Nagainis P A, Nakagawa C H, Baron S L, Fuller S A, Chandler H M, Hurrell J G
Clin Chim Acta. 1986 Nov 15;160(3):273-9. doi: 10.1016/0009-8981(86)90194-4.
A quantitative capillary tube enzyme immunoassay (CTEIA) method for the determination of human urinary chorionic gonadotropin (hCG) has been developed. The method utilizes an antibody-coated capillary tube through which the test fluid is passed and a urease-labelled second antibody in an immunometric format. Any hCG in the test solution is 'captured' by the immobilized antibody which is hybridoma derived and specific for the beta-subunit of hCG. The second hCG-specific antibody, conjugated to the enzyme urease, is used to detect the captured hCG on the internal surface of the capillary tube. The amount of urease bound to the surface is determined by the introduction of a substrate solution containing urea and the pH indicator bromothymol blue. The rate of colour change, from yellow to blue, caused by the release of ammonia from urea by urease, is determined in a spectrophotometer using a cell holder adapted to accommodate capillary tubes. The initial rate of absorbance change is directly proportional to the concentration of hCG in the sample in the range 0-100 mIU/ml. The test can detect concentrations of hCG as low as 10 mIU/ml in a total elapsed time of 5 min.
已开发出一种用于测定人尿绒毛膜促性腺激素(hCG)的定量毛细管酶免疫测定(CTEIA)方法。该方法利用包被抗体的毛细管,测试液通过该毛细管,以及采用免疫比浊法的脲酶标记二抗。测试溶液中的任何hCG被固定化抗体“捕获”,该固定化抗体源自杂交瘤,对hCG的β亚基具有特异性。与脲酶偶联的第二种hCG特异性抗体用于检测毛细管内表面捕获的hCG。通过引入含有尿素和pH指示剂溴百里酚蓝的底物溶液来测定结合到表面的脲酶量。由脲酶使尿素释放氨引起的颜色从黄色到蓝色的变化速率,在使用适合容纳毛细管的样品池架的分光光度计中测定。吸光度变化的初始速率在0 - 100 mIU/ml范围内与样品中hCG的浓度成正比。该测试在总耗时5分钟内可检测低至10 mIU/ml的hCG浓度。