Beijing National Laboratory for Molecular Sciences, Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
Adv Sci (Weinh). 2022 May;9(16):e2200732. doi: 10.1002/advs.202200732. Epub 2022 Mar 27.
Photothermal therapy based on conjugated polymers represents a promising antibacterial strategy but still possesses notable limitations. Herein, degradable pseudo conjugated polymers (PCPs) containing photothermal molecular backbones and reactive oxygen species (ROS)-sensitive thioketal bonds are designed. Triphenylphosphine (PPh ) is introduced into PCPs to generate phosphonium-based PCPs (pPCPs), which further assembled with hyaluronic acid into pPCP nanoparticles (pPCP-NPs). pPCP-NPs with quaternary phosphonium cations selectively anchor on and destroy bacterial cell membranes through electrostatic action. Under 1064 nm laser irradiation, pPCP-NPs (pPCP-NPs/+L) produce near-infrared-II (NIR-II) photothermal antibacterial effect, thereby killing bacteria in a sustained manner. pPCP-NPs are readily degraded upon ROS abundant at infection sites, therefore exhibiting enough biosafety. pPCP-NPs/+L display an almost 100% bacterial inhibition rate in vitro and resultin a nearly complete recovery of bacteria-induced mouse wounds. A further metabolomics analysis denotes that pPCP-NPs/+L work in a concerted way to induce bacterial DNA damage, inhibit bacterial carbon/nitrogen utilization and amino acid/nucleotide synthesis. Taken together, degradable pPCP-NPs with both NIR-II photothermal effect and cationic phosphonium structural bacteriostasis provide a new avenue for antibiotics-alternative anti-infection therapy.
基于共轭聚合物的光热疗法是一种很有前途的抗菌策略,但仍存在显著的局限性。本文设计了含有光热分子骨架和活性氧(ROS)敏感硫缩酮键的可降解假共轭聚合物(PCPs)。将三苯基膦(PPh )引入 PCPs 中,生成基于膦的 PCPs(pPCPs),然后将其与透明质酸进一步组装成 pPCP 纳米颗粒(pPCP-NPs)。带季铵阳离子的 pPCP-NPs 通过静电作用选择性地锚定在细菌细胞膜上并破坏它们。在 1064nm 激光照射下,pPCP-NPs(pPCP-NPs/+L)产生近红外二区(NIR-II)光热抗菌效应,从而持续杀死细菌。pPCP-NPs 在感染部位富含 ROS 时很容易降解,因此具有足够的生物安全性。pPCP-NPs/+L 在体外对细菌的抑制率几乎达到 100%,并使细菌诱导的小鼠伤口几乎完全愈合。进一步的代谢组学分析表明,pPCP-NPs/+L 协同作用诱导细菌 DNA 损伤,抑制细菌碳/氮利用和氨基酸/核苷酸合成。总之,具有 NIR-II 光热效应和阳离子膦结构抑菌作用的可降解 pPCP-NPs 为抗生素替代抗感染治疗提供了新途径。