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DOI码：10.1021/acs.analchem.5c03410

发表刊物：Analytical Chemistry

摘要：Precise classification of lung adenocarcinoma (LUAD) subtypes is very important for determining surgical necessity and strategy. There is an urgent need to develop a noninvasive and accurate method to improve the accuracy of preoperative diagnosis. Programmed death-ligand-1 (PD-L1)-expressing exosomes are pivotal biomarkers for monitoring the LUAD progression. Nevertheless, most previously reported sensors are limited by sensitivity, which makes it challenging to differentiate LUAD subtypes. Herein, we synthesized silver nanoparticle-decorated graphitic carbon nitride (g-C3N4@AgNPs) nanosheets dual-functionalized with 8-amino-5-chloro-2,3-dihydro-7-phenylpyrido-[3,4-d]-pyridazine-1,4-dione (L012) and Co2+ (GALC) via an in situ growth strategy. The composite exhibited a strong CL intensity and stability. This was attributed to the fact that g-C3N4 not only enriched a large amount of L012 but also catalyzed the generation of reactive OH• together with Co2+, synergistically amplifying the CL signal. On this basis, a CL immunosensor for detecting PD-L1-expressing exosomes was constructed, using PD-L1 antibody-modified GALC as a CL immunoprobe and Fe3O4@TiO2 nanoparticle as a capture platform for exosomes. The optimized immunosensor exhibited exceptional sensitivity, with a low limit of detection of 28.1 particles/mL and a wide linear range of 4.28 × 102–4.28 × 106 particles/mL, outperforming previously reported sensors. Clinical evaluation using 50 serum samples revealed statistically significant differences in PD-L1-expressing exosome levels among healthy individuals, minimally invasive adenocarcinoma patients, and invasive adenocarcinoma patients (P < 0.0001), with excellent discriminatory ability (AUC = 0.947). This work not only achieves the ultrasensitive detection of PD-L1-expressing exosomes at the individual level but also presents a facile, noninvasive, and accurate method for LUAD diagnosis and subtype classification.

第一作者：郑可颖

合写作者：李丹阳,张婼娴,张文灿,王慢莉,郑天骅

论文类型：期刊论文

通讯作者：魏熹,崔华

学科门类：理学

文献类型：J

卷号：97

期号：32

页面范围：17833–17840

是否译文：否

发表时间：2025-08-06

收录刊物：SCI

发布期刊链接：https://pubs.acs.org/doi/10.1021/acs.analchem.5c03410?ref=PDF