Ito Kaori, Yamamoto Takayuki, Oyama Yuriko, Tsuruma Rieko, Saito Eriko, Saito Yoshikazu, Ozu Takeshi, Honjoh Tsutomu, Adachi Reiko, Sakai Shinobu, Akiyama Hiroshi, Shoji Masahiro
Morinaga Institute of Biological Science, Inc., Sachiura 2-1-16, Kanazawa-ku, Yokohama, 236-0003, Japan.
National Institute of Health Sciences, Setagaya-ku, Tokyo, 158-8501, Japan.
Anal Bioanal Chem. 2016 Sep;408(22):5973-84. doi: 10.1007/s00216-016-9438-7. Epub 2016 Mar 14.
Enzyme-linked immunosorbent assay (ELISA) is commonly used to determine food allergens in food products. However, a significant number of ELISAs give an erroneous result, especially when applied to highly processed food. Accordingly, an improved ELISA, which utilizes an extraction solution comprising the surfactant sodium lauryl sulfate (SDS) and reductant 2-mercaptoethanol (2-ME), has been specially developed to analyze food allergens in highly processed food by enhancing analyte protein extraction. Recently, however, the use of 2-ME has become undesirable. In the present study, a new extraction solution containing a human- and eco-friendly reductant, which is convenient to use at the food manufacturing site, has been established. Among three chemicals with different reducing properties, sodium sulfite, tris(3-hydroxypropyl)phosphine, and mercaptoethylamine sodium sulfite was selected as a 2-ME substitute. The protein extraction ability of SDS/0.1 M sodium sulfite solution was comparable to that of SDS/2-ME solution. Next, the ELISA performance for egg, milk, wheat, peanut, and buckwheat was evaluated by using model-processed foods and commercially available food products. The data showed that the SDS/0.1 M sulfite ELISA significantly correlated with the SDS/2-ME ELISA for all food allergens examined (p < 0.01), thereby establishing the validity of the SDS/0.1 M sulfite ELISA performance. Furthermore, the new SDS/0.1 M sulfite solution was investigated for its applicability to the lateral-flow (LF) test. The result demonstrated the successful analysis of food allergens in processed food, showing consistency with the SDS/0.1 M sulfite ELISA results. Accordingly, a harmonized analysis system for processed food comprising a screening LF test and a quantitative ELISA with identical extraction solution has been established. The ELISA based on the SDS/0.1 M sulfite extraction solution has now been authorized as the revised official method for food allergen analysis in Japan.
酶联免疫吸附测定(ELISA)通常用于测定食品中的食物过敏原。然而,大量的ELISA会给出错误结果,尤其是应用于高度加工食品时。因此,一种改进的ELISA已被专门开发出来,它使用了一种包含表面活性剂十二烷基硫酸钠(SDS)和还原剂2-巯基乙醇(2-ME)的提取溶液,通过增强分析物蛋白质提取来分析高度加工食品中的食物过敏原。然而,最近2-ME的使用变得不可取。在本研究中,已经建立了一种含有对人和环境友好的还原剂的新提取溶液,该溶液在食品生产现场使用方便。在三种具有不同还原特性的化学物质中,亚硫酸钠、三(3-羟丙基)膦和巯基乙胺亚硫酸钠中,亚硫酸钠被选为2-ME的替代品。SDS/0.1M亚硫酸钠溶液的蛋白质提取能力与SDS/2-ME溶液相当。接下来,通过使用模型加工食品和市售食品来评估ELISA对鸡蛋、牛奶、小麦、花生和荞麦的性能。数据表明,对于所有检测的食物过敏原,SDS/0.1M亚硫酸盐ELISA与SDS/2-ME ELISA显著相关(p<0.01),从而确立了SDS/0.1M亚硫酸盐ELISA性能的有效性。此外还研究了新的SDS/0.1M亚硫酸盐溶液在侧流(LF)检测中的适用性。结果表明成功分析了加工食品中的食物过敏原,与SDS/0.1M亚硫酸盐ELISA结果一致。因此,已经建立了一个用于加工食品的统一分析系统,该系统包括一个筛选LF检测和一个使用相同提取溶液的定量ELISA。基于SDS/0.1M亚硫酸盐提取溶液的ELISA现已被批准为日本食品过敏原分析的修订官方方法。