Lönnberg M, Carlsson J
Center for Surface Biotechnology, Uppsala, S-751 23, Sweden.
Anal Biochem. 2001 Jun 15;293(2):224-31. doi: 10.1006/abio.2001.5130.
This work describes the use of the combination of carbon black as an antibody label, a membrane-based immunochromatographic device, and a flatbed scanner as a quantitative test system. The scanner detected 0.4-345 ng carbon black/mm(2) on a nitrocellulose membrane (0.2-170 amol carbon black/mm(2)) with an imprecision (coefficient of variation, CV) lower than 2% for the carbon black determination and a detection limit of 0.04 ng carbon black/mm(2) (0.02 amol/mm(2)). The detection ability was compared to that obtained with alkaline phosphatase (ALP) using a substrate yielding a chemiluminescent signal (0.02 amol ALP/well), beta-galactosidase using a substrate yielding a fluorescent signal (0.3 amol beta-galactosidase/well), and horseradish peroxidase (HRP) using a substrate yielding a colored signal (5 amol HRP/microtiter well). The carbon black immunochromatographic test for immunoglobulin E (IgE) showed a detection limit of 0.13 pM IgE (0.01 kU/L) after a testing time of 10 min. The scanner detection imprecision for the IgE determination was 0.6% CV in the range 1-10 kU IgE/L when 2.3 mm(2) was used for detection and 1% CV when 0.19 mm(2) was used. A flatbed scanner is an inexpensive instrument with multiple uses, which now also includes the sensitive evaluation of immunoassays.
本研究描述了将炭黑用作抗体标记物、基于膜的免疫层析装置和平板扫描仪组合作为定量检测系统的应用。该扫描仪可在硝酸纤维素膜上检测到0.4 - 345 ng炭黑/mm²(0.2 - 170 amol炭黑/mm²),炭黑测定的不精密度(变异系数,CV)低于2%,检测限为0.04 ng炭黑/mm²(0.02 amol/mm²)。将该检测能力与使用产生化学发光信号的底物的碱性磷酸酶(ALP)(0.02 amol ALP/孔)、使用产生荧光信号的底物的β - 半乳糖苷酶(0.3 amolβ - 半乳糖苷酶/孔)以及使用产生显色信号的底物的辣根过氧化物酶(HRP)(5 amol HRP/微量滴定孔)的检测能力进行了比较。免疫球蛋白E(IgE)的炭黑免疫层析试验在10分钟的检测时间后显示检测限为0.13 pM IgE(0.01 kU/L)。当使用2.3 mm²进行检测时,IgE测定的扫描仪检测不精密度在1 - 10 kU IgE/L范围内为0.6% CV,当使用0.19 mm²时为1% CV。平板扫描仪是一种具有多种用途的廉价仪器,现在还包括免疫分析的灵敏评估。