Urusov Alexandr E, Petrakova Alina V, Vozniak Maxim V, Zherdev Anatoly V, Dzantiev Boris B
Bach Institute of Biochemistry of the Russian Academy of Sciences, Leninsky Prospect 33, Moscow 119071, Russia.
IL Test-Pushchino Ltd., Gruzovaya Street 1g, Pushchino 142290, Moscow Region, Russia.
Sensors (Basel). 2014 Nov 18;14(11):21843-57. doi: 10.3390/s141121843.
The main limitations of microplate-based enzyme immunoassays are the prolonged incubations necessary to facilitate heterogeneous interactions, the complex matrix and poorly soluble antigens, and the significant sample dilutions often required because of the presence of organic extractants. This study presents the use of antibody immobilization on the surface of magnetic particles to overcome these limitations in the detection of the mycotoxin, aflatoxin B1. Features of the proposed system are a high degree of nanoparticle dispersion and methodologically simple immobilization of the antibodies by adsorption. Reactions between the immobilized antibodies with native and labeled antigens are conducted in solution, thereby reducing the interaction period to 5 min without impairing the analytical outcome. Adsorption of immunoglobulins on the surface of magnetic nanoparticles increases their stability in aqueous-organic media, thus minimizing the degree of sample dilution required. Testing barley and maize extracts demonstrated a limit of aflatoxin B1 detection equal to 20 pg/mL and total assay duration of 20 min. Using this method, only the 3-fold dilution of the initial methanol/water (60/40) extraction mixture in the microplate wells is necessary. The proposed pseudo-homogeneous approach could be applied toward immunodetection of a wide range of compounds.
基于微孔板的酶免疫测定的主要局限性在于,为促进异相相互作用需要长时间孵育,存在复杂基质和难溶性抗原,以及由于有机萃取剂的存在常常需要大量样品稀释。本研究介绍了通过将抗体固定在磁性颗粒表面来克服这些局限性,以检测霉菌毒素黄曲霉毒素B1。所提出系统的特点是纳米颗粒高度分散,并且通过吸附固定抗体的方法简单。固定化抗体与天然和标记抗原之间的反应在溶液中进行,从而将相互作用时间缩短至5分钟,而不影响分析结果。免疫球蛋白吸附在磁性纳米颗粒表面可提高其在水-有机介质中的稳定性,从而将所需样品稀释程度降至最低。对大麦和玉米提取物的检测表明,黄曲霉毒素B1的检测限为20 pg/mL,总检测时间为20分钟。使用该方法,在微孔板孔中仅需将初始甲醇/水(60/40)萃取混合物稀释3倍。所提出的准均相方法可应用于多种化合物的免疫检测。
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