Pettersson K S, Söderholm J R
Wallac Immunodiagnostic Research Laboratory, Turku, Finland.
Clin Chem. 1990 Nov;36(11):1928-33.
A rapid, sensitive two-site immunometric assay for human lutropin (LH), with two monoclonal antibodies directed against the beta subunit, has been developed with time-resolved fluorescence as the detection principle. The cross-reactivities with human thyrotropin and human follitropin are negligible and that with human choriogonadotropin is 1% in the standard two-step protocol. Free beta subunits of LH are also detected. Besides the standard procedure (45 + 15 min), more rapid alternative protocols (15 + 15 min or 30 min in one step) have also been evaluated. The minimum detectable dose per well is approximately 1 amol (10(-18) mol), corresponding to less than 0.01 int. unit/L, for a sample volume of 25 microL and less than 0.001 int. unit/L for 200-microL samples. The intra- and interassay CV is less than 6% for LH concentrations from 0.2 to 250 int. units/L. With 200-microL sample volumes, intra-assay variation is less than 6% at 0.04 int. unit/L and interassay variation is 7% at 0.05 int. unit/L. The very high sensitivity and reproducibility of the presented method enables assay of low prepubertal and of suppressed LH concentrations, and represents a clear improvement over currently available immunoassays.
已开发出一种快速、灵敏的人促黄体生成素(LH)双位点免疫分析方法,该方法采用针对β亚基的两种单克隆抗体,以时间分辨荧光作为检测原理。在标准两步法中,与人促甲状腺激素和人促卵泡激素的交叉反应可忽略不计,与人绒毛膜促性腺激素的交叉反应为1%。还可检测LH的游离β亚基。除了标准程序(45 + 15分钟)外,还评估了更快速的替代方案(一步法15 + 15分钟或30分钟)。对于25微升的样品体积,每孔的最低检测剂量约为1阿摩尔(10^(-18)摩尔),相当于低于0.01国际单位/升,对于200微升的样品则低于0.001国际单位/升。对于0.2至250国际单位/升的LH浓度,批内和批间变异系数均小于6%。对于200微升的样品体积,在0.04国际单位/升时批内变异小于6%,在0.05国际单位/升时批间变异为7%。所提出方法的极高灵敏度和重现性使得能够检测青春期前低水平和受抑制的LH浓度,并且相对于目前可用的免疫分析方法有明显改进。