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作 者:贾慧勤[1] 丁焕中[1] 刘晓云 李小红[1] 张炳旭[1] 鲁晓雄[1]
机构地区:[1]华南农业大学兽医学院,广州510642 [2]广州万孚生物技术股份有限公司,广州510641
出 处:《中国兽药杂志》2013年第6期20-23,共4页Chinese Journal of Veterinary Drug
摘 要:为改进和完善免疫检测呋喃唑酮代谢物方法,制备了抗呋喃唑酮代谢物(AOZ)特异性抗体。采用对醛基苯甲酸对AOZ进行衍生化得到CPAOZ,还原CPAOZ结构中的C=N双键得到半抗原,半抗原用N-羟基琥珀酰亚胺活化酯法与BSA偶联制备免疫原,免疫新西兰大白兔制得特异性抗体,采用间接(竞争)ELISA法评价抗血清效价及特异性。结果显示,试验获得了较高效价(1∶1280000)的抗AOZ血清,AOZ半抑制浓度为5.9 ng/mL;抗血清与结构类似物呋喃它酮代谢物的交叉反应率仅为0.76%,与呋喃妥因代谢物和呋喃西林代谢物无交叉反应;利用该抗体建立的间接竞争ELISA检测法,AOZ在1~27 ng/mL与抑制率呈线性关系。结果表明,该特抗体虽然灵敏度较低,却对AOZ而非AOZ衍生物有特异性,可为畜产品中AOZ残留检测提供新的思路和方法。In order to prepare specific antibody against 3 - amino - 2 - oxazolidinone ( AOZ), a metabolite of furazolidone, AOZ was activated by 4 - formylbenzoic acid and then reduced the schiff base, then conjugated with BSA via EDC/NHS as immunogen. Rabbits were immunized with immunogen; antisera were evaluated by indirect (competitive) ELISA (IC -ELISA). Antisera titer was 1 : 1280000 and ICs0 was 5.9 ng/mL. The antisera had hardly cross - reaction with AMOZ, AHD and SEM. An IC - ELISA was developed for the determination of AOZ in the linear range of 1 -27 ng/mL. Although the sensitivity is not high, the new antibodies with high specificity against AOZ not AOZ derivatives were obtained in this study which would provide a new thought and method for the detection of AOZ in livestock and poultry products.
关 键 词:呋喃唑酮代谢物 特异性抗体 间接(竞争)ELISA
分 类 号:S859.84[农业科学—临床兽医学]
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