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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Electrochemiluminescence cytosensing platform based on Ru(bpy)32 @ silica -Au nanocomposite as luminophore and AuPd nanoparticles as coreaction accelerator for in situ evaluation of intracellular H2O2
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Electrochemiluminescence cytosensing platform based on Ru(bpy)32 @ silica -Au nanocomposite as luminophore and AuPd nanoparticles as coreaction accelerator for in situ evaluation of intracellular H2O2

机译:基于Ru(BPY)32的电化学发光胞嘧度平台32 @ Silica -U纳米复合材料作为发光体和AUPD纳米粒子作为植物促进剂,用于对细胞内H2O2进行原位评估

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摘要

An electrochemiluminescence (ECL) cytosensor was fabricated onto a microfluidic paper-based analytical device (p-PAD) in order to detect hydrogen peroxide (H2O2) which was released from tumor cells. The ECL probe Ru (bpy)32 @silica-Au nanocomposite (Ru@SiO2-Au) was fabricated and served as ECL reagent. The ECL of Ru@ Si02-Au nanocomposite was quenched by the ferrocene (Fc). AuPd nanoparticles (AuPd NPs), which were modified on the paper working electrode (PWE), were served as the catalyst of H2O2 to produce hydroxyl radicals ("OH) for cleaving Fc-labelled DNA to achieve "signal-on", and AuPd NPs also severed as coreaction accelerator. H202 was released from cells under the stimulation of phorbol myristate acetate. Fc-labelled DNA strand was cleaved via "OH. Fc molecule departed from the PWE surface, The ECL could be recovered. An ECL cytosensor on a 3D origami device was constructed. The ECL response of the Ru@Si02-Au-Fc system was related to the number of cells. The ECL intensity was quantitatively related with the logarithm of MCF-7 cells number and H202 concentration, the detection limit was 30 cells mL-1. As a consequence, this work provided a really low-cost and disposable p-PAD for sensitive detection of intracellular H202. What's more, this work had potential application value for studying cellular biology and pathophysiology.
机译:将电化学发光(ECL)胞嘧度(ECL)胞嘧度被制成微流体纸的分析装置(P垫),以检测从肿瘤细胞释放的过氧化氢(H 2 O 2)。 ECL探针Ru(BPY)32 @ Silica-Au纳米复合材料(Ru / @ SiO2-Au)制成并用作ECL试剂。用二茂铁(Fc)淬灭Ru @ SiO 2-Au纳米复合物的ECL。在纸张工作电极(PWE)上改性的AUPD纳米颗粒(AUPD NPS)用作H 2 O 2的催化剂,以产生羟基自由基(“OH),用于切割Fc标记的DNA以获得”信号 - on“,以及AUPD NPS也被切断为必修促进剂。H202在刺激磷肌酐醋酸盐的刺激下从细胞中释放。通过“哦,溶解Fc标记的DNA链。 Fc分子从PWE表面偏离PWE,可以回收ECL。构建了3D Origami设备上的ECL胞子传感器。 RU @ SI02-AU-FC系统的ECL响应与单元数有关。 ECL强度与MCF-7细胞数和H202浓度的对数定量相关,检测极限为30细胞ML-1。因此,这项工作提供了一种非常低成本和一次性P焊盘,用于细胞内H202的敏感性检测。更重要的是,这项工作具有研究蜂窝生物学和病理生理学的潜在应用价值。

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