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Multiresidue Determination of Saraftoxacin, Difloxacin, Norfloxacin, and Pefloxacin in Fish using an Enzyme-Linked Immunosorbent Assay

机译:使用酶联免疫吸附测定法测定鱼类糖酸胞外毒素,二氧化酮,诺氟沙星和Pefloxacin

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An indirect competitive ELISA (icELISA) method for multiresidue determination of Fluoroquinolones (FQs) residues in fish samples has been developed. For this purpose, Sarafloxacin (SAR) was employed to synthesize the immunogen and coating antigen through EDC conjugation method, and cell fusion technology was used to produce anti-SAR monoclonal antiobdy. Based on the square matrix titration, an icELISA method was established. The dynamic range for Sarafloxacin in assay buffer was from 0.004 to 18 ng/mL, with LOD and IC_(50) value of 0.002 ng/mL and 0.32 ng/mL, respectively. After optimization, the physiological pH (7.4) was selected for the immunoassays, and this assay could tolerate up to 10% acetonitrile. The results of this assay showed a high cross-reactivity to Difloxacin (85.5%), Norfloxacin (61.7%), and Pefloxacin (34.8%). Under the 10-fold dilution in authentic fish samples, the regression curve equations for Sarafloxacin, Difloxacin, Norfloxacin and Pefloxacin were y = 1.0114x-0.4003, R~2= 0.9901; y = 0.9782x + 0.2754, R~2= 0.9807; y = 0.9892x +0.0489, R~2= 0.9843; and y = 0.9797x +0.8017, R~2= 0.9844, respectively. The results suggest this immunoassay can be used for simultaneous detecting four kinds of FQs in fish samples.
机译:已经开发出一种间接竞争力的ELISA(ICELISA)用于多留法测定鱼类样品中的氟喹诺酮酮(FQS)残留物的方法。为此目的,使用Sarafloxacin(SAR)通过EDC缀合方法合成免疫原和涂层抗原,并使用细胞融合技术产生抗SAR单克隆抗抗体。基于方矩阵滴定,建立了ICELISA方法。测定缓冲液中Sarafloxacin的动态范围为0.004至18ng / ml,含量和IC_(50)值分别为0.002ng / ml和0.32ng / ml。优化后,选择用于免疫测定的生理pH(7.4),该测定可耐受高达10%的乙腈。该测定结果表明,对二醇辛酸(85.5%),NORFLOXACIN(61.7%)和Pefloxacin(34.8%)的高交叉反应性。在正宗鱼类样品中的10倍稀释下,Sarafloxacin,Difloxacin,Norfloxacin和Pefloxacin的回归曲线方程是Y = 1.0114×0.4003,R〜2 = 0.9901; y = 0.9782x + 0.2754,R〜2 = 0.9807; Y = 0.9892x +0.0489,R〜2 = 0.9843;和y = 0.9797x +0.8017,r〜2 = 0.9844分别。结果表明该免疫测定可用于同时检测鱼类样品中的四种FQS。

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