Suppr超能文献

能够释放治疗性气体的抗菌 PDT 纳米平台,用于协同增强治疗深部感染。

Antibacterial PDT nanoplatform capable of releasing therapeutic gas for synergistic and enhanced treatment against deep infections.

机构信息

State Key Laboratory on Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, Changchun, 130012, China.

Department of Oral Implantology, Jilin Provincial Key Laboratory of Sciences and Technology for Stomatology Nanoengineering, Hospital of Stomatology, Jilin University, Changchun, 130021, China.

出版信息

Theranostics. 2022 Feb 28;12(6):2580-2597. doi: 10.7150/thno.70277. eCollection 2022.

Abstract

Antibacterial photodynamic therapy (aPDT) has emerged as an attractive treatment option for efficient removal of pathogenic bacteria. However, aPDT in deep tissue will encounter difficulties such as limited light penetration depth, insufficient oxygen (O) supply and inability to eliminate inflammation introduced by bacteria, which hinders its clinical application. Herein, the near infrared (NIR) strategy of simultaneously generating O and CO was developed for aPDT based antibacterial therapy and mitigation of deep infection inflammation. We prepared NIR-mediated multifunctional aPDT nanoplatform (POS-UCNPs/ICG) producing therapeutic gas of O and CO. The CO, O and ROS generation of the nanoplatform were characterized by dye probes, respectively. The antibacterial activity and anti-inflammation of POS-UCNPs/ICG were demonstrated and . In addition, the therapeutic effects were serially analyzed by immunofluorescence staining, Masson's staining, hematoxylin and eosin staining, colony formation units (CFU) and so on. NIR-mediated multifunctional aPDT nanoplatform was realized by combining the up-conversion nanoparticles (UCNPs) and partially oxidized SnS (POS) nanosheets (NSs) as well as indocyanine green (ICG). Using a single 808 nm light, aPDT can be achieved via ICG molecules, meanwhile, O/CO can be generated by POS NSs through upconversion light excitation. During the aPDT process, O can enhance aPDT, while CO can regulate inflammation through the PI3K/NF-κB pathway. Therefore, POS-UCNPs/ICG groups had a highest percentage of healing area up to 91.55±1.26% in mouse abscess model. Due to enhanced aPDT and anti-inflammatory collaborative therapy, the POS-UCNPs/ICG composites showed remarkably accelerated recovery in animal abscess models. Such NIR light responsive nanoplatform with optimized antibacterial capacity and immunomodulatory functions is promising for clinical therapeutics of bacteria-induced infections.

摘要

抗菌光动力疗法(aPDT)作为一种有效的去除致病菌的治疗方法,已经引起了人们的关注。然而,深部组织中的 aPDT 会遇到一些困难,如有限的光穿透深度、供氧不足以及无法消除细菌引起的炎症等,这些都阻碍了其临床应用。在此,我们开发了一种近红外(NIR)策略,通过同时产生 O 和 CO,为基于 aPDT 的抗菌治疗和缓解深部感染炎症提供了可能。我们制备了一种近红外介导的多功能 aPDT 纳米平台(POS-UCNPs/ICG),该平台可以产生 O 和 CO 两种治疗气体。通过染料探针分别对纳米平台的 CO、O 和 ROS 的产生进行了表征。通过 、 和 等实验,证明了 POS-UCNPs/ICG 的抗菌活性和抗炎作用。此外,还通过免疫荧光染色、Masson 染色、苏木精和伊红染色、集落形成单位(CFU)等方法对 进行了连续分析。通过将上转换纳米粒子(UCNPs)和部分氧化的 SnS(POS)纳米片(NSs)以及吲哚菁绿(ICG)结合在一起,实现了 NIR 介导的多功能 aPDT 纳米平台。通过使用 808nm 单波长光,ICG 分子可以实现 aPDT,同时,POS NSs 通过上转换光激发可以产生 O/CO。在 aPDT 过程中,O 可以增强 aPDT,而 CO 可以通过 PI3K/NF-κB 途径调节炎症。因此,在小鼠脓肿模型中,POS-UCNPs/ICG 组的愈合面积百分比最高,达到 91.55±1.26%。由于增强的 aPDT 和抗炎协同治疗,POS-UCNPs/ICG 复合材料在动物脓肿模型中表现出了显著的恢复速度。这种具有优化抗菌能力和免疫调节功能的近红外光响应纳米平台有望应用于细菌感染的临床治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3890/8965476/dc84266de3d7/thnov12p2580g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验