Quinn R P, Good S S, Gerald L, Sabatka J J
Anal Biochem. 1983 Oct 1;134(1):16-25. doi: 10.1016/0003-2697(83)90257-9.
A direct radioimmunoassay for the detection of A134U in biological fluids and extracts has been developed. The entire assay, including scintillation counting, is performed using 12 X 55-mm centrifuge tubes and results in a sensitive, reliable, and relatively inexpensive procedure. The log-logit transformation is linear over a range of 1 to 30 pmol per sample. Intra-assay precision was found to be excellent with a coefficient of variation ranging from 4.1 to 14.5% for the standard curve with plasma and a coefficient of variation ranging from 4.0 to 17.8% for the standard curve with urine. Interassay precision and accuracy were also found to be good. With the antisera chosen for use, no cross-reactivity was found with acyclovir or its two known metabolites, while some cross-reactivity was seen with the corresponding two derivatives of A134U. Only very minor cross-reactivities were seen with a small number of other compounds out of a large number tested.
已开发出一种用于检测生物体液和提取物中A134U的直接放射免疫测定法。整个测定过程,包括闪烁计数,均使用12×55毫米的离心管进行,结果是一种灵敏、可靠且相对便宜的方法。对数-对数转换在每个样品1至30皮摩尔的范围内呈线性。测定内精密度极佳,血浆标准曲线的变异系数为4.1%至14.5%,尿液标准曲线的变异系数为4.0%至17.8%。测定间精密度和准确性也良好。在所选用的抗血清中,未发现与阿昔洛韦或其两种已知代谢物有交叉反应,而与A134U的相应两种衍生物有一些交叉反应。在大量测试的其他化合物中,仅发现与少数几种有非常轻微的交叉反应。