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通过锂和铥共掺杂及活性核壳结构增强上转换纳米粒子的红色发射用于微小RNA的灵敏检测

Enhanced red emission of upconversion nanoparticles via Li and Tm codoping and active core-shell construction for sensitive detection of miRNAs.

作者信息

Li Yingchao, Tu Canzhao, Chen Qianshun, Lin Yingying, Li Baoming, Lyu Haixia

机构信息

College of Materials Science and Engineering, Fuzhou University, Fuzhou, 350108, China.

Department of Thoracic Surgery, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou University Affiliated Provincial Hospital, Fuzhou, 350001, China.

出版信息

Anal Chim Acta. 2025 Jan 15;1335:343429. doi: 10.1016/j.aca.2024.343429. Epub 2024 Nov 17.

Abstract

The overexpression of microRNA-222 (miRNA-222) is closely related to many human diseases, so the development of biosensors to detect this biomarker will contribute to the diagnosis of related diseases. Here, a simple, sensitive and specific fluorescence assay for the detection of miRNA-222 was developed using red-emitting upconversion nanoparticle (UCNP) as the donor and a DNA hairpin with black hole quencher-2 (BHQ-2) as the acceptor. Li and Tm-doped UCNP with a strong emission peak at 654 nm was obtained by changing the doped ion ratio and constructing core-shell structures. Under optimal conditions, the linear range for detecting miRNA-222 is 0.5-2.5 nM and the limit of detection is as low as 0.077 nM without any complicated amplification strategy. Finally, the proposed assay was applied for the detection of miRNA-222 in serum samples. The results obtained were similar to those of the standard method, and the spiked recoveries were in the range of 97.62%-102.14 %, suggesting that the proposed method has practical value in a complex biological sample matrix.

摘要

微小RNA-222(miRNA-222)的过表达与许多人类疾病密切相关,因此开发用于检测这种生物标志物的生物传感器将有助于相关疾病的诊断。在此,利用发红光的上转换纳米颗粒(UCNP)作为供体,以及带有黑洞猝灭剂-2(BHQ-2)的DNA发夹作为受体,开发了一种简单、灵敏且特异的用于检测miRNA-222的荧光测定法。通过改变掺杂离子比例并构建核壳结构,获得了在654 nm处具有强发射峰的锂和铥掺杂的UCNP。在最佳条件下,检测miRNA-222的线性范围为0.5 - 2.5 nM,无需任何复杂的扩增策略,检测限低至0.077 nM。最后,将所提出的测定法应用于血清样品中miRNA-222的检测。所得结果与标准方法的结果相似,加标回收率在97.62% - 102.14%范围内,表明所提出的方法在复杂生物样品基质中具有实用价值。

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