Maeda Y, Setoguchi T, Katsuki T, Ishikawa E
J Lipid Res. 1979 Nov;20(8):960-5.
A bile acid disappearance test using an enzyme immunoassay for ursodeoxycholic acid (UDCA) is presented. The immunoassay employs an antiserum produced in rabbits with UDCA coupled by amide linkage to egg albumin. An antigen (UDCA)-enzyme (beta-D-galactosidase) complex was prepared by adding the N-hydroxy-succinimide ester of UDCA to beta-D-galactosidase in a molar ratio of 5000:1. The anti-UDCA serum was coupled to glass beads and a competitive reaction between bile acids and UDCA coupled to the enzyme on the glass beads was measured by determining enzyme activity. One bead was used for each test tube. Thus it was convenient to wash and transfer the bead to a fresh test tube after incubation. The procedure requires 2.5 hr at 30 degrees C for the competitive reaction and enzyme assay. Using a 1:100 dilution of anti-serum, the intensity of fluorescence of 4-methylumbelliferone produced from 4-methylumbelliferyl-beta-D-galactoside by the enzyme decreased linearly with a logarithmic increase of UDCA concentration over a range of from 0.1 to 10 pmnd taurine conjugates, and good recovery data were obtained. The development of the enzyme immunoassay using glass beads shortens analysis time; furthermore, the method makes it possible to detect obstructive jaundice in rabbits before the serum bilirubin level is elevated.
本文介绍了一种使用熊去氧胆酸(UDCA)酶免疫测定法的胆汁酸消失试验。该免疫测定法采用兔抗血清,其中UDCA通过酰胺键与卵清蛋白偶联。通过将UDCA的N-羟基琥珀酰亚胺酯以5000:1的摩尔比添加到β-D-半乳糖苷酶中,制备了抗原(UDCA)-酶(β-D-半乳糖苷酶)复合物。将抗UDCA血清偶联到玻璃珠上,并通过测定酶活性来测量胆汁酸与偶联在玻璃珠上的酶的UDCA之间的竞争反应。每个试管使用一个珠子。因此,在孵育后清洗并将珠子转移到新的试管中很方便。该过程在30℃下进行竞争反应和酶测定需要2.5小时。使用1:100稀释的抗血清,在0.1至10 pmnd牛磺酸结合物范围内,酶从4-甲基伞形酮基-β-D-半乳糖苷产生的4-甲基伞形酮的荧光强度随UDCA浓度的对数增加而线性下降,并获得了良好的回收率数据。使用玻璃珠的酶免疫测定法的发展缩短了分析时间;此外,该方法能够在兔血清胆红素水平升高之前检测出梗阻性黄疸。