Nanoparticle-aptamer based cytosensing for the detection of human non-small cell lung cancer cells†

IF 2.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Lianju Chen, Rong Yang, Wenwei Li, Xu Wen, Yue Li, Jiaming Tang, Jing Hu and Qiming Kou
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引用次数: 0

Abstract

This study reports a simple and rapid aptamer-based sensor platform designed for the sensitive and selective detection of human non-small cell lung cancer (NSCLC) cells. Under standard conditions, gold nanoparticles (AuNPs) remain dispersed and exhibit a characteristic peak at 520 nm. However, the addition of sodium chloride (NaCl) destabilizes the charge of the solution, leading to the aggregation of AuNPs. The AS1411 aptamer can adsorb onto the surface of AuNPs, effectively preventing their aggregation. In the presence of A549 cells, the AS1411 aptamer is induced to form stable G-tetrads, which allows for specific binding to the cells and results in the aggregation of AuNPs in the NaCl solution. This proposed aptasensor platform demonstrates high specificity for A549 cells when compared to other control human normal cells. The method exhibits a dynamic range of 101 to 106 cells per mL, with a detection limit of 7 cells per mL.

Abstract Image

基于纳米粒子适体的细胞传感检测人类非小细胞肺癌细胞。
本研究报道了一种简单快速的基于适配体的传感器平台,用于灵敏和选择性地检测人类非小细胞肺癌(NSCLC)细胞。在标准条件下,金纳米颗粒(AuNPs)保持分散,并在520 nm处呈现特征峰。然而,氯化钠(NaCl)的加入使溶液的电荷不稳定,导致aunp聚集。AS1411适体可以吸附在AuNPs表面,有效阻止其聚集。在A549细胞存在的情况下,AS1411适体被诱导形成稳定的g -四分体,这允许与细胞特异性结合,并导致AuNPs在NaCl溶液中聚集。与其他对照人类正常细胞相比,该拟合体传感器平台对A549细胞具有高特异性。该方法动态范围为101 ~ 106个细胞/ mL,检测限为7个细胞/ mL。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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