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一种基于多分支局部催化发夹组装和光子晶体的原位外泌体微小RNA传感生物芯片。

An in situ exosomal miRNA sensing biochip based on multi-branched localized catalytic hairpin assembly and photonic crystals.

作者信息

Wu Tingting, Liu Xushun, Chen Hanjun, Liu Ying, Cao Yu

机构信息

College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, PR China.

College of Chemistry and Chemical Engineering, Hubei University, Wuhan, 430062, PR China.

出版信息

Biosens Bioelectron. 2023 Feb 15;222:115013. doi: 10.1016/j.bios.2022.115013. Epub 2022 Dec 14.

Abstract

Exosomal microRNAs (miRNAs) are emerging as attractive non-invasive and reliable biomarkers for disease diagnosis. In situ exosomal miRNA detection can avoid laborious and time-consuming exosome lysis, RNA extraction and effectively improve the accuracy. However, in situ exosomal miRNA detection is hampered by the low abundance of the targets and low permeability of the probes. Herein, an in situ exosomal miRNA sensing biochip based on multi-branched localized catalytic hairpin assembly (MLCHA) and photonic crystals (PCs) was proposed. The MLCHA probes could penetrate into the exosomes nondestructively due to its rigidity and generate amplified fluorescence signal upon recognizing the target miRNA. And then, the fluorescence signal was further enhanced by PCs to improve the sensitivity. The developed biosensor can not only detect exosomal miRNA in a concentration-dependent manner but also distinguish samples from cancer state and healthy state, which is potential for non-invasive clinical diagnostics.

摘要

外泌体微小RNA(miRNA)正成为疾病诊断中颇具吸引力的非侵入性且可靠的生物标志物。原位外泌体miRNA检测可避免繁琐且耗时的外泌体裂解、RNA提取,并有效提高准确性。然而,原位外泌体miRNA检测受到靶标丰度低和探针通透性低的阻碍。在此,提出了一种基于多分支局部催化发夹组装(MLCHA)和光子晶体(PCs)的原位外泌体miRNA传感生物芯片。MLCHA探针因其刚性可无损穿透外泌体,并在识别靶标miRNA时产生放大的荧光信号。然后,PCs进一步增强荧光信号以提高灵敏度。所开发的生物传感器不仅能以浓度依赖方式检测外泌体miRNA,还能区分癌症状态和健康状态的样本,具有非侵入性临床诊断的潜力。

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