Lessing J B, Peyser M R, Gilad S, Amit A, Kogosowski A, Yovel I, Barak Y, David M P
Fertil Steril. 1987 Sep;48(3):450-3. doi: 10.1016/s0015-0282(16)59416-3.
A simple, rapid, and sensitive solid-phase immunoassay procedure for the determination of estrone-3-glucuronide (E1-3-G), which uses chemiluminescence as the end point in unextracted morning urine, is described. Thirty-one patients undergoing induction of ovulation in an in vitro fertilization (IVF) unit participated in the study. From day 3 of the menstrual cycle until the day of hCG administration, morning blood samples and morning urine specimens were collected for the determination of serum 17 beta-estradiol (E2) and urine E1-3-G, respectively. A good correlation was noted between E2 measured by radioimmunoassay (RIA) and the E1-3-G measured by chemiluminescence immunoassay (CIA), from day 5 up to the day of hCG administration (0.6 less than r less than 0.85, P less than 0.001). It is evident from this study that the CIA measurement of E1-3-G in morning urine is an accurate and rapid (2.5 hours) method and is convenient for monitoring induction of ovulation with human menopausal gonadotropins.
本文描述了一种简单、快速且灵敏的固相免疫分析方法,用于测定雌酮-3-葡萄糖醛酸苷(E1-3-G),该方法以化学发光作为未提取晨尿的终点检测。31名在体外受精(IVF)单元接受排卵诱导的患者参与了该研究。从月经周期的第3天到注射人绒毛膜促性腺激素(hCG)当天,分别采集早晨血液样本和早晨尿液样本,用于测定血清17β-雌二醇(E2)和尿液E1-3-G。从第5天到注射hCG当天,通过放射免疫分析(RIA)测定的E2与通过化学发光免疫分析(CIA)测定的E1-3-G之间存在良好的相关性(0.6<r<0.85,P<0.001)。从这项研究可以明显看出,早晨尿液中E1-3-G的CIA测定是一种准确、快速(2.5小时)的方法,便于监测人绝经期促性腺激素诱导的排卵。