Meng Jie, Zhang Peng, Liu Qingjie, Ran Pan, Xie Shuang, Wei Junwu, Li Xiaohong
Institute of Biomedical Engineering, College of Medicine, Southwest Jiaotong University, Chengdu 610031, PR China; Key Laboratory of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031, PR China.
Key Laboratory of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu 610031, PR China.
Acta Biomater. 2023 May;162:20-31. doi: 10.1016/j.actbio.2023.03.012. Epub 2023 Mar 16.
Antibacterial electrotherapy is currently activated by external electric field or self-powered generators, but usually needs complicated power management circuits. Herein, near-infrared illumination (NIR) of pyroelectric nanoparticles (NPs) produces a built-in electric field to address the effectiveness and safety concerns in the antibacterial treatment. Janus tBT@PDA NPs were obtained by capping polydopamine (PDA) on tetragonal BaTiO (tBT) NPs through defining the polymerization time, followed by ciprofloxacin (CIP) loading on the PDA caps to fabricate Janus tBT@PDA-Cip NPs. NIR illumination of PDA caps creates temperature variations on tBT NPs to generate photothermal and pyroelectric effects. Finite element simulation reveals a pyroelectric potential of over 1 V and sufficient reactive oxygen species (ROS) are produced to exhibit pyroelectric dynamic therapy (PEDT). The elevated temperature on one side of the Janus NPs produces thermophoretic force to drive NP motion, which enhances interactions with bacteria and overcomes limitations in the short action distance and lifespan of ROS. The pyroelectric field accelerates CIP release through weakening the π-π stacking and electrostatic interaction with PDA and also interrupts membrane potentials of bacteria to enhance CIP invasion into bacteria. The synergistic antibacterial effect of pyroelectric tBT@PDA-Cip NPs causes the fully recovery of S. aureus-infected skin wounds and regeneration of intact epidermis, blood vessels and hair follicles, while no obvious pathological change or inflammatory lesion is detected in the major organs. Thus, the pyroelectric Janus nanomotors demonstrate synergistic PEDT/photothermal/antibiotic effects to enhance antibacterial efficacy while avoiding the necessity of excessive heat, ROS and antibiotic doses. STATEMENT OF SIGNIFICANCE: Antibacterial treatment is challenged by antibiotics-derived side effects and the evolution of resistant strains. Phototherapy is commonly associated with excessive heat and oxidative stress, and their combinations with other agents are especially encouraged to strengthen antibacterial efficacy while alleviating the associated side effects. Electric field is another activator to generate antibacterial abilities, but usually requires complicated power management and bulk electrodes, making it inconvenient in a biological setup. To address these challenges, we propose a strategy to generate microelectric field on nanoparticles themselves and achieve synergistic electrodynamic-photothermal-antibiotic therapies. The pyroelectric effect weakens interactions between nanoparticles and antibiotics to accelerate drug release, and the built-in pyroelectric field increases membrane fluidity to enhance bacterial uptake of antibiotics.
抗菌电疗法目前由外部电场或自供电发电机激活,但通常需要复杂的电源管理电路。在此,热释电纳米颗粒(NPs)的近红外光照(NIR)产生一个内置电场,以解决抗菌治疗中的有效性和安全性问题。通过定义聚合时间,在四方相钛酸钡(tBT)纳米颗粒上包覆聚多巴胺(PDA),得到Janus tBT@PDA NPs,然后在PDA帽上负载环丙沙星(CIP),制备Janus tBT@PDA-Cip NPs。PDA帽的近红外光照在tBT纳米颗粒上产生温度变化,以产生光热和热释电效应。有限元模拟显示热释电势超过1 V,并且产生了足够的活性氧(ROS)以展现热释电动态疗法(PEDT)。Janus纳米颗粒一侧升高的温度产生热泳力以驱动纳米颗粒运动,这增强了与细菌的相互作用,并克服了ROS的短作用距离和短寿命的限制。热释电场通过削弱与PDA的π-π堆积和静电相互作用来加速CIP释放,并且还中断细菌的膜电位以增强CIP向细菌内的侵入。热释电tBT@PDA-Cip NPs的协同抗菌作用导致金黄色葡萄球菌感染的皮肤伤口完全愈合,完整的表皮、血管和毛囊再生,而在主要器官中未检测到明显的病理变化或炎性病变。因此,热释电Janus纳米马达展现出协同的PEDT/光热/抗生素效应,以增强抗菌功效,同时避免过度的热、ROS和抗生素剂量的必要性。重要性声明:抗菌治疗受到抗生素副作用和耐药菌株进化的挑战。光疗通常与过热和氧化应激相关,特别鼓励将它们与其他药物联合使用,以增强抗菌功效同时减轻相关副作用。电场是产生抗菌能力的另一种激活剂,但通常需要复杂的电源管理和大体积电极,这使得其在生物环境中使用不便。为应对这些挑战,我们提出一种在纳米颗粒自身上产生微电场并实现协同电动力学-光热-抗生素疗法的策略。热释电效应削弱纳米颗粒与抗生素之间的相互作用以加速药物释放,并且内置的热释电场增加膜流动性以增强细菌对抗生素的摄取。