Qiao Jing, Liu Zhi, Purro Max, Xiong May P
Department of Pharmaceutical & Biomedical Sciences, College of Pharmacy, University of Georgia, Athens, GA 30602-2352, USA.
Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison, Madison, WI 53705-2222, USA.
J Mater Chem B. 2018 Sep 7;6(33):5353-5361. doi: 10.1039/C8TB01610K. Epub 2018 Jul 31.
Bacteria are now becoming more resistant to most conventional antibiotics. Approaches for the treatment of multidrug-resistant bacterial infections are urgently required. Cationic polymers have broad-spectrum antibacterial activity but can also induce non-specific damage to mammalian cells. Herein, we report on the design of cationic polyrotaxanes (cPRs) with variable charge densities. cPRs were prepared by conjugating neutral ethanolamine and cationic ethylenediamine at various ratios onto threaded alpha-cyclodextrins and their antimicrobial and cytocompatible properties were investigated in vitro. In contact with Gram-negative bacteria, cPRs can disrupt the bacterial outer membrane integrity via electrostatic interactions and penetrate into the cytosol. The ability of cPRs to serve as potentiators at sub-MIC concentrations, to enhance the permeability and activity of poorly permeable antibiotics such as vancomycin, erythromycin and rifampicin, was also investigated against Gram-negative PAO1 and ATCC 25922.
细菌现在对大多数传统抗生素的耐药性越来越强。迫切需要治疗多重耐药细菌感染的方法。阳离子聚合物具有广谱抗菌活性,但也会对哺乳动物细胞造成非特异性损伤。在此,我们报告了具有可变电荷密度的阳离子聚轮烷(cPRs)的设计。通过将中性乙醇胺和阳离子乙二胺以不同比例共轭到穿线的α-环糊精上制备了cPRs,并在体外研究了它们的抗菌和细胞相容性特性。与革兰氏阴性菌接触时,cPRs可通过静电相互作用破坏细菌外膜完整性并渗透到细胞质中。还针对革兰氏阴性菌PAO1和ATCC 25922研究了cPRs在亚MIC浓度下作为增效剂,增强万古霉素、红霉素和利福平这类渗透性差的抗生素的渗透性和活性的能力。