Andreou V G, Nikolelis D P
Department of Chemistry, University of Athens, Greece.
Anal Chem. 1998 Jun 1;70(11):2366-71. doi: 10.1021/ac9712097.
This work describes a technique for the rapid and sensitive electrochemical flow injection monitoring of aflatoxin M1 (AFM1) using stabilized systems of filter-supported bilayer lipid membranes (BLMs). Injections of AFM1 were made into flowing streams of a carrier electrolyte solution, and a transient current signal with a duration of seconds reproducibly appeared less than 10 s after exposure of the lipid membranes to the toxin. The magnitude of this signal was linearly related to the concentration of AFM1, with detection limits at the subnanomolar level. The mechanism of signal generation was investigated by differential scanning calorimetric experiments. The technique was applied for the rapid flow injection determination of AFM1 in milk and milk preparations. The effect of potent interferences such as proteins and lipids was investigated, and the results show that interferences from these milk constituents can be eliminated by modulation of the flow rate of the carrier solution so as not to allow adsorption of these compounds in BLMs. AFM1 could be determined in continuous flowing systems with a rate of at least 4 samples min-1. Repetitive cycles of injection of AFM1 showed no signal degradation during each cycle.
这项工作描述了一种使用滤膜支撑的双层脂质膜(BLM)稳定系统对黄曲霉毒素M1(AFM1)进行快速灵敏的电化学流动注射监测的技术。将AFM1注入载流电解质溶液的流动流中,在脂质膜暴露于毒素后不到10秒,会重复出现持续数秒的瞬态电流信号。该信号的大小与AFM1的浓度呈线性关系,检测限处于亚纳摩尔水平。通过差示扫描量热实验研究了信号产生的机制。该技术用于牛奶和奶制品中AFM1的快速流动注射测定。研究了蛋白质和脂质等强干扰物的影响,结果表明,通过调节载液流速以防止这些化合物吸附在BLM中,可以消除这些牛奶成分的干扰。AFM1可以在连续流动系统中以至少每分钟4个样品的速率进行测定。重复注射AFM1的循环在每个循环中均未出现信号降解。