Laboratorio Antidoping Federazione Medico Sportiva Italiana, Largo Giulio Onesti, Rome, Italy.
Electrophoresis. 2011 Oct;32(20):2915-8. doi: 10.1002/elps.201100178. Epub 2011 Sep 16.
A specific, sensitive and rapid analytical procedure based on capillary electrophoresis with UV/Vis detection at 405 and 415 nm was developed and validated to detect human haemoglobin and haemoglobin-based oxygen carriers (Hemopure®, Oxyglobin® and Polyheme®) in blood samples collected for doping control. The electrophoretic separation, based on capillary dynamic coating, was achieved in less than 10 min. The effects of capillary temperature, injection conditions and initial ramping were investigated. The optimum separation voltage was 25 kV with a capillary temperature of 20 °C, initial ramping of 1 kV/s and an injection pressure of 0.5 psi for 10 s. The removal of haptoglobin using anti-human haptoglobin antibody prior to the analysis was mandatory to increase the specificity of the analysis. Sufficient resolution between endogenous haemoglobin variants and the three haemoglobin-based oxygen carriers here investigated was obtained, thus allowing discrimination between a normal haemolysed sample and a sample in which Oxyglobin®, Hemopure® or Polyheme® is present. Good repeatability of migration times (CV% less than 1), peak resolution and adequate sensitivity (limit of detection: 2.5 mg/mL) was obtained.
建立并验证了一种基于毛细管电泳-紫外/可见光检测(检测波长 405nm 和 415nm)的特异性强、灵敏度高、快速的分析方法,用于检测兴奋剂检测采血管中采集的血液样本中的人血红蛋白和血红蛋白类氧载体(Hemopure®、Oxyglobin®和 Polyheme®)。在不到 10 分钟的时间内,通过毛细管动态涂层实现电泳分离。考察了毛细管温度、进样条件和初始线性 ramp 的影响。最佳分离电压为 25kV,毛细管温度为 20°C,初始线性 ramp 为 1kV/s,进样压力为 0.5psi 持续 10s。在分析前使用抗人结合珠蛋白抗体去除结合珠蛋白是提高分析特异性的必要条件。本方法可充分分离内源性血红蛋白变异体和三种血红蛋白类氧载体,从而能够区分正常溶血样本和含有 Oxyglobin®、Hemopure®或 Polyheme®的样本。该方法具有良好的迁移时间重现性(CV%小于 1%)、峰分辨率和足够的灵敏度(检测限:2.5mg/mL)。