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下一个前沿领域:揭示对抗多重耐药细菌的新方法。

The Next Frontier: Unveiling Novel Approaches for Combating Multidrug-Resistant Bacteria.

作者信息

Mallari Praveen, Rostami Leila D, Alanko Ida, Howaili Fadak, Ran Meixin, Bansal Kuldeep K, Rosenholm Jessica M, Salo-Ahen Outi M H

机构信息

Department of Zoology, Indira Gandhi National Tribal University, Amarkantak, Madhya Pradesh, 484887, India.

Pharmaceutical Sciences Laboratory, Faculty of Science and Engineering, Pharmacy, Åbo Akademi University, 20520, Turku, Finland.

出版信息

Pharm Res. 2025 Jun 16. doi: 10.1007/s11095-025-03871-x.

DOI:10.1007/s11095-025-03871-x
PMID:40524025
Abstract

BACKGROUND

The rapid occurrence of bacterial antibiotic resistance poses a significant threat to public health worldwide. Since particularly multidrug-resistant (MDR) pathogens are becoming untreatable with currently available antibiotics, new treatment modalities must be deployed.

OBJECTIVES

This review explores the recent advancements and the enduring challenges in new antibacterial development for drug-resistant organisms.

RESULTS

We describe how bacterial resistance to antibiotics arises and discuss why the traditional drug discovery routes are inefficient. The best alternative strategies to overcome these challenges might include exploring new bacterial pathways, utilizing compounds with antibacterial activities from the human microbiome, and repurposing existing drugs. Moreover, novel drug delivery mechanisms that leverage, for example, nanotechnology-based carriers may be breakthrough ideas that can increase antibiotic efficacy and, at the same time, reduce toxicity. Current clinical trials of next-generation drugs indicate that some treatments possess excellent potential to overcome the MDR issue.

CONCLUSION

Despite the substantial obstacles to getting bench findings to the patient, numerous scientists are still working towards this goal. Both the application of antibiotic stewardship principles and timely considerations through the regulatory pathways are needed to release the next generation of antibiotics that are suitable for the fight against superbugs.

摘要

背景

细菌抗生素耐药性的迅速出现对全球公共卫生构成了重大威胁。由于特别是多重耐药(MDR)病原体正变得无法用目前可用的抗生素治疗,因此必须采用新的治疗方式。

目的

本综述探讨了耐药生物体新型抗菌药物研发的最新进展和持续存在的挑战。

结果

我们描述了细菌对抗生素的耐药性是如何产生的,并讨论了传统药物发现途径效率低下的原因。克服这些挑战的最佳替代策略可能包括探索新的细菌途径、利用来自人类微生物群的具有抗菌活性的化合物以及重新利用现有药物。此外,利用例如基于纳米技术的载体的新型药物递送机制可能是能够提高抗生素疗效并同时降低毒性的突破性想法。目前下一代药物的临床试验表明,一些治疗方法具有克服多重耐药问题的巨大潜力。

结论

尽管将实验室研究结果应用于患者存在重大障碍,但众多科学家仍在朝着这一目标努力。需要应用抗生素管理原则并通过监管途径及时进行考量,以推出适合对抗超级细菌的下一代抗生素。

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本文引用的文献

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Optimizing the production and efficacy of antimicrobial bioactive compounds from in combating multi-drug-resistant pathogens.优化来自……的抗微生物生物活性化合物在对抗多重耐药病原体方面的生产及功效。 (注:原文中“from”后面似乎缺少具体内容)
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Novel inhibition of sortase A by plantamajoside: implications for controlling multidrug-resistant infections.大车前苷对分选酶A的新型抑制作用:对控制多重耐药感染的意义。
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Eicosapentaenoic acid enhances intestinal stem cell-mediated colonic epithelial regeneration by activating the LSD1-WNT signaling pathway.
二十碳五烯酸通过激活LSD1-WNT信号通路增强肠道干细胞介导的结肠上皮再生。
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Discovery, synthesis, and antibacterial activity of novel myrtucommulone analogs as inhibitors of DNA gyrase and topoisomerase IV.新型桃金娘烯醛类似物作为DNA促旋酶和拓扑异构酶IV抑制剂的发现、合成及抗菌活性
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Unveiling the Antimycobacterial Potential of Novel 4-Alkoxyquinolines: Insights into Selectivity, Mechanism of Action, and Exposure.揭示新型4-烷氧基喹啉的抗分枝杆菌潜力:对选择性、作用机制和暴露情况的见解
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Discovery and optimization of tetrahydroacridine derivatives as a novel class of antibiotics against multidrug-resistant Gram-positive pathogens by targeting type I signal peptidase and disrupting bacterial membrane.通过靶向I型信号肽酶和破坏细菌膜来发现和优化四氢吖啶衍生物作为一类新型抗多重耐药革兰氏阳性病原体的抗生素。
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Challenges and opportunities in engineering next-generation 3D microelectronic devices: improved performance and higher integration density.下一代3D微电子器件的工程挑战与机遇:性能提升与更高集成密度
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A Comprehensive Review of Antimicrobial Agents Against Clinically Important Bacterial Pathogens: Prospects for Phytochemicals.针对临床重要细菌病原体的抗菌剂综合综述:植物化学物质的前景
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Anti-bacteria, anti-biofilm, and anti-virulence activity of the synthetic compound MTEBT-3 against carbapenem-resistant Klebsiella pneumoniae strains ST3984.合成化合物 MTEBT-3 对碳青霉烯类耐药肺炎克雷伯菌 ST3984 的抗细菌、抗生物膜和抗毒力活性。
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