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Recent developments in doping testing for erythropoietin

机译:促红细胞生成素的兴奋剂检测的最新进展

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The constant development of new erythropoiesis-stimulating agents (ESAs), since the first introduction of recombinant erythropoietin (rhEpo) for clinical use, has also necessitated constant development of methods for detecting the abuse of these substances. Doping with ESAs is prohibited according to the World Anti-Doping Code and its prohibited list of substances and methods. Since the first publication of a direct and urine-based detection method in 2000, which uses changes in the Epo isoform profile as detected by isoelectric focusing in polyacrylamide slab gels (IEF-PAGE), the method has been constantly adapted to the appearance of new ESAs (e.g., Dynepo, Mircera). Blood had to be introduced as an additional matrix, because Mircera (a PEGylated Epo) is best confirmed in serum or plasma after immunoaffinity purification. A Mircera ELISA was developed for fast screening of sera. With the appearance of Dynepo and copy epoetins, the additional application of sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE or equivalent) became necessary. The haematological module of the Athlete Biological Passport is the latest development in multivariable indirect testing for ESA doping. The article summarizes the main strategies currently used in Epo anti-doping testing with special focus on new developments made between 2009 and 2010.
机译:自从首次将重组促红细胞生成素(rhEpo)引入临床以来,新的促红细胞生成刺激剂(ESA)的不断开发,还需要不断开发检测这些物质滥用的方法。根据《世界反兴奋剂条例》及其禁止的物质和方法清单,严禁使用ESA进行掺杂。自2000年首次发表基于尿液的直接和直接检测方法以来,该方法利用了通过等电聚焦在聚丙烯酰胺平板凝胶(IEF-PAGE)中检测到的Epo亚型分布的变化,该方法一直在不断适应新的出现ESA(例如,Dynepo,Mircera)。必须将血液作为其他基质引入,因为在免疫亲和纯化后,最好在血清或血浆中确认Mircera(一种PEG化的Epo)。开发了Mircera ELISA用于快速筛选血清。随着Dynepo和依泊汀的出现,有必要另外应用十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE或等效方法)。运动员生物护照的血液学模块是ESA兴奋剂多变量间接测试的最新进展。本文总结了Epo反兴奋剂测试中目前使用的主要策略,特别关注了2009年至2010年之间的最新进展。

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