引导金属β-内酰胺酶抑制剂药物开发的复杂性。

IF 3.6 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nakita Reddy, Alessandra Moraes Balieiro, José Rogério A. Silva, Christiaan A. Gouws, Awelani Mutshembele, Per I. Arvidsson, Hendrik G. Kruger, Thavendran Govender and Tricia Naicker
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引用次数: 0

摘要

抗生素耐药率的上升,特别是在具有金属β-内酰胺酶(MBLs)的碳青霉烯耐药肠杆菌中,突出了对有效的MBL抑制剂(MBLIs)的迫切需要。驾驭mbli药物开发的复杂性需要解决阻碍其进展的重大挑战。尽管在临床前开发方面做出了许多努力,但缺乏标准化的方法导致了差异,阻碍了潜在的mbli从研究到临床应用的转化。令人担忧的是,只有一种金属β-内酰胺酶抑制候选药物处于预注册开发阶段。本综述强调需要在MBLI开发的关键方面达成全球共识,包括标准化的体外测试、完善的动物模型、统一的毒性评估、一致的药代动力学数据和统一的计算机方法。它还提出了应对这些挑战的解决方案,旨在弥合研究与临床应用之间的差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Navigating the complexities of drug development for metallo-β-lactamase inhibitors

Navigating the complexities of drug development for metallo-β-lactamase inhibitors

The rising antibiotic resistance rates, especially among carbapenem-resistant Enterobacterales with metallo-β-lactamases (MBLs), highlight the urgent need for effective MBL inhibitors (MBLIs). Navigating the complexities of drug development for MBLIs requires addressing the significant challenges that have hindered its progress. Despite numerous efforts in pre-clinical development, the lack of standardized approaches has led to disparities, stalling the translation of potential MBLIs from research into clinical use. Alarmingly, there is only one metallo-β-lactamase inhibitory candidate in the pre-registration phase of development. This review highlights the need for a global consensus on key aspects of MBLI development, including standardized in vitro testing, refined animal models, harmonized toxicity assessments, consistent pharmacokinetic data, and uniform in silico methods. It also proposes solutions to these challenges, aiming to bridge the gap between research and clinical application.

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来源期刊
CiteScore
5.80
自引率
2.40%
发文量
129
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