Parr M K, Geyer H, Reinhart U, Schänzer W
Institute of Biochemistry, German Sport University Cologne.
Food Addit Contam. 2004 Jul;21(7):632-40. doi: 10.1080/02652030410001701602.
Recent studies showed that non-hormonal supplements such as vitamins, minerals and amino acids can contain anabolic androgenic steroids not declared on the labels of the products. These undeclared substances (often prohormones of testosterone or 19-nortestosterone) can cause health risks to consumers and might lead to positive results in sports doping control, especially for the nandrolone metabolite norandrosterone. The analysis of nutritional supplements for anabolic steroids has proven to be rather difficult due to the different matrices in the various products. To conduct a broad-based analysis, a few robust methods capable of analysing various matrices are needed. To obtain a sensitive gas chromatography-mass spectrometry (GC-MS) analysis, a method including extraction and purification of the analytes followed by GC-MS analysis of the trimethylsilyl (TMS) derivatives of the steroids was developed. The limit of detection was improved by the addition of a mixture of 1-N,N-diisopropylamino-n-alkanes (DIPAs) to the final extract. In pure creatine monohydrate powder the limits of detection were demonstrated to be 0.1 ng microg (-1) for dehydroepiandrosterone (DHEA) and estr-4-ene-3beta,17beta-diol, 0.7 ng g(-1) for 5alpha-androstane-3beta,17beta-diol and androsta-1,4-diene-3,17-dione, 1 ng g(-1) for estr-5-ene-3beta,17beta-diol, estr-4-ene-3,17-dione, 19-nortestosterone, androst-4-ene-3, 17-dione and testosterone, and 2 ng g(-1) for androst-4-ene-3beta,17beta-diol and androst-5-ene-3beta,17beta-diol. The recovery (determined at 200 ng g(-1)) ranged from 32% for 19-nortestosterone to 92% for androst-5-ene-3beta,17beta-diol. During the investigation of different nutritional supplements, several analytical difficulties occurred. Aspects of homogenization, extraction, separation, derivatization and GC-MS measurement as well as strategies for the solution of problems arising were optimized. For quantitative measurements of the steroids in nutritional supplements, deuterated internal standards of the specific steroids or standard addition are necessary to compensate for matrix effects.
最近的研究表明,维生素、矿物质和氨基酸等非激素补充剂可能含有产品标签上未标明的合成代谢雄激素类固醇。这些未标明的物质(通常是睾酮或19-去甲睾酮的前体激素)会给消费者带来健康风险,并且可能导致在运动兴奋剂检测中出现阳性结果,尤其是对于诺龙代谢物去甲雄酮而言。由于各种产品中的基质不同,对营养补充剂中的合成代谢类固醇进行分析已被证明相当困难。为了进行广泛的分析,需要一些能够分析各种基质的可靠方法。为了获得灵敏的气相色谱 - 质谱(GC-MS)分析结果,开发了一种方法,该方法包括对分析物进行提取和纯化,然后对类固醇的三甲基硅烷基(TMS)衍生物进行GC-MS分析。通过在最终提取物中添加1-N,N-二异丙基氨基 - n - 烷烃(DIPAs)混合物提高了检测限。在纯肌酸一水合物粉末中,脱氢表雄酮(DHEA)和雌甾 - 4 - 烯 - 3β,17β - 二醇的检测限为0.1 ng μg⁻¹,5α - 雄甾烷 - 3β,17β - 二醇和雄甾 - 1,4 - 二烯 - 3,17 - 二酮的检测限为0.7 ng g⁻¹,雌甾 - 5 - 烯 - 3β,17β - 二醇、雌甾 - 4 - 烯 - 3,17 - 二酮、19 - 去甲睾酮、雄甾 - 4 - 烯 - 3,17 - 二酮和睾酮的检测限为1 ng g⁻¹,雄甾 - 4 - 烯 - 3β,17β - 二醇和雄甾 - 5 - 烯 - 3β,17β - 二醇的检测限为2 ng g⁻¹。回收率(在200 ng g⁻¹下测定)范围从19-去甲睾酮的32%到雄甾 - 5 - 烯 - 3β,17β - 二醇的92%。在对不同营养补充剂的调查过程中,出现了几个分析难题。对匀浆、提取、分离、衍生化和GC-MS测量等方面以及解决出现问题的策略进行了优化。对于营养补充剂中类固醇的定量测量,特定类固醇的氘代内标或标准加入法对于补偿基质效应是必要的。