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Enhancing the sensitivity of localized surface plasmon resonance (LSPR) biosensors using nanorods and DNA aptamers

机译:使用纳米棒和DNA适体的局部表面等离子体共振(LSPR)生物传感器增强敏感性

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Localized surface plasmon resonance (LSPR) biosensors have drawn much attention for their promising application in point-of-care diagnostics. While surface plasmon resonance (SPR) biosensing systems have been well developed, LSPR systems have the advantages of simpler and more compact setups. The LSPR peak shifts caused by the binding of molecules to the LSPR substrates, however, are usually smaller than 1 nm if no signal amplification mechanism is used. When using nanoparticles to enhance the sensitivity of LSPR biosensors, because of the short field penetration depth, the nanoparticles should be very close to the LSPR substrate to induce significant shifts in the LSPR peak position. In this study, we used DNA aptamers and gold nanorods to significantly increase the change in the LSPR peak position with the concentration of the target molecules. We have successfully used the proposed mechanism to detect 0.1 nM interferon-gamma (IFN-γ), a biomarker related to the diagnosis of latent tuberculosis infection. The calibration curves obtained in pure buffers and serum-containing buffers show that accurate detection can be achieved even when the sample is from complex biological fluids such as serum. Because of the enhancement in the sensitivity by the proposed sensing scheme, it is possible to use a low-cost spectrometer to build a LSPR biosensing system.
机译:局部表面等离子体共振(LSPR)生物传感器对他们在护理点诊断中的有前途的应用中汲取了很多关注。虽然表面等离子体共振(SPR)生物传感系统已经发育良好,但LSPR系统具有更简单更紧凑的设置。然而,如果没有使用信号放大机构,则由分子与LSPR基质的结合引起的LSPR峰值偏移通常小于1nm。当使用纳米颗粒增强LSPR生物传感器的灵敏度时,由于短场穿透深度,纳米颗粒应该非常接近LSPR衬底,以引起LSPR峰位置的显着变化。在这项研究中,我们使用DNA适体和金纳米棒以显着增加LSPR峰位置的变化与靶分子的浓度。我们已成功使用所提出的机制来检测0.1nm干扰素-γ(IFN-γ),生物标志物,与潜在结核感染的诊断有关。在纯缓冲液和含血清缓冲液中获得的校准曲线表明,即使样品来自诸如血清的复杂生物流体,也可以实现精确的检测。由于所提出的感测方案的灵敏度提高,可以使用低成本光谱仪来构建LSPR生物调位系统。

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