Liu Y, Naaktgeboren N, Heip J, Devroey P, Temmerman M, Verhoeven N, Van Steirteghem A C
Ann Biol Clin (Paris). 1984;42(6):419-25.
Three commercially available RIA kits for serum and urinary LH were assessed for their usefulness to detect endogenous LH rise in patients receiving ovarian stimulation as part of an in vitro fertilization treatment for infertility. Prerequisites included a turn-around time of 5 hours for an assay of 100 tubes. The following parameters were evaluated: reproducibility of standard curve, sensitivity, precision profile, within- and between-assay precision, analytical drift, recovery and linearity. The Amerlex LH RIA kit was selected because of superior precision profiles, higher precision and better recovery tests.
对三种市售的血清和尿液促黄体生成素放射免疫分析试剂盒进行了评估，以检测接受卵巢刺激作为不育症体外受精治疗一部分的患者体内内源性促黄体生成素的升高情况。前提条件包括100管检测的周转时间为5小时。评估了以下参数：标准曲线的重现性、灵敏度、精密度曲线、批内和批间精密度、分析漂移、回收率和线性。由于具有卓越的精密度曲线、更高的精密度和更好的回收率测试，选择了Amerlex促黄体生成素放射免疫分析试剂盒。
