Han Seung-Mok, Cho Joung-Hwan, Cho Il-Hoon, Paek Eui-Hwan, Oh Hee-Bok, Kim Bong-Su, Ryu Chunsun, Lee Kyunghee, Kim Young-Kee, Paek Se-Hwan
Program for Bio-Microsystem Technology, Korea University, 1, 5-ka Anam-dong, Sungbuk-ku, Seoul 136-701, South Korea.
Anal Chim Acta. 2007 Mar 21;587(1):1-8. doi: 10.1016/j.aca.2007.01.028. Epub 2007 Jan 20.
A plastic ELISA-on-a-chip (EOC) employing the concept of cross-flow immuno-chromatographic analysis was applied to the measurement of botulinum neurotoxin A (BoNT/A) as agent for bio-terrorism. Two monoclonal antibodies specific to the heavy chain of the toxin were raised and identified to form sandwich binding complexes as the pair with the analyte. For the construction of an immuno-strip, one was utilized as the capture antibody immobilized onto nitrocellulose membrane and the other as the detection coupled to an enzyme, horseradish peroxidase. The two plates of EOC used in this study were fabricated by injection molding of polycarbonate to improve the reproducibility of manufacture and, after inclusion of the immuno-strip, bonded using a UV-sensitive adhesive. Under optimal conditions of analysis, the chip produced a color signal in proportion to the analyte dose and the signal was quantified using a detector equipped with a digital camera. From the dose-response curve, the detection limit of BoNT/A was 2.0 ng mL(-1), approximately five times more sensitive than a commercial-version detection kit employing colloidal gold tracer.
一种采用错流免疫色谱分析概念的塑料芯片酶联免疫吸附测定法(EOC)被应用于检测作为生物恐怖主义制剂的肉毒杆菌神经毒素A(BoNT/A)。制备并鉴定了两种针对该毒素重链的单克隆抗体,它们与分析物形成夹心结合复合物。为构建免疫试纸条,一种抗体用作捕获抗体固定在硝酸纤维素膜上,另一种与辣根过氧化物酶偶联用作检测抗体。本研究中使用的两片EOC芯片通过聚碳酸酯注塑成型制造,以提高制造的可重复性,在装入免疫试纸条后,用紫外线敏感粘合剂进行粘合。在最佳分析条件下,芯片产生与分析物剂量成比例的颜色信号,并使用配备数码相机的检测器对信号进行定量。根据剂量 - 反应曲线,BoNT/A的检测限为2.0 ng mL⁻¹,比采用胶体金示踪剂的商业版检测试剂盒灵敏度高约五倍。