2023
DOI: 10.1021/acs.analchem.3c00057
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Minimizing Cross-Reactivity for the Chemiluminescent Lateral Flow Immunoassay of Cardiac Troponin I Based on PEGylation of Gold Nanoparticles

Abstract: Lateral flow immunoassays (LFIAs) have been employed extensively for the rapid, accurate, and portable detection of protein biomarkers in healthcare. However, the cross-reactivity, especially in the multiplexed detection, leads to false-positive errors that would further limit their practical applications. In this work, we report a highly sensitive and accurate chemiluminescent LFIA based on the synthesis of the Au nanoparticle–antibody–horseradish peroxidase–polyethylene glycol conjugate for detecting cardiac… Show more

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Cited by 11 publications
(1 citation statement)
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“…In the gradient concentration (0.02–20 ng mL –1 ) spiked recovery test, no outliers and false positive/negative results were found to occur, and the test results showed a high degree of consistency between the two methods, suggesting that the developed test protocol was able to accurately determine the concentration of cTnI in the actual samples from humans (Figure E). , In addition, clinical samples collected from potential patients were evaluated for accuracy according to the test protocol and the ELISA kit, and again no significant differences were found between the two test protocols, and the t exp were both less than 2.78, thus further defining the accuracy of the developed test protocol for evaluating cTnI targets (Table S4). In addition, a comparison of the test protocols that had reported for cTnI targets revealed that the game theory-based test protocol we developed could match or even outperform them in terms of dynamic response range and detection limit (Figure F). …”
Section: Resultsmentioning
confidence: 99%
“…In the gradient concentration (0.02–20 ng mL –1 ) spiked recovery test, no outliers and false positive/negative results were found to occur, and the test results showed a high degree of consistency between the two methods, suggesting that the developed test protocol was able to accurately determine the concentration of cTnI in the actual samples from humans (Figure E). , In addition, clinical samples collected from potential patients were evaluated for accuracy according to the test protocol and the ELISA kit, and again no significant differences were found between the two test protocols, and the t exp were both less than 2.78, thus further defining the accuracy of the developed test protocol for evaluating cTnI targets (Table S4). In addition, a comparison of the test protocols that had reported for cTnI targets revealed that the game theory-based test protocol we developed could match or even outperform them in terms of dynamic response range and detection limit (Figure F). …”
Section: Resultsmentioning
confidence: 99%