School of Chemical and Biomedical Engineering, Nanyang Technological University (NTU), 62 Nanyang Drive, Singapore 637459, Singapore.
Centre for Antimicrobial Bioengineering, NTU, Singapore 637459, Singapore.
ACS Appl Mater Interfaces. 2021 Jan 20;13(2):3237-3245. doi: 10.1021/acsami.0c20881. Epub 2021 Jan 6.
Cationic polymers are promising antibacterial agents because bacteria have a low propensity to develop resistance against them, but they usually have low biocompatibility because of their hydrophobic moieties. Herein, we report a new biodegradable and biocompatible chitosan-derived cationic antibacterial polymer, 2,6-diamino chitosan (2,6-DAC). 2,6-DAC shows excellent broad-spectrum antimicrobial activity with minimum inhibitory concentrations (MICs) of 8-32 μg/mL against clinically relevant and multidrug-resistant (MDR) bacteria including , , , , , and . Furthermore, 2,6-DAC shows an excellent synergistic effect with various clinically relevant antibiotics proved by decreasing the MICs of the antibiotics against MDR and methicillin-resistant to <1 μg/mL. In vivo biocompatibility of 2,6-DAC is proved by a dosage of 100 mg/kg compound via oral administration and 25 mg/kg compound via intraperitoneal injection to mice; 2,6-DAC does not cause any weight loss and any significant change in liver and kidney biomarkers or the important blood electrolytes. The combinations of 2,6-DAC together with novobiocin and rifampicin show >2.4 log reduction of in murine intraperitoneal and lung infection models. The novel chitosan derivative, 2,6-DAC, can be utilized as a biocompatible broad-spectrum cationic antimicrobial agent alone or in synergistic combination with various antibiotics.
阳离子聚合物是很有前途的抗菌剂,因为细菌对它们产生耐药性的倾向较低,但由于其疏水性部分,它们通常生物相容性较低。在此,我们报告了一种新型可生物降解和生物相容的壳聚糖衍生阳离子抗菌聚合物,2,6-二氨基壳聚糖(2,6-DAC)。2,6-DAC 对临床相关和多药耐药(MDR)细菌表现出优异的广谱抗菌活性,最低抑菌浓度(MIC)为 8-32μg/mL,包括 、 、 、 、 和 。此外,2,6-DAC 与各种临床相关抗生素表现出优异的协同作用,通过降低抗生素对 MDR 和耐甲氧西林 的 MIC 值至 <1μg/mL 来证明。通过口服给予 100mg/kg 化合物和腹腔内注射 25mg/kg 化合物,证明了 2,6-DAC 的体内生物相容性;2,6-DAC 不会导致体重减轻,也不会导致肝和肾生物标志物或重要血液电解质发生任何显著变化。2,6-DAC 与新生霉素和利福平的组合在小鼠腹腔和肺部感染模型中使 的减少量超过 2.4 对数。新型壳聚糖衍生物 2,6-DAC 可单独用作生物相容的广谱阳离子抗菌剂,也可与各种抗生素协同组合使用。