Berk L S, Imperio N, Eby W C
Ther Drug Monit. 1986;8(1):111-4. doi: 10.1097/00007691-198603000-00019.
The usefulness of the enzyme multiplied immunoassay quantitative single test (EMIT QST) gentamicin assay was assessed for gentamicin analysis in patient sera. The EMIT QST reagents are in powder form in a single, premeasured vial and are run on a thermoregulated sample processor that controls mixing and timing steps. The results of the clinical evaluation showed that the standard curve was stable throughout a 26-day study period. Within-run precision on 20 replicates at 4.0 micrograms/ml yielded a coefficient of variation (CV) of 5.6%; between-run precision on 66 analyses at 6.0 micrograms/ml over a 152-day period yielded a CV of 4.0%. Mean recovery through the range of the standard curve with 10 spiked patient samples was 102%. Comparative analysis with radioimmunoassay of 95 patient samples showed a correlation of 0.97, with y = 0.93x - 0.03. It was concluded that the EMIT QST gentamicin assay is an appropriate, rapid methodology for patient gentamicin analysis.
对酶放大免疫测定定量单项试验(EMIT QST)庆大霉素检测法在患者血清中庆大霉素分析的实用性进行了评估。EMIT QST试剂为粉末状,装于单个预先测量好的小瓶中,并在可控制混合和计时步骤的温度调节样品处理器上运行。临床评估结果表明,在为期26天的研究期间,标准曲线保持稳定。在4.0微克/毫升浓度下进行20次重复测量的批内精密度产生的变异系数(CV)为5.6%;在152天内对6.0微克/毫升浓度进行66次分析的批间精密度产生的CV为4.0%。对10份加标的患者样本在标准曲线范围内的平均回收率为102%。对95份患者样本进行的与放射免疫测定的对比分析显示,相关性为0.97,y = 0.93x - 0.03。得出的结论是,EMIT QST庆大霉素检测法是一种适用于患者庆大霉素分析的快速方法。