Lam Michael T, Le Chris X
Environmental Health Sciences Program, Department of Public Health Sciences, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, AB, Canada T6G 2G3.
Analyst. 2002 Dec;127(12):1633-7. doi: 10.1039/b206531b.
A competitive immunoassay using capillary electrophoresis with laser-induced fluorescence was developed for vancomycin. Capillary electrophoresis using a Tris-glycine running buffer provided adequate separation of the antibody-bound from the unbound fluorescent probe (tracer) in less than 4 min. Laser-induced fluorescence polarization (LIFP) provided high sensitivity detection and simultaneous monitoring of fluorescence intensity and polarization. A fluorescence polarization value of 0.30 confirmed the formation of the antibody-tracer complex. Calibration curves showed a working linear range of 2-3 orders of magnitude with a minimum detectable concentration of 0.98 ng mL(-1) (or 1.1 fg vancomycin). Clinical samples obtained from patients undergoing vancomycin treatment were analyzed for vancomycin and the results correlated well with a standard immunoassay based on latex particle detection that was routinely used by a hospital laboratory. Only 1/10 of the reagents were needed as compared with the standard immunoassay.
开发了一种采用毛细管电泳结合激光诱导荧光的竞争性免疫分析法用于测定万古霉素。使用Tris-甘氨酸运行缓冲液的毛细管电泳在不到4分钟的时间内就能充分分离结合抗体的荧光探针(示踪剂)和未结合的荧光探针。激光诱导荧光偏振(LIFP)提供了高灵敏度检测以及对荧光强度和偏振的同时监测。荧光偏振值为0.30证实了抗体-示踪剂复合物的形成。校准曲线显示工作线性范围为2至3个数量级,最低检测浓度为0.98 ng mL⁻¹(或1.1 fg万古霉素)。对接受万古霉素治疗的患者的临床样本进行万古霉素分析,结果与医院实验室常规使用的基于乳胶颗粒检测的标准免疫分析法相关性良好。与标准免疫分析法相比,所需试剂仅为其1/10。