Jensen A L, Høier R, Poulsen J S
Department of Clinical Studies, Royal Veterinary and Agricultural University, Frederiksberg, Denmark.
Zentralbl Veterinarmed A. 1992 Dec;39(10):741-6. doi: 10.1111/j.1439-0442.1992.tb00238.x.
The purpose of the present study was to modify a previously evaluated enzyme linked immunosorbent assay (Larsson and Lumsden, 1980) for the determination of the thyroxine (T4) concentration in canine plasma samples. The test kit Enzymun-Test(Boehringer Mannheim) for determination of T4 concentrations in human plasma was used in connection with the analyzer system Enzymun-Test(Boehringer Mannheim) System ES-33. The assay protocol originally used by Larsson and Lumsden (1980) was modified by including an additional standard, prolongation of the incubation period for the immunoreaction and the enzymeassay, and reduction of the amount of T4 conjugate. The intra- and interassay coefficient of variations ranged from 3.8% to 12.5%. The detection limit of the assay was 3.9 nmol/l which is well below the T4 concentration observed in plasma from healthy dogs, and the T4 concentrations determined in plasma from healthy dogs before and 3 hours after administration of TRH (38.0 +/- 7.4 nmol/l and 51.8 +/- 8.5 nmol/l, respectively) were comparable to those reported in the literature.
本研究的目的是对先前评估过的酶联免疫吸附测定法(Larsson和Lumsden,1980年)进行改进,以测定犬血浆样本中的甲状腺素(T4)浓度。用于测定人血浆中T4浓度的酶免疫检测试剂盒(宝灵曼公司)与酶免疫检测分析仪系统(宝灵曼公司ES-33系统)配套使用。对Larsson和Lumsden(1980年)最初使用的测定方案进行了修改,增加了一个标准品,延长了免疫反应和酶测定的孵育时间,并减少了T4偶联物的用量。批内和批间变异系数在3.8%至12.5%之间。该测定法的检测限为3.9 nmol/l,远低于健康犬血浆中观察到的T4浓度,并且在给予促甲状腺激素释放激素(TRH)之前和之后3小时,健康犬血浆中测定的T4浓度(分别为38.0±7.4 nmol/l和51.8±8.5 nmol/l)与文献报道的结果相当。