多功能无序二氧化钛纳米针通过杀死细菌和调节骨免疫微环境防止假体周围感染并增强骨整合。

IF 12.4 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Theranostics Pub Date : 2024-09-16 eCollection Date: 2024-01-01 DOI:10.7150/thno.98219
Yangmengfan Chen, Liqiang Zhou, Ming Guan, Shue Jin, Peng Tan, Xiaoxue Fu, Zongke Zhou
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引用次数: 0

摘要

理由:全髋关节置换术(THA)和全膝关节置换术(TKA)是治疗终末期骨关节炎的有效干预措施;然而,假体周围感染是关节置换术的一种破坏性并发症。为了安全地预防假体周围感染并增强骨整合,我们采用了表面修饰策略来杀灭细菌、调节骨免疫微环境并改善新骨形成。方法:我们采用水热法制造了带有无序二氧化钛纳米针(TNN)涂层的仿生昆虫翅膀。在TNN上包覆贻贝启发的聚多巴胺(PDA)和抗菌银纳米粒子(AgNPs),命名为AgNPs-PDA@TNN,以提高其生物相容性和长效杀菌能力。利用扫描电镜、原子力显微镜、XPS 光谱和水接触试验对工程试样的理化性质进行了评估。利用 RT-qPCR、Western 印迹、活/死染色、免疫荧光染色等方法评估了工程试样的生物相容性、杀菌能力以及对巨噬细胞和成骨分化的影响。结果AgNPs-PDA@TNN与巨噬细胞具有良好的生物相容性,并具有促进M2巨噬细胞极化的免疫调节能力。此外,AgNPs-PDA@TNN 还能改善 AgNPs 引起的细胞毒性,促进细胞扩散,增加 BMSCs 的成骨和基质沉积。此外,AgNPs-PDA@TNN 通过仿生纳米结构和包覆的 AgNPs 显示出对大肠杆菌和金黄色葡萄球菌的杀菌能力。各种成像分析表明,AgNPs-PDA@TNN 增强了杀菌能力,并改善了体内新骨的形成。H&E、革兰氏和马森染色证实,骨形成得到改善,炎症、感染和纤维化包裹减少。免疫荧光染色证实了 AgNPs-PDA@TNN 在体内的免疫调节能力。结论仿生昆虫翅膀AgNPs-PDA@TNN涂层具有杀菌特性、免疫调节能力和更强的骨整合能力。因此,这种多维仿生植入体表面有望成为预防假体周围感染的一种新策略。
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Multifunctionally disordered TiO2 nanoneedles prevent periprosthetic infection and enhance osteointegration by killing bacteria and modulating the osteoimmune microenvironment.

Rationale: Total hip arthroplasty (THA) and total knee arthroplasty (TKA) are effective interventions for end-stage osteoarthritis; however, periprosthetic infection is a devastating complication of arthroplasty. To safely prevent periprosthetic infection and enhance osteointegration, the surface modification strategy was utilized to kill bacteria, modulate the osteoimmune microenvironment, and improve new bone formation. Methods: We used the hydrothermal method to fabricate a bionic insect wing with the disordered titanium dioxide nanoneedle (TNN) coating. The mussel-inspired poly-dopamine (PDA) and antibacterial silver nanoparticles (AgNPs) were coated on TNN, named AgNPs-PDA@TNN, to improve the biocompatibility and long-lasting bactericidal capacity. The physicochemical properties of the engineered specimen were evaluated with SEM, AFM, XPS spectrum, and water contact assay. The biocompatibility, bactericidal ability, and the effects on macrophages and osteogenic differentiation were assessed with RT-qPCR, Western blotting, live/dead staining, immunofluorescent staining, etc. Results: The AgNPs-PDA@TNN were biocompatible with macrophages and exhibited immunomodulatory ability to promote M2 macrophage polarization. In addition, AgNPs-PDA@TNN ameliorated the cytotoxicity caused by AgNPs, promoted cell spreading, and increased osteogenesis and matrix deposition of BMSCs. Furthermore, AgNPs-PDA@TNN exhibited bactericidal ability against E. coli and S. aureus by the bionic nanostructure and coated AgNPs. Various imaging analyses indicated the enhanced bactericidal ability and improved new bone formation by AgNPs-PDA@TNN in vivo. H&E, Gram, and Masson staining, verified the improved bone formation, less inflammation, infection, and fibrosis encapsulation. The immunofluorescence staining confirmed the immunomodulatory ability of AgNPs-PDA@TNN in vivo. Conclusion: The bionic insect wing AgNPs-PDA@TNN coating exhibited bactericidal property, immunomodulatory ability, and enhanced osteointegration. Thus, this multidimensional bionic implant surface holds promise as a novel strategy to prevent periprosthetic infection.

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来源期刊
Theranostics
Theranostics MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
25.40
自引率
1.60%
发文量
433
审稿时长
1 months
期刊介绍: Theranostics serves as a pivotal platform for the exchange of clinical and scientific insights within the diagnostic and therapeutic molecular and nanomedicine community, along with allied professions engaged in integrating molecular imaging and therapy. As a multidisciplinary journal, Theranostics showcases innovative research articles spanning fields such as in vitro diagnostics and prognostics, in vivo molecular imaging, molecular therapeutics, image-guided therapy, biosensor technology, nanobiosensors, bioelectronics, system biology, translational medicine, point-of-care applications, and personalized medicine. Encouraging a broad spectrum of biomedical research with potential theranostic applications, the journal rigorously peer-reviews primary research, alongside publishing reviews, news, and commentary that aim to bridge the gap between the laboratory, clinic, and biotechnology industries.
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