Wilkinson A P, Denning D W, Morgan M R
AFRC Institute of Food Research, Norwich Laboratory, UK.
Food Addit Contam. 1988 Oct-Dec;5(4):609-19. doi: 10.1080/02652038809373725.
A rapid, simple method for the determination of aflatoxin in human serum using anti-aflatoxin antisera in an indirect, double antibody microtitration plate enzyme-linked immunosorbent assay (ELISA) is described. Direct assay of serum necessitated the availability of a large sample volume, due to the presence of 'non-specific' interference. Addition of methanol to sera removed the interference enabling the analysis to be performed on small volumes (0.5 ml) of serum. The sensitivity of the assay is 20 pg ml-1. Total assay time, including sample preparation, is 4.5 h. No aflatoxin was found in any of the UK samples analysed.
本文描述了一种快速、简便的方法,该方法利用抗黄曲霉毒素抗血清,通过间接双抗体微量滴定板酶联免疫吸附测定法(ELISA)来测定人血清中的黄曲霉毒素。由于存在“非特异性”干扰,直接检测血清需要大量样本。向血清中加入甲醇可消除干扰,从而能够对少量(0.5毫升)血清进行分析。该测定方法的灵敏度为20皮克/毫升。包括样品制备在内的总测定时间为4.5小时。在分析的任何英国样品中均未发现黄曲霉毒素。