Vilja P, Wichmann L, Isola J, Tuohimaa P
Department of Biomedical Sciences, University of Tampere, Finland.
Clin Chem. 1988 Aug;34(8):1585-90.
This noncompetitive avidin-biotin assay for lutropin (LH) in urine is based on the use of solid-phase, monoclonal antibodies, avidin-biotin binding, and enzyme label. The detection limit for LH is 0.5 int. unit/L. Performance time is 2 h. Intra- and interassay CVs were 4.2% and 6.2%, respectively. The assay is more specific for intact LH than are RIAs, and the results are unambiguous as compared with those by RIAs. LH is stable for a week in refrigerated urine; thus urine is a convenient sample material in follow-up studies for clinical ovulation timing. This rapid and sensitive nonisotopic LH assay avoids the disadvantages of blood samples. The assay provides clinically relevant predictions of ovulation timing from the amount of hormone measured in a 3-h urine specimen.
这种用于检测尿液中促黄体生成素(LH)的非竞争性抗生物素蛋白-生物素分析法基于固相、单克隆抗体、抗生物素蛋白-生物素结合以及酶标记技术。LH的检测限为0.5国际单位/升。检测时间为2小时。批内和批间变异系数分别为4.2%和6.2%。与放射免疫分析法(RIA)相比,该分析法对完整的LH更具特异性,且结果与RIA法相比更明确。LH在冷藏尿液中可稳定保存一周;因此,在临床排卵时间的后续研究中,尿液是一种方便的样本材料。这种快速灵敏的非同位素LH分析法避免了血样检测的缺点。该分析法可根据3小时尿液样本中测得的激素量提供与临床相关的排卵时间预测。