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Detection of Aflatoxin B1 Based on a Porous Anodized Aluminum Membrane Combined with Surface-Enhanced Raman Scattering Spectroscopy

机译:多孔阳极氧化铝膜结合表面增强拉曼散射光谱技术检测黄曲霉毒素B1

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摘要

An Aflatoxin B (AFB ) biosensor was fabricated via an Ag nanoparticles assembly on the surface of a porous anodized aluminum (PAA) membrane. First, the Raman reporter 4-Aminothiophenol (4-ATP) and DNA (partially complementary to AFB aptamer) were attached to the surface of Ag nanoparticles (AgNPs) by chemical bonding to form a 4-ATP-AgNPs-DNA complex. Similarly, the surface of a PAA membrane was functionalized with an AFB aptamer. Then, the PAA surface was functionalized with 4-ATP-AgNPs-DNA through base complementary pairing to form AgNPs-PAA sensor with a strong Raman signal. When AFB was added, AgNPs would be detached from the PAA surface because of the specific binding between AFB and the aptamer, resulting in a reduction in Raman signals. The detection limit of the proposed biosensor is 0.009 ng/mL in actual walnut and the linear range is 0.01–10 ng/mL. The sensor has good selectivity and repeatability; it can be applied to the rapid qualitative and quantitative detection of AFB .
机译:黄曲霉毒素B(AFB)生物传感器是通过在多孔阳极氧化铝(PAA)膜表面上的Ag纳米颗粒组装而成的。首先,通过化学键合将拉曼报告基因4-氨基硫酚(4-ATP)和DNA(与AFB适体部分互补)附着到Ag纳米颗粒(AgNPs)的表面,形成4-ATP-AgNPs-DNA复合物。类似地,用AFB适体对PAA膜的表面进行功能化。然后,通过碱基互补配对用4-ATP-AgNPs-DNA对PAA表面进行功能化,以形成具有强拉曼信号的AgNPs-PAA传感器。当添加AFB时,由于AFB与适体之间的特异性结合,AgNPs将与PAA表面分离,从而导致拉曼信号降低。拟议中的生物传感器在实际核桃中的检出限为0.009 ng / mL,线性范围为0.01–10 ng / mL。该传感器具有良好的选择性和重复性;可用于AFB的快速定性和定量检测。

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