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用于miRNA绝对定量的光谱编码微凝胶的流入实时检测。

In-flow real-time detection of spectrally encoded microgels for miRNA absolute quantification.

作者信息

Dannhauser David, Causa Filippo, Battista Edmondo, Cusano Angela M, Rossi Domenico, Netti Paolo A

机构信息

Center for Advanced Biomaterials for Healthcare@CRIB, Istituto Italiano di Tecnologia (IIT) , Largo Barsanti e Matteucci 53, 80125 Naples, Italy.

出版信息

Biomicrofluidics. 2016 Dec 6;10(6):064114. doi: 10.1063/1.4967489. eCollection 2016 Nov.

Abstract

We present an in-flow ultrasensitive fluorescence detection of microRNAs (miRNAs) using spectrally encoded microgels. We researched and employed a viscoelastic fluid to achieve an optimal alignment of microgels in a straight measurement channel and applied a simple and inexpensive microfluidic layout, allowing continuous fluorescence signal acquisitions with several emission wavelengths. In particular, we chose microgels endowed with fluorescent emitting molecules designed for multiplex spectral analysis of specific miRNA types. We analysed in a -real-time manner 80 microgel particles a minute at sample volumes down to a few microliters, achieving a miRNA detection limit of 202 fM in microfluidic flow conditions. Such performance opens up new routes for biosensing applications of particles within microfluidic devices.

摘要

我们展示了一种使用光谱编码微凝胶对微小RNA(miRNA)进行流入式超灵敏荧光检测的方法。我们研究并采用了一种粘弹性流体,以在直的测量通道中实现微凝胶的最佳排列,并应用了一种简单且廉价的微流体布局,从而能够以多种发射波长连续采集荧光信号。特别地,我们选择了带有为特定miRNA类型的多重光谱分析而设计的荧光发射分子的微凝胶。我们在微流体流动条件下,以每分钟80个微凝胶颗粒的速度实时分析低至几微升的样品体积,实现了202 fM的miRNA检测限。这样的性能为微流体装置内颗粒的生物传感应用开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc62/5148760/8e7afaf41585/BIOMGB-000010-064114_1-g001.jpg

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