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本文引用的文献

1
Re-shaping the coffee ring.重塑咖啡环。
Angew Chem Int Ed Engl. 2012 Mar 12;51(11):2546-8. doi: 10.1002/anie.201108008. Epub 2012 Jan 25.
2
Optofluidic fluorescent imaging cytometry on a cell phone.手机上的光流荧光成像细胞术。
Anal Chem. 2011 Sep 1;83(17):6641-7. doi: 10.1021/ac201587a. Epub 2011 Aug 2.
3
Gold nanoparticle enhanced electrochemiluminescence of CdS thin films for ultrasensitive thrombin detection.金纳米粒子增强的 CdS 薄膜电化学发光法用于超灵敏凝血酶检测。
Anal Chem. 2011 Jun 1;83(11):4004-11. doi: 10.1021/ac200616g. Epub 2011 May 5.
4
Nanochromatography driven by the coffee ring effect.基于咖啡环效应的纳米色谱分析。
Anal Chem. 2011 Mar 15;83(6):1871-3. doi: 10.1021/ac102963x. Epub 2011 Feb 2.
5
Portable, battery-operated, low-cost, bright field and fluorescence microscope.便携式、电池供电、低成本、明场和荧光显微镜。
PLoS One. 2010 Aug 4;5(8):e11890. doi: 10.1371/journal.pone.0011890.
6
Applications of aptamers as sensors.适体作为传感器的应用。
Annu Rev Anal Chem (Palo Alto Calif). 2009;2:241-64. doi: 10.1146/annurev.anchem.1.031207.112851.
7
Signal-on electrochemiluminescence biosensor for thrombin based on target-induced conjunction of split aptamer fragments.基于靶标诱导的分裂适体片段连接的凝血酶信号电化学发光生物传感器。
Chem Commun (Camb). 2010 Aug 14;46(30):5563-5. doi: 10.1039/c0cc00932f. Epub 2010 Jun 7.
8
Coffee-ring effect-based three dimensional patterning of micro/nanoparticle assembly with a single droplet.基于咖啡环效应的单液滴中微/纳颗粒组装的三维图案化。
Langmuir. 2010 Jul 20;26(14):11690-8. doi: 10.1021/la101110t.
9
Minimal size of coffee ring structure.咖啡环结构的最小尺寸。
J Phys Chem B. 2010 Apr 29;114(16):5269-74. doi: 10.1021/jp912190v.
10
Gold nanoparticles doped conducting polymer nanorod electrodes: ferrocene catalyzed aptamer-based thrombin immunosensor.金纳米粒子掺杂导电聚合物纳米棒电极:基于二茂铁催化的适体的凝血酶免疫传感器。
Anal Chem. 2009 Aug 15;81(16):6604-11. doi: 10.1021/ac900285v.

咖啡环适体传感器用于快速蛋白质检测。

Coffee ring aptasensor for rapid protein detection.

机构信息

Department of Bioengineering, University of California, Riverside, California 92521, United States.

出版信息

Langmuir. 2013 Jul 2;29(26):8440-6. doi: 10.1021/la400224a. Epub 2013 Apr 15.

DOI:10.1021/la400224a
PMID:23540796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4131697/
Abstract

We introduce a new biosensing platform for rapid protein detection that combines one of the simplest methods for biomolecular concentration, coffee ring formation, with a sensitive aptamer-based optical detection scheme. In this approach, aptamer beacons are utilized for signal transduction where a fluorescence signal is emitted in the presence of the target molecule. Signal amplification is achieved by concentrating aptamer-target complexes within liquid droplets, resulting in the formation of coffee ring "spots". Surfaces with various chemical coatings were utilized to investigate the correlation among surface hydrophobicity, concentration efficiency, and signal amplification. On the basis of our results, we found that the increase in the coffee ring diameter with larger droplet volumes is independent of surface hydrophobicity. Furthermore, we show that highly hydrophobic surfaces produce enhanced particle concentration via coffee ring formation, resulting in signal intensities 6-fold greater than those on hydrophilic surfaces. To validate this biosensing platform for the detection of clinical samples, we detected α-thrombin in human serum and 4-fold-diluted whole blood. Coffee ring spots from serum and blood produced detection signals up to 40 times larger than those from samples in liquid droplets. Additionally, this biosensor exhibits a lower limit of detection of 2 ng/mL (54 pM) in serum, and 4 ng/mL (105 pM) in blood. On the basis of its simplicity and high performance, this platform demonstrates immense potential as an inexpensive diagnostic tool for the detection of disease biomarkers, particularly for use in developing countries that lack the resources and facilities required for conventional biodetection practices.

摘要

我们介绍了一种新的生物传感平台,用于快速蛋白质检测,该平台将生物分子浓度的最简单方法之一(咖啡环形成)与基于敏感适体的光学检测方案相结合。在这种方法中,适体信标用于信号转导,在存在靶分子的情况下发出荧光信号。通过将适体-靶复合物浓缩在液滴内来实现信号放大,从而形成咖啡环“斑点”。利用各种化学涂层的表面来研究表面疏水性、浓度效率和信号放大之间的相关性。根据我们的结果,我们发现随着液滴体积的增大,咖啡环直径的增加与表面疏水性无关。此外,我们表明,疏水性表面通过咖啡环形成产生增强的颗粒浓度,从而产生比亲水性表面强 6 倍的信号强度。为了验证这种用于检测临床样本的生物传感平台,我们检测了人血清中的α-凝血酶和 4 倍稀释的全血。来自血清和血液的咖啡环斑点产生的检测信号比液滴中的样品大 40 倍。此外,该生物传感器在血清中的检测下限为 2 ng/mL(54 pM),在血液中的检测下限为 4 ng/mL(105 pM)。基于其简单性和高性能,该平台展示了作为廉价诊断工具用于检测疾病生物标志物的巨大潜力,特别是在缺乏常规生物检测所需资源和设施的发展中国家。