丝胶辅助绿色合成纳米金作为治疗细菌感染的广谱抗菌和生物膜破坏剂。

IF 6.6 2区 医学 Q1 NANOSCIENCE & NANOTECHNOLOGY
International Journal of Nanomedicine Pub Date : 2025-03-19 eCollection Date: 2025-01-01 DOI:10.2147/IJN.S494616
Rui Cai, Qian Cheng, Jiayu Zhao, Peirong Zhou, Zhaodan Wu, Xuemin Ma, Yajuan Hu, Huiyue Wang, Xiaorong Lan, Jing Zhou, Gang Tao
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引用次数: 0

摘要

背景:全球每年有数千万人死于伤口感染,近80%的组织感染与细菌生物膜有关。然而,过度使用抗生素会导致细菌耐药性。因此,开发简单有效的杀灭细菌和去除生物膜的策略至关重要。方法:以丝胶为还原剂和稳定剂合成丝胶金纳米粒子(Ser-Au NPs),并对其在不同pH和盐浓度条件下的胶体稳定性进行测试。随后,将Ser-Au NPs与2-巯基-1-甲基咪唑(MMI)结合,合成了功能金纳米复合材料(Ser-Au@MMI)。采用MIC法、抑菌活性法检测Ser-Au@MMI的抑菌效果,CCK-8法检测其体外细胞毒性。通过荧光显微镜和扫描电镜观察其体外抗生物膜作用。最后,在体内大鼠感染创面模型中测定Ser-Au@MMI的抗感染治疗效果。结果:丝胶作为合成Ser-Au NPs的还原剂和稳定剂,在不同的pH和盐浓度条件下均表现出优异的胶体稳定性。TEM, EDS和XPS分析证实了Ser-Au@MMI的成功合成。由于MMI和AuNP的协同作用,它表现出较高的抗菌活性,通过破坏细菌细胞壁和结构的完整性来达到杀菌效果。此外,Ser-Au@MMI10 (HAuCl4:MMI =1:10)浓度(64 μg/mL)能有效破坏铜绿假单胞菌、枯草芽孢杆菌、大肠杆菌和金黄色葡萄球菌等4种细菌形成的生物膜并杀死它们,但对小鼠成纤维细胞(L929)细胞无细胞毒性。感染创面模型显示Ser-Au@MMI10在体内加速感染创面愈合。结论:Ser-Au@MMI纳米复合材料制备工艺简单、环境友好,具有杀菌效果好、毒性低的优点,具有作为广谱抗菌剂和生物膜破坏剂在医疗保健领域的应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sericin-Assisted Green Synthesis of Gold Nanoparticles as Broad-Spectrum Antimicrobial and Biofilm-Disrupting Agents for Therapy of Bacterial Infection.

Background: Tens of millions of people die from wound infections globally each year, and nearly 80% of tissue infections are associated with bacterial biofilms. However, overuse of antibiotics can lead to bacterial resistance. Therefore, it is critical to develop simple and effective strategies to kill bacteria and remove biofilms.

Methods: The present study used sericin as a reducing and stabilizing agent to synthesize sericin-gold nanoparticles (Ser-Au NPs) and tested its colloidal stability under different pH and salt concentration conditions. Subsequently, functional gold nanocomposites (Ser-Au@MMI) were synthesized by combining Ser-Au NPs with 2-mercapto-1-methylimidazole (MMI). The antimicrobial effect of Ser-Au@MMI was checked by MIC, antimicrobial activity test, and in vitro cytotoxicity was assessed using CCK-8 assay. In vitro anti-biofilm effect was observed by fluorescence microscopy and SEM. Finally, the anti-infective therapeutic efficacy of Ser-Au@MMI was determined in an in vivo rat-infected wound model.

Results: Sericin as a reducing and stabilizing agent to synthesize Ser-Au NPs exhibited excellent colloidal stability under different pH and salt concentration conditions. The TEM, EDS, and XPS analyses confirmed the successful synthesis of Ser-Au@MMI. It exhibited higher antibacterial activity due to the synergistic effect of MMI and AuNP, which can achieve a bactericidal effect by destroying the integrity of bacterial cell walls and structure. In addition, Ser-Au@MMI10 (HAuCl4:MMI =1:10) concentration (64 μg/mL) could effectively disrupt biofilms formed by four species of bacteria and kill them, including P. aeruginosa, B. subtilis, E. coli, and S. aureus, but was not cytotoxic to mouse fibroblasts (L929) cells. Infected wound modeling showed that Ser-Au@MMI10 accelerated infected wound healing in vivo.

Conclusion: Ser-Au@MMI nanocomposites are prepared through a facile and environmentally friendly strategy and have the advantages of excellent bactericidal effect and low toxicity, which has the potential for application as a broad-spectrum antimicrobial agent and biofilm disrupting agent in healthcare.

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来源期刊
International Journal of Nanomedicine
International Journal of Nanomedicine NANOSCIENCE & NANOTECHNOLOGY-PHARMACOLOGY & PHARMACY
CiteScore
14.40
自引率
3.80%
发文量
511
审稿时长
1.4 months
期刊介绍: The International Journal of Nanomedicine is a globally recognized journal that focuses on the applications of nanotechnology in the biomedical field. It is a peer-reviewed and open-access publication that covers diverse aspects of this rapidly evolving research area. With its strong emphasis on the clinical potential of nanoparticles in disease diagnostics, prevention, and treatment, the journal aims to showcase cutting-edge research and development in the field. Starting from now, the International Journal of Nanomedicine will not accept meta-analyses for publication.
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