Schneider E, Usleber E, Dietrich R, Märtlbauer E
Institut für Tierärztliche Nahrungsmittelkunde, Justus-Liebig-Universität, Ludwigstrasse 21, D-35390, Gießen.
Mycotoxin Res. 2001 Jun;17 Suppl 2:170-3. doi: 10.1007/BF03036429.
Antibodies against ochratoxin A were produced in rabbits after immunization with an ochratoxin A-keyhole limpet hemocyanine conjugate. The immunogen was found to be very efficient, and high antibody titers were detected in the sera of all immunized rabbits. In a competitive enzyme immunoassay using ochratoxin A-horseradish peroxidase as the labelled antigen, low levels of ochratoxin A in buffer solution could be detected. The mean standard curve detection limit and 50% inhibition level of the optimized assay were at 15 pg/ml and 50 pg/ml, respectively. Relative cross-reactivity of ochratoxin B was found to be 2%. With these characteristics, this novel enzyme immunoassay should be useful for the routine detection of ochratoxin A in food and in biological samples at levels well below 1 ng/g.
用赭曲霉毒素A-钥孔戚血蓝蛋白偶联物免疫家兔后,产生了抗赭曲霉毒素A的抗体。发现该免疫原非常有效,在所有免疫家兔的血清中均检测到高抗体滴度。在使用赭曲霉毒素A-辣根过氧化物酶作为标记抗原的竞争性酶免疫测定中,可检测到缓冲溶液中低水平的赭曲霉毒素A。优化后的测定方法的平均标准曲线检测限和50%抑制水平分别为15 pg/ml和50 pg/ml。发现赭曲霉毒素B的相对交叉反应率为2%。基于这些特性,这种新型酶免疫测定法应有助于常规检测食品和生物样品中含量远低于1 ng/g的赭曲霉毒素A。