Antigen detection based on background fluorescence quenching immunochromatographic assay

2014 ◽  
Vol 841 ◽  
pp. 44-50 ◽  
Author(s):  
Xiangjun Chen ◽  
Yangyang Xu ◽  
Jinsheng Yu ◽  
Jiutong Li ◽  
Xuelei Zhou ◽  
...  
2017 ◽  
Vol 2017 ◽  
pp. 1-7 ◽  
Author(s):  
Xiaoxia Wu ◽  
Xiaofeng Tian ◽  
Lihua Xu ◽  
Jiutong Li ◽  
Xinxia Li ◽  
...  

Harsh demanding has been exposed on the concentration of aflatoxin M1 (AFM1) and chloramphenicol (CAP) in milk. In this study, we developed a new method based on background fluorescence quenching immunochromatographic assay (bFQICA) to detect AFM1 and CAP in milk. The detection limit for AFM1 was 0.0009 ng/mL, while that for the CAP was 0.0008 ng/mL. The assay variability was determined with 3 AFM1 standards (i.e., 0.25 ng/mL, 0.5 ng/mL, and 1.0 ng/mL), and the actual detection value was 0.2497, 0.5329, and 1.0941, respectively. For the assay variability of 3 CAP standards (i.e., 0.10 ng/mL, 0.30 ng/mL, and 0.50 ng/mL), the actual detection value was 0.0996, 0.3096, and 0.4905, respectively. The recovery rate of AFM1 was 99.7%–101.7%, while that for CAP was 95.3%–97.6%. For the test stability, AFM1 and CAP showed satisfactory test stability even at month 5. Compared with the sensitivity of liquid chromatography-mass spectrometry (LC-MS) method, no statistical difference was noticed in results of the bFQICA. Our method is convenient for the detection of AFM1 and CAP in milk with a test duration of about 8 minutes. Additionally, an internal WiFi facility is provided in the system allowing for quick connection and storage in the intelligent cell phone.


2016 ◽  
Vol 8 (3) ◽  
pp. 627-631 ◽  
Author(s):  
Ganggang Zhang ◽  
Minghui Chen ◽  
Daofeng Liu ◽  
Yonghua Xiong ◽  
Ronghua Feng ◽  
...  

β2-Adrenergic agonists are banned in China and other areas in the world.


2019 ◽  
Vol 38 (2) ◽  
pp. 172-180 ◽  
Author(s):  
Wei Zhang ◽  
Junlei Chen ◽  
Xinxia Li ◽  
Yuwen Wang ◽  
Jiutong Li

SummaryBackgroundTo establish a fast and simple quantitative method for detection of heart-type fatty acid-binding protein (H-FABP) in serum based on a background fluorescence quenching immunochromatographic assay.MethodsA detection card based on the double-antibody sandwich double-antibody method with background fluorescence quenching was developed for quantitative measurement of H-FABP in serum. The optimal concentrations of control for coating the test and control lines were determined as well as the concentrations of gold-labeled antibodies used in preparing the detection system. The detection method for H-FABP in serum was established and validated using real-world clinical samples.ResultsThe optimal concentrations of labeling antibody and coating antibody were 5.0 μg/mL and 1.0 mg/mL, respectively. The test card had a sensitivity of 1.15 ng/mL over a linear concentration range of 0–100 ng/mL. Based on three batches prepared for testing the card, the relative standard deviation (RSD) within batches was less than 15% without a significant difference (P=0.942). The detection method was tested against common interfering substances in serum, such as bilirubin, triglyceride and serum anticoagulants ethylenediamine tetraacetic acid (EDTA), heparin, and sodium citrate, and no significant cross-reaction was detected. The test method was further validated with 50 clinical serum samples, and the test results were comparable with standard reference detection methods with good correlation (R=0.95).ConclusionOur study presents a new method with strong specificity and sensitivity for the detection of H-FABP in serum, which could promote H-FABP detection in a broad range of applications.


2009 ◽  
Vol 158 (1-2) ◽  
pp. 160-164 ◽  
Author(s):  
Angela Yumico Mikawa ◽  
Sandra Antonia Tagliavini Santos ◽  
Flávia Regina Kenfe ◽  
Flávio Henrique da Silva ◽  
Paulo Inácio da Costa

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