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Flow injection monitoring of aflatoxin M-1 in cheese using filter-supported bilayer lipid membranes with incorporated DNA

机译:使用结合了DNA的滤膜支持的双层脂质膜对奶酪中的黄曲霉毒素M-1进行流动注射监测

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This work describes a technique for the rapid and sensitive electrochemical flow injection monitoring of aflatoxin M-1 (AFM(1)) in cheese samples. Stabilized filter-supported bilayer lipid membranes (BLMs) were used as detectors Single stranded DNA oligomers terminated with alkyl chains (dT(20)-C-16) were incorporated into the membranes to control surface electrostatic properties. The incorporation of dT(20)-C-16 in BLMs lowered the detection limit for the detection of this toxin by one to four orders of magnitude as compared with the detection limit obtained in the absence of DNA. Therefore, it is now possible to continuously monitor this toxin at concentrations that approached those that could be of interest as set by the U.S. Food and Drug Administration and most European countries. The work described herein takes a significant step towards development of a detector of greater practical potential by demonstrating that the incorporation of C-16-ssDNA into lipid membranes results in a combination of properties that provides for a much more sensitive and robust detection system. Injections of AFM(1) were made into flowing streams of a 0.1 M KCI electrolyte solution, and a transient current signal with duration of seconds reproducibly appeared in about 12 s after exposure of the detector element to the toxin. The magnitude of this signal was linearly related to the concentration of AFM(1) with detection limits at subnanomolar level. The effect of interferents such as proteins and lipids was investigated. It was determined that interferences from proteins could be eliminated by adjustment of the flow rate of the carrier electrolyte solution. The technique was applied for the rapid flow injection determination of aflatoxin MI in cheese samples. AFM(1) could be determined in continuous flowing systems with a rate of at least 3 samples min(-1). Repetitive cycles of injection of AFM(1) have shown no signal degradation during each cycle for experiments that attempted over 30 cycles of detection. [References: 25]
机译:这项工作描述了一种快速,灵敏的电化学流动注射监测奶酪样品中黄曲霉毒素M-1(AFM(1))的技术。稳定的过滤器支持的双层脂质膜(BLM)用作检测器将烷基链终止的单链DNA寡聚物(dT(20)-C-16)掺入膜中以控制表面静电性能。与不存在DNA的检测限相比,在BLM中掺入dT(20)-C-16可使该毒素的检测限降低1-4个数量级。因此,现在有可能以接近美国食品药品监督管理局和大多数欧洲国家设定的浓度连续监测这种毒素。本文所述的工作通过证明将C-16-ssDNA掺入脂质膜可产生多种特性组合,从而朝着具有更大实用潜力的检测器的发展迈出了重要的一步,从而提供了更加灵敏且坚固的检测系统。将AFM(1)注入到0.1 M KCI电解质溶液的流动物流中,在将检测器元件暴露于毒素后约12 s内,可重复出现几秒钟的瞬态电流信号。该信号的大小与AFM(1)的浓度线性相关,检测极限在亚纳摩尔水平。研究了蛋白质和脂质等干扰物的作用。已确定可以通过调节载体电解质溶液的流速来消除蛋白质的干扰。该技术用于奶酪样品中黄曲霉毒素MI的快速流动注射测定。可以在连续流动系统中以至少3个样本min(-1)的速率确定AFM(1)。重复注射AFM(1)的循环显示,在尝试进行30个以上检测循环的实验的每个循环中,没有信号衰减。 [参考:25]

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