Quinn R P, Gerald L, Tadepalli S
J Immunoassay. 1987;8(2-3):247-65. doi: 10.1080/15321818708057025.
A direct radioimmunoassay for the detection of desciclovir (DCV)(2) in biological fluids has been developed. The radioimmunoassay was validated by comparing results obtained from human plasma samples analyzed by both this RIA and a gas chromatographic method. None of the crossreactivities noted interfere with the assay system. Although the succinylated antigen has a slightly higher affinity constant, the non-succinylated tritiated antigen was chosen for routine use. The assay is sensitive with an I50 value of 20 nM and with a lower limit of detection of about 3 nM. Intra-assay precision gave sample coefficients of variation which ranged from 2.2 to 9.6% for the standard curve with human plasma and from 2.0 to 8.2% for the standard curve with human urine. Inter-assay precision and accuracy were within acceptable limits.
已开发出一种用于检测生物体液中去甲阿昔洛韦(DCV)(2)的直接放射免疫测定法。通过比较该放射免疫测定法和气相色谱法分析人血浆样品所得结果,对该放射免疫测定法进行了验证。所观察到的交叉反应性均不干扰测定系统。虽然琥珀酰化抗原的亲和常数略高,但仍选择非琥珀酰化的氚化抗原用于常规检测。该测定法灵敏度高,半数抑制浓度(I50)值为20 nM,检测下限约为3 nM。批内精密度给出的样品变异系数,人血浆标准曲线范围为2.2%至9.6%,人尿标准曲线范围为2.0%至8.2%。批间精密度和准确性在可接受范围内。