Ran Luoxiao, Lu Bitao, Qiu Haoyu, Zhou Guofang, Jiang Jing, Hu Enling, Dai Fangyin, Lan Guangqian
State Key Laboratory of Silkworm Genome Biology, College of Sericulture, Textile and Biomass Sciences, Southwest University, Chongqing, 400715, China.
Chongqing General Hospital, University of Chinese Academy of Sciences No.118, Xingguang Avenue, Liangjiang New Area, Chongqing, China.
Bioact Mater. 2021 Mar 1;6(9):2956-2968. doi: 10.1016/j.bioactmat.2021.01.032. eCollection 2021 Sep.
The increase in the number of resistant bacteria caused by the abuse of antibiotics and the emergence of biofilms significantly reduce the effectiveness of antibiotics. Bacterial infections are detrimental to our life and health. To reduce the abuse of antibiotics and treat biofilm-related bacterial infections, a biomimetic nano-antibacterial system, RBCM-NW-G namely, that controls the release of antibiotics through near infrared was prepared. The hollow porous structure and the high surface activity of nanoworms are used to realize antibiotic loading, and then, biomimetics are applied with red blood cell membranes (RBCM). RBCM-NW-G, which retains the performance of RBCM, shows enhanced permeability and retention effects. Fluorescence imaging in mice showed the effective accumulation of RBCM-NW-G at the site of infection. In addition, the biomimetic nanoparticles showed a longer blood circulation time and good biocompatibility. Anti-biofilm test results showed damage to biofilms due to a photothermal effect and a highly efficient antibacterial performance under the synergy of the photothermal effect, silver iron, and antibiotics. Finally, by constructing a mouse infection model, the great potential of RBCM-NW-G in the treatment of in vivo infections was confirmed.
抗生素滥用导致的耐药菌数量增加以及生物膜的出现,显著降低了抗生素的有效性。细菌感染对我们的生命和健康有害。为减少抗生素滥用并治疗与生物膜相关的细菌感染,制备了一种通过近红外控制抗生素释放的仿生纳米抗菌系统,即RBCM-NW-G。利用纳米蠕虫的中空多孔结构和高表面活性实现抗生素负载,然后将红细胞膜(RBCM)应用于仿生学。保留了RBCM性能的RBCM-NW-G显示出增强的渗透和滞留效应。小鼠体内的荧光成像显示RBCM-NW-G在感染部位有效积累。此外,仿生纳米颗粒显示出更长的血液循环时间和良好的生物相容性。抗生物膜测试结果表明,由于光热效应以及光热效应、银铁和抗生素协同作用下的高效抗菌性能,生物膜受到了破坏。最后,通过构建小鼠感染模型,证实了RBCM-NW-G在体内感染治疗中的巨大潜力。