Varlet-Marie Emmanuelle, Ashenden Michael, Lasne Françoise, Sicart Marie-Therese, Marion Benedicte, de Ceaurriz Jacques, Audran Michel
Biophysical & Bioanalysis Laboratory, Faculty of Pharmacy, University Montpellier I, Montpellier, France.
Clin Chem. 2004 Apr;50(4):723-31. doi: 10.1373/clinchem.2003.026591. Epub 2004 Feb 5.
Hemoglobin-based oxygen carriers (HBOCs) are being developed as potential substitutes for the oxygen-carrying functions of erythrocytes, but athletes may obtain and experiment with HBOCs as an illicit means of enhancing oxygen transport. An electrophoretic technique has been developed to screen for the presence of HBOCs in blood samples (Lasne et al. Clin Chem 2004;50:410-5). Interest has focused on complementary methods that can provide legally defensible scientific evidence for the presence of HBOCs in blood samples collected for doping control.
The aim of this research was to develop a size-exclusion SEC-HPLC technique to identify in plasma or serum samples the presence of HBOCs that are currently under development. This method was also used to detect a polymerized bovine hemoglobin (Hemopure) after infusion in 12 healthy males.
The chromatograms of all HBOCs tested were clearly separated from the 54-min peak associated with human hemoglobin dimers. It was possible to differentiate between the different HBOC products based solely on their chromatographic profiles, provided they were at high concentrations. Differences were discernible not only based on the presence (or absence) of peaks, but also the separation between respective peaks. The profiles for serum samples collected from the men immediately after infusion of Hemopure showed a distinctive profile. The shape of the chromatographic profile remained consistent for at least 48 h.
Under the analytical conditions reported here, SEC-HPLC was able to separate native hemoglobin from the modified hemoglobin molecules present in each of the HBOC products studied. In tandem with electrophoretic screening, SEC-HPLC provides evidence of the presence of HBOCs and can therefore be regarded as a method that satisfies the criteria for use in an antidoping control setting.
基于血红蛋白的氧载体(HBOCs)正被开发用作红细胞氧运输功能的潜在替代品,但运动员可能会获取并使用HBOCs作为增强氧运输的非法手段。已开发出一种电泳技术来筛查血样中HBOCs的存在(Lasne等人,《临床化学》2004年;50:410 - 5)。人们关注的焦点在于能够为兴奋剂检测所采集血样中HBOCs的存在提供具有法律依据的科学证据的补充方法。
本研究的目的是开发一种尺寸排阻SEC - HPLC技术,以鉴定血浆或血清样本中目前正在研发的HBOCs的存在。该方法还用于检测12名健康男性输注聚合牛血红蛋白(Hemopure)后的情况。
所有测试的HBOCs的色谱图均与54分钟时与人血红蛋白二聚体相关的峰明显分开。仅根据色谱图就有可能区分不同的HBOC产品,前提是它们处于高浓度。差异不仅基于峰的存在(或不存在),还基于各个峰之间的分离情况。在输注Hemopure后立即从这些男性采集的血清样本的图谱显示出独特的特征。色谱图的形状至少在48小时内保持一致。
在此处报告的分析条件下,SEC - HPLC能够将天然血红蛋白与所研究的每种HBOC产品中存在的修饰血红蛋白分子分开。与电泳筛查相结合,SEC - HPLC为HBOCs的存在提供了证据,因此可被视为一种满足反兴奋剂检测使用标准的方法。