Study of the urinary metabolites of 17ɑ-methyl-19-nortestosterone in human using gas chromatography - mass spectrometry. Preliminary results.

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY
R Montes de Oca Porto, D Martinez Brito, O Terrero Serrano, M T Correa Vidal
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引用次数: 0

Abstract

1. 17ɑ-methyl-19-nortestosterone (MNT), a steroid prohibited in sport, has been marketed since the 1990s, however their use is increasingly, mainly because it is contained in nutritional supplements. The study of the metabolism of the prohibited substances for athletes allows to identify new metabolites that could increase the veracity of the results. This work studied preliminary the in-vivo metabolism of MNT.

2. The study was conducted after a single oral administration dose using the simple quadrupole mass spectrometry coupled to gas chromatography and considering the steroids classic metabolic reactions.

3. Nine MNT metabolites were detected in urine. Mass spectra and fragmentation patterns were proposed for each metabolite. In addition to MNT, the detection of four metabolites corroborated what is described in the specialised literature. However, to our knowledge, four other metabolites have not been explicitly described. According to the time-course, three metabolites were still detected at 96-, 84- and 72-hours port-administration. These detection windows can increase by using other instrumentations such as a triple quadrupole mass spectrometer with multiple reaction monitoring acquisition mode.

用气相色谱-质谱法研究人尿中17 -甲基-19-去甲睾酮的代谢产物。初步结果。
1. 17 -甲基-19-去甲睾酮(MNT)是一种被禁止在运动中使用的类固醇,自20世纪90年代以来一直在市场上销售,但它们的使用越来越多,主要是因为它含有在营养补充剂中。对运动员禁用物质代谢的研究可以识别新的代谢物,从而提高结果的准确性。本文对MNT.2的体内代谢进行了初步研究。本研究是在单次口服给药后使用简单的四极杆质谱联用气相色谱法进行的,并考虑了类固醇的经典代谢反应。尿中检测到9种MNT代谢物。提出了每种代谢物的质谱和碎片化模式。除了MNT外,四种代谢物的检测证实了专业文献中所描述的内容。然而,据我们所知,其他四种代谢物尚未被明确描述。根据时间过程,在给药后96、84和72小时仍检测到三种代谢物。这些检测窗口可以通过使用其他仪器,如三重四极杆质谱仪与多反应监测采集模式增加。
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来源期刊
Xenobiotica
Xenobiotica 医学-毒理学
CiteScore
3.80
自引率
5.60%
发文量
96
审稿时长
2 months
期刊介绍: Xenobiotica covers seven main areas, including:General Xenobiochemistry, including in vitro studies concerned with the metabolism, disposition and excretion of drugs, and other xenobiotics, as well as the structure, function and regulation of associated enzymesClinical Pharmacokinetics and Metabolism, covering the pharmacokinetics and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in manAnimal Pharmacokinetics and Metabolism, covering the pharmacokinetics, and absorption, distribution, metabolism and excretion of drugs and other xenobiotics in animalsPharmacogenetics, defined as the identification and functional characterisation of polymorphic genes that encode xenobiotic metabolising enzymes and transporters that may result in altered enzymatic, cellular and clinical responses to xenobioticsMolecular Toxicology, concerning the mechanisms of toxicity and the study of toxicology of xenobiotics at the molecular levelXenobiotic Transporters, concerned with all aspects of the carrier proteins involved in the movement of xenobiotics into and out of cells, and their impact on pharmacokinetic behaviour in animals and manTopics in Xenobiochemistry, in the form of reviews and commentaries are primarily intended to be a critical analysis of the issue, wherein the author offers opinions on the relevance of data or of a particular experimental approach or methodology
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