Vitali Valentina, Zineddu Stefano, Messori Luigi
Department of Chemistry "Ugo Schiff", University of Florence Sesto Fiorentino 50019 Italy
RSC Adv. 2025 Jan 9;15(2):748-753. doi: 10.1039/d4ra07449a.
Due to their considerable chemical diversity, metal compounds are attracting increasing and renewed attention from the scientific and medical communities as potential antimicrobial agents to combat the growing problem of antibiotic resistance. The development of metal compounds as antimicrobial agents typically follows classical drug discovery procedures and suffers from the same problems; indeed, these procedures can be very expensive and time-consuming, and carry an intrinsically high risk of failure. Here, we show how some established drug discovery approaches can be conveniently and successfully applied to antimicrobial metal compounds to provide some shortcuts for faster clinical translation of new treatments. Specifically, we refer to (i) drug repurposing, (ii) drug combination and (iii) drug targeting by bioconjugation; some relevant examples will be illustrated.
由于其显著的化学多样性,金属化合物作为对抗日益严重的抗生素耐药性问题的潜在抗菌剂,正吸引着科学界和医学界越来越多的关注并重新受到重视。将金属化合物开发为抗菌剂通常遵循经典的药物发现程序,并且存在同样的问题;实际上,这些程序可能非常昂贵且耗时,并且本质上失败风险很高。在此,我们展示了一些既定的药物发现方法如何能够方便且成功地应用于抗菌金属化合物,以为新治疗方法更快地转化为临床应用提供一些捷径。具体而言,我们指的是(i)药物重新利用,(ii)药物联合以及(iii)通过生物偶联进行药物靶向;将举例说明一些相关实例。