Tobin T, Tai H H, Tai C L, Houtz P K, Dai M R, Woods W E, Yang J M, Weckman T J, Chang S L, Blake J W
Maxwell H. Gluck Equine Research Center, University of Kentucky, Lexington 40546-0099.
Res Commun Chem Pathol Pharmacol. 1988 Apr;60(1):97-115.
We have developed and evaluated a one step enzyme-linked immunosorbent assay (ELISA) test for fentanyl as part of a panel of pre- and post-race tests for narcotic analgesics in racing horses. This ELISA test detects fentanyl with an I-50 of about 100 pg/ml. The test is economical in that it can be read with an inexpensive spectrophotometer, or even by eye. The test is rapid, and ten samples, a normal pre-race complement, can be analyzed in about twenty minutes. The test readily detects the presence of fentanyl or its metabolites in equine blood and urine from two and twenty-four hours respectively after administration of sub-therapeutic doses. The two antibodies evaluated also cross-react with the methylated analogs of fentanyl, sufetanil and carfentanil and the test detected these drugs shortly after their administration to horses. When introduced into routine screening, this test, in combination with another immunoassay test previously described, yielded 10 sufentanil positives. As such this test is capable of both improving the quality and reducing the cost of pre-race and post-race testing for fentanyl and a number of its congeners in racing horses.
我们已研发并评估了一种用于检测芬太尼的一步式酶联免疫吸附测定(ELISA)试验,作为赛马麻醉性镇痛药赛前和赛后检测项目的一部分。这种ELISA试验检测芬太尼的半数抑制浓度(IC50)约为100 pg/ml。该试验经济实惠,因为它可以用一台价格低廉的分光光度计读取结果,甚至肉眼也能读取。该试验速度很快,大约20分钟就能分析10个样本,这是正常的赛前样本量。该试验能够轻松检测出在给予亚治疗剂量后两小时和二十四小时的马血和马尿中芬太尼或其代谢物的存在。所评估的两种抗体也与芬太尼的甲基化类似物舒芬太尼和卡芬太尼发生交叉反应,并且该试验在给马施用这些药物后不久就能检测到它们。当将此试验引入常规筛查时,与之前描述的另一种免疫测定试验相结合,检测出了10例舒芬太尼阳性病例。因此,该试验能够提高赛马中芬太尼及其多种同系物赛前和赛后检测的质量并降低成本。