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Preclinical development of Ramizol an antibiotic belonging to a new class for the treatment of Clostridium difficile colitis

机译:雷米唑的临床前开发一种新的抗生素用于治疗艰难梭菌结肠炎

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摘要

Antibiotic-resistant bacteria is a major threat to human health and is predicted to become the leading cause of death from disease by 2050. Despite the recent resurgence of research and development in the area, few antibiotics have reached the market, with most of the recently approved antibiotics corresponding to new uses for old antibiotics, or structurally similar derivatives thereof. We have recently reported an in silico approach that led to the design of an entirely new class of antibiotics for the bacteria-specific mechanosensitive ion channel of large conductance: MscL. Here, we present the preclinical development of one such antibiotic, Ramizol, a first generation antibiotic belonging to that class. We present the lack of interaction between Ramizol and other mammalian channels adding credibility to its MscL selectivity. We determine the pharmacokinetic profile in a rat model and show <0.1% of Ramizol is absorbed systemically. We show this non-systemic nature of the antibiotic translates to over 70% survival of hamsters in a Clostridium difficile colitis model. Lastly, initial in vitro data indicate that resistance to Ramizol occurs at a low frequency. In conclusion, we establish the potential of Ramizol as an effective new treatment for C. difficile associated disease.
机译:抗生素抗药性细菌是对人类健康的主要威胁,预计到2050年将成为疾病致死的主要原因。尽管该地区的研究和开发最近复苏,但几乎没有抗生素进入市场,其中大多数是最近批准的抗生素,对应于旧抗生素的新用途,或其结构类似的衍生物。我们最近报道了一种计算机方法,该方法导致针对大电导的细菌特异性机械敏感离子通道设计了全新的抗生素类:MscL。在这里,我们介绍了一种此类抗生素拉米佐的临床前开发,该药物属于该类别。我们目前在Ramizol和其他哺乳动物渠道之间缺乏相互作用,为其MscL选择性增加了可信度。我们确定了大鼠模型的药代动力学特征,并显示<0.1%的雷米唑被全身吸收。我们显示这种非系统性的抗生素转化为艰难梭菌结肠炎模型中仓鼠的70%以上的存活率。最后,最初的体外数据表明,对雷米唑的抗药性较低。总之,我们建立了雷米唑作为艰难梭菌相关疾病的有效新疗法的潜力。

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