Liang Zhuoying, Liu Wenkang, Wang Ziqiang, Zheng Peilian, Liu Wei, Zhao Jianfu, Zhong Yunlong, Zhang Yan, Lin Jing, Xue Wei, Yu Siming
Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Guangdong Provincial Engineering and Technological Research Center for Drug Carrier Development, Department of Biomedical Engineering, Jinan University, Guangzhou 510632, China.
Department of Pharmacy, Jinan University, Guangzhou 510632, China.
Acta Biomater. 2022 Apr 15;143:428-444. doi: 10.1016/j.actbio.2022.02.029. Epub 2022 Feb 26.
Recently, nitric oxide (NO) has received increasing interest in combat against bacteria-induced infections because of its ability to sensitize and enhance the antibacterial effectiveness of many therapeutic approaches such as antibiotics. However, high-efficient loading and controlled release of NO remain a big challenge. In the present work, a type of gold nanostar/hollow polydopamine Janus nanostructure (GNS/HPDA JNPs) with precise near infrared (NIR)-controlled NO release property was fabricated using a facile seed-mediated method. Upon NIR laser irradiation, the NO-releasing GNS/HPDA JNPs (GNS/HPDA-BNN6) exhibited a synergistic photothermal and NO antibacterial effect by significantly inhibiting the growth and biofilm formation of both Gram-negative and Gram-positive bacterial strains, including methicillin-resistant Staphylococcus aureus (MRSA). An in-depth mechanism study revealed that two pathways were mainly involved in the synergistic photothermal and NO antibacterial effect. In one pathway, the synergistic effect severely destroyed the bacterial membrane by causing leakage of intracellular components such as DNA. In another pathway, the synergistic effect largely disturbed bacterial metabolism by regulating relative metabolic genes, followed by enhancing ROS generation to cause intracellular GSH depletion and DNA damage. More importantly, the synergistic effect significantly diminished the drug resistance of MRSA by downregulating the expression of the drug-resistant gene mecA and some relative multidrug efflux pumps (e.g., SepA and Tet38). An in vivo evaluation using a rat model with MRSA-infected wounds indicated that the synergistic photothermal and NO effect of GNS/HPDA-BNN6 can effectively eliminate MRSA from wounds, thereby alleviating inflammation and promoting wound healing. STATEMENT OF SIGNIFICANCE: Multidrug-resistant (MDR) bacteria have become a big threat to mankind, and therefore, the development of innovative antibacterial agents with high antibacterial efficiency is urgently required. Nanomaterial-mediated nitric oxide (NO) therapy is a promising strategy to effectively combat MDR bacteria through a synergistic antibacterial effect. Here, a gold nanostar/hollow polydopamine Janus nanostructure with precise near infrared (NIR) light-controlled NO release property (GNS/HPDA-BNN6) was developed. Both in vitro and in vivo evaluations demonstrated that GNS/HPDA-BNN6 could effectively eliminate methicillin-resistant Staphylococcus aureus (MRSA) from infected wounds and promote wound healing through a synergistic photothermal and NO therapeutic effect. Remarkably, the synergistic effect significantly diminished the drug resistance of MRSA by downregulating the expression of some drug-resistant genes and multidrug efflux pumps.
近年来,一氧化氮(NO)因其能够增强和提高多种治疗方法(如抗生素)的抗菌效果,在对抗细菌感染方面受到越来越多的关注。然而,高效负载和可控释放NO仍然是一个巨大的挑战。在本研究中,我们采用一种简便的种子介导法制备了一种具有精确近红外(NIR)控制的NO释放特性的金纳米星/中空聚多巴胺Janus纳米结构(GNS/HPDA JNPs)。在近红外激光照射下,释放NO的GNS/HPDA JNPs(GNS/HPDA-BNN6)通过显著抑制革兰氏阴性和革兰氏阳性细菌菌株(包括耐甲氧西林金黄色葡萄球菌(MRSA))的生长和生物膜形成,展现出协同的光热和NO抗菌作用。深入的机制研究表明,协同的光热和NO抗菌作用主要涉及两条途径。在一条途径中,协同作用通过导致细胞内成分(如DNA)泄漏,严重破坏细菌膜。在另一条途径中,协同作用通过调节相关代谢基因,极大地干扰细菌代谢,随后增强活性氧生成,导致细胞内谷胱甘肽耗竭和DNA损伤。更重要的是,协同作用通过下调耐药基因mecA和一些相关多药外排泵(如SepA和Tet38)的表达,显著降低了MRSA的耐药性。使用MRSA感染伤口的大鼠模型进行的体内评估表明,GNS/HPDA-BNN6的协同光热和NO作用可以有效地从伤口清除MRSA,从而减轻炎症并促进伤口愈合。重要性声明:多重耐药(MDR)细菌已成为人类的重大威胁,因此,迫切需要开发具有高抗菌效率的创新抗菌剂。纳米材料介导的一氧化氮(NO)疗法是一种通过协同抗菌作用有效对抗MDR细菌的有前景的策略。在此,我们开发了一种具有精确近红外(NIR)光控NO释放特性的金纳米星/中空聚多巴胺Janus纳米结构(GNS/HPDA-BNN6)。体外和体内评估均表明,GNS/HPDA-BNN6可以通过协同的光热和NO治疗作用,有效地从感染伤口清除耐甲氧西林金黄色葡萄球菌(MRSA)并促进伤口愈合。值得注意的是,协同作用通过下调一些耐药基因和多药外排泵的表达,显著降低了MRSA的耐药性。