Tamate K, Charleton M, Gosling J P, Egan D, Ishikawa M, Fottrell P F, Kane M M
National Diagnostics Centre-Bioresearch Ireland, University College, Galway, Ireland.
Clin Chem. 1997 Jul;43(7):1159-64.
We developed a direct microtiter plate enzyme immunoassay to measure estradiol-17 beta in saliva. The assay has a commercially available monoclonal antibody, raised against estradiol-17 beta-6-carboxymethyloximebovine serum albumin, and a homologous horseradish peroxidase conjugate measured colorimetrically. The detection limit (equivalent to B0-3 SD) is 365 amol/well or 7.3 pmol/L when 50-microL samples are assayed. Cross-reactivity with estrone and estriol, testosterone, or progesterone is < 0.2%. Estradiol-17 beta was measured in daily samples over five natural menstrual cycles and eight cycles stimulated as a preliminary to in vitro fertilization, and the concentrations and fluctuations found agreed with previously published data. This method gives results in approximately 3 h and may be useful for fertility monitoring and management.
我们开发了一种直接酶标板酶免疫分析法来测定唾液中的雌二醇-17β。该分析方法使用一种市售的单克隆抗体,它是针对雌二醇-17β-6-羧甲基肟牛血清白蛋白产生的,还有一种同源辣根过氧化物酶偶联物,通过比色法进行检测。当检测50微升样品时,检测限(相当于B0-3标准差)为365阿摩尔/孔或7.3皮摩尔/升。与雌酮、雌三醇、睾酮或孕酮的交叉反应率<0.2%。在五个自然月经周期和八个体外受精前促排卵周期的日常样本中测定了雌二醇-17β,所发现的浓度和波动情况与先前发表的数据一致。该方法大约3小时即可得出结果,可能有助于生育监测和管理。