Shimizu H, Hosoda K, Mizumoto M, Kuroki Y, Sato H, Kataoka K, Hagisawa M, Fujimoto S, Akino T
Department of Biochemistry, Sapporo Medical College.
Tohoku J Exp Med. 1989 Mar;157(3):269-78. doi: 10.1620/tjem.157.269.
A simple, improved immunoassay for the determination of human surfactant protein A (SP-A) in human amniotic fluid was developed. The immunoreaction with a monoclonal antibody PC6-immobilized plastic bead, peroxidase-labeled monoclonal antibody PE10 and amniotic fluid sample diluting in the buffer containing 0.6% sodium dodecyl sulfate/2% Triton X-100, was carried out simultaneously at 45 degrees C for 30 min in test tubes. After washing the bead with 2% skimmilk in phosphate buffered saline containing 1% Triton X-100, the peroxidase reaction was developed by adding the substrate reagent and the absorbance was measured. The amniotic fluid obtained at full term was used as a standard instead of purified SP-A, because of the stability of the antigenicity. This immunoassay method was used to measure SP-A in 69 samples of amniotic fluid from 22 to 41 weeks of gestation. The result indicated that the SP-A values obtained by the present immunoassay can be used for predicting the fetal lung maturity. This simplified monoclonal immunoassay completed the measurement within 1 hr, and so it could be used routinely in clinical laboratory.
开发了一种简单、改进的免疫测定法,用于测定人羊水中的人表面活性蛋白A(SP-A)。在含有0.6%十二烷基硫酸钠/2% Triton X-100的缓冲液中稀释的羊水产样品,与固定在塑料珠上的单克隆抗体PC6、过氧化物酶标记的单克隆抗体PE10进行免疫反应,在试管中于45℃同时进行30分钟。用含有1% Triton X-100的磷酸盐缓冲盐水中的2%脱脂乳洗涤珠子后,加入底物试剂进行过氧化物酶反应并测量吸光度。由于抗原性的稳定性,足月获得的羊水被用作标准品而非纯化的SP-A。该免疫测定法用于测量妊娠22至41周的69份羊水样品中的SP-A。结果表明,通过本免疫测定法获得的SP-A值可用于预测胎儿肺成熟度。这种简化的单克隆免疫测定法在1小时内完成测量,因此可在临床实验室常规使用。