Place J D, Thompson S G, Clements H M, Ott R A, Jensen F C
Antimicrob Agents Chemother. 1983 Aug;24(2):246-51. doi: 10.1128/AAC.24.2.246.
The current substrate-labeled fluorescent immunoassay for gentamicin has been modified by substituting monoclonal antibodies for conventional antiserum to gentamicin. The standard curve generated with gentamicin monoclonal antibody was essentially linear from 0 to 12 micrograms/ml, could detect 0.4 micrograms of gentamicin per ml, and had overall intra- and interassay precision values (coefficients of variation) of 1.9 and 5.0%, respectively. The substrate-labeled fluorescent immunoassay produced with gentamicin monoclonal antibody gave results with clinical specimens comparable (r = 0.991) to those obtained with the commercially available substrate-labeled fluorescent immunoassay and also with an enzyme immunoassay, a radioimmunoassay, and a fluorescent immunoassay. This technologically state-of-the-art assay employs both a nonisotopic label and monoclonal antibodies. It offers excellent precision, sensitivity, lot-to-lot reproducibility, linearity, and reagent stability.
目前用于庆大霉素检测的底物标记荧光免疫分析法进行了改进,用庆大霉素单克隆抗体替代了传统的抗血清。用庆大霉素单克隆抗体生成的标准曲线在0至12微克/毫升范围内基本呈线性,可检测出每毫升0.4微克的庆大霉素,批内和批间精密度值(变异系数)分别为1.9%和5.0%。用庆大霉素单克隆抗体制备的底物标记荧光免疫分析法对临床标本的检测结果与市售底物标记荧光免疫分析法以及酶免疫分析法、放射免疫分析法和荧光免疫分析法所得结果具有可比性(r = 0.991)。这种技术先进的检测方法采用了非同位素标记和单克隆抗体。它具有出色的精密度、灵敏度、批间重现性、线性和试剂稳定性。