Preparation of a highly specific and sensitive monoclonal antibody against tilmicosin and its application in lateral flow immunoassay

被引:0
|
作者
Youyi Wang
Qingyue Li
Guanghua Liang
Huayun Li
Zizhe Li
Tian Gao
Lianjun Song
Xianqing Huang
Dapeng Peng
Xiya Zhang
机构
[1] Henan Agricultural University,Henan Engineering Technology Research Center of Food Processing and Circulation Safety Control, College of Food Science and Technology
[2] Development Center of Livestock and Veterinary,Henan Province Measurement Standard and Product Quality Inspection and Testing Center
[3] Fuling District,National Reference Laboratory of Veterinary Drug Residues
[4] Guancheng District,undefined
[5] Huazhong Agricultural University,undefined
来源
One Health Advances | / 1卷 / 1期
关键词
Hapten design; Monoclonal antibody; High sensitivity; Tilmicosin; Lateral flow immunoassay;
D O I
10.1186/s44280-023-00032-w
中图分类号
学科分类号
摘要
To reduce the false positive results caused by cross reactivity of the antibodies with other structural analogues, it is crucial to prepare a high specificity and sensitivity antibody against target for developing an accurate immunoassay. In this study, tilmicosin (TM) was selected as a model molecule. Firstly, two-dimensional similarity, electrostatic potential energy, mulliken atomic charges and overlapping of different haptens with TM were calculated using Gaussian 09W and Discovery studio, and the newly designed TM-HS was selected as the optimal hapten. Furthermore, a monoclonal antibody (mAb 12C8) was produced with the half maximal inhibitory concentration (IC50) of 0.36 ng/mL, and negligible cross-reactivity (CR) with other antibiotics. Finally, a lateral flow immunoassay (LFA) for the detection of TM based on amorphous carbon nanoparticles (ACNPs) labeled mAb 12C8 was developed by the reflectance value under natural light. The recoveries of TM ranged from 83.18% to 103.25% with a coefficient of variation (CV) < 12.47%. The results showed that the cut-off value of TM in milk samples was 1 ng/mL, and the limits of detection (LODs) for chicken muscle, bovine muscle, porcine muscle and porcine liver samples were 5.23, 5.98, 6.85 and 7.31 μg/kg, respectively. In addition, 40 real samples were tested by the LFA, and the detection results were consisted with that of high-performance liquid chromatography-UV detector (HPLC–UV). Those results indicated that the developed LFA is an accurate and useful tool for on-site screening of TM in milk and animal tissues.
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