Journal
BIOMEDICAL OPTICS EXPRESS
Volume 13, Issue 8, Pages 4102-4117Publisher
Optica Publishing Group
DOI: 10.1364/BOE.463612
Keywords
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Funding
- National Natural Science Foundation of China
- Social Development Foundation of Jiangsu
- Natural Science Foundation of the Jiangsu Higher Education Institutions of China
- [81701825]
- [BE2018684]
- [17KJB416012]
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A high-throughput surface-enhanced Raman scattering-based lateral flow assay is proposed for accurate quantification of ctDNA associated with head and neck squamous cell carcinoma. The method combines high-performing SERS probes and target-specific signal amplification strategy, enabling fast and parallel detection of multiple samples.
Circulating tumor DNA (ctDNA) has recently emerged as an ideal target for biomarker analytes. Thus, the development of rapid and ultrasensitive ctDNA detection methods is essential. In this study, a high-throughput surface-enhanced Raman scattering (SERS)-based lateral flow assay (LFA) strip is proposed. The aim of this method is to achieve accurate quantification of TP53 and PIK3CA E545K, two types of ctDNAs associated with head and neck squamous cell carcinoma (HNSCC), particularly for point-of-care testing (POCT). Raman reporters and hairpin DNAs are used to functionalize the Pd-Au core-shell nanorods (Pd-AuNRs), which serve as the SERS probes. During the detection process, the existence of targets could open the hairpins on the surface of Pd-AuNRs and trigger the first step of catalytic hairpin assembly (CHA) amplification. The next stage of CHA amplification is initiated by the hairpins prefixed on the test lines, generating numerous hot spots to enhance the SERS signal significantly. By the combination of high-performing SERS probes and a target-specific signal amplification strategy, TP53 and PIK3CA E545K are directly quantified in the range of 100 aM-1 nM, with the respective limits of detection (LOD) calculated as 33.1 aM and 20.0 aM in the PBS buffer and 37.8 aM and 23.1 aM in human serum, which are significantly lower than for traditional colorimetric LFA methods. The entire detection process is completed within 45 min, and the multichannel design realizes the parallel detection of multiple groups of samples. Moreover, the analytical performance is validated, including reproducibility, uniformity, and specificity. Finally, the SERS-LFA biosensor is employed to analyze the expression levels of TP53 and PIK3CA E545K in the serum of patients with HNSCC. The results are verified as consistent with those of qRT-PCR. Thus, the SERS-LFA biosensor can be considered as a noninvasive liquid biopsy assay for clinical cancer diagnosis.(c) 2022 Optica Publishing Group under the terms of the Optica Open Access Publishing Agreement
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