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首页> 外文期刊>Journal of the American Society for Mass Spectrometry >A New Strategy for Highly Sensitive Immunoassay Based on Single-Particle Mode Detection by Inductively Coupled Plasma Mass Spectrometry
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A New Strategy for Highly Sensitive Immunoassay Based on Single-Particle Mode Detection by Inductively Coupled Plasma Mass Spectrometry

机译:基于电感耦合等离子体质谱单颗粒模式检测的高灵敏度免疫测定新策略

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摘要

A highly sensitive immunoassay is proposed based on time-resolved inductively coupled plasma mass spectrometry with nanoparticles as tags to antibody. Instead of using traditional integral mode detection, the transient signals induced by the flash of ions in the plasma torch from the ionization of nanoparticles tagged on antibody were recorded in a time-resolved mode. Since, under certain conditions, the frequency of transient signals is directly correlated to the concentration of nanoparticle tags, the concentration of nanoparticle-tagged antibodies can be quantified by the frequency of transient signals. With the present instrument setup, gold nanoparticle (Au-NP) tags, as small as about 15 nm in diameter, can be detected. This protocol is evaluated for a competitive immunoassay and the linear range for a-fetoprotein is 0.016-6.8 mu g/L (between 20 and 80% inhibition). The limit of quantification is 0.016 mu g/L (20% inhibition, IC20) with a relative standard deviation of 4.2% (20% inhibition, 4 replicates) for a-fetoprotein. The present strategy provides a sensitive readout method for nanoparticle tags, which is quite promising for numerous applications in immunoassay, DNA hybridization, and other biological analyses. (J Am Soc Mass Spectrom 2009, 20, 1096-1103).
机译:基于时间分辨的电感耦合等离子体质谱法,以纳米颗粒作为抗体标签,提出了一种高灵敏度的免疫测定方法。代替使用传统的积分模式检测,以时间分辨模式记录由血浆炬中的离子闪光引起的瞬态信号,该瞬态信号是由标记在抗体上的纳米粒子的电离引起的。由于在某些条件下,瞬态信号的频率与纳米标签的浓度直接相关,因此可以通过瞬态信号的频率来量化带有纳米颗粒标签的抗体的浓度。使用本仪器设置,可以检测到直径约15 nm的金纳米颗粒(Au-NP)标签。评估该方案用于竞争性免疫测定,α-甲胎蛋白的线性范围为0.016-6.8μg / L(20%至80%抑制)。甲胎蛋白的定量限为0.016μg / L(20%抑制,IC20),相对标准偏差为4.2%(20%抑制,重复4次)。本策略为纳米标签提供了灵敏的读出方法,对于免疫测定,DNA杂交和其他生物学分析中的许多应用而言,这是非常有前途的。 (J Am Soc Mass Spectrom 2009,20,1096-1103)。

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