Dotti C
Quad Sclavo Diagn. 1975 Jun;11(2):334-44.
The experimental determination of the operative parameters of two radioimmunoassay (RIA) systems for the determination of triiodothyronine (T3) level directly in serum is described. The two systems differ both for the agents blocking the aspecific T3-serum protein bindings (sulphonic acid, 8-aniline, 1-Naphtalene in borate buffer: bor-ANS-RIA and Merthiolate in phosphate buffer: PO4-Merth-RIA) and for the methods adopted for compensating the aspecific serum interferences (T3,4 free serum for bor-ANS-RIA and Human Serum Albumine HSA 8% for PO4-Merth-RIA. The tracers are T3-I125 (spec. act. 500 Ci/g for bor-ANS-RIA and 1000 Ci/g for PO4-Merth-RIA). The antisera have been raised in rabbit (T3-bovine SA conjugate for bor-ANS-RIA and T3-HSA conjugate for PO4-Merth-RIA). The incubation conditions are 2degreesC X 24 h for bor-ANS-RIA and room temp. X 2 h for PO4-Merth-RIA. For both systems, the Bound-Free (B-F) separations are carried out by charcoal-dextrane adsorption, 4 mg/tube, 10 min contact. Indicatively, the lowest detection limits of the two systems are about 8 pg T3 for ANS and about 6 pg T3 for Merth. Evidence of parallelism and even superimposition is provided for both assays between the dose-response curve and the serum dilution curve. The calibration curves of the employed antisera are reported (final titres: 1/1000 for ANS and 1/2500 for Merth). 4 different incubation conditions for ANS and 2 for Merth are described and the reasons of choice of the mentioned conditions statistically elucidated. Acceptable statistical comparison between "sample-blank" and the "blank" of the diluents of the employed standard preparations are presented and discussed. F-countings vs. B-countings functions are reported (regression line -- equations: F = 0.93 B + 0.07, n = 15, r = 0.993 for ANS and F = 0.95 B -- 0.02, n = 14, r = 0.992 for Merth) demonstrating the possibility of alternative countings. The recovery regression lines (found f vs. expected e) have equations: f = 1.01 e + 0.08, n = 10, r = 0.999 for ANS and f = 1.08 e -- 1.64, n = 9, r = 0.995 for Merth, implying a practically quantitative recovery in both cases. Thyroxine (T4) cross reaction study has been undertaken under a quite new optics re-calculating the regression lines -- equations of the T3 recovery in the presence of added T4; in that case, the following equations are valid: f = 1.05 e + 0,13, n = 10, r = 0.992 for ANS and f = 1.07 e + 2.26, n = 18, r = 0,985 for Merth. Reducing the maximum added T4 to 1 ng/tube, the cross reaction can be considered as negligible. T3 levels for normal subjects are finally reported: 1.50 +/- 0.80, n= 37 for ANS and 1.40 +/- 0.68, n = 40 for Merth (ng T3/ml, means +/- 2SD).
本文描述了直接测定血清中三碘甲状腺原氨酸(T3)水平的两种放射免疫分析(RIA)系统操作参数的实验测定。这两种系统的不同之处在于,用于阻断非特异性T3-血清蛋白结合的试剂(硼酸盐缓冲液中的磺酸、8-苯胺、1-萘:硼-ANS-RIA和磷酸盐缓冲液中的硫柳汞:PO4-Merth-RIA)以及用于补偿非特异性血清干扰的方法(硼-ANS-RIA用游离T3、T4血清,PO4-Merth-RIA用8%人血清白蛋白HSA)。两种系统的示踪剂均为T3-I125(硼-ANS-RIA的比活度为500 Ci/g,PO4-Merth-RIA的比活度为1000 Ci/g)。两种抗血清均由兔制备(硼-ANS-RIA用T3-牛血清白蛋白偶联物,PO4-Merth-RIA用T3-HSA偶联物)。硼-ANS-RIA的孵育条件为2℃×24小时,PO4-Merth-RIA的孵育条件为室温×2小时。对于两种系统,均采用4mg/管的活性炭-葡聚糖吸附法进行结合-游离(B-F)分离,接触10分钟。两种系统的最低检测限分别约为8pg T3(ANS法)和约6pg T3(Merth法)。两种分析方法的剂量-反应曲线和血清稀释曲线均呈现平行性甚至重叠性。报告了所用抗血清的校准曲线(最终滴度:ANS为1/1000,Merth为1/2500)。描述了ANS的4种不同孵育条件和Merth的2种孵育条件,并从统计学角度阐明了选择上述条件的原因。给出并讨论了“样品-空白”与所用标准制剂稀释剂“空白”之间可接受的统计比较结果。报告了F计数与B计数的函数关系(回归线——方程:ANS为F = 0.93B + 0.07,n = 15,r = 0.993;Merth为F = 0.95B - 0.02,n = 14,r = 0.992),证明了交替计数的可能性。回收回归线(实测值f与预期值e)的方程为:ANS为f = 1.01e + 0.08,n = 10,r = 0.999;Merth为f = 1.08e - 1.64,n = 9,r = 0.995,这意味着两种情况下的回收几乎是定量的。在全新的视角下进行了甲状腺素(T4)交叉反应研究,重新计算了添加T4时T3回收的回归线——方程;在这种情况下,以下方程成立:ANS为f = 1.05e + 0.13,n = 10,r = 0.992;Merth为f = 1.07e + 2.26,n = 18,r = 0.985。将最大添加T4量降至1ng/管时,交叉反应可视为可忽略不计。最后报告了正常受试者的T3水平:ANS法为1.50±0.80,n = 37;Merth法为1.40±0.68,n = 40(ng T3/ml,均值±2SD)。