纳米团簇
荧光
DNA
检出限
胞嘧啶
化学
自愈水凝胶
选择性
组合化学
聚集诱导发射
纳米技术
生物物理学
材料科学
色谱法
生物化学
高分子化学
生物
物理
催化作用
量子力学
作者
Elnaz Ahmadi-Sangachin,Morteza Hosseini,Javad Mohammadnejad
标识
DOI:10.1016/j.snb.2023.134012
摘要
Here, a platform consisting of a fluorescent DNA-functionalized hydrogel was created for the measurement of miRNA-141. In the presence of the target, the closed cytosine-rich loop of the three-segment branched DNA structure is formed as a useful template to create fluorescent silver nanoclusters (AgNCs). Then, aggregation-induced emission of AgNCs occurs in the hydrogel, and enhanced fluorescence is observed. Instead of acrylate-modified DNA, we used unmodified penta-adenine (A5) DNA strands for incorporation into polyacrylamide hydrogel in this method. By raising the concentration of target microRNA 141 (miR-141) under optimal conditions, the silver nanocluster's fluorescence intensities increased linearly from 5 pM to 100 nM, with a detection limit (LOD) of 2 pM. In addition, a selectivity analysis against the target demonstrates that the proposed analytical technique has good selectivity for miR-141. Since the creation of nanoclusters only occurs in the presence of the target sequence, this technique has shown significant potential for sensitive, selective, and label-free miRNA detection for clinical disease diagnosis and biomedical applications.
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