对市售产品和兴奋剂检测尿样中的奥司他林进行手性分析

Oliver Krug , Mario Thevis
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引用次数: 0

摘要

世界反兴奋剂机构(WADA)列为体育禁用的各种物质都含有一个或多个手性中心。烯诺巴马((2S)-3-(4-氰基苯氧基)-N-[4-氰基-3-(三氟甲基)苯基]-2-羟基-2-甲基丙酰胺、S-奥司他林、S-22、MK-2866、GTx-024、VERU-024)就是其中一种。虽然奥司他林不是一种已获批准的药物,但它可以通过互联网供应商轻易买到,迄今为止,我们还不知道这些产品中使用了多少 R-奥司他林、S-奥司他林或两者的混合物。同样,在运动药物检测项目中,也没有关于尿样中出现不良分析结果的信息,因此,本试验研究旨在建立一种检测方法,以初步了解 R- 和 S-ostarine 在市售产品和真实兴奋剂检测尿样中的存在情况。本文介绍了一种手性液相色谱-质谱检测方法,该方法采用了含茶碱(手性)的固定相,可区分奥司他林的 R-和 S-对映体。分析前对奥司他林产品进行提取和稀释,而尿液样本则通过酶水解后的液-液萃取进行分析。在购买的 5 种产品中,只有 2 种含有奥司他林。在这两种产品和没收的产品中,只发现了奥司他林 S-对映体。此外,对 5 份含有目标分析物的真实兴奋剂检查尿样进行了手性分析,也证实只存在 S-奥司他林对映体。事实证明,所开发的方法适用于奥司他林对映体的分离,这为非法药物生产、贩运和兴奋剂检查等方面提供了更多信息,特别是当需要更多有助于确定药物或药物残留来源的细节时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chiral analysis of ostarine in commercially available products and doping control urine samples

Chiral analysis of ostarine in commercially available products and doping control urine samples

Various substances classified as prohibited in sport by the World Anti-Doping Agency (WADA) comprise one or more chiral centers. One such substance is enobosarm ((2S)-3-(4-cyanophenoxy)-N-[4-cyano-3-(trifluoromethyl)phenyl]-2‑hydroxy-2-methylpropanamide, S-ostarine, S-22, MK-2866, GTx-024, VERU-024). Although ostarine is not an approved drug, it has been readily available via Internet-based suppliers, and to date it is unknown to what extent R-ostarine, S-ostarine, or a mixture of both is used in these products. Likewise, such information is not available with regards to urine samples that returned an adverse analytical finding in the context of sports drug testing programs and, hence, this pilot-study aimed at establishing a test method to provide first insights into the presence of R- and S-ostarine in commercially available products and in authentic doping control urine samples.

Here, a chiral liquid chromatographic - mass spectrometric method, employing a teicoplanin-containing (chiral) stationary phase that allows the differentiation of R- and S-enantiomers of ostarine, is presented. Ostarine products were extracted and diluted prior to analysis, while urine samples were prepared for analysis by enzymatic hydrolysis followed by liquid-liquid extraction.

Seven products declaring to contain ostarine were investigated, five of which were ordered via the Internet and two were confiscated and made available by a customs authority. Only 2 of the 5 purchased products contained ostarine. In these two products and the confiscated products, only the ostarine S-enantiomer was found. Further, five authentic doping control urine samples containing the target analyte were subjected to chiral analysis, also confirming the sole presence of the S-ostarine enantiomer.

The developed approach proved suitable for the separation of ostarine enantiomers, which adds further information e.g. in the context of illicit drug production, trafficking, and doping controls, especially when additional details are desirable that might assist in determining the origin of a drug or drug residue.

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Journal of chromatography open
Journal of chromatography open Analytical Chemistry
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