Development of a second-generation Testosterone synthesis route via biocatalysis

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Abstract

Testosterone is a male hormone which is being manufactured in pharmaceutical industry for many years. Testosterone is the primary sex hormone and anabolic steroid in males. It is also used as a drug to treat male hypogonadism, gender dysphoria, bone loss, certain types of breast cancer, prostate cancer and hypersexuality [01]. It may also be used to increase athletic ability in the form of doping. Most of the time the current manufacturing routes start from 4 androstene 3,17 dione which is chemically converted to Testosterone by a reduction reaction. In this article we present the development of a second-generation route towards Testosterone via Biocatalysis, using an oxidoreductase enzyme. This results in a more sustainable API Testosterone. The overall PMI decreases from 69 to 44. Consequently, the enzymatic route reduces the environmental impact based on material use by 36%. Via proteomics principles we have been able to develop a generally applicable in-house analysis/method to prove absence of residual enzyme with a detection limit as low as 1 ppm.
通过生物催化的第二代睾酮合成途径的发展
睾酮是一种男性激素,已在制药行业生产多年。睾酮是男性体内主要的性激素和合成代谢类固醇。它也被用作治疗男性性腺功能减退、性别焦虑、骨质流失、某些类型的乳腺癌、前列腺癌和性欲亢进的药物。它也可能以兴奋剂的形式被用来提高运动能力。大多数时候,目前的制造路线从4雄烯3,17二酮开始,通过还原反应将其化学转化为睾酮。在这篇文章中,我们介绍了通过氧化还原酶生物催化合成睾酮的第二代途径。这导致API睾酮更可持续。整体PMI从69降至44。因此,酶的途径减少了36%的基于材料使用的环境影响。通过蛋白质组学原理,我们已经能够开发出一种普遍适用的内部分析/方法来证明残留酶的缺失,检测限低至1ppm。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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