College of Chemistry and Chemical Engineering, Xinyang Normal University, Xinyang, 464000, China.
Mikrochim Acta. 2022 May 10;189(6):217. doi: 10.1007/s00604-022-05309-2.
An ultrasensitive fluorescence assay strategy on the basis of carbon dots (CDs) and cDNA-modified gold nanoparticles (AuNP-cDNA) was developed for the determination of microRNA-21 (miRNA-21) via internal filtering effect (IFE). Positively charged CDs (PEI-CDs), the fluorophores in IFE, were synthesized via a hydrothermal method using polyethyleneimine (PEI) as surface ligand. The maximum emission wavelength is located at 500 nm under the excitation of 410 nm. AuNPs, the absorbers, were modified with single-stranded DNA (cDNA), which is completely complementary to miRNA-21. The fluorescence of PEI-CDs is quenched due to the assembly of PEI-CDs and AuNPs-cDNA. In the presence of miRNA-21, the hybridization between miRNA-21 and cDNA causes the release of PEI-CDs and the recovery of fluorescence intensity.The fluorescence recovery degree is linearly correlated with the logarithm of miRNA-21 concentration in the range of 1-1000 fM. This method can be applied to determine miRNA-21 in real serum samples, and the detection results are in well agreement with those of qRT-PCR. The determination of miRNA-21 spiked into diluted human serum samples displays satisfactory recovery within the range 88.44-112.7%, which confirmed the reliability for miRNAs detection in real samples.
基于碳点 (CDs) 和 cDNA 修饰的金纳米粒子 (AuNP-cDNA) 的超灵敏荧光分析策略,通过内滤效应 (IFE) 用于测定 microRNA-21 (miRNA-21)。正电荷 CDs (PEI-CDs),IFE 中的荧光团,通过水热法使用聚乙烯亚胺 (PEI) 作为表面配体合成。在 410nm 激发下,最大发射波长位于 500nm 处。AuNPs 被修饰为单链 DNA (cDNA),其完全与 miRNA-21 互补。由于 PEI-CDs 和 AuNPs-cDNA 的组装,PEI-CDs 的荧光被猝灭。在 miRNA-21 的存在下,miRNA-21 与 cDNA 之间的杂交导致 PEI-CDs 的释放和荧光强度的恢复。荧光恢复程度与 miRNA-21 浓度的对数在 1-1000 fM 范围内呈线性相关。该方法可用于测定真实血清样品中的 miRNA-21,检测结果与 qRT-PCR 吻合良好。在稀释的人血清样品中添加 miRNA-21 的测定显示出 88.44-112.7%的范围内令人满意的回收率,这证实了在真实样品中检测 miRNAs 的可靠性。