Department of Pathology, Microbiology and Immunology, University of South Carolina, School of Medicine, Columbia, South Carolina 29209, United States.
ACS Appl Mater Interfaces. 2020 May 13;12(19):21221-21230. doi: 10.1021/acsami.9b19712. Epub 2020 Jan 15.
New antimicrobial agents are needed to address ever-increasing antimicrobial resistance and a growing epidemic of infections caused by multidrug resistant pathogens. We design nanostructured antimicrobial copolymers containing multicyclic natural products that bear facial amphiphilicity. Bile acid based macromolecular architectures of these nanostructures can interact preferentially with bacterial membranes. Incorporation of polyethylene glycol into the copolymers not only improved the colloidal stability of nanostructures but also increased the biocompatibility. This study investigated the effects of facial amphiphilicity, polymer architectures, and self-assembled nanostructures on antimicrobial activity. Advanced nanostructures such as spheres, vesicles, and rod-shaped aggregates are formed in water from the facial amphiphilic cationic copolymers via supramolecular interactions. These aggregates were particularly interactive toward Gram-positive and Gram-negative bacterial cell membranes and showed low hemolysis against mammalian cells.
需要新的抗菌剂来应对不断增加的抗菌耐药性和由多药耐药病原体引起的感染流行。我们设计了含有多环天然产物的纳米结构抗菌共聚物,这些产物具有面两亲性。这些纳米结构的基于胆汁酸的大分子结构可以优先与细菌膜相互作用。将聚乙二醇掺入共聚物中不仅提高了纳米结构的胶体稳定性,而且提高了生物相容性。本研究考察了面两亲性、聚合物结构和自组装纳米结构对抗菌活性的影响。通过超分子相互作用,从具有面两亲性的阳离子共聚物在水中形成了高级纳米结构,如球体、囊泡和棒状聚集体。这些聚集体对革兰氏阳性和革兰氏阴性细菌细胞膜特别具有交互作用,并对哺乳动物细胞的溶血作用较低。