Synthesis and characterization of hyperbranched polyesters from polyethylene glycol and citric acid: structural insights and antibiotic resistance mitigation against drug-resistant bacterial strains†

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Aniruddha Mukherjee, Sonai Dutta, Reetika Sarkar, Sayan Basak, Srijoni Sengupta, Subhadeep Chakraborty, Anirban Mukherjee, Payel Biswas, Satish Kumar and Abhijit Bandyopadhyay
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Abstract

The escalating global threat of microbial diseases and antibiotic resistance has spurred research into innovative polymeric materials with potent antimicrobial properties, driven by the impact on healthcare systems worldwide and the increasing resistance of conventional drugs. Multidrug-resistant (MDR) bacteria pose a significant challenge to global health, endangering vulnerable patients and critical medical procedures, with profound economic implications. Addressing antibiotic resistance requires a multifaceted approach, including exploring new drug formulations like natural and hyperbranched polymers. A promising strategy involves combining synthetic hyperbranched polymers with existing drugs to eliminate resistant cells and impede biofilm formation more effectively within a shorter timeframe, offering a cost-effective alternative for treating antibiotic-resistant infections. Innovative polyesters derived from polyethylene glycol and citric acid show potential as nanoscale antibiotics due to their biocompatibility, biodegradability, and antibacterial activity. With this as the context, our study aims to synthesize hyperbranched polyesters by controlling gelation and optimizing branching with strategic adjustments of citric acid mole composition relative to PEG. It was also found that antimicrobial studies revealed the efficacy of these polyesters against Gram-positive and Gram-negative bacteria, particularly in specific formulations. We envision that combining sublethal doses of these polyesters with conventional antibiotics resulted in synergistic effects, enhancing antimicrobial activity and biofilm eradication without promoting resistance development.

Abstract Image

聚乙二醇和柠檬酸超支化聚酯的合成和表征:对耐药菌株的结构见解和抗生素耐药性缓解
微生物疾病和抗生素耐药性的全球威胁不断升级,在对全球医疗保健系统的影响和传统药物耐药性不断增加的推动下,刺激了对具有强大抗菌性能的创新聚合物材料的研究。耐多药(MDR)细菌对全球健康构成重大挑战,危及脆弱患者和关键医疗程序,并产生深远的经济影响。解决抗生素耐药性需要多方面的方法,包括探索新的药物配方,如天然和超支化聚合物。一个有希望的策略是将合成的超支化聚合物与现有药物结合起来,在更短的时间内更有效地消除耐药细胞并阻碍生物膜的形成,为治疗抗生素耐药感染提供了一种经济有效的替代方案。从聚乙二醇和柠檬酸中提取的新型聚酯由于其生物相容性、可生物降解性和抗菌活性,显示出作为纳米级抗生素的潜力。在此背景下,我们的研究旨在通过对柠檬酸摩尔组成相对于PEG的战略性调整来控制凝胶化和优化支化,从而合成超支化聚酯。还发现,抗菌研究揭示了这些聚酯对革兰氏阳性和革兰氏阴性细菌的功效,特别是在特定配方中。我们设想将亚致死剂量的这些聚酯与常规抗生素结合使用,产生协同效应,增强抗菌活性和生物膜根除,而不会促进耐药性的发展。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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