State Key Laboratory of Pathogen and Biosecurity, Institute of Microbiology and Epidemiology, Academy of Military Medical Sciences, No. 20 Dongda Street, Fengtai District, Beijing 100071, People's Republic of China.
J Food Prot. 2012 Jan;75(1):112-7. doi: 10.4315/0362-028X.JFP-11-252.
In the present study, we developed a convenient, rapid, and sensitive immunochromatographic (IC) test strip to detect abrin in assay buffer and spiked abrin in test food samples. The abrin IC test strip was based on a sandwich format consisting of a monoclonal antibody and a polyclonal antibody. The anti-abrin A chain monoclonal antibody from mice was immobilized on a porous nitrocellulose membrane as a capture antibody, while the anti-abrin polyclonal antibody from rabbits was conjugated to colloidal gold particles, serving as a detection antibody. Both visual observation and quantitative analysis indicated that the lower detection of the strip was about 3 ng/ml when abrin was directly spiked into milk, orange juice, and drinking water at a concentration of 3 to 60 ng/ml; the analytical recovery rate was 92.2 to 128%. With this method, abrin spiked into food could be detected in less than 10 min. Moreover, the IC test strip showed no cross-reaction with the closely related phytotoxin ricin. Therefore, our test strip is an ideal candidate for the development of a kit for rapid and quantitative detection of abrin in food samples.
在本研究中,我们开发了一种方便、快速、灵敏的免疫层析(IC)测试条,用于检测检测缓冲液中的蓖麻毒素和测试食品样品中的添加蓖麻毒素。蓖麻毒素 IC 测试条基于夹心型结构,由单克隆抗体和多克隆抗体组成。来自小鼠的抗蓖麻毒素 A 链单克隆抗体被固定在多孔硝酸纤维素膜上作为捕获抗体,而来自兔子的抗蓖麻毒素多克隆抗体则与胶体金颗粒偶联,作为检测抗体。无论是通过肉眼观察还是定量分析,均表明当直接将蓖麻毒素以 3 至 60 ng/ml 的浓度添加到牛奶、橙汁和饮用水中时,该条带的最低检测下限约为 3ng/ml;分析回收率为 92.2%至 128%。使用这种方法,不到 10 分钟即可检测到添加到食物中的蓖麻毒素。此外,IC 测试条与密切相关的植物毒素相思豆毒素没有交叉反应。因此,我们的测试条是开发用于快速定量检测食品样品中蓖麻毒素试剂盒的理想候选物。