Falsified and problematic methandienone products available online: active pharmaceutical ingredient identification by portable Raman spectrometers and quantification by ultra-high-performance liquid chromatography–Fourier transform mass spectrometry

Robin Schreiber, Manami Hori, Chisato Takahashi, Mohammad Sofiqur Rahman, Ayane Nakao, Shu Zhu, Feiyu Zhu, Naoko Yoshida, Keiko Maekawa, Kazuko Kimura
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Abstract

This study aimed on the one hand to clarify the quality, authenticity, safety, and other issues related to products of the anabolic-androgenic steroid methandienone advertised on the Internet and personally imported to Japan and on the other hand to evaluate the use of two portable Raman spectrometers in identifying the active pharmaceutical ingredient (API). The study found that all n = 15 samples purchased from 14 websites were problematic regarding their package, labeling, and/or content. Specifically, one sample (6.7%) was confirmed falsified, twelve samples (80%) were found either to be falsified or unlicensed as pharmaceutical product, and two samples (13.3%) were received without information on the manufacturers’ physical address or country of origin, with one sample (6.7%) having no labeling or other accompanying information at all. Both Raman spectrometers were able to identify the API in all samples as confirmed and quantified by ultra-high-performance liquid chromatography–Fourier transform mass spectrometry. Twelve samples contained on average less than 90% of the declared API content. By contacting national regulatory authorities in 44 countries, methandienone products were found to be approved in 1 country and not approved in 21 countries. To prevent health hazards and abuse, measures against the acquisition of anabolic-androgenic steroids from unknown sources are required. Portable Raman spectrometers may be suitable for the non-destructive and quick identification of methandienone in tablets.
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网上销售的假冒和问题甲地孕酮产品:利用便携式拉曼光谱仪鉴定活性药物成分并利用超高效液相色谱-傅立叶变换质谱法进行定量
本研究一方面旨在澄清互联网上宣传的、个人进口到日本的合成代谢雄激素类固醇美雄酮产品的质量、真实性、安全性和其他相关问题,另一方面旨在评估使用两台便携式拉曼光谱仪鉴定活性药物成分 (API) 的情况。研究发现,从 14 个网站购买的所有 n = 15 个样品在包装、标签和/或含量方面都存在问题。具体来说,1 个样品(6.7%)被证实是伪造的,12 个样品(80%)被发现是伪造的或未经许可的药品,2 个样品(13.3%)没有制造商的实际地址或原产国信息,1 个样品(6.7%)没有任何标签或其他附带信息。经超高效液相色谱-傅立叶变换质谱法确认和定量,两种拉曼光谱仪都能识别所有样品中的原料药。12 个样品中的原料药含量平均不到申报含量的 90%。通过与 44 个国家的国家监管机构联系,发现 1 个国家批准了甲地孕酮产品,21 个国家未批准。为防止危害健康和滥用,需要采取措施防止从不明来源获取合成代谢雄性类固醇。便携式拉曼光谱仪可能适用于对药片中的甲地孕酮进行非破坏性的快速鉴定。
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