Aguilar Zoraida P, Sirisena Mali
Vegrandis, LLC, 700 W. Research Ctr. Blvd., ENRC 1208, Fayetteville, AR 72701, USA.
Anal Bioanal Chem. 2007 Sep;389(2):507-15. doi: 10.1007/s00216-007-1448-z. Epub 2007 Jul 18.
Picogram levels of antibodies against the protective antigen (PA) of Bacillus anthracis were detected in an automated electrochemical sandwich-type enzyme-linked immunosorbant assay. The antibodies were captured and detected using an 8 x 3 array of 50-microm-diameter cavities. The reagent and sample volumes were as low as 200 nL in a less than 25-min assay from capture to signal generation. The electrochemical detection of the antibodies was demonstrated at 0.05-10 microg/mL containing only 10-5,000 pg antibodies. The limit of detection is 10 fg for a 200-nL sample. Detection of anti-PA immunoglobulin G performed in spiked normal human serum and fresh whole human blood did not show a significant difference from detection in a buffer. The initial automation of the assay involved the use of a digital syringe pump for the delivery of reagents to the capture surface.
在自动电化学夹心型酶联免疫吸附测定中检测到了皮克水平的抗炭疽芽孢杆菌保护性抗原(PA)抗体。使用直径为50微米的8×3阵列微孔捕获并检测抗体。从捕获到信号产生的检测过程不到25分钟,试剂和样品体积低至200纳升。在仅含有10 - 5000皮克抗体的0.05 - 10微克/毫升浓度下证明了抗体的电化学检测。对于200纳升样品,检测限为10飞克。在加标的正常人血清和新鲜全血中进行的抗PA免疫球蛋白G检测与在缓冲液中的检测没有显著差异。该检测的初步自动化涉及使用数字注射泵将试剂输送到捕获表面。