Author: Chen, Cuicui; Guo, Xiaoxiao; Liang, Huankun; Ning, Bo; Li, Jiexing; Zhong, Shuhai; Liu, Xipan; Li, Laiqing
Title: Determination of parvovirus antibodies in canine serum using magnetic beadâ€based chemiluminescence immunoassay Cord-id: l7qui35s Document date: 2019_5_30
ID: l7qui35s
Snippet: Canine parvovirus type 2 (CPVâ€2), as a highly contagious and potentially fatal disease of dogs and many other carnivores, usually causes severe gastroenteritis and myocarditis. Therefore, it is very necessary and urgent to have an accurate method to determine the CPVâ€2 antibodies (CPVâ€2â€Ab) in canine samples. Here, a magnetic bead–based chemiluminescence immunoassay was established and optimized to detect the concentration of CPVâ€2â€Ab in serum. And a commercial assay was also used
Document: Canine parvovirus type 2 (CPVâ€2), as a highly contagious and potentially fatal disease of dogs and many other carnivores, usually causes severe gastroenteritis and myocarditis. Therefore, it is very necessary and urgent to have an accurate method to determine the CPVâ€2 antibodies (CPVâ€2â€Ab) in canine samples. Here, a magnetic bead–based chemiluminescence immunoassay was established and optimized to detect the concentration of CPVâ€2â€Ab in serum. And a commercial assay was also used to evaluate the consistency with our method. After optimization of the detective system, the CPVâ€2â€Ab was captured by CPVâ€antigenâ€magnetic bead (8.3 µg/mL); then combined with the conjugation of antiâ€canine IgG antibodyâ€acridinium ester (0.36 µg/mL). Finally, collected the signal (read the luminosity) after 1 H reaction time. The linear correlation coefficient (R(2)) is 0.9924. The limit of detection (sensitivity) is 0.36 ng/mL (the linear dynamic range: 1.32–93.75 ng/mL), and the average recovery is 100.89% without crossâ€reactions with other canine viral antibodies. The results’ correlation between commercial assays and this method is 0.9888. This immunoassay establishes that it has high sensitivity, accuracy, and specificity in clinical analysis, indicating that this method could be suitable for quantitative detection of CPVâ€2â€Ab and evaluation of vaccination effect.
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