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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >A plasmonic colorimetric strategy for biosensing through enzyme guided growth of silver nanoparticles on gold nanostars
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A plasmonic colorimetric strategy for biosensing through enzyme guided growth of silver nanoparticles on gold nanostars

机译:通过酶引导的银纳米粒子在金纳米星上的生长来进行生物传感的等离子体比色法

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A plasmonic colorimetric strategy was designed for sensitive detection of biomolecules through enzyme guided silver nanoparticles (AgNPs) growth on gold nanostars (AuNS). The growth of AgNPs on AuNS led to a substantial blue shift of the localized surface plasmon resonance (LSPR) peak and the color change of AuNS from blue to dark blue, purple and ultimately orange. Both the LSPR blueshift wavelength and the color of detection solution containing AuNS, Ag+ and ascorbic acid 2-phosphate (AAP) depend on the amount of enzyme that catalyzed the dephosphorylation of AAP to reduce Ag+ on AuNS surface. Thus this strategy could be used for LSPR and naked-eye detections of both the enzyme such as alkaline phosphatase (ALP) and other biomolecules involved in biorecognition events using ALP as a tag. The LSPR detection method for ALP showed a linear range from 1.0 pM to 25 nM with a detection limit of 0.5 pM. Using DNA as a mode target molecule, this technique showed a detection range from 10 fM to 50 pM DNA with a detection limit of 2.6 fM through the convenient combination with hybridization chain reaction amplification. The proposed plasmonic colorimetric strategy could be extended as a general analytical platform for design of immunosensors and aptasensors with ALP as a label. (C) 2015 Elsevier B.V. All rights reserved.
机译:设计了等离子比色策略,用于通过在金纳米星(AuNS)上酶促银纳米颗粒(AgNPs)的生长来灵敏检测生物分子。 AgNPs在AuNS上的生长导致局部表面等离振子共振(LSPR)峰发生明显的蓝移,并且AuNS的颜色从蓝色变为深蓝色,紫色并最终变为橙色。 LSPR蓝移波长和包含AuNS,Ag +和抗坏血酸2-磷酸(AAP)的检测溶液的颜色均取决于催化AAP脱磷酸以还原AuNS表面上Ag +的酶的量。因此,该策略可用于LSPR和肉眼检测酶(例如碱性磷酸酶(ALP))以及使用ALP作为标签参与生物识别事件的其他生物分子。用于ALP的LSPR检测方法显示出1.0 pM至25 nM的线性范围,检测限为0.5 pM。通过将DNA用作模式目标分子,该技术通过与杂交链反应扩增的便捷结合,显示了10 fM至50 pM DNA的检测范围,检测限为2.6 fM。拟议的等离子比色策略可以扩展为设计以ALP为标记的免疫传感器和适体传感器的通用分析平台。 (C)2015 Elsevier B.V.保留所有权利。

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