanomotors and materials based on synthetic biology as well as biomedical imaging and targeting.
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