LoC-SERS detection platform based on targeted signal anchoring mechanism, high-sensitivity detection of protein biomarkers in precancerous lesions of gastric cancer
Yanwen Zhuang , Feng Lu , Xiaoyong Wang , Jie Yao , Yong Wan , Shichen Qin , Xiaowei Cao , Jinxin Sheng
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引用次数: 0
Abstract
In this study, a novel lab-on-a-chip surface-enhanced Raman scattering (LoC-SERS) analysis platform was developed based on chip laboratory for monitoring precancerous lesions of GC. The platform integrated graphene-like Au nano-hexagonal arrays (Au NHAs) as a high-efficiency plasma substrate with the highly integrated microarray chip as an ideal system for sensitive recognition and rapid quantification of matrix metalloproteinase-9 (MMP-9) and interleukin-6 (IL-6) based on the targeted signal anchoring mechanism. Au NHAs were surface modified to form a double stranded structure with aptamer chains and single stranded DNA1 (ssDNA1), Au nanobipyramid with Ag shell (Au NBP@Ag) surface modified single stranded DNA2 (ssDNA2) and Raman signaling molecules. When the target is present, the aptamer specifically captures the target protein and detaches from the Au NHAs surface, exposing ssDNA1 and ssDNA2 to pair and bind. This resulted in the Au NBP@Ag probe carrying the signaling molecule anchoring to the surface of Au NHAs, thereby enhancing the SERS signal. The platform demonstrated excellent detection efficiency and could complete detection tasks within 20 min. The platform can detect MMP-9 and IL-6 at levels down to the pg/mL order of magnitude, demonstrating excellent detection sensitivity. In addition, the platform has the capability of simultaneous dual-target detection, demonstrating good clinical applicability and accuracy when testing real serum samples. Overall, this platform provides an efficient solution for early diagnosis and progression monitoring of precancerous lesions of GC, further providing a scientific basis for clinical decision-making and intervention.
期刊介绍:
Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome.
Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.