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一种用于唾液中病毒抗原快速灵敏检测的实时酶联适配体分析方法(RT-eELAA),采用电化学读数。

A Real-Time Enzyme-Linked Aptamer Assay (RT-eELAA) for Rapid and Sensitive Detection of Viral Antigens in Saliva Using Electrochemical Readout.

作者信息

Adhikari Bal Ram, Wang Qing, Li Jiuxing, Sen Payel, Zhang Zijie, Gu Jimmy, Salena Bruno J, Yamamura Deborah, Li Yingfu, Soleymani Leyla

机构信息

Department of Engineering Physics, McMaster University, Hamilton L8S 4L8, Canada.

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton L8S 4L8, Canada.

出版信息

Anal Chem. 2025 Jul 1;97(25):13698-13706. doi: 10.1021/acs.analchem.5c02555. Epub 2025 Jun 13.

Abstract

Despite the need for reliable rapid antigen tests for infectious disease diagnostics, tests that combine rapid answer-to-result times with high sensitivity and specificity remain elusive. A major challenge in developing such tests is the loss of performance of analytical assays in clinical samples. Herein, we developed a rapid antigen test based on a real-time electrochemical sandwich assay for detecting SARS-CoV-2 and Influenza A in saliva. This assay used aptamers for both target capture and signal transduction and produced limits of detection of 301 and 743 copies/mL for SARS-CoV-2 and Influenza A, respectively. When evaluating this assay with clinical saliva samples, we encountered major issues in distinguishing between positive and negative samples. In response, we developed a revised method to interrogate each clinical sample with a pair of electrochemical detectors modified, respectively, with a functional aptamer or a nonfunctional aptamer mutant. This method enabled us to normalize the signal response measured from each clinical sample with a reference signal, overcoming the previously encountered challenge and resulting in a clinical sensitivity of 100% and a specificity of 100% when analyzing 20 saliva samples that were collected and tested for COVID-19.

摘要

尽管传染病诊断需要可靠的快速抗原检测,但能将快速出结果时间与高灵敏度和特异性相结合的检测方法仍然难以实现。开发此类检测方法的一个主要挑战是临床样本中分析检测的性能损失。在此,我们开发了一种基于实时电化学夹心检测法的快速抗原检测方法,用于检测唾液中的新型冠状病毒2(SARS-CoV-2)和甲型流感病毒。该检测法使用适体进行靶标捕获和信号转导,对SARS-CoV-2和甲型流感病毒的检测限分别为301和743拷贝/毫升。在用临床唾液样本评估该检测法时,我们在区分阳性和阴性样本方面遇到了重大问题。作为回应,我们开发了一种改进方法,用分别用功能性适体或非功能性适体突变体修饰的一对电化学检测器对每个临床样本进行检测。这种方法使我们能够用参考信号对每个临床样本测得的信号响应进行归一化,克服了之前遇到的挑战,在分析20份为新冠病毒病采集和检测的唾液样本时,临床灵敏度达到100%,特异性达到100%。

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