杨兴东,曲扬,王趁趁,毋丽华,何贝贝,王小慧,胡骁飞.间接竞争酶联免疫吸附测定法快速筛查药酒中双氯芬酸[J].食品安全质量检测学报,2024,15(16):39-44
间接竞争酶联免疫吸附测定法快速筛查药酒中双氯芬酸
Indirect competitive enzyme-linked immunosorbent assay for rapid screening of diclofenac in medicinal liquor
投稿时间:2024-07-31  修订日期:2024-08-28
DOI:
中文关键词:  双氯芬酸  合成抗原  单克隆抗体  酶联免疫吸附测定法  药酒
英文关键词:Diclofenac  synthetic antigen  monoclonal antibody  enzyme-linked immunosorbent assay  medicinal liquor
基金项目:河南省科技攻关项目(212102110094)、周口师范学院中青年骨干教师资助项目
作者单位
杨兴东 周口师范学院 
曲扬 周口师范学院生命科学与农学学院 
王趁趁 周口师范学院生命科学与农学学院 
毋丽华 周口师范学院生命科学与农学学院 
何贝贝 周口师范学院生命科学与农学学院 
王小慧 周口师范学院生命科学与农学学院 
胡骁飞 河南省农业科学院动物免疫学重点实验室 
AuthorInstitution
YANG Xing-Dong College of Life Science and Agriculture,Zhoukou Normal University 
QU Yang College of Life Science and Agriculture,Zhoukou Normal University 
WANG Chen-Chen College of Life Science and Agriculture,Zhoukou Normal University 
WU Li-Hua College of Life Science and Agriculture,Zhoukou Normal University 
HE Bei-Bei College of Life Science and Agriculture,Zhoukou Normal University 
WANG Xiao-Hui College of Life Science and Agriculture,Zhoukou Normal University 
HU Xiao-Fei Key Laboratory of Animal Immunology,Henan Academy of Agricultural Sciences 
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中文摘要:
      目的 建立间接竞争酶联免疫吸附测定法快速筛查药酒中双氯芬酸(diclofenac, DCF)。方法 采用活性酯法和混合酸酐法分别将DCF与载体蛋白耦合, 得到DCF的免疫原和检测抗原。采用DCF-牛血清白蛋白免疫BALB/c小鼠, 随后用杂交瘤等技术制备抗DCF单克隆抗体(monoclonal antibody, mAb), 基于DCF mAb建立了间接竞争ELISA方法, 对该检测方法的性能(准确度、精密度和特异性)进行鉴定。结果 紫外扫描结果表明DCF已成功与载体蛋白偶联; 获得最优株抗DCF的杂交瘤细胞株(4B9), 其IC50值为0.61 ng/mL; 该检测方法在药酒中的DCF平均添加回收率为85.9%, 其批间变异系数(coefficient of variation, CV)(5.3%~9.7%)均大于批内CV(4.9%~9.1%), 与类似物(酮洛芬、阿司匹林、吲哚美辛、布洛芬、舒林酸、萘普生、罗非昔布)没有交叉反应。结论 本研究建立的间接竞争ELISA法为DCF在药酒中的残留提供了一种新的筛查手段。
英文摘要:
      Objective To establish an indirect competitive enzyme-linked immunosorbent assay for rapid screening diclofenac (DCF) in medicinal liquor. Methods DCF was coupled to carrier protein using the active ester method and the mixed anhydride method to obtain DCF immunogen and detection antigen. BALB/c mice were immunized with DCF-bovine serum albumin, and then anti-DCF monoclonal antibody (mAb) was prepared by hybridoma technology. An indirect competitive ELISA method was established based on DCF mAb, and the performance (accuracy, precision and specificity) of the detection method was evaluated. Results UV scanning results showed that DCF was successfully coupled to the carrier protein; the optimal hybridoma cell line (4B9) against DCF was obtained, with an IC50 value of 0.61 ng/mL; the average recovery rate of DCF added in medicinal liquor by this detection method was 85.9%, and the coefficient of variation (CV) for intra-assay (5.3%~9.7%) was greater than the CV for inter-assay (4.9%~9.1%), and there was no cross-reaction with analogues (ketoprofen, aspirin, indomethacin, ibuprofen, sulindac, naproxen, and rofecoxib). Conclusion The indirect competitive ELISA method established in this study provides a new screening method for DCF residues in medicinal liquor.
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