δ13C values of urinary 19-norandrosterone in antidoping samples and potential for adverse findings from boar offal consumption

IF 2.6 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Drug Testing and Analysis Pub Date : 2023-03-16 DOI:10.1002/dta.3470
Vinod S. Nair, John D. Howa, Matthew S. Morrison, Lacey Beggs, Thane Campbell, Matthew Fedoruk, Brian Ahrens, Daniel Eichner
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引用次数: 2

Abstract

19-Norandrosterone (19NA) is the preferred urinary target compound to identify doping with nandrolone or related 19-norsteroids. At concentrations between 2.5 and 15 ng/mL, isotope ratio mass spectrometry (IRMS) is required to establish exogenous origin of urinary 19NA. An absolute difference of 3‰ between urinary 19NA and an endogenous reference compound (ERC) constitutes a finding for exogenous origin of 19NA. Over the last 3 years, 77 samples containing urinary 19NA between 2.5 and 15 ng/mL were analyzed at our laboratory. The measured δ13C values for 19NA ranged from −29.5‰ to −16.8‰. In comparison, the δ13C values for the corresponding urinary ERCs ranged from −22.4‰ to −16.2‰. Due to the considerable overlap in values between the target compound and the natural range of urinary ERCs, it can be challenging to distinguish between endogenous and exogenous origins of urinary 19NA. In addition, it is well known that consumption of offal from non-castrated pigs can produce 19NA in urine. To determine whether this could cause a positive IRMS finding under the current IRMS positivity criteria, meat from non-castrated boars fed a mixture of corn and soy was consumed by 13 volunteers. Two volunteers produced 19NA findings above 2.5 ng/mL, and the measured isotope values, while inconsistent with documented 19-norsteroid preparations, did meet IRMS positivity criteria. However, these increases in 19NA urinary concentrations were short-lived due to rapid elimination. Timely follow-up collections may help support a claim for dietary exposure when low urinary concentrations of 19NA with pseudo-endogenous isotope values are observed.

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反兴奋剂样品中尿19-去雄酮的δ 13c值和食用猪内脏的潜在不良结果。
19-去甲雄酮(19NA)是鉴别诺龙或相关19-去甲甾类兴奋剂的首选尿液靶标化合物。浓度在2.5 - 15ng /mL之间时,需要同位素比质谱法(IRMS)来确定尿19NA的外源性来源。尿19NA与内源性对照化合物(ERC)的绝对差异为3‰,表明19NA是外源性来源。在过去的3年中,在我们的实验室分析了77例尿19NA在2.5至15 ng/mL之间的样本。19NA的δ 13c值为-29.5‰~ -16.8‰。相比之下,相应的尿ERCs的δ 13c值在-22.4‰~ -16.2‰之间。由于目标化合物的值与尿ERCs的自然范围有相当大的重叠,因此区分尿19NA的内源性和外源性来源可能具有挑战性。此外,众所周知,食用未阉割猪的内脏可在尿液中产生19NA。为了确定这是否会导致目前IRMS阳性标准下的IRMS阳性结果,13名志愿者食用了饲喂玉米和大豆混合物的未阉割公猪的肉。两名志愿者的19NA检测结果高于2.5 ng/mL,测量的同位素值虽然与文献记载的19-去甲类固醇制剂不一致,但确实符合IRMS阳性标准。然而,尿中19NA浓度的增加是短暂的,因为它能迅速消除。及时的随访收集可能有助于支持膳食暴露的主张,当观察到低尿浓度的19NA与伪内源性同位素值。
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来源期刊
Drug Testing and Analysis
Drug Testing and Analysis BIOCHEMICAL RESEARCH METHODS-CHEMISTRY, ANALYTICAL
CiteScore
5.90
自引率
24.10%
发文量
191
审稿时长
2.3 months
期刊介绍: As the incidence of drugs escalates in 21st century living, their detection and analysis have become increasingly important. Sport, the workplace, crime investigation, homeland security, the pharmaceutical industry and the environment are just some of the high profile arenas in which analytical testing has provided an important investigative tool for uncovering the presence of extraneous substances. In addition to the usual publishing fare of primary research articles, case reports and letters, Drug Testing and Analysis offers a unique combination of; ‘How to’ material such as ‘Tutorials’ and ‘Reviews’, Speculative pieces (‘Commentaries’ and ‘Perspectives'', providing a broader scientific and social context to the aspects of analytical testing), ‘Annual banned substance reviews’ (delivering a critical evaluation of the methods used in the characterization of established and newly outlawed compounds). Rather than focus on the application of a single technique, Drug Testing and Analysis employs a unique multidisciplinary approach to the field of controversial compound determination. Papers discussing chromatography, mass spectrometry, immunological approaches, 1D/2D gel electrophoresis, to name just a few select methods, are welcomed where their application is related to any of the six key topics listed below.
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