Sadler W A, Lynskey C P, Dawson K P
Anal Biochem. 1984 Dec;143(2):272-82. doi: 10.1016/0003-2697(84)90663-8.
Pairs of radioimmunoassays, each of which include a two-dimensional matrix of standards, have been previously employed to resolve specificity problems in steroid immunoassay. In this study the bivariate radioimmunoassay principle has been applied to simultaneous measurement of plasma antidiuretic hormone, arginine vasopressin, and the synthetic antidiuretic agent 1-deamino-8-D-arginine vasopressin (desmopressin), by utilizing two arginine vasopressin antisera which show significantly different cross-reactivities with the synthetic analog. Data processing consists of mathematical representation of two curved dose-response surfaces followed by solution of this pair of nonlinear simultaneous equations for the unknown arginine vasopressin and desmopressin concentrations. Details of numerical procedures are given in the Appendix. The assay appears entirely adequate in terms of sensitivity, accuracy, and precision for measurement of these antidiuretic agents in clinical samples. No evidence of significant covariance in estimated concentrations could be detected but precision of estimation is (not unexpectedly) a function of the concentration of both agents. The plasma disappearance half-time of desmopressin (probably the second of a biphasic disappearance) was estimated as 37 min in one normal subject, which is in good agreement with a previously reported value of 30 min.
成对的放射免疫测定法,每种都包括一个二维标准矩阵,以前曾用于解决类固醇免疫测定中的特异性问题。在本研究中,双变量放射免疫测定原理已应用于同时测量血浆抗利尿激素、精氨酸加压素和合成抗利尿剂1-去氨基-8-D-精氨酸加压素(去氨加压素),方法是利用两种与合成类似物交叉反应性显著不同的精氨酸加压素抗血清。数据处理包括两个曲线剂量反应表面的数学表示,然后求解这对非线性联立方程以确定未知的精氨酸加压素和去氨加压素浓度。数值程序的详细信息见附录。该测定法在临床样本中测量这些抗利尿剂的灵敏度、准确性和精密度方面似乎完全足够。未检测到估计浓度存在显著协方差的证据,但估计的精密度(不出所料)是两种药物浓度的函数。在一名正常受试者中,去氨加压素的血浆消除半衰期(可能是双相消除的第二个阶段)估计为37分钟,这与先前报道的30分钟值非常一致。