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Assaying Biomarkers via Real-Time Measurements of the Effective Relaxation Time of Biofunctionalized Magnetic Nanoparticles Associated with Biotargets

机译:通过实时测量与生物靶标相关联的生物功能化磁性纳米颗粒的有效弛豫时间来测定生物标志物

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An assay of biomarkers consisting of alpha-fetoprotein (AFP) is reported. Real-time measurements of the effective relaxation timeτeff, when the biofunctionalized magnetic nanoparticles (BMNs) were conjugating with biotargets, were made. The BMNs are anti-alpha-fetoprotein (antiAFP) coated onto dextran-coated iron oxide nanoparticles labeled as Fe3O4-antiAFP. It was found that the effective relaxation time,τeff, increases as the association of AFP and Fe3O4-antiAFP evolves. We attribute this to the enhanced Brownian motion of BMNs when magnetic clusters are present during the conjugation. We found that saturation magnetization,Ms, increases when the concentration of AFP increases. This is due to the fact that more magnetic clusters are associated in the reagent, and therefore theMsincreases when the concentration of AFP increases. The change of effective relaxation time and saturation magnetization shows a behavior of logistic function, which provides a foundation for assaying an unknown amount of biomolecules. Thus, we demonstrate sensitive platforms for detecting AFP by characterizingτeff. The detection platform is robust and easy to use and shows promise for further use in assaying a broad number of biomarkers.
机译:报道了由甲胎蛋白(AFP)组成的生物标志物的测定。当生物功能化的磁性纳米粒子(BMN)与生物靶标结合时,进行有效弛豫时间τeff的实时测量。将BMNs包被在标记为Fe3O4-antiAFP的葡聚糖包被的氧化铁纳米粒子上的抗甲胎蛋白(antiAFP)。发现有效弛豫时间τeff随着AFP和Fe 3 O 4 -antiAFP的缔合的发展而增加。我们将其归因于共轭过程中存在磁簇时BMNs的布朗运动增强。我们发现,随着AFP浓度的增加,饱和磁化强度Ms会增加。这是由于以下事实:试剂中会结合更多的磁簇,因此当AFP浓度增加时M会增加。有效弛豫时间和饱和磁化强度的变化显示了逻辑函数的行为,这为测定未知量的生物分子提供了基础。因此,我们展示了通过表征eff来检测AFP的敏感平台。该检测平台坚固耐用且易于使用,显示出有望用于分析多种生物标志物的前景。

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