Target triggered G4 catalytic network via HCR-mediated hydrogel assembly for multi-model analysis of microRNA efficiently

Mingli Su , Jun Yang , Ruiwen Wang , Jiabao Yang , Fahui Wang , Jiamin Qin , Weiguo Yang , Qing-Chun Deng , Chengyi Xiong , Wen-Bin Liang
{"title":"Target triggered G4 catalytic network via HCR-mediated hydrogel assembly for multi-model analysis of microRNA efficiently","authors":"Mingli Su ,&nbsp;Jun Yang ,&nbsp;Ruiwen Wang ,&nbsp;Jiabao Yang ,&nbsp;Fahui Wang ,&nbsp;Jiamin Qin ,&nbsp;Weiguo Yang ,&nbsp;Qing-Chun Deng ,&nbsp;Chengyi Xiong ,&nbsp;Wen-Bin Liang","doi":"10.1016/j.asems.2025.100158","DOIUrl":null,"url":null,"abstract":"<div><div>With the advancement of hierarchical diagnosis and treatment systems, there is an increasing demand for rapid, user-friendly, and cost-effective approaches for disease analysis and prognosis monitoring. MicroRNAs (miRNAs), as vital biomarkers for early-stage disease diagnosis, pose substantial analytical challenges due to their small molecular size, low endogenous abundance, and high sequence homology among different species. Traditional methods such as Northern blotting and real-time ​polymerase chain reaction (RT-PCR) are limited by their complexity, lengthy procedures, and reliance on specialized instruments, making them less suitable for point-of-care (POC) applications. To address these challenges, we propose a portable and efficient POC analytical platform by utilizing a G4 catalytic network triggered by miRNA-155 through hybridization chain reaction (HCR)-mediated hydrogel assembly. A highly sensitive analysis was achieved for concentrations of 500 pM and 100 ​nM, with a limit of detection (LOD) of 138 pM, which demonstrated the method's capability for precise detection at low concentrations. Additionally, based on the color development reaction, its image information <em>via</em> RGB analysis could be used to achieve ternary precise quantitative analysis, thereby improving the analysis sensitivity and portability. This innovative platform provides a simple, cost-effective, and customizable solution for miRNA detection, opening new avenues for home-based bioanalysis and early disease diagnosis in resource-limited or remote settings.</div></div>","PeriodicalId":100036,"journal":{"name":"Advanced Sensor and Energy Materials","volume":"4 4","pages":"Article 100158"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Sensor and Energy Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2773045X25000251","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

With the advancement of hierarchical diagnosis and treatment systems, there is an increasing demand for rapid, user-friendly, and cost-effective approaches for disease analysis and prognosis monitoring. MicroRNAs (miRNAs), as vital biomarkers for early-stage disease diagnosis, pose substantial analytical challenges due to their small molecular size, low endogenous abundance, and high sequence homology among different species. Traditional methods such as Northern blotting and real-time ​polymerase chain reaction (RT-PCR) are limited by their complexity, lengthy procedures, and reliance on specialized instruments, making them less suitable for point-of-care (POC) applications. To address these challenges, we propose a portable and efficient POC analytical platform by utilizing a G4 catalytic network triggered by miRNA-155 through hybridization chain reaction (HCR)-mediated hydrogel assembly. A highly sensitive analysis was achieved for concentrations of 500 pM and 100 ​nM, with a limit of detection (LOD) of 138 pM, which demonstrated the method's capability for precise detection at low concentrations. Additionally, based on the color development reaction, its image information via RGB analysis could be used to achieve ternary precise quantitative analysis, thereby improving the analysis sensitivity and portability. This innovative platform provides a simple, cost-effective, and customizable solution for miRNA detection, opening new avenues for home-based bioanalysis and early disease diagnosis in resource-limited or remote settings.

Abstract Image

目标通过hcr介导的水凝胶组装触发G4催化网络,高效地进行microRNA的多模型分析
随着分级诊断和治疗系统的发展,人们对快速、用户友好、成本效益高的疾病分析和预后监测方法的需求日益增加。MicroRNAs (miRNAs)作为早期疾病诊断的重要生物标志物,由于其小分子大小、低内源丰度和不同物种之间的高序列同源性,给分析带来了巨大挑战。传统的方法,如Northern印迹和实时聚合酶链反应(RT-PCR),由于其复杂性、冗长的程序和对专用仪器的依赖而受到限制,使其不太适合护理点(POC)应用。为了解决这些问题,我们提出了一种便携式高效的POC分析平台,该平台利用miRNA-155通过杂交链反应(HCR)介导的水凝胶组装触发的G4催化网络。在500 pM和100 nM的浓度下获得了高灵敏度分析,检测限(LOD)为138 pM,证明了该方法在低浓度下的精确检测能力。此外,基于显色反应,通过RGB分析,其图像信息可用于三元精确定量分析,从而提高分析灵敏度和便携性。这一创新平台为miRNA检测提供了一种简单、经济、可定制的解决方案,为资源有限或偏远地区的家庭生物分析和早期疾病诊断开辟了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信