Kharga Kusum, Jha Shubhang, Vishwakarma Tanvi, Kumar Lokender
School of Biotechnology, Faculty of Applied Sciences and Biotechnology, Shoolini University, Himachal Pradesh, India.
School of Bioengineering and Food Technology, Faculty of Applied Sciences and Biotechnology, Shoolini University, Himachal Pradesh, India.
Crit Rev Microbiol. 2025 Feb;51(1):44-83. doi: 10.1080/1040841X.2024.2321480. Epub 2024 Feb 29.
Antibiotics have remained the cornerstone for the treatment of bacterial infections ever since their discovery in the twentieth century. The uproar over antibiotic resistance among bacteria arising from genome plasticity and biofilm development has rendered current antibiotic therapies ineffective, urging the development of innovative therapeutic approaches. The development of antibiotic resistance among bacteria has further heightened the clinical failure of antibiotic therapy, which is often linked to its low bioavailability, side effects, and poor penetration and accumulation at the site of infection. In this review, we highlight the potential use of siderophores, antibodies, cell-penetrating peptides, antimicrobial peptides, bacteriophages, and nanoparticles to smuggle antibiotics across impermeable biological membranes to achieve therapeutically relevant concentrations of antibiotics and combat antimicrobial resistance (AMR). We will discuss the general mechanisms which each delivery system functions and how it can be tailored to deliver antibiotics against the paradigm of mechanisms underlying antibiotic resistance.
自20世纪发现抗生素以来,抗生素一直是治疗细菌感染的基石。细菌因基因组可塑性和生物膜形成而产生的抗生素耐药性引发了轩然大波,使得当前的抗生素疗法失效,这促使人们开发创新的治疗方法。细菌中抗生素耐药性的发展进一步加剧了抗生素治疗的临床失败,这通常与其低生物利用度、副作用以及在感染部位的低渗透和积累有关。在这篇综述中,我们强调了铁载体、抗体、细胞穿透肽、抗菌肽、噬菌体和纳米颗粒在将抗生素偷运过不可渗透的生物膜以达到治疗相关浓度的抗生素并对抗抗菌耐药性(AMR)方面的潜在用途。我们将讨论每种递送系统发挥作用的一般机制,以及如何根据抗生素耐药性潜在机制的范式对其进行调整以递送抗生素。